US20090321364A1 - Systems and methods for filtering nanowires - Google Patents

Systems and methods for filtering nanowires Download PDF

Info

Publication number
US20090321364A1
US20090321364A1 US12/105,525 US10552508A US2009321364A1 US 20090321364 A1 US20090321364 A1 US 20090321364A1 US 10552508 A US10552508 A US 10552508A US 2009321364 A1 US2009321364 A1 US 2009321364A1
Authority
US
United States
Prior art keywords
nanowire
solution
passage
filter
flow
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/105,525
Inventor
Michael A. Spaid
Manfred Heidecker
Pierre-Marc Allemand
Frank Wallace
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Cambrios Technologies Corp
Cambrios Film Solutions Corp
Original Assignee
Cambrios Technologies Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39620244&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=US20090321364(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Cambrios Technologies Corp filed Critical Cambrios Technologies Corp
Priority to US12/105,525 priority Critical patent/US20090321364A1/en
Assigned to CAMBRIOS TECHNOLOGIES CORPORATION reassignment CAMBRIOS TECHNOLOGIES CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SPAID, MICHAEL A., ALLEMAND, PIERRE-MARC, HEIDECKER, MANFRED, WALLACE, FRANK
Publication of US20090321364A1 publication Critical patent/US20090321364A1/en
Assigned to CAM HOLDING CORPORATION reassignment CAM HOLDING CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHAMP GREAT INTERNATIONAL CORPORATION
Abandoned legal-status Critical Current

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B5/00Non-insulated conductors or conductive bodies characterised by their form
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00Apparatus or processes for manufacturing printed circuits
    • H05K3/22Secondary treatment of printed circuits
    • H05K3/24Reinforcing the conductive pattern
    • H05K3/245Reinforcing conductive patterns made by printing techniques or by other techniques for applying conductive pastes, inks or powders; Reinforcing other conductive patterns by such techniques
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y10/00Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L29/00Semiconductor devices adapted for rectifying, amplifying, oscillating or switching, or capacitors or resistors with at least one potential-jump barrier or surface barrier, e.g. PN junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof  ; Multistep manufacturing processes therefor
    • H01L29/40Electrodes ; Multistep manufacturing processes therefor
    • H01L29/41Electrodes ; Multistep manufacturing processes therefor characterised by their shape, relative sizes or dispositions
    • H01L29/413Nanosized electrodes, e.g. nanowire electrodes comprising one or a plurality of nanowires
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L31/00Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
    • H01L31/18Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
    • H01L31/1884Manufacture of transparent electrodes, e.g. TCO, ITO
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00Apparatus or processes for manufacturing printed circuits
    • H05K3/22Secondary treatment of printed circuits
    • H05K3/24Reinforcing the conductive pattern
    • H05K3/245Reinforcing conductive patterns made by printing techniques or by other techniques for applying conductive pastes, inks or powders; Reinforcing other conductive patterns by such techniques
    • H05K3/247Finish coating of conductors by using conductive pastes, inks or powders
    • H05K3/249Finish coating of conductors by using conductive pastes, inks or powders comprising carbon particles as main constituent
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1343Electrodes
    • G02F1/13439Electrodes characterised by their electrical, optical, physical properties; materials therefor; method of making
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L29/00Semiconductor devices adapted for rectifying, amplifying, oscillating or switching, or capacitors or resistors with at least one potential-jump barrier or surface barrier, e.g. PN junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof  ; Multistep manufacturing processes therefor
    • H01L29/02Semiconductor bodies ; Multistep manufacturing processes therefor
    • H01L29/06Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions
    • H01L29/0657Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions characterised by the shape of the body
    • H01L29/0665Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions characterised by the shape of the body the shape of the body defining a nanostructure
    • H01L29/0669Nanowires or nanotubes
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K1/00Printed circuits
    • H05K1/02Details
    • H05K1/09Use of materials for the conductive, e.g. metallic pattern
    • H05K1/092Dispersed materials, e.g. conductive pastes or inks
    • H05K1/097Inks comprising nanoparticles and specially adapted for being sintered at low temperature
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K2201/00Indexing scheme relating to printed circuits covered by H05K1/00
    • H05K2201/01Dielectrics
    • H05K2201/0104Properties and characteristics in general
    • H05K2201/0108Transparent
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K2201/00Indexing scheme relating to printed circuits covered by H05K1/00
    • H05K2201/02Fillers; Particles; Fibers; Reinforcement materials
    • H05K2201/0203Fillers and particles
    • H05K2201/0242Shape of an individual particle
    • H05K2201/026Nanotubes or nanowires
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00Organic light-emitting devices
    • H10K50/80Constructional details
    • H10K50/805Electrodes
    • H10K50/81Anodes
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/20Carbon compounds, e.g. carbon nanotubes or fullerenes
    • H10K85/221Carbon nanotubes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy

Definitions

  • This description generally relates to the field of nanowire manufacturing, and more particularly to filtering solutions containing nanowires.
  • Conductive and non-conductive nanowires may be used in a variety of applications. These high aspect ratio nano-structures may be used to form transparent conductors, similar to those manufactured currently using indium tin oxide (ITO). They may prove useful in quantum computing, sensing applications, flexible electronics and integration with biotechnology. In addition, they may someday be used to create high speed, high density microprocessors.
  • ITO indium tin oxide
  • a method of filtering a solution containing nanowires and a first set of contaminant particles comprises: providing the solution; generating a flow of the solution; and filtering the solution by directing the flow through a passage defining an aperture having a width less than at least one dimension of the first set of contaminant particles.
  • a nanowire filtering system comprises: a source container for holding a solution containing nanowires and a first set of contaminant particles; and a nanowire filter passage communicatively coupled to the source container for receiving the solution, the nanowire filter passage defined at least in part by: a first plate; and a second plate disposed adjacent the first plate with a minimum separation distance between the first plate and the second plate of less than at least one dimension of the first set of contaminant particles.
  • a method of filtering a solution containing nanowires comprises: providing the solution; generating a primary flow of the solution; and filtering the solution by directing the primary flow over a micro-structured surface configured to filter the solution.
  • a nanowire filtering system comprises: a source container for holding a solution containing nanowires; and a nanowire filter communicatively coupled to the source container for receiving the solution, the nanowire filter including: a rotatable tube defining a passage for the solution; a micro-structured surface lining an inside of the rotatable tube; a substantially helical surface adjacent the micro-structured surface and extending at least partially into the passage; and a drive member adapted to turn the rotatable tube.
  • a nanowire filtering system comprises: a source container for holding a solution containing nanowires; and a nanowire filter communicatively coupled to the source container for receiving the solution, the nanowire filter including: an elongate channel defining a passage for the solution flowing along a long axis, the elongate channel having a lower surface including a plurality of parallel ridges disposed at an angle to the long axis; wherein the plurality of parallel ridges at least partially define a plurality of openings from the elongate channel.
  • a nanowire filtering system comprises: a source container for holding a solution containing nanowires; and a nanowire filter communicatively coupled to the source container for receiving the solution, the nanowire filter including: an elongate channel defining a passage for the solution; and a collection chamber defined in part by an outer surface of the elongate channel, the collection chamber communicatively coupled to the elongate channel via a plurality of openings having an average diameter of greater than 5 ⁇ m.
  • FIG. 1 is a schematic diagram of a nanowire filtering system, according to one illustrated embodiment.
  • FIG. 2 is a schematic diagram of another nanowire filtering system, according to another illustrated embodiment.
  • FIG. 3 is a perspective view of an example micro-structured nanowire filter, according to one illustrated embodiment.
  • FIG. 4 is a longitudinal cross-section of the nanowire filter of FIG. 3 .
  • FIG. 5 is radial cross-section of the nanowire filter of FIG. 3 .
  • FIG. 6 is a perspective view of another example micro-structured nanowire filter, according to one illustrated embodiment.
  • FIG. 7 is a bottom view of the nanowire filter of FIG. 6 .
  • FIG. 8 is a perspective view of another example micro-structured nanowire filter, according to one illustrated embodiment.
  • FIG. 9 is a front view of the nanowire filter of FIG. 8 .
  • FIG. 10 illustrates schematically nanowires and other nano-particles flowing in a solution over the nanowire filter of FIG. 8 .
  • FIG. 11 is a perspective view of another example micro-structured nanowire filter, according to one illustrated embodiment, with inner portions of the nanowire filter shown in dashed lines.
  • FIG. 12 is a radial cross-section of the nanowire filter of FIG. 11 .
  • FIG. 13 is a longitudinal cross-section of the nanowire filter of FIG. 11 .
  • FIG. 14 is a perspective view of another example micro-structured nanowire filter, according to one illustrated embodiment.
  • FIG. 15 is a top view of the nanowire filter of FIG. 14 .
  • FIG. 16 is an enlarged, schematic view of a bottom surface of the nanowire filter of FIG. 14 in operation.
  • FIG. 17 is a perspective view of an example nanowire filter having a narrow aperture, according to one illustrated embodiment.
  • FIG. 18 is a cross-section of the nanowire filter of FIG. 17 .
  • FIG. 19 illustrates schematically nanowires and other particles flowing in a solution through the nanowire filter of FIG. 17 .
  • FIG. 20 is a perspective view of an example micro-structured nanowire filter having a narrow aperture, according to one illustrated embodiment.
  • FIG. 21 is a bottom view of the nanowire filter of FIG. 20 .
  • FIG. 22 is a perspective view of another example nanowire filter having a narrow aperture, according to one illustrated embodiment.
  • FIG. 23 is a cross-sectional, schematic view of the nanowire filter of FIG. 22 in operation.
  • FIG. 24 is a top view of the nanowire filter of FIG. 22 .
  • FIG. 25 is a perspective view of another example nanowire filter having a narrow aperture, according to one illustrated embodiment.
  • FIG. 26 is a side view of the nanowire filter of FIG. 25 .
  • FIG. 27 is a perspective view of another example nanowire filter having a narrow aperture, according to one illustrated embodiment.
  • FIG. 28 is a side view of the nanowire filter of FIG. 27 .
  • FIG. 29 is a perspective view of another example nanowire filter having a plurality of narrow apertures, according to one illustrated embodiment.
  • FIG. 30 is a side view of the nanowire filter of FIG. 29 .
  • FIG. 31 is a flow diagram illustrating a method of filtering a solution containing nanowires using a micro-structured nanowire filter, according to one illustrated embodiment
  • FIG. 32 is a flow diagram illustrating another method of filtering a solution containing nanowires using a nanowire filter having a narrow aperture, according to another illustrated embodiment.
  • FIG. 1 illustrates an exemplary nanowire filtering system 10 .
  • the nanowire filtering system 10 comprises a source container 12 , a pump 14 and a nanowire filter 16 .
  • the components of the nanowire filtering system 10 function together to filter a solution containing nanowires, removing undesirable contaminant particles and/or solvent from the solution to achieve a more uniform solution of high aspect ratio nanowires.
  • the source container 12 may comprise any of a variety of containers for holding a solution containing nanowires.
  • the source container 12 may comprise a stainless steel or glass vessel, within which the nanowires were formed.
  • the source container 12 may simply comprise tubing through which the solution containing nanowires may travel.
  • the solution containing nanowires within the source container 12 may comprise any liquid carrying nanowires.
  • the solution containing the nanowires may come directly from a synthesis reaction prior to any formulation.
  • the solution containing nanowires may include, by weight, from 0.0025% to 0.1% surfactant (e.g., a preferred range is from 0.0025% to 0.05% of ZONYL® FSO-100), from 0.02% to 4% viscosity modifier (e.g., a preferred range is 0.02% to 0.5% of hydroxypropyl methyl cellulose (“HPMC”)), from 94.5% to 99.0% solvent and from 0.05% to 1.4% nanowires.
  • surfactant e.g., a preferred range is from 0.0025% to 0.05% of ZONYL® FSO-100
  • 0.02% to 4% viscosity modifier e.g., a preferred range is 0.02% to 0.5% of hydroxypropyl methyl cellulose (“HPMC”)
  • HPMC hydroxyprop
  • Suitable surfactants include ZONYL® FSN, ZONYL® FSO, ZONYL® FSH, TRITON® (x100, x114, x45), DYNOLTM (604, 607), n-Dodecyl b-D-maltoside and Novek.
  • suitable viscosity modifiers include HPMC, methyl cellulose, xanthan gum, polyvinyl alcohol, carboxy methyl cellulose, and hydroxy ethyl cellulose.
  • suitable solvents include water, alcohol (e.g., isopropanol), ketones, ether, or hydrocarbon or aromatic solvents (e.g., benzene, toluene or xylene).
  • the solvent may be volatile, having a boiling point of no more than 200° C., no more than 150° C., or no more than 100° C.
  • the amount of solvent can be adjusted to provide a desired viscosity and concentration of nanowires in the solution.
  • different pumps 14 and different nanowire filters 16 may function optimally on different concentration solutions.
  • the relative ratios of the other ingredients may remain the same.
  • the ratio of the surfactant to the viscosity modifier may be kept in the range of about 80 to about 0.01; the ratio of the viscosity modifier to the nanowires may remain in the range of about 5 to about 0.000625; and the ratio of the nanowires to the surfactant may be in the range of about 560 to about 5.
  • the viscosity range for the nanowire solution may be from 1 to 100 cP.
  • a number of contaminant particles and other structures may also be present in the solution, including low aspect ratio nano-particles (e.g., short rods, discs or spheres) made from the same material as the nanowires, as well as synthesis catalysts, reaction byproducts and unreacted precursors. For many applications, the presence of such contaminant particles may be undesirable.
  • low aspect ratio nano-particles e.g., short rods, discs or spheres
  • synthesis catalysts e.g., reaction byproducts and unreacted precursors.
  • nanowire refers generally to a nano-structure having a high aspect ratio (e.g., higher than 10).
  • non-metallic nanowires include, but are not limited to, carbon nanotubes (CNTs), metal oxide nanowires, conductive polymer fibers and the like.
  • Metallic nanowires may comprise elemental metals, metal alloys or metal compounds. Suitable metal nanowires can be based on any metal or combinations and/or alloys of metals, including without limitation, silver, gold, copper, nickel, gold-plated silver, gold-silver alloys, platinum, and palladium.
  • At least one cross-sectional dimension of a nanowire is less than 500 nm. In another embodiment, at least one cross-sectional dimension of a nanowire is less than 200 nm, and in yet another embodiment, at least one cross-sectional dimension is less than 100 nm.
  • the nanowire may have an aspect ratio (length:diameter) of greater than 10. In another embodiment, the aspect ratio may be greater than 50. In yet another embodiment, the aspect ratio may be greater than 100. Nanowires may have aspect ratios anywhere in the range of 10 to 100,000.
  • the nanowires can be prepared by any of a number of methods.
  • large-scale production of silver nanowires of uniform size may be carried out according to the methods described in, e.g., Xia, Y. et al., Chem. Mater . (2002), vol. 14, 4736-4745, and Xia, Y. et al., Nanoletters (2003) vol. 3(7), 955-960, the contents of which are hereby incorporated herein by reference in their entirety.
  • silver nanowires may be synthesized in a batch process by the reduction of silver nitrate in propylene glycol.
  • the chemistry of such a process is described in co-pending U.S. patent application Ser. No. 11/766,552, titled METHODS OF CONTROLLING NANOSTRUCTURE FORMATIONS AND SHAPES, filed Jun. 21, 2007, the contents of which are hereby incorporated herein by reference in their entirely.
  • Nanowire formation may be accomplished by the use of a surface active polymer (e.g., polyvinylpyrrolidone (“PVP”)) and chloride (e.g., added in the form of tetra-n-butylammonium chloride (“TBAC”)).
  • PVP polyvinylpyrrolidone
  • TBAC tetra-n-butylammonium chloride
  • the process may be carried out in an agitated, jacketed glass reactor including glass impellers, an automated temperature controller, a small glass feed vessel (which may also be agitated), and a precision metering pump.
  • Propylene glycol, PVP, and TBAC may first be added to the reactor and heated to a target temperature (e.g., 100° C.) under agitation. Meanwhile, a solution of silver nitrate and propylene glycol may be prepared in the small glass feed vessel. Once the silver nitrate is fully dissolved, and the reactor has stabilized at the target temperature, the silver n
  • the solution may then react under agitation at atmospheric pressure. As the reaction progresses, nano-particles may form first, followed by nanowires that grow to the desired length and width. Nano-particles may be indicated by an orange-brown or brown-green color, and, as nanowires form, the mixture may become increasingly grey and metallic in appearance.
  • the reaction may be quenched by the rapid addition of water, which both cools the reaction mixture and inhibits further reaction. Reaction temperature, reaction time, and silver nitrate addition rate may be varied to control the dimensions of the resulting nanowires.
  • the reactor may be cleaned using a clean-in-place system consisting of a spray ball and a persistaltic pump. Residue from previous reactions may have adverse effects on the synthesis process.
  • Propylene glycol was first added to a 30 L glass reactor. PVP and TBAC were also added to the glass reactor. The agitator for the glass reactor was turned to 100 rpm, and the solution in the glass reactor was heated to 100° C. While the solution was heating, propylene glycol and silver nitrate were premixed in a 4 L glass feed vessel until all of the solids were dissolved. Once the solution in the reactor reached a stable 100° C., the propylene glycol/silver nitrate solution were added to the reactor via a metering pump. 900 mL of propylene glycol and silver nitrate were added to the reactor at an addition rate of 45 mL/min for 20 minutes. Starting a timer at the start of the silver nitrate addition, the solution was mixed for 4 hours in the reactor before the heating was turned off and the reaction quenched with deionized water.
  • the average length of the resulting silver nanowires was 24 ⁇ m with a standard deviation of 15 ⁇ m.
  • the average width of the resulting silver nanowires was 65 nm with a standard deviation of 14 nm.
  • the estimated yield of silver converted into silver nanowires was 50 wt %.
  • nanowires may be prepared using biological templates (or biological scaffolds) that can be mineralized.
  • biological materials such as viruses and phages can function as templates to create metal nanowires.
  • the biological templates can be engineered to exhibit selective affinity for a particular type of material, such as a metal or a metal oxide. More detailed descriptions of biofabrication of nanowires can be found in, e.g., Mao, C. B. et al., “Virus-Based Toolkit for the Directed Synthesis of Magnetic and Semiconducting Nanowires,” (2004) Science, 303, 213-217; Mao, C. B. et al., “Viral Assembly of Oriented Quantum Dot Nanowires,” (2003) PNAS , vol. 100, no. 12, 6946-6951; U.S. patent application Ser. No. 10/976,179 and U.S. provisional patent application Ser. No. 60/680,491, all of which are hereby incorporated herein by reference in their entireties.
  • the resulting solution may be a polydisperse solution containing a mixture of contaminant particles and nanowires of various shapes and sizes.
  • purification may be desirable in order to achieve a more uniform solution of high aspect ratio nanowires.
  • solubilized ion contaminants e.g., Cl ⁇ , Ag+, NO 3 ⁇
  • exchange of the solvent may be desirable based on the particular application for the nanowire solution.
  • the source container 12 may serve as the reactor within which the nanowires are formed.
  • a solution containing nanowires may be generated in another container/reactor and be subsequently transferred to the source container 12 .
  • the solution containing nanowires need not comprise the solution within which the nanowires were originally formed.
  • the nanowire filtering system 10 may be used to filter any solution containing nanowires.
  • the nanowire filtering system 10 may include a pump 14 to generate a flow of the solution containing nanowires from the source container 12 to the nanowire filter 16 .
  • the pump 14 may comprise any of a variety of liquid pumps.
  • the pump 14 may comprise a bellows pump, a centrifugal pump, a diaphragm pump, a drum pump, a flexible liner/impeller pump, a gear pump, a peristaltic pump, a piston pump, a progressing cavity pump, a rotary lobe pump, a rotary vane pump, etc.
  • the nanowire filtering system 10 may not include a pump.
  • a flow of the solution containing nanowires may be generated by gravity.
  • the pump 14 may be incorporated into the nanowire filter 16 .
  • the nanowire filter 16 may comprise any of a variety of filters configured to separate nanowires from contaminant particles and other nano-structures.
  • the nanowire filter 16 may be further configured to separate the nanowires from a solvent in order to facilitate a solvent exchange.
  • the nanowire filter 16 may be configured to yield a retentate 18 , which comprises a more uniform solution containing nanowires, and a filtrate (not shown), which may comprise solvent and/or the contaminant particles filtered from the solution.
  • the retentate 18 may have a higher weight percentage of nanowires than the flow of solution 20 entering the nanowire filter 16 . As discussed below with reference to FIGS.
  • the nanowire filter 16 may include a plurality of micro-structures and/or may include one or more narrow apertures configured to filter the solution.
  • the nanowire filter 16 may also, in some embodiments, comprise a plurality of nanowire filters arranged in parallel or in series to filter the solution containing nanowires.
  • the nanowire filter 16 may filter out nanowires having aspect ratios below a certain threshold.
  • the nanowire filter 16 may generally filter out nanowires having aspect ratios lower than 100.
  • the aspect ratio targeted by a particular nanowire filter 16 may be selected based upon an application for the solution.
  • the retentate 18 may be collected in a container (not shown) for subsequent processing or use.
  • the retentate 18 may be added to a solvent useful in coating formulations.
  • a nanowire filtering system 22 may recirculate the retentate 18 from the nanowire filter 16 back to the source container 12 for further filtering. In such an embodiment, the filtering and subsequent recirculating of the solution containing nanowires may continue for a predetermined time period, or until the solution containing nanowires has reached a desired purity.
  • solvent may also be added to the nanowire filtering system 22 (e.g., at the source container 12 ) as the retentate 18 is recirculated.
  • the filtering, recirculating, and addition of a new solvent may continue until the solution containing nanowires achieves a predetermined concentration of the new solvent.
  • FIG. 3 is a perspective view of a micro-structured nanowire filter 300 , which may be used in the nanowire filtering system 10 or the nanowire filtering system 22 .
  • FIGS. 4 and 5 present longitudinal and radial cross-sections, respectively, of the nanowire filter 300 to facilitate an understanding of its inner structure.
  • the nanowire filter 300 comprises an elongate channel 302 having an entrance 308 and an exit 310 and defining a passage for a primary flow (designated by the arrow 301 ) of the solution containing nanowires.
  • the elongate channel 302 may include a micro-structured surface between the entrance 308 and exit 310 having a plurality of openings 306 defined therethrough.
  • the elongate channel 302 is surrounded by a plurality of collection chambers 304 communicatively coupled to the elongate channel 302 by the plurality of openings 306 .
  • the nanowire filter 300 may, of course, be formed from a variety of different materials, including metallic and non-metallic materials, and may be coupled to the rest of the nanowire filtering system 10 by any of a variety of fluid connectors, tubes and/or conduits.
  • micro-structures configured to filter the solution.
  • the terms micro-structures and micro-structured may reference any small structures formed in, on or through a surface that may interfere with a fluid flow.
  • micro-structures may refer to structures having at least one dimension less than 1 cm.
  • the micro-structures comprise the plurality of openings 306 .
  • micro-structures may comprise a plurality of niches, valleys, detents, peaks, protrusions, etc.
  • Other examples of micro-structures and micro-structured surfaces are presented with reference to FIGS. 6-16 .
  • the size, arrangement and configuration of the openings 306 may be varied to filter different contaminant particles.
  • the size of the openings 306 may be chosen based at least in part on the desired length/diameter/aspect ratio of the nanowires, the size/aspect ratio of the contaminant particles that should be filtered from the solution as well as a viscosity and flow rate of the solvent.
  • the openings 306 may have an average diameter greater than 5 ⁇ m because the expected filtrate may have a diameter up to approximately 5 ⁇ m. In another embodiment, the openings 306 may have an average diameter greater than 10 ⁇ m.
  • the nanowire filter 300 may filter out more contaminant particles and solvent on each pass. However, with larger openings 306 , the nanowire filter 300 may also become less selective, and more nanowires may be lost in the filtrate.
  • the elongate channel 302 may be approximately 3 cm in diameter, and approximately 50 cm long. In other embodiments, the length and diameter of the elongate channel 302 may be varied. As the elongate channel 302 is lengthened or its diameter made smaller, a greater amount of filtrate may be separated from the primary flow of solution as the solution passes through the nanowire filter 300 . However, a greater quantity of nanowires may also be lost in the filtrate. The length, diameter and geometry of the elongate channel 302 may therefore be varied to achieve desired characteristics for the nanowire filter 300 .
  • the elongate channel 302 may comprise a cylindrical passage, and the openings 306 may extend along the entire surface of this cylindrical passage.
  • the elongate channel 302 may have a variety of shapes, and the openings 306 may be formed on only a portion of the channel's surface.
  • the openings 306 may be formed only along a bottom half of the surface of the elongate channel 302 , as the filtrate may preferentially flow through these openings 306 by gravity.
  • the openings 306 may be formed along only a portion of the entire length of the elongate channel 302 .
  • eight collection chambers 304 are defined at least in part by an outer surface of the elongate channel 302 .
  • the eight collection chambers 304 may be separated by radially extending fins extending from the outer surface of the elongate channel 302 to an outer wall 312 of the nanowire filter 300 .
  • the collection chambers 304 may be configured differently.
  • more or fewer collection chambers 304 may be formed around the elongate channel 302 , and they may have different geometries.
  • the collection chambers 304 need not be integrally formed with the elongate channel 302 .
  • the elongate channel 302 may be suspended over one or more collection chambers, and, in operation, the filtrate emerging from the openings 306 of the elongate channel 302 may fall into the collection chambers.
  • a primary flow 301 of the solution may pass through the entrance 308 , through the elongate channel 302 and emerge from the exit 310 as retentate 18 .
  • the plurality of openings 306 may create a secondary flow of at least a portion of the solution, i.e., the filtrate, through the plurality of openings 306 and into the collection chambers 304 .
  • the collection chambers 304 may transfer the secondary flow to a filtrate container (not shown).
  • the nanowires may be equal to or smaller than the diameter of the filtered contaminant particles, the nanowires (due to their high aspect ratio) may substantially align with the primary flow 301 passing through the elongate channel 302 , and this alignment may inhibit or effectively prevent the nanowires from passing through the plurality of openings 306 .
  • the primary flow 301 of the solution through the elongate channel 302 may be greater than the secondary flow through the plurality of openings 306 into the collection chambers 304 to take advantage of this alignment.
  • the primary flow 301 may be at least 100 times greater than the secondary flow of the solution. This relatively high flow rate through the elongate channel 302 may help to align the nanowires with the primary flow 301 and prevent the nanowires from inadvertently passing through the plurality of openings 306 .
  • the primary flow rate may be correspondingly increased to help prevent nanowires from slipping through the enlarged openings 306 .
  • the size of the openings 306 and the primary flow rate through the elongate channel 302 may be varied in different embodiments of the nanowire filter 300 in order to change its filtering characteristics.
  • FIG. 6 is a perspective view of another micro-structured nanowire filter 600 that operates similarly to the nanowire filter 300 of FIGS. 3-5 .
  • FIG. 7 is a bottom view of the nanowire filter 600 .
  • the nanowire filter 600 comprises an elongate channel 606 having an entrance 608 and an exit 610 and defining a passage for a primary flow (designated by the arrow 601 ) of the solution containing nanowires.
  • the elongate channel 606 may, in turn, be defined at least in part by a micro-structured surface 602 comprising a plurality of openings 604 .
  • the openings 604 may have an average diameter of approximately 5 ⁇ m, and the elongate channel 606 may be approximately 50 cm in length.
  • the size and shape of the openings 604 , the size and shape of the elongate channel 606 , and the primary flow rate of the solution may be varied to achieve desired filtering characteristics.
  • an average height of the solution passing over the micro-structured surface 602 may also be varied to achieve the desired filtering characteristics.
  • a primary flow 601 of the solution may pass through the entrance 608 , through the elongate chamber 606 and emerge from the exit 610 as retentate 18 .
  • the plurality of openings 604 may create a secondary flow of filtrate out from the elongate chamber 606 .
  • the nanowires in the solution may substantially align with the primary flow 601 passing through the elongate chamber 606 , and this alignment may inhibit or effectively prevent the nanowires from passing through the plurality of openings 604 .
  • a trough or another type of collection chamber may be disposed beneath the micro-structured surface 602 to collect the filtrate.
  • the elongate chamber 606 may be coupled to at least one collection chamber in an arrangement similar to that of the nanowire filter 300 .
  • FIG. 8 is a perspective view
  • FIG. 9 is a front view of another example micro-structured nanowire filter 800 .
  • the nanowire filter 800 comprises a frame 802 defining a generally V-shaped trough between an entrance 804 and an exit 806 that may direct a primary flow (designated by the arrow 801 ) of the solution containing nanowires over a micro-structured surface 808 supported by the frame 802 .
  • the micro-structured surface 808 may, in one embodiment, comprise a plurality of surface protrusions and pores.
  • the frame 802 may comprise a metallic plate bent into the desired V-shape. In other embodiments, the frame 802 may comprise other materials, such as plastics.
  • the frame 802 may also have other shapes for directing the primary flow 801 of the solution. For example, the frame 802 may define a cylindrical or a U shape.
  • the micro-structured surface 808 may be defined by filter paper.
  • the filter paper may be any type of filter paper configured to filter the solution containing nanowires.
  • the filter paper may have a porosity of greater than 5 ⁇ m because the expected filtrate may have a diameter up to approximately 5 ⁇ m.
  • the filter paper may have a porosity of greater than 10 ⁇ m.
  • the porosity of the filter paper may be varied, as described above to achieve particular filtering characteristics.
  • the micro-structured surface 808 may be defined by a more permanent filtering substrate.
  • an inner surface of the frame 802 itself may have small protrusions defined thereon.
  • a primary flow 801 of the solution may pass through the entrance 804 , over the micro-structured surface 808 and emerge from the exit 806 as retentate 18 .
  • More compact contaminant particles which may tend to have lower drag in a flowing solution, may be pulled by gravity towards the micro-structured surface 808 , where they may be trapped by the micro-structures.
  • more massive contaminant particles may sediment more quickly out of the solution, while smaller contaminant particles may sediment more slowly.
  • the dimensions and arrangement of the nanowire filter 800 may be configured to filter different sizes of the contaminant particles as desired. Meanwhile, the nanowires in the solution may substantially align with the primary flow 801 , and this alignment may inhibit or effectively prevent the nanowires from being trapped by the micro-structured surface 808 .
  • a flow rate of the primary flow 801 of the solution may be monitored and controlled to ensure that the nanowire filter 800 is, indeed, preferentially filtering out the more compact, low aspect ratio particles. If the flow rate is too high, even the low aspect ratio contaminant particles may emerge as retentate 18 . However, if the flow rate is too low, high aspect ratio nanowires may settle out of the solution onto the bottom of the nanowire filter 800 .
  • FIG. 10 A schematic view of the microscopic filtering process is illustrated in FIG. 10 .
  • the nanowires 1002 may be generally aligned with the primary flow 801 of the solution while low aspect ratio contaminant particles 1006 are trapped by the micro-structures 1008 .
  • the nanowire filter 800 may trap filtrate within the micro-structures 1008 .
  • the primary flow 801 of the solution may be stopped, and a separate cleaning solution passed over the micro-structured surface 808 to eliminate the filtrate.
  • the micro-structured surface 808 may be occasionally replaced. For example, new filter paper may replace the old filter paper. Other methods of cleaning the micro-structured surface 808 may be used in other embodiments.
  • the micro-structured surface 808 may be cleaned periodically, according to some time interval, or may be cleaned after a certain amount of solution has been filtered. In another embodiment, the micro-structured surface 808 may be cleaned when the performance of the nanowire filter 800 has degraded by a certain amount.
  • FIG. 11 is a perspective view of another example micro-structured nanowire filter 1100 , with interior portions of the nanowire filter 1100 illustrated in dashed lines.
  • FIGS. 12 and 13 present radial and longitudinal cross-sections, respectively, of the nanowire filter 1100 to facilitate a greater understanding of its inner structure.
  • the nanowire filter 1100 comprises a rotatable tube 1102 having an entrance 1110 and an exit 1112 and defining a passage for a primary flow (designated by the arrow 1101 ) of the solution containing nanowires.
  • a micro-structured surface 1108 lines an inside of the rotatable tube 1102 .
  • the rotatable tube 1102 may also have disposed therein a substantially helical element 1104 and may be coupled to a drive member 1106 for rotating the rotatable tube 1102 about a longitudinal axis.
  • the rotatable tube 1102 may be formed from any metallic or non-metallic materials.
  • the size and shape of the rotatable tube 1102 may also be varied to achieve desired filtering characteristics.
  • the micro-structured surface 1108 lining the rotatable tube 1102 may comprise filter paper.
  • the filter paper may be any type of filter paper configured to filter the solution.
  • the filter paper may have a porosity of greater than 5 ⁇ m because the expected filtrate may have a diameter up to approximately 5 ⁇ m.
  • the filter paper may have a porosity of greater than 10 ⁇ m.
  • the porosity of the filter paper may be varied, as described above.
  • the micro-structured surface 1108 may be defined by an inner surface of the rotatable tube 1102 itself.
  • the rotatable tube 1102 may include a plurality of openings (not shown) that comprise the micro-structures.
  • the substantially helical element 1104 may be arranged adjacent the micro-structured surface 1108 and may comprise a strip of fluid impermeable material wound around an interior of the rotatable tube 1102 .
  • the substantially helical element 1104 may be formed integrally with or may be separate from the rotatable tube 1102 .
  • the substantially helical element 1104 is illustrated as extending only a short way into the passage defined by the rotatable tube 1102 . However, in other embodiments, the substantially helical element 1104 may extend much further.
  • the substantially helical element 1104 may have a height approximately equal to a radius of the rotatable tube 1102 .
  • the drive member 1106 may comprise any appropriate combination of a motor and fittings adapted to turn the rotatable tube 1102 .
  • the drive member 1106 may be configured to turn the rotatable tube 1102 at a variable angular velocity.
  • the drive member 1106 may turn the rotatable tube 1102 in a counter-clockwise direction (from the vantage point of FIG. 12 ).
  • the primary flow 1101 of the solution may be maintained at a level lower than a height of the substantially helical element 1104 , such that the solution cannot pass over the barrier represented by the substantially helical element 1104 .
  • the solution may be driven through the rotatable tube 1102 by the substantially helical element 1104 , and thus, a flow rate of the solution may be controlled by the drive member 1106 .
  • low aspect ratio contaminant particles which may tend to have lower drag in a flowing solution, may be pulled by gravity towards the micro-structured surface 1108 , where they may be trapped by micro-structures. Meanwhile, nanowires in the solution may substantially align with the primary flow 1101 , and this alignment may inhibit or effectively prevent the nanowires from being trapped by the micro-structured surface 1108 .
  • micro-structured surface 1108 It may be desirable to occasionally clean the micro-structured surface 1108 to maintain the filtering efficiency of the nanowire filter 1100 .
  • the primary flow of the solution may be stopped, and a separate cleaning solution passed over the micro-structured surface 1108 to eliminate the filtrate.
  • the micro-structured surface 1108 may be occasionally replaced. For example, new filter paper may replace the old filter paper. Other methods of cleaning the micro-structured surface 1108 may be used in other embodiments.
  • the micro-structured surface 1108 may be cleaned periodically, according to some time interval, or after a certain amount of solution has been filtered. In another embodiment, the micro-structured surface 1108 may be cleaned when the performance of the nanowire filter 1100 has degraded by a certain amount.
  • FIG. 14 is a perspective view
  • FIG. 15 is a top view of another micro-structured nanowire filter 1400 .
  • the nanowire filter 1400 may include an elongate channel 1402 having an entrance 1410 and an exit 1412 and defining a passage for a primary flow (designated by the arrow 1401 ) of the solution containing nanowires along a long axis 1404 .
  • the elongate channel 1402 may further include a micro-structured, bottom surface 1406 having a plurality of parallel ridges oriented at an angle to the long axis 1404 .
  • the elongate channel 1402 may be integral with or may be formed separately from the micro-structured surface 1406 .
  • walls 1414 , 1416 of the elongate channel 1402 as well as the micro-structured surface 1406 may be formed from any of a variety of metallic or non-metallic materials.
  • the elongate channel 1402 may have any of a number of other shapes and configurations.
  • the elongate channel 1402 may be fully enclosed, forming a generally rectangular cross-sectional shape.
  • the micro-structures of the bottom surface 1406 may comprise a plurality of parallel ridges (and corresponding valleys) that form a non-right angle with the long axis 1404 .
  • the ridges may at least partially define a plurality of fluid passages ending at a plurality of secondary openings 1408 from the elongate channel 1402 .
  • the plurality of secondary openings 1408 may, in one embodiment, allow filtrate to exit the elongate channel 1402 .
  • the ridges may be configured differently. For example, they need not be parallel, and, in one embodiment, the ridges may be oriented at a right angle to the long axis 1404 .
  • the parallel ridges may also be separated by a distance greater than 5 ⁇ m because the expected filtrate may have a diameter up to approximately 5 ⁇ m. In another embodiment, the parallel ridges may be separated by a distance greater than 10 ⁇ m.
  • a cross-section of the valleys formed by the ridges may be approximately square, such that the valleys are deeper than 5 ⁇ m or 10 ⁇ m in respective embodiments.
  • the size and shape of the ridges, the size and shape of the elongate channel 1402 , and the primary flow rate of the solution may be varied to achieve desired filtering characteristics.
  • FIG. 16 an enlarged, schematic view of the micro-structured surface 1406 of the nanowire filter 1400 is illustrated in operation.
  • a primary flow 1401 of the solution may flow across the micro-structured surface 1406 , and thereby across the plurality of parallel ridges.
  • the parallel ridges may then create a plurality of secondary flows 1604 , as filtrate from the solution is diverted by the parallel ridges through the secondary openings 1408 .
  • These secondary flows 1604 containing filtrate may or may not be collected in collection chambers (not shown). Since the filtrate may thus be diverted away from the nanowire filter 1400 , the nanowire filter 1400 may remain relatively clear of the filtrate. Thus, there may be a reduced need to clean the nanowire filter 1400 .
  • the plurality of parallel ridges may filter low aspect ratio contaminant particles from the nanowires due to the different drag characteristics of these particles in a fluid flow.
  • FIG. 17 is a perspective view
  • FIG. 18 is a cross-section of a nanowire filter 1700 having a narrow aperture 1708 , which filter may be used in the nanowire filtering system 10 or the nanowire filtering system 22 .
  • the nanowire filter 1700 may comprise a first plate 1702 and a second plate 1704 disposed adjacent the first plate 1702 .
  • the first and second plates 1702 , 1704 may at least partially define a passage 1706 extending through the filter, the passage 1706 having an entrance 1710 and an exit 1712 .
  • the passage 1706 defines an aperture 1708 having a width W less than at least one dimension of a set of contaminant particles.
  • the nanowire filter 1700 may be formed from a variety of different materials.
  • the nanowire filter 1700 may comprise a molded plastic.
  • the nanowire filter 1700 may be formed from stainless steel.
  • the nanowire filter 1700 may comprise stainless steel first and second plates 1702 , 1704 separated by relatively hard micro- or nano-particles (e.g., silica). In one embodiment, a plurality of such plates may be stacked one upon the other in order to achieve a high flow rate through the nanowire filter 1700 .
  • the first plate 1702 and the second plate 1704 are substantially parallel and define a separation distance between them of less than at least one dimension of a set of contaminant particles. Since the separation distance between the two plates 1702 , 1704 is substantially invariant, the aperture 1708 may coincide with the entrance 1710 to the nanowire filter 1700 .
  • the aperture 1708 may have a width W selected to filter out the set of contaminant particles having at least one dimension greater than the width.
  • the aperture 1708 may have a width W less than 2 ⁇ m, in order to filter out particles having a diameter greater than 2 ⁇ m.
  • the aperture 1708 may have a width W less than 1 ⁇ m, or less than 0.5 ⁇ m, in order to filter out contaminant particles having greater dimensions.
  • the width W of the aperture 1708 may be varied in different embodiments to filter out different sets of contaminant particles, while allowing nanowires to pass through the filter 1700 unimpeded.
  • the length L of the aperture 1708 may also be varied to pass more or less solution. In one embodiment, a very long aperture 1708 may be used to enable a greater flow of solution through the passage 1706 of the nanowire filter 1700 .
  • nanowires in the solution may substantially align with the flow through the passage 1706 of the nanowire filter 1700 .
  • the nanowires may present a relatively small cross-section.
  • the nanowires may have an average diameter ranging from 20 to 200 nm.
  • the nanowires may be as long as, or longer than, the width W, the narrow cross-section of the nanowires may enable the nanowires to align with the flow and pass through the nanowire filter 1700 .
  • FIG. 19 A schematic view of the nanowire filter 1700 in operation is illustrated in FIG. 19 .
  • the first plate 1702 is illustrated transparently, in order to schematically show the nanowires 1902 in the solution aligned with a flow 1906 through the nanowire filter 1700 .
  • low aspect ratio contaminant particles 1904 (which may, for example, have a diameter approximately equal to a length of the nanowires) may be “captured” at the aperture 1708 , unable to pass through the nanowire filter 1700 with the rest of the retentate 18 .
  • the nanowire filter 1700 is illustrated as comprising two substantially parallel plates forming an aperture 1708 sized to prevent large diameter contaminant particles from passing therethrough, other configurations are, of course, possible.
  • the nanowire filter 1700 may include any other aperture shape (e.g., circular, elliptical, triangular) having at least one width less than at least one dimension of a set of contaminant particles.
  • the nanowire filter 1700 may comprise a plurality of cylindrical passages, each of the passages having a diameter less than the at least one dimension of the set of contaminant particles.
  • the nanowire filter 1700 may build up filtrate at the aperture 1708 , which may eventually become clogged by these large contaminant particles. As a result, it may be desirable to “de-clog” the filter 1700 by occasionally removing these particles from the aperture 1708 in order to maintain the filtering efficiency of the nanowire filter 1700 .
  • the primary flow of the solution (designated by the arrow 1906 ) may be occasionally stopped and the nanowire filter 1700 removed for cleaning.
  • the primary flow 1906 of the solution may be stopped, and a reverse flow (not shown) of a liquid generated through the passage 1706 in order to dislodge the larger particles from the aperture 1708 .
  • a reverse flow of the solution itself may be periodically generated through the passage 1706 in order to dislodge the larger particles from the aperture 1708 .
  • This reverse flow may also be coupled with an external cleaning, ultrasonic energy, or another mechanism to ensure that the filtered contaminant particles are well-separated from the aperture 1708 and do not immediately re-clog the nanowire filter 1700 .
  • the solution may flow through the nanowire filter 1700 in both directions, a net flow may be directed from the entrance 1710 to the exit 1712 of the nanowire filter 1700 .
  • the nanowire filter 1700 may be de-clogged periodically, according to some time interval. In another embodiment, the nanowire filter 1700 may be de-clogged after a certain amount of solution has been filtered. In yet another embodiment, the nanowire filter 1700 may be de-clogged when the performance of the nanowire filter 1700 (as measured, for example, by a flow rate of the primary flow 1906 through the nanowire filter 1700 ) has degraded by a certain amount.
  • FIG. 20 is a perspective view
  • FIG. 21 is a bottom view of another nanowire filter 2000 having a narrow aperture 2008 defined at least in part by a top plate 2002 and a bottom plate 2004 .
  • the nanowire filter 2000 may be configured similarly to the nanowire filter 1700 , except that the bottom plate 2004 may further include a plurality of openings 2010 .
  • the plurality of openings 2010 may be considered micro-structures. In other embodiments, different micro-structures may be used in conjunction with a narrow aperture to form other nanowire filters.
  • the nanowire filter 2000 may filter out larger contaminant particles at the aperture 2008 and may filter out smaller contaminant particles via the openings 2010 in the bottom plate 2004 .
  • the nanowire filter 2000 may effectively combine the filtering capabilities of the nanowire filter 1700 with the filtering capabilities of, for example, the nanowire filter 600 .
  • the flow rate, solution composition and dimensions of the components of the nanowire filter 2000 may be varied to optimize one or both of these filtering capabilities.
  • FIG. 22 is a perspective view of another nanowire filter 2200 having a narrow aperture 2208 .
  • FIGS. 23 and 24 illustrate a cross-sectional view and a top view of the nanowire filter 2200 , respectively.
  • the nanowire filter 2200 may comprise a top plate 2202 and a bottom plate 2204 disposed adjacent the top plate 2202 .
  • the top plate 2202 and the bottom plate 2204 may at least partially define a passage 2216 extending through the nanowire filter 2200 .
  • the passage 2216 defines at least one aperture 2208 having a width less than at least one dimension of a set of contaminant particles.
  • the top plate 2202 may further include an entrance 2212 therethrough.
  • the entrance 2212 may define an opening through which a primary flow (designated by the arrows 2201 ) of the solution may be directed.
  • a conduit 2214 for the solution may be coupled to the entrance 2212 in order to guide a primary flow 2201 of the solution from the source container 12 into the nanowire filter 2200 .
  • the nanowire filter 2200 may be formed from a variety of different materials.
  • the nanowire filter 2200 may comprise a molded plastic.
  • the nanowire filter 2200 may be formed from stainless steel.
  • the top plate 2202 and the bottom plate 2204 are substantially parallel and define a separation distance between them of less than at least one dimension of a set of contaminant particles.
  • the aperture 2208 having a width W may coincide with the entrance 2212 of the nanowire filter 2200 and may have a generally cylindrical shape, as illustrated by the dashed lines of FIG. 23 .
  • the size and configuration of the aperture 2208 and the position of the plates 2202 , 2204 may be varied to filter out particular contaminant particles from the solution.
  • the solution containing nanowires may flow outwards from the entrance 2212 between the two plates 2202 , 2204 .
  • nanowires in the solution may align with the primary flow 2201 through the nanowire filter 2200 , while large, low aspect ratio, contaminant particles may be prevented from passing radially outwards between the top and bottom plates 2202 , 2204 .
  • the nanowire filter 2200 may build up filtrate at the aperture 2208 .
  • the nanowire filter 2200 may be occasionally de-clogged to maintain its filtering efficiency.
  • FIG. 25 is a perspective view
  • FIG. 26 is a side view of another nanowire filter 2500 having a narrow aperture 2508 .
  • the nanowire filter 2500 may comprise a first plate 2502 and a second plate 2504 disposed adjacent the first plate 2502 .
  • the first and second plates 2502 , 2504 may converge, such that a passage 2506 extending through the nanowire filter 2500 may narrow between an entrance 2510 and an exit 2512 .
  • the aperture 2508 may be defined at the exit 2512 and may have a width less than at least one dimension of a set of contaminant particles.
  • the nanowire filter 2500 may be configured and may function similarly to the nanowire filter 1700 .
  • the size and configuration of the components of the nanowire filter 2500 may be varied depending on the desired filtering characteristics.
  • each particle may be captured at that portion of the passage 2506 having a width approximately equal to that particle's diameter.
  • the entrance 2510 of the nanowire filter 2500 has a width of 10 ⁇ m and the exit 2512 has a width of 1 ⁇ m, then 5 ⁇ m particles may be captured somewhere near the middle of the passage 2506 , and 1.1 ⁇ m particles may be captured very close to the exit 2512 .
  • the nanowire filter 2500 may filter out contaminant particles along its entire length. Thus, it may take longer for the nanowire filter 2500 to become clogged.
  • FIG. 27 is a perspective view
  • FIG. 28 is a side view of another nanowire filter 2700 having a narrow aperture 2708 .
  • the nanowire filter 2700 may comprise a first plate 2702 , a second plate 2704 disposed adjacent the first plate 2702 , and a passage 2706 defined between the two plates 2702 , 2704 .
  • the passage 2706 may define at least one aperture 2708 approximately halfway through having a width less than at least one dimension of a set of contaminant particles.
  • the nanowire filter 2700 may have an aperture 2708 arranged substantially anywhere along the passage 2706 defined between the two plates 2702 , 2704 , and the plates 2702 , 2704 may have a variety of different shapes and configurations.
  • the nanowire filter 2700 may function generally similarly to the nanowire filter 2500 described above.
  • FIG. 29 is a perspective view
  • FIG. 30 is a side view of another nanowire filter 2900 having a plurality of narrow apertures 2908 , 2928 and 2938 .
  • the nanowire filter 2900 may comprise a first plate 2902 and a second plate 2904 disposed adjacent the first plate 2902 .
  • the two plates 2902 , 2904 may at least partially define a passage having an entrance 2910 and an exit 2912 , and may at least partially define an aperture 2908 having a width less than at least one dimension of a first set of contaminant particles (e.g., 2 ⁇ m).
  • the nanowire filter 2900 may further comprise a third plate 2922 and a fourth plate 2924 disposed adjacent the third plate 2922 .
  • the two plates 2922 , 2924 may at least partially define a second passage having a second entrance 2926 and a second exit 2927 , and may at least partially define a second aperture 2928 having a width less than at least one dimension of a second set of contaminant particles (e.g., 1 ⁇ m).
  • the second set of contaminant particles may have at least one dimension smaller than the at least one dimension of the first set of contaminant particles.
  • the nanowire filter 2900 may comprise a fifth plate 2932 and a sixth plate 2934 disposed adjacent the fifth plate 2932 .
  • the two plates 2932 , 2934 may at least partially define a third passage having a third entrance 2936 and a third exit 2937 , and may at least partially define a third aperture 2938 having a width less than at least one dimension of a third set of contaminant particles (e.g., 0.5 ⁇ m).
  • the third set of contaminant particles may have at least one dimension smaller than the at least one dimension of the second set of contaminant particles.
  • more or fewer apertures of various sizes may be used to filter out particular sets of contaminant particles.
  • the nanowire filter 2900 may function generally similarly to the nanowire filter 2500 described above.
  • the nanowire filter 2900 may filter out contaminant particles having diameters larger than 2 ⁇ m at the first aperture 2908 , other contaminant particles having diameters between 1 and 2 ⁇ m at the second aperture 2928 and still more contaminant particles having diameters between 0.5 and 1 ⁇ m at the third aperture 2938 .
  • FIG. 31 illustrates a flow diagram for a method 3100 of filtering a solution containing nanowires using a micro-structured nanowire filter, according to one embodiment.
  • This method 3100 will be discussed primarily in the context of the nanowire filter 300 incorporated into the nanowire filtering system 10 . However, it may be understood that the acts disclosed herein may also be executed using a variety of other micro-structured nanowire filters (e.g., nanowire filters 600 , 800 , 1100 , 1400 , and 2000 ), in accordance with the described method.
  • the method begins at 3102 , when a solution containing nanowires is provided.
  • the solution containing nanowires may comprise the solution within which the nanowires were formed.
  • the solution within which the nanowires were formed may have already undergone a variety of processing and/or filtering acts.
  • the solution containing nanowires may comprise a polydisperse solution including a variety of particles and nano-structures in addition to the desired nanowires.
  • a variety of different solutions may be filtered in different embodiments, including different percentages of nanowires, different solvents and additives, different shapes and types of low aspect ratio particles, etc.
  • the nanowire filtering system 10 and, in particular, the nanowire filter 300 may be configured differently.
  • a primary flow of the solution is generated.
  • the primary flow of the solution may be generated by any of a variety of mechanisms.
  • a pump 14 as illustrated in FIG. 1 , may be used to generate the primary flow of the solution.
  • the primary flow of the solution may be generated by gravity from the source container 12 .
  • a pressure differential e.g., a source pressurized tank
  • a flow rate of this primary flow may also be varied in different embodiments, depending on the configuration of the nanowire filter 300 , the source container 12 , a pump 14 , tubes and conduits connecting these components, a target filtration rate, etc.
  • the solution is filtered by directing the primary flow over a micro-structured surface configured to filter the solution.
  • the primary flow may be directed over the micro-structured surface in a variety of ways.
  • a plurality of tubes, connectors, valves and other fluid conduits may direct the primary flow towards, and subsequently over the micro-structured surface.
  • the primary flow may be directed over the micro-structured surface, at least in part, by structures (such as the interior walls of the elongate channel 302 ) within the nanowire filter 300 itself.
  • the flow rate of the primary flow may also be varied in order to control an average height of the solution above the micro-structured surface.
  • the micro-structured surface may comprise any of a variety of microstructures.
  • the nanowire filter 300 may include a plurality of openings 306 .
  • the nanowire filter 800 may include a micro-structured surface 808 having a plurality of microscopic protrusions and pores.
  • the nanowire filter 1400 may comprise a plurality of parallel ridges.
  • micro-structures may include any small structures formed in, on or through a surface that may interfere with a fluid flow. The micro-structures are preferably configured to filter the solution by removing undesirable contaminant particles. Examples of suitable configurations are described above in greater detail with reference to the exemplary micro-structured nanowire filters.
  • the retentate 18 emerging from the nanowire filter 300 may comprise a more uniform solution of nanowires. Meanwhile, the filtrate from the solution may flow away from the micro-structured surface and thereby away from the nanowire filter 300 . In other embodiment, the filtrate may be captured and held by the micro-structured surface (e.g., as illustrated in FIGS. 8-10 ).
  • directing the primary flow over the micro-structured surface may further comprise creating a secondary flow through the plurality of openings 306 .
  • the secondary flow through the plurality of openings 306 may include both solvent and low aspect ratio contaminant particles.
  • a flow rate of the primary flow may be selected to be at least 10 times greater than a flow rate of the secondary flow.
  • a flow rate of the primary flow may be at least 100 times greater than a flow rate of the secondary flow.
  • directing the primary flow over the micro-structured surface may further comprise creating a secondary flow directed away from the primary flow of the solution via a plurality of fluid passages defined by a plurality of parallel ridges.
  • a flow rate of the primary flow may be selected to be at least 10 times greater than a flow rate of the secondary flow.
  • a flow rate of the primary flow may be at least 100 times greater than a flow rate of the secondary flow.
  • the primary flow of the solution may also be occasionally stopped, and a cleaning solution may be passed over the micro-structured surface.
  • a cleaning solution may be passed over the micro-structured surface.
  • this act of passing the cleaning solution over the micro-structured surface may be desirable to mitigate or prevent the build-up of filtrate and any resulting degradation in filtering efficiency.
  • the primary flow may be stopped and the cleaning solution applied periodically, according to some time interval.
  • these acts may be performed after a certain amount of solution has been filtered.
  • these acts may be performed when the performance of the nanowire filter has degraded by a certain amount.
  • the retentate 18 may be collected, liquid may be added, and the retentate 18 may be recirculated over the micro-structured surface.
  • An exemplary nanowire filtering system 22 for performing such acts is illustrated in FIG. 2 .
  • the retentate 18 may be collected in a variety of ways.
  • a second pump (not illustrated) may generate a flow of the retentate 18 from the nanowire filter 16 back to the source container 12 , where it may be collected.
  • replacement solvent may be added.
  • an inlet (not shown) may combine additional solvent with the retentate 18 before the retentate 18 is collected at the source container 12 .
  • the additional solvent may be added directly to the source container 12 (e.g., at a rate generally corresponding to the loss of filtrate from the solution).
  • the retentate 18 may be recirculated over the micro-structured surface a number of times. In one embodiment, for example, the retentate 18 may be recirculated a pre-determined number of times calibrated to approximately filter the solution to a desired purity. In another embodiment, a purity of the retentate 18 (corresponding, for example, to the percentage weight of nanowires in the retentate 18 or to a percentage concentration of replacement solvent) may be tested periodically or continuously, in order to determine whether or not to continue recirculating the retentate 18 over the micro-structured surface. Once a desired purity is reached, the recirculation of the retentate 18 may be stopped, and the solution collected in the source container 12 .
  • FIG. 32 illustrates a flow diagram for an alternative method 3200 of filtering a solution containing nanowires using a nanowire filter having a narrow aperture, according to one embodiment.
  • This method 3200 will be discussed in the context of the nanowire filter 1700 incorporated into the nanowire filtering system 10 . However, it may be understood that the acts disclosed herein may also be executed using a variety of other nanowire filters having narrow apertures (e.g., nanowire filters 2000 , 2200 , 2500 , 2700 , and 2900 ), in accordance with the described method.
  • the method begins at 3202 , when a solution containing nanowires and a first set of contaminant particles is provided.
  • the solution containing nanowires may comprise the solution within which the nanowires were formed.
  • the solution within which the nanowires were formed may have already undergone a variety of processing and/or filtering acts.
  • a flow of the solution is generated.
  • the flow of the solution may be generated by any of a variety of mechanisms, as described above with respect to act 3104 .
  • the solution is filtered by directing the flow through a passage defining an aperture having a width less than at least one dimension of the first set of contaminant particles.
  • the flow may be directed through the passage in any of a variety of ways.
  • a plurality of tubes, connectors, valves and other fluid conduits may direct the flow towards and through the passage.
  • the passage and the aperture defined thereby may comprise any of a variety of shapes and configurations.
  • a pair of parallel plates 1702 , 1704 may at least partially define a passage having a generally rectangular cross-section.
  • the passage may define circular, elliptical, triangular or irregularly shaped apertures.
  • the nanowire filter 1700 may eventually become clogged by filtrate collecting at the entrance 1710 to the passage.
  • the flow of the solution may therefore occasionally be stopped, a reverse flow of a liquid generated, and the reverse flow directed through the passage in a direction opposite to the flow of the solution.
  • a cleaning solution e.g., water
  • a reverse flow of the solution itself may occasionally be generated.
  • the pump 14 may be configured to pump in both a forward and reverse direction and may periodically switch direction in order to drive the solution back and forth through the nanowire filter 1700 .
  • a flow rate of the forward flow of the solution, and a flow rate of the reverse flow may be chosen such that there is a net flow of the solution towards the exit 1712 of the passage (i.e., in the forward direction).
  • potential clogging of the nanowire filter 1700 may be avoided or at least delayed by the periodic flushing of the entrance 1710 .
  • the reverse flow may be generated periodically, according to some time interval, or may be generated after a certain amount of solution has been filtered.
  • the reverse flow may be generated when the performance of the nanowire filter 1700 has degraded by a certain amount.
  • the reverse flow may be generated based on a reduction in a forward flow rate of the solution.
  • the nanowire filter 16 may further include a tortuous path filter (not illustrated) located upstream from the aperture 1708 .
  • the tortuous path filter may comprise any type of tortuous path filter.
  • the tortuous path filter may be configured similarly to a beta pure depth filter, manufactured by 3M, with a nominal pore size of 125 ⁇ m.
  • the flow of the solution may be further directed to a second passage defining a second aperture having a width less than at least one dimension of a second set of contaminant particles (e.g., 1 ⁇ m), and may then be directed to a third passage defining a third aperture having a width less than at least one dimension of a third set of contaminant particles (e.g., 0.5 ⁇ m) (as illustrated in FIG. 29 ).
  • the flow of the solution may be directed first through the first passage, then through the second passage, and then through the third passage.

Abstract

In order to filter a solution containing nanowires, a flow of the solution is generated and directed through a passage defining an aperture having a narrow width. Alternatively, a flow of the solution may be generated and directed over a micro-structured surface configured to filter the solution.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application claims the benefit under 35 U.S.C. § 119(e) of U.S. provisional patent application Ser. No. 60/913,231, filed Apr. 20, 2007, the content of which application is herein incorporated by reference in its entirety.
  • BACKGROUND
  • 1. Technical Field
  • This description generally relates to the field of nanowire manufacturing, and more particularly to filtering solutions containing nanowires.
  • 2. Description of the Related Art
  • Conductive and non-conductive nanowires may be used in a variety of applications. These high aspect ratio nano-structures may be used to form transparent conductors, similar to those manufactured currently using indium tin oxide (ITO). They may prove useful in quantum computing, sensing applications, flexible electronics and integration with biotechnology. In addition, they may someday be used to create high speed, high density microprocessors.
  • Current methods of manufacturing such nanowires often result in polydisperse solutions containing a mixture of structures of various shapes and sizes. These structures may include reaction byproducts, unreacted precursors, synthesis catalysts, etc., in addition to nanowires having the desired dimensions. In many applications, a more uniform solution of high aspect ratio nanowires is desirable. For example, depending on the size and amount, low aspect ratio nano-structures may tend to worsen the optical properties (e.g., higher haze, lower contrast ratio and lower transmission) in transparent conductors without improving conductivity. In addition, the solvent used in the manufacturing process may be unsuitable for later applications of the nanowires. For example, a solvent useful in nanowire synthesis may need to be exchanged before applying the nanowires in a surface coating.
  • Unfortunately, many conventional methods of separating/filtering particles and solvents (e.g., tortuous path filtration, conventional filtration, chromatography, sedimentation, centrifugation, etc.) are inefficient for or incapable of separating high aspect ratio nanowires from other structures in a solution.
  • Accordingly, there remains a need to effectively filter nanowires from a solution containing both nanowires and other structures. There is also a need to effectively exchange the solvent in a solution containing nanowires.
  • BRIEF SUMMARY OF THE INVENTION
  • In one embodiment, a method of filtering a solution containing nanowires and a first set of contaminant particles comprises: providing the solution; generating a flow of the solution; and filtering the solution by directing the flow through a passage defining an aperture having a width less than at least one dimension of the first set of contaminant particles.
  • In another embodiment, a nanowire filtering system comprises: a source container for holding a solution containing nanowires and a first set of contaminant particles; and a nanowire filter passage communicatively coupled to the source container for receiving the solution, the nanowire filter passage defined at least in part by: a first plate; and a second plate disposed adjacent the first plate with a minimum separation distance between the first plate and the second plate of less than at least one dimension of the first set of contaminant particles.
  • In yet another embodiment, a method of filtering a solution containing nanowires comprises: providing the solution; generating a primary flow of the solution; and filtering the solution by directing the primary flow over a micro-structured surface configured to filter the solution.
  • In another embodiment, a nanowire filtering system comprises: a source container for holding a solution containing nanowires; and a nanowire filter communicatively coupled to the source container for receiving the solution, the nanowire filter including: a rotatable tube defining a passage for the solution; a micro-structured surface lining an inside of the rotatable tube; a substantially helical surface adjacent the micro-structured surface and extending at least partially into the passage; and a drive member adapted to turn the rotatable tube.
  • In yet another embodiment, a nanowire filtering system comprises: a source container for holding a solution containing nanowires; and a nanowire filter communicatively coupled to the source container for receiving the solution, the nanowire filter including: an elongate channel defining a passage for the solution flowing along a long axis, the elongate channel having a lower surface including a plurality of parallel ridges disposed at an angle to the long axis; wherein the plurality of parallel ridges at least partially define a plurality of openings from the elongate channel.
  • In yet another embodiment, a nanowire filtering system comprises: a source container for holding a solution containing nanowires; and a nanowire filter communicatively coupled to the source container for receiving the solution, the nanowire filter including: an elongate channel defining a passage for the solution; and a collection chamber defined in part by an outer surface of the elongate channel, the collection chamber communicatively coupled to the elongate channel via a plurality of openings having an average diameter of greater than 5 μm.
  • BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS
  • In the drawings, identical reference numbers identify similar elements or acts. The sizes and relative positions of elements in the drawings are not necessarily drawn to scale. For example, the shapes of various elements and angles are not drawn to scale, and some of these elements are arbitrarily enlarged and positioned to improve drawing legibility. Further, the particular shapes of the elements as drawn are not intended to convey any information regarding the actual shape of the particular elements, and have been selected solely for ease of recognition in the drawings.
  • FIG. 1 is a schematic diagram of a nanowire filtering system, according to one illustrated embodiment.
  • FIG. 2 is a schematic diagram of another nanowire filtering system, according to another illustrated embodiment.
  • FIG. 3 is a perspective view of an example micro-structured nanowire filter, according to one illustrated embodiment.
  • FIG. 4 is a longitudinal cross-section of the nanowire filter of FIG. 3.
  • FIG. 5 is radial cross-section of the nanowire filter of FIG. 3.
  • FIG. 6 is a perspective view of another example micro-structured nanowire filter, according to one illustrated embodiment.
  • FIG. 7 is a bottom view of the nanowire filter of FIG. 6.
  • FIG. 8 is a perspective view of another example micro-structured nanowire filter, according to one illustrated embodiment.
  • FIG. 9 is a front view of the nanowire filter of FIG. 8.
  • FIG. 10 illustrates schematically nanowires and other nano-particles flowing in a solution over the nanowire filter of FIG. 8.
  • FIG. 11 is a perspective view of another example micro-structured nanowire filter, according to one illustrated embodiment, with inner portions of the nanowire filter shown in dashed lines.
  • FIG. 12 is a radial cross-section of the nanowire filter of FIG. 11.
  • FIG. 13 is a longitudinal cross-section of the nanowire filter of FIG. 11.
  • FIG. 14 is a perspective view of another example micro-structured nanowire filter, according to one illustrated embodiment.
  • FIG. 15 is a top view of the nanowire filter of FIG. 14.
  • FIG. 16 is an enlarged, schematic view of a bottom surface of the nanowire filter of FIG. 14 in operation.
  • FIG. 17 is a perspective view of an example nanowire filter having a narrow aperture, according to one illustrated embodiment.
  • FIG. 18 is a cross-section of the nanowire filter of FIG. 17.
  • FIG. 19 illustrates schematically nanowires and other particles flowing in a solution through the nanowire filter of FIG. 17.
  • FIG. 20 is a perspective view of an example micro-structured nanowire filter having a narrow aperture, according to one illustrated embodiment.
  • FIG. 21 is a bottom view of the nanowire filter of FIG. 20.
  • FIG. 22 is a perspective view of another example nanowire filter having a narrow aperture, according to one illustrated embodiment.
  • FIG. 23 is a cross-sectional, schematic view of the nanowire filter of FIG. 22 in operation.
  • FIG. 24 is a top view of the nanowire filter of FIG. 22.
  • FIG. 25 is a perspective view of another example nanowire filter having a narrow aperture, according to one illustrated embodiment.
  • FIG. 26 is a side view of the nanowire filter of FIG. 25.
  • FIG. 27 is a perspective view of another example nanowire filter having a narrow aperture, according to one illustrated embodiment.
  • FIG. 28 is a side view of the nanowire filter of FIG. 27.
  • FIG. 29 is a perspective view of another example nanowire filter having a plurality of narrow apertures, according to one illustrated embodiment.
  • FIG. 30 is a side view of the nanowire filter of FIG. 29.
  • FIG. 31 is a flow diagram illustrating a method of filtering a solution containing nanowires using a micro-structured nanowire filter, according to one illustrated embodiment
  • FIG. 32 is a flow diagram illustrating another method of filtering a solution containing nanowires using a nanowire filter having a narrow aperture, according to another illustrated embodiment.
  • DETAILED DESCRIPTION OF THE INVENTION
  • In the following description, certain specific details are set forth in order to provide a thorough understanding of various disclosed embodiments. However, one skilled in the relevant art will recognize that embodiments may be practiced without one or more of these specific details, or with other methods, components, materials, etc. In other instances, well-known structures and methodologies associated with nanowires, filters, pumps, and fluid dynamics have not been shown or described in detail to avoid unnecessarily obscuring descriptions of the embodiments.
  • Unless the context requires otherwise, throughout the specification and claims which follow, the word “comprise” and variations thereof, such as, “comprises” and “comprising” are to be construed in an open, inclusive sense, that is, as “including, but not limited to.”
  • Reference throughout this specification to “one embodiment” or “an embodiment” means that a particular feature, structure or characteristic described in connection with the embodiment is included in at least one embodiment. Thus, the appearances of the phrases “in one embodiment” or “in an embodiment” in various places throughout this specification are not necessarily all referring to the same embodiment. Furthermore, the particular features, structures, or characteristics may be combined in any suitable manner in one or more embodiments.
  • As used in this specification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise. It should also be noted that the term “or” is generally employed in its sense including “and/or” unless the context clearly dictates otherwise.
  • The headings and Abstract of the Disclosure provided herein are for convenience only and do not interpret the scope or meaning of the embodiments.
  • Description of an Exemplary Nanowire Filtering System
  • FIG. 1 illustrates an exemplary nanowire filtering system 10. As illustrated, the nanowire filtering system 10 comprises a source container 12, a pump 14 and a nanowire filter 16. In one embodiment, the components of the nanowire filtering system 10 function together to filter a solution containing nanowires, removing undesirable contaminant particles and/or solvent from the solution to achieve a more uniform solution of high aspect ratio nanowires.
  • The source container 12 may comprise any of a variety of containers for holding a solution containing nanowires. For example, the source container 12 may comprise a stainless steel or glass vessel, within which the nanowires were formed. In another embodiment, the source container 12 may simply comprise tubing through which the solution containing nanowires may travel.
  • The solution containing nanowires within the source container 12 may comprise any liquid carrying nanowires. In one example, the solution containing the nanowires may come directly from a synthesis reaction prior to any formulation. The solution containing nanowires may include, by weight, from 0.0025% to 0.1% surfactant (e.g., a preferred range is from 0.0025% to 0.05% of ZONYL® FSO-100), from 0.02% to 4% viscosity modifier (e.g., a preferred range is 0.02% to 0.5% of hydroxypropyl methyl cellulose (“HPMC”)), from 94.5% to 99.0% solvent and from 0.05% to 1.4% nanowires. Representative examples of suitable surfactants include ZONYL® FSN, ZONYL® FSO, ZONYL® FSH, TRITON® (x100, x114, x45), DYNOL™ (604, 607), n-Dodecyl b-D-maltoside and Novek. Examples of suitable viscosity modifiers include HPMC, methyl cellulose, xanthan gum, polyvinyl alcohol, carboxy methyl cellulose, and hydroxy ethyl cellulose. Examples of suitable solvents include water, alcohol (e.g., isopropanol), ketones, ether, or hydrocarbon or aromatic solvents (e.g., benzene, toluene or xylene). In addition, the solvent may be volatile, having a boiling point of no more than 200° C., no more than 150° C., or no more than 100° C.
  • The amount of solvent can be adjusted to provide a desired viscosity and concentration of nanowires in the solution. For example, different pumps 14 and different nanowire filters 16 may function optimally on different concentration solutions. In one embodiment, however, the relative ratios of the other ingredients may remain the same. In particular, the ratio of the surfactant to the viscosity modifier may be kept in the range of about 80 to about 0.01; the ratio of the viscosity modifier to the nanowires may remain in the range of about 5 to about 0.000625; and the ratio of the nanowires to the surfactant may be in the range of about 560 to about 5. In one embodiment, the viscosity range for the nanowire solution may be from 1 to 100 cP.
  • A number of contaminant particles and other structures may also be present in the solution, including low aspect ratio nano-particles (e.g., short rods, discs or spheres) made from the same material as the nanowires, as well as synthesis catalysts, reaction byproducts and unreacted precursors. For many applications, the presence of such contaminant particles may be undesirable.
  • As used herein, a “nanowire” refers generally to a nano-structure having a high aspect ratio (e.g., higher than 10). Examples of non-metallic nanowires include, but are not limited to, carbon nanotubes (CNTs), metal oxide nanowires, conductive polymer fibers and the like. Metallic nanowires may comprise elemental metals, metal alloys or metal compounds. Suitable metal nanowires can be based on any metal or combinations and/or alloys of metals, including without limitation, silver, gold, copper, nickel, gold-plated silver, gold-silver alloys, platinum, and palladium.
  • In one embodiment, at least one cross-sectional dimension of a nanowire is less than 500 nm. In another embodiment, at least one cross-sectional dimension of a nanowire is less than 200 nm, and in yet another embodiment, at least one cross-sectional dimension is less than 100 nm. As noted above, the nanowire may have an aspect ratio (length:diameter) of greater than 10. In another embodiment, the aspect ratio may be greater than 50. In yet another embodiment, the aspect ratio may be greater than 100. Nanowires may have aspect ratios anywhere in the range of 10 to 100,000.
  • The nanowires can be prepared by any of a number of methods. In one embodiment, large-scale production of silver nanowires of uniform size may be carried out according to the methods described in, e.g., Xia, Y. et al., Chem. Mater. (2002), vol. 14, 4736-4745, and Xia, Y. et al., Nanoletters (2003) vol. 3(7), 955-960, the contents of which are hereby incorporated herein by reference in their entirety.
  • In another embodiment, silver nanowires may be synthesized in a batch process by the reduction of silver nitrate in propylene glycol. The chemistry of such a process is described in co-pending U.S. patent application Ser. No. 11/766,552, titled METHODS OF CONTROLLING NANOSTRUCTURE FORMATIONS AND SHAPES, filed Jun. 21, 2007, the contents of which are hereby incorporated herein by reference in their entirely.
  • Nanowire formation may be accomplished by the use of a surface active polymer (e.g., polyvinylpyrrolidone (“PVP”)) and chloride (e.g., added in the form of tetra-n-butylammonium chloride (“TBAC”)). The process may be carried out in an agitated, jacketed glass reactor including glass impellers, an automated temperature controller, a small glass feed vessel (which may also be agitated), and a precision metering pump. Propylene glycol, PVP, and TBAC may first be added to the reactor and heated to a target temperature (e.g., 100° C.) under agitation. Meanwhile, a solution of silver nitrate and propylene glycol may be prepared in the small glass feed vessel. Once the silver nitrate is fully dissolved, and the reactor has stabilized at the target temperature, the silver nitrate mixture may be added to the reactor at a controlled rate
  • The solution may then react under agitation at atmospheric pressure. As the reaction progresses, nano-particles may form first, followed by nanowires that grow to the desired length and width. Nano-particles may be indicated by an orange-brown or brown-green color, and, as nanowires form, the mixture may become increasingly grey and metallic in appearance. Once the target nanowire morphology is achieved (e.g., as determined by dark field optical microscopy), the reaction may be quenched by the rapid addition of water, which both cools the reaction mixture and inhibits further reaction. Reaction temperature, reaction time, and silver nitrate addition rate may be varied to control the dimensions of the resulting nanowires.
  • Following reaction, the reactor may be cleaned using a clean-in-place system consisting of a spray ball and a persistaltic pump. Residue from previous reactions may have adverse effects on the synthesis process.
  • Example 30 kg Nanowire Synthesis
  • Raw Material Weight % Quantity
    Propylene Glycol 79.0% 23700 g
    PVP 0.5% 150 g
    TBAC 0.01% 3.0 g
    AgNO3 0.83% 250 g
    Propylene Glycol 3.0% 900 g
    (added with AgNO3)
    Deionized Water 16.7% 5000 g
  • Propylene glycol was first added to a 30 L glass reactor. PVP and TBAC were also added to the glass reactor. The agitator for the glass reactor was turned to 100 rpm, and the solution in the glass reactor was heated to 100° C. While the solution was heating, propylene glycol and silver nitrate were premixed in a 4 L glass feed vessel until all of the solids were dissolved. Once the solution in the reactor reached a stable 100° C., the propylene glycol/silver nitrate solution were added to the reactor via a metering pump. 900 mL of propylene glycol and silver nitrate were added to the reactor at an addition rate of 45 mL/min for 20 minutes. Starting a timer at the start of the silver nitrate addition, the solution was mixed for 4 hours in the reactor before the heating was turned off and the reaction quenched with deionized water.
  • The average length of the resulting silver nanowires was 24 μm with a standard deviation of 15 μm. The average width of the resulting silver nanowires was 65 nm with a standard deviation of 14 nm. The estimated yield of silver converted into silver nanowires was 50 wt %.
  • Alternatively, nanowires may be prepared using biological templates (or biological scaffolds) that can be mineralized. For example, biological materials such as viruses and phages can function as templates to create metal nanowires. In certain embodiments, the biological templates can be engineered to exhibit selective affinity for a particular type of material, such as a metal or a metal oxide. More detailed descriptions of biofabrication of nanowires can be found in, e.g., Mao, C. B. et al., “Virus-Based Toolkit for the Directed Synthesis of Magnetic and Semiconducting Nanowires,” (2004) Science, 303, 213-217; Mao, C. B. et al., “Viral Assembly of Oriented Quantum Dot Nanowires,” (2003) PNAS, vol. 100, no. 12, 6946-6951; U.S. patent application Ser. No. 10/976,179 and U.S. provisional patent application Ser. No. 60/680,491, all of which are hereby incorporated herein by reference in their entireties.
  • Regardless of the exact methodology used for nanowire synthesis, the resulting solution may be a polydisperse solution containing a mixture of contaminant particles and nanowires of various shapes and sizes. For many applications, purification may be desirable in order to achieve a more uniform solution of high aspect ratio nanowires. In some embodiments, solubilized ion contaminants (e.g., Cl−, Ag+, NO3−) that might lead to nanowire degradation should also be removed. In addition, exchange of the solvent may be desirable based on the particular application for the nanowire solution.
  • In one embodiment, the source container 12 may serve as the reactor within which the nanowires are formed. However, in other embodiments, a solution containing nanowires may be generated in another container/reactor and be subsequently transferred to the source container 12. In yet another embodiment, the solution containing nanowires need not comprise the solution within which the nanowires were originally formed. Thus, the nanowire filtering system 10 may be used to filter any solution containing nanowires.
  • As illustrated, the nanowire filtering system 10 may include a pump 14 to generate a flow of the solution containing nanowires from the source container 12 to the nanowire filter 16. The pump 14 may comprise any of a variety of liquid pumps. For example, the pump 14 may comprise a bellows pump, a centrifugal pump, a diaphragm pump, a drum pump, a flexible liner/impeller pump, a gear pump, a peristaltic pump, a piston pump, a progressing cavity pump, a rotary lobe pump, a rotary vane pump, etc.
  • In another embodiment, the nanowire filtering system 10 may not include a pump. For example, in one embodiment, a flow of the solution containing nanowires may be generated by gravity. In another embodiment, the pump 14 may be incorporated into the nanowire filter 16.
  • The nanowire filter 16 may comprise any of a variety of filters configured to separate nanowires from contaminant particles and other nano-structures. The nanowire filter 16 may be further configured to separate the nanowires from a solvent in order to facilitate a solvent exchange. In one embodiment, the nanowire filter 16 may be configured to yield a retentate 18, which comprises a more uniform solution containing nanowires, and a filtrate (not shown), which may comprise solvent and/or the contaminant particles filtered from the solution. The retentate 18 may have a higher weight percentage of nanowires than the flow of solution 20 entering the nanowire filter 16. As discussed below with reference to FIGS. 3-30, the nanowire filter 16 may include a plurality of micro-structures and/or may include one or more narrow apertures configured to filter the solution. The nanowire filter 16 may also, in some embodiments, comprise a plurality of nanowire filters arranged in parallel or in series to filter the solution containing nanowires.
  • In one embodiment, the nanowire filter 16 may filter out nanowires having aspect ratios below a certain threshold. For example, in one embodiment, the nanowire filter 16 may generally filter out nanowires having aspect ratios lower than 100. The aspect ratio targeted by a particular nanowire filter 16 may be selected based upon an application for the solution.
  • In one embodiment, the retentate 18 may be collected in a container (not shown) for subsequent processing or use. For example, in one embodiment, the retentate 18 may be added to a solvent useful in coating formulations. In another embodiment, as illustrated in FIG. 2, a nanowire filtering system 22 may recirculate the retentate 18 from the nanowire filter 16 back to the source container 12 for further filtering. In such an embodiment, the filtering and subsequent recirculating of the solution containing nanowires may continue for a predetermined time period, or until the solution containing nanowires has reached a desired purity. In order to maintain a viscosity of the solution or in order to effect a solvent exchange, solvent (not shown) may also be added to the nanowire filtering system 22 (e.g., at the source container 12) as the retentate 18 is recirculated. In one embodiment, the filtering, recirculating, and addition of a new solvent may continue until the solution containing nanowires achieves a predetermined concentration of the new solvent.
  • Description of an Exemplary Micro-Structured Nanowire Filter
  • FIG. 3 is a perspective view of a micro-structured nanowire filter 300, which may be used in the nanowire filtering system 10 or the nanowire filtering system 22. FIGS. 4 and 5 present longitudinal and radial cross-sections, respectively, of the nanowire filter 300 to facilitate an understanding of its inner structure. As illustrated, the nanowire filter 300 comprises an elongate channel 302 having an entrance 308 and an exit 310 and defining a passage for a primary flow (designated by the arrow 301) of the solution containing nanowires. The elongate channel 302 may include a micro-structured surface between the entrance 308 and exit 310 having a plurality of openings 306 defined therethrough. In one embodiment, the elongate channel 302 is surrounded by a plurality of collection chambers 304 communicatively coupled to the elongate channel 302 by the plurality of openings 306. The nanowire filter 300 may, of course, be formed from a variety of different materials, including metallic and non-metallic materials, and may be coupled to the rest of the nanowire filtering system 10 by any of a variety of fluid connectors, tubes and/or conduits.
  • The plurality of openings 306 through the surface of the elongate channel 302 are micro-structures configured to filter the solution. The terms micro-structures and micro-structured may reference any small structures formed in, on or through a surface that may interfere with a fluid flow. For example, micro-structures may refer to structures having at least one dimension less than 1 cm. In the illustrated embodiment, the micro-structures comprise the plurality of openings 306. However, in other embodiments, micro-structures may comprise a plurality of niches, valleys, detents, peaks, protrusions, etc. Other examples of micro-structures and micro-structured surfaces are presented with reference to FIGS. 6-16.
  • The size, arrangement and configuration of the openings 306 may be varied to filter different contaminant particles. In one embodiment, the size of the openings 306 may be chosen based at least in part on the desired length/diameter/aspect ratio of the nanowires, the size/aspect ratio of the contaminant particles that should be filtered from the solution as well as a viscosity and flow rate of the solvent. For example, the openings 306 may have an average diameter greater than 5 μm because the expected filtrate may have a diameter up to approximately 5 μm. In another embodiment, the openings 306 may have an average diameter greater than 10 μm. As the diameter of the openings 306 increases, a greater secondary flow may be generated through the openings 306, and the nanowire filter 300 may filter out more contaminant particles and solvent on each pass. However, with larger openings 306, the nanowire filter 300 may also become less selective, and more nanowires may be lost in the filtrate.
  • In one embodiment, the elongate channel 302 may be approximately 3 cm in diameter, and approximately 50 cm long. In other embodiments, the length and diameter of the elongate channel 302 may be varied. As the elongate channel 302 is lengthened or its diameter made smaller, a greater amount of filtrate may be separated from the primary flow of solution as the solution passes through the nanowire filter 300. However, a greater quantity of nanowires may also be lost in the filtrate. The length, diameter and geometry of the elongate channel 302 may therefore be varied to achieve desired characteristics for the nanowire filter 300.
  • In one embodiment, as illustrated, the elongate channel 302 may comprise a cylindrical passage, and the openings 306 may extend along the entire surface of this cylindrical passage. Of course, in other embodiments, other configurations are possible. The elongate channel 302 may have a variety of shapes, and the openings 306 may be formed on only a portion of the channel's surface. For example, in one embodiment, the openings 306 may be formed only along a bottom half of the surface of the elongate channel 302, as the filtrate may preferentially flow through these openings 306 by gravity. In another embodiment, the openings 306 may be formed along only a portion of the entire length of the elongate channel 302.
  • As illustrated, eight collection chambers 304 are defined at least in part by an outer surface of the elongate channel 302. The eight collection chambers 304 may be separated by radially extending fins extending from the outer surface of the elongate channel 302 to an outer wall 312 of the nanowire filter 300. Of course, in other embodiments, the collection chambers 304 may be configured differently. In one embodiment, more or fewer collection chambers 304 may be formed around the elongate channel 302, and they may have different geometries. In another embodiment, the collection chambers 304 need not be integrally formed with the elongate channel 302. For example, the elongate channel 302 may be suspended over one or more collection chambers, and, in operation, the filtrate emerging from the openings 306 of the elongate channel 302 may fall into the collection chambers.
  • During operation, a primary flow 301 of the solution may pass through the entrance 308, through the elongate channel 302 and emerge from the exit 310 as retentate 18. Meanwhile, the plurality of openings 306 may create a secondary flow of at least a portion of the solution, i.e., the filtrate, through the plurality of openings 306 and into the collection chambers 304. In one embodiment, the collection chambers 304 may transfer the secondary flow to a filtrate container (not shown).
  • Although the diameter of the nanowires may be equal to or smaller than the diameter of the filtered contaminant particles, the nanowires (due to their high aspect ratio) may substantially align with the primary flow 301 passing through the elongate channel 302, and this alignment may inhibit or effectively prevent the nanowires from passing through the plurality of openings 306. In one embodiment, the primary flow 301 of the solution through the elongate channel 302 may be greater than the secondary flow through the plurality of openings 306 into the collection chambers 304 to take advantage of this alignment. For example, in one embodiment, the primary flow 301 may be at least 100 times greater than the secondary flow of the solution. This relatively high flow rate through the elongate channel 302 may help to align the nanowires with the primary flow 301 and prevent the nanowires from inadvertently passing through the plurality of openings 306.
  • In one embodiment, if the diameter of the openings 306 is increased, the primary flow rate may be correspondingly increased to help prevent nanowires from slipping through the enlarged openings 306. Thus, the size of the openings 306 and the primary flow rate through the elongate channel 302 may be varied in different embodiments of the nanowire filter 300 in order to change its filtering characteristics.
  • Description of Another Exemplary Micro-Structured Nanowire Filter
  • FIG. 6 is a perspective view of another micro-structured nanowire filter 600 that operates similarly to the nanowire filter 300 of FIGS. 3-5. FIG. 7 is a bottom view of the nanowire filter 600. In one embodiment, the nanowire filter 600 comprises an elongate channel 606 having an entrance 608 and an exit 610 and defining a passage for a primary flow (designated by the arrow 601) of the solution containing nanowires. The elongate channel 606 may, in turn, be defined at least in part by a micro-structured surface 602 comprising a plurality of openings 604.
  • In one embodiment, the openings 604 may have an average diameter of approximately 5 μm, and the elongate channel 606 may be approximately 50 cm in length. Of course, as described above with respect to the nanowire filter 300, the size and shape of the openings 604, the size and shape of the elongate channel 606, and the primary flow rate of the solution may be varied to achieve desired filtering characteristics. In addition, an average height of the solution passing over the micro-structured surface 602 may also be varied to achieve the desired filtering characteristics.
  • In operation, a primary flow 601 of the solution may pass through the entrance 608, through the elongate chamber 606 and emerge from the exit 610 as retentate 18. Meanwhile, the plurality of openings 604 may create a secondary flow of filtrate out from the elongate chamber 606. The nanowires in the solution may substantially align with the primary flow 601 passing through the elongate chamber 606, and this alignment may inhibit or effectively prevent the nanowires from passing through the plurality of openings 604.
  • In one embodiment, a trough or another type of collection chamber (not shown) may be disposed beneath the micro-structured surface 602 to collect the filtrate. In another embodiment, the elongate chamber 606 may be coupled to at least one collection chamber in an arrangement similar to that of the nanowire filter 300.
  • Description of Yet Another Exemplary Micro-Structured Nanowire Filter
  • FIG. 8 is a perspective view, and FIG. 9 is a front view of another example micro-structured nanowire filter 800. As illustrated, the nanowire filter 800 comprises a frame 802 defining a generally V-shaped trough between an entrance 804 and an exit 806 that may direct a primary flow (designated by the arrow 801) of the solution containing nanowires over a micro-structured surface 808 supported by the frame 802. The micro-structured surface 808 may, in one embodiment, comprise a plurality of surface protrusions and pores.
  • In one embodiment, the frame 802 may comprise a metallic plate bent into the desired V-shape. In other embodiments, the frame 802 may comprise other materials, such as plastics. The frame 802 may also have other shapes for directing the primary flow 801 of the solution. For example, the frame 802 may define a cylindrical or a U shape.
  • In one embodiment, the micro-structured surface 808 may be defined by filter paper. The filter paper may be any type of filter paper configured to filter the solution containing nanowires. For example, the filter paper may have a porosity of greater than 5 μm because the expected filtrate may have a diameter up to approximately 5 μm. In another embodiment, the filter paper may have a porosity of greater than 10 μm. The porosity of the filter paper may be varied, as described above to achieve particular filtering characteristics.
  • In other embodiments, the micro-structured surface 808 may be defined by a more permanent filtering substrate. For example, an inner surface of the frame 802 itself may have small protrusions defined thereon.
  • In operation, a primary flow 801 of the solution may pass through the entrance 804, over the micro-structured surface 808 and emerge from the exit 806 as retentate 18. More compact contaminant particles, which may tend to have lower drag in a flowing solution, may be pulled by gravity towards the micro-structured surface 808, where they may be trapped by the micro-structures. Of course, more massive contaminant particles may sediment more quickly out of the solution, while smaller contaminant particles may sediment more slowly. The dimensions and arrangement of the nanowire filter 800 may be configured to filter different sizes of the contaminant particles as desired. Meanwhile, the nanowires in the solution may substantially align with the primary flow 801, and this alignment may inhibit or effectively prevent the nanowires from being trapped by the micro-structured surface 808.
  • In one embodiment, a flow rate of the primary flow 801 of the solution may be monitored and controlled to ensure that the nanowire filter 800 is, indeed, preferentially filtering out the more compact, low aspect ratio particles. If the flow rate is too high, even the low aspect ratio contaminant particles may emerge as retentate 18. However, if the flow rate is too low, high aspect ratio nanowires may settle out of the solution onto the bottom of the nanowire filter 800.
  • A schematic view of the microscopic filtering process is illustrated in FIG. 10. As shown, the nanowires 1002 may be generally aligned with the primary flow 801 of the solution while low aspect ratio contaminant particles 1006 are trapped by the micro-structures 1008.
  • As may be understood with reference to FIG. 10, the nanowire filter 800 may trap filtrate within the micro-structures 1008. As a result, it may be desirable to occasionally clean the micro-structured surface 808 to maintain the filtering efficiency of the nanowire filter 800. In one embodiment, the primary flow 801 of the solution may be stopped, and a separate cleaning solution passed over the micro-structured surface 808 to eliminate the filtrate. In another embodiment, the micro-structured surface 808 may be occasionally replaced. For example, new filter paper may replace the old filter paper. Other methods of cleaning the micro-structured surface 808 may be used in other embodiments.
  • The micro-structured surface 808 may be cleaned periodically, according to some time interval, or may be cleaned after a certain amount of solution has been filtered. In another embodiment, the micro-structured surface 808 may be cleaned when the performance of the nanowire filter 800 has degraded by a certain amount.
  • Description of Yet Another Exemplary Micro-Structured Nanowire Filter
  • FIG. 11 is a perspective view of another example micro-structured nanowire filter 1100, with interior portions of the nanowire filter 1100 illustrated in dashed lines. FIGS. 12 and 13 present radial and longitudinal cross-sections, respectively, of the nanowire filter 1100 to facilitate a greater understanding of its inner structure. As illustrated, the nanowire filter 1100 comprises a rotatable tube 1102 having an entrance 1110 and an exit 1112 and defining a passage for a primary flow (designated by the arrow 1101) of the solution containing nanowires. A micro-structured surface 1108 lines an inside of the rotatable tube 1102. The rotatable tube 1102 may also have disposed therein a substantially helical element 1104 and may be coupled to a drive member 1106 for rotating the rotatable tube 1102 about a longitudinal axis.
  • The rotatable tube 1102 may be formed from any metallic or non-metallic materials. The size and shape of the rotatable tube 1102 may also be varied to achieve desired filtering characteristics.
  • In one embodiment, the micro-structured surface 1108 lining the rotatable tube 1102 may comprise filter paper. The filter paper may be any type of filter paper configured to filter the solution. For example, the filter paper may have a porosity of greater than 5 μm because the expected filtrate may have a diameter up to approximately 5 μm. In another embodiment, the filter paper may have a porosity of greater than 10 μm. The porosity of the filter paper may be varied, as described above. In another embodiment, the micro-structured surface 1108 may be defined by an inner surface of the rotatable tube 1102 itself. For example, the rotatable tube 1102 may include a plurality of openings (not shown) that comprise the micro-structures.
  • In one embodiment, the substantially helical element 1104 may be arranged adjacent the micro-structured surface 1108 and may comprise a strip of fluid impermeable material wound around an interior of the rotatable tube 1102. The substantially helical element 1104 may be formed integrally with or may be separate from the rotatable tube 1102. The substantially helical element 1104 is illustrated as extending only a short way into the passage defined by the rotatable tube 1102. However, in other embodiments, the substantially helical element 1104 may extend much further. For example, in some embodiments, the substantially helical element 1104 may have a height approximately equal to a radius of the rotatable tube 1102.
  • The drive member 1106 may comprise any appropriate combination of a motor and fittings adapted to turn the rotatable tube 1102. In one embodiment, the drive member 1106 may be configured to turn the rotatable tube 1102 at a variable angular velocity.
  • In operation, in order to drive a primary flow 1101 of the solution containing nanowires through the entrance 1110 and out the exit 1112 of the rotatable tube 1102, the drive member 1106 may turn the rotatable tube 1102 in a counter-clockwise direction (from the vantage point of FIG. 12). The primary flow 1101 of the solution may be maintained at a level lower than a height of the substantially helical element 1104, such that the solution cannot pass over the barrier represented by the substantially helical element 1104. As the rotatable tube 1102 turns in a counter-clockwise direction, the solution may be driven through the rotatable tube 1102 by the substantially helical element 1104, and thus, a flow rate of the solution may be controlled by the drive member 1106.
  • As described above with reference to FIG. 10, low aspect ratio contaminant particles, which may tend to have lower drag in a flowing solution, may be pulled by gravity towards the micro-structured surface 1108, where they may be trapped by micro-structures. Meanwhile, nanowires in the solution may substantially align with the primary flow 1101, and this alignment may inhibit or effectively prevent the nanowires from being trapped by the micro-structured surface 1108.
  • It may be desirable to occasionally clean the micro-structured surface 1108 to maintain the filtering efficiency of the nanowire filter 1100. In one embodiment, the primary flow of the solution may be stopped, and a separate cleaning solution passed over the micro-structured surface 1108 to eliminate the filtrate. Alternatively, the micro-structured surface 1108 may be occasionally replaced. For example, new filter paper may replace the old filter paper. Other methods of cleaning the micro-structured surface 1108 may be used in other embodiments.
  • The micro-structured surface 1108 may be cleaned periodically, according to some time interval, or after a certain amount of solution has been filtered. In another embodiment, the micro-structured surface 1108 may be cleaned when the performance of the nanowire filter 1100 has degraded by a certain amount.
  • Description of Another Exemplary Micro-Structured Nanowire Filter
  • FIG. 14 is a perspective view, and FIG. 15 is a top view of another micro-structured nanowire filter 1400. As illustrated, the nanowire filter 1400 may include an elongate channel 1402 having an entrance 1410 and an exit 1412 and defining a passage for a primary flow (designated by the arrow 1401) of the solution containing nanowires along a long axis 1404. The elongate channel 1402 may further include a micro-structured, bottom surface 1406 having a plurality of parallel ridges oriented at an angle to the long axis 1404.
  • The elongate channel 1402 may be integral with or may be formed separately from the micro-structured surface 1406. In one embodiment, walls 1414, 1416 of the elongate channel 1402 as well as the micro-structured surface 1406 may be formed from any of a variety of metallic or non-metallic materials. Although illustrated as generally U-shaped, the elongate channel 1402 may have any of a number of other shapes and configurations. In one embodiment, the elongate channel 1402 may be fully enclosed, forming a generally rectangular cross-sectional shape.
  • The micro-structures of the bottom surface 1406 may comprise a plurality of parallel ridges (and corresponding valleys) that form a non-right angle with the long axis 1404. In one embodiment, the ridges may at least partially define a plurality of fluid passages ending at a plurality of secondary openings 1408 from the elongate channel 1402. The plurality of secondary openings 1408 may, in one embodiment, allow filtrate to exit the elongate channel 1402. Of course, in other embodiments, the ridges may be configured differently. For example, they need not be parallel, and, in one embodiment, the ridges may be oriented at a right angle to the long axis 1404.
  • The parallel ridges may also be separated by a distance greater than 5 μm because the expected filtrate may have a diameter up to approximately 5 μm. In another embodiment, the parallel ridges may be separated by a distance greater than 10 μm. A cross-section of the valleys formed by the ridges may be approximately square, such that the valleys are deeper than 5 μm or 10 μm in respective embodiments. The size and shape of the ridges, the size and shape of the elongate channel 1402, and the primary flow rate of the solution may be varied to achieve desired filtering characteristics.
  • Turning to FIG. 16, an enlarged, schematic view of the micro-structured surface 1406 of the nanowire filter 1400 is illustrated in operation. As shown, a primary flow 1401 of the solution may flow across the micro-structured surface 1406, and thereby across the plurality of parallel ridges. The parallel ridges may then create a plurality of secondary flows 1604, as filtrate from the solution is diverted by the parallel ridges through the secondary openings 1408. These secondary flows 1604 containing filtrate may or may not be collected in collection chambers (not shown). Since the filtrate may thus be diverted away from the nanowire filter 1400, the nanowire filter 1400 may remain relatively clear of the filtrate. Thus, there may be a reduced need to clean the nanowire filter 1400.
  • As discussed above, the plurality of parallel ridges may filter low aspect ratio contaminant particles from the nanowires due to the different drag characteristics of these particles in a fluid flow.
  • Description of an Exemplary Nanowire Filter Having a Narrow Aperture
  • FIG. 17 is a perspective view, and FIG. 18 is a cross-section of a nanowire filter 1700 having a narrow aperture 1708, which filter may be used in the nanowire filtering system 10 or the nanowire filtering system 22. The nanowire filter 1700 may comprise a first plate 1702 and a second plate 1704 disposed adjacent the first plate 1702. The first and second plates 1702, 1704 may at least partially define a passage 1706 extending through the filter, the passage 1706 having an entrance 1710 and an exit 1712. In one embodiment, the passage 1706 defines an aperture 1708 having a width W less than at least one dimension of a set of contaminant particles.
  • The nanowire filter 1700 may be formed from a variety of different materials. In one embodiment, the nanowire filter 1700 may comprise a molded plastic. In another embodiment, the nanowire filter 1700 may be formed from stainless steel. In yet another embodiment, the nanowire filter 1700 may comprise stainless steel first and second plates 1702, 1704 separated by relatively hard micro- or nano-particles (e.g., silica). In one embodiment, a plurality of such plates may be stacked one upon the other in order to achieve a high flow rate through the nanowire filter 1700.
  • In one embodiment, the first plate 1702 and the second plate 1704 are substantially parallel and define a separation distance between them of less than at least one dimension of a set of contaminant particles. Since the separation distance between the two plates 1702, 1704 is substantially invariant, the aperture 1708 may coincide with the entrance 1710 to the nanowire filter 1700.
  • The aperture 1708 may have a width W selected to filter out the set of contaminant particles having at least one dimension greater than the width. For example, in one embodiment, the aperture 1708 may have a width W less than 2 μm, in order to filter out particles having a diameter greater than 2 μm. In another embodiment, the aperture 1708 may have a width W less than 1 μm, or less than 0.5 μm, in order to filter out contaminant particles having greater dimensions. As the width W of the aperture 1708 is decreased, the flow through the nanowire filter 1700 may also decrease, and the nanowire filter 1700 may filter out more contaminant particles. The width W of the aperture 1708 may be varied in different embodiments to filter out different sets of contaminant particles, while allowing nanowires to pass through the filter 1700 unimpeded.
  • The length L of the aperture 1708 may also be varied to pass more or less solution. In one embodiment, a very long aperture 1708 may be used to enable a greater flow of solution through the passage 1706 of the nanowire filter 1700.
  • In general, as with the micro-structured nanowire filters described above, nanowires in the solution may substantially align with the flow through the passage 1706 of the nanowire filter 1700. Thus, as the nanowires approach the aperture 1708, they may present a relatively small cross-section. For example, in one embodiment, the nanowires may have an average diameter ranging from 20 to 200 nm. Although, the nanowires may be as long as, or longer than, the width W, the narrow cross-section of the nanowires may enable the nanowires to align with the flow and pass through the nanowire filter 1700.
  • A schematic view of the nanowire filter 1700 in operation is illustrated in FIG. 19. The first plate 1702 is illustrated transparently, in order to schematically show the nanowires 1902 in the solution aligned with a flow 1906 through the nanowire filter 1700. Meanwhile, low aspect ratio contaminant particles 1904 (which may, for example, have a diameter approximately equal to a length of the nanowires) may be “captured” at the aperture 1708, unable to pass through the nanowire filter 1700 with the rest of the retentate 18.
  • Although the nanowire filter 1700 is illustrated as comprising two substantially parallel plates forming an aperture 1708 sized to prevent large diameter contaminant particles from passing therethrough, other configurations are, of course, possible. In one embodiment, the nanowire filter 1700 may include any other aperture shape (e.g., circular, elliptical, triangular) having at least one width less than at least one dimension of a set of contaminant particles. In another embodiment, the nanowire filter 1700 may comprise a plurality of cylindrical passages, each of the passages having a diameter less than the at least one dimension of the set of contaminant particles.
  • As illustrated in FIG. 19, the nanowire filter 1700 may build up filtrate at the aperture 1708, which may eventually become clogged by these large contaminant particles. As a result, it may be desirable to “de-clog” the filter 1700 by occasionally removing these particles from the aperture 1708 in order to maintain the filtering efficiency of the nanowire filter 1700. In one embodiment, the primary flow of the solution (designated by the arrow 1906) may be occasionally stopped and the nanowire filter 1700 removed for cleaning. In another embodiment, the primary flow 1906 of the solution may be stopped, and a reverse flow (not shown) of a liquid generated through the passage 1706 in order to dislodge the larger particles from the aperture 1708. Indeed, in one embodiment, a reverse flow of the solution itself may be periodically generated through the passage 1706 in order to dislodge the larger particles from the aperture 1708. This reverse flow may also be coupled with an external cleaning, ultrasonic energy, or another mechanism to ensure that the filtered contaminant particles are well-separated from the aperture 1708 and do not immediately re-clog the nanowire filter 1700. Although the solution may flow through the nanowire filter 1700 in both directions, a net flow may be directed from the entrance 1710 to the exit 1712 of the nanowire filter 1700.
  • In one embodiment, the nanowire filter 1700 may be de-clogged periodically, according to some time interval. In another embodiment, the nanowire filter 1700 may be de-clogged after a certain amount of solution has been filtered. In yet another embodiment, the nanowire filter 1700 may be de-clogged when the performance of the nanowire filter 1700 (as measured, for example, by a flow rate of the primary flow 1906 through the nanowire filter 1700) has degraded by a certain amount.
  • Description of an Exemplary Micro-Structured Nanowire Filter Having a Narrow Aperture
  • FIG. 20 is a perspective view, and FIG. 21 is a bottom view of another nanowire filter 2000 having a narrow aperture 2008 defined at least in part by a top plate 2002 and a bottom plate 2004. The nanowire filter 2000 may be configured similarly to the nanowire filter 1700, except that the bottom plate 2004 may further include a plurality of openings 2010. As described above with reference to the other micro-structured nanowire filters, the plurality of openings 2010 may be considered micro-structures. In other embodiments, different micro-structures may be used in conjunction with a narrow aperture to form other nanowire filters.
  • In operation, the nanowire filter 2000 may filter out larger contaminant particles at the aperture 2008 and may filter out smaller contaminant particles via the openings 2010 in the bottom plate 2004. Thus, the nanowire filter 2000 may effectively combine the filtering capabilities of the nanowire filter 1700 with the filtering capabilities of, for example, the nanowire filter 600. The flow rate, solution composition and dimensions of the components of the nanowire filter 2000 may be varied to optimize one or both of these filtering capabilities.
  • Description of Another Exemplary Nanowire Filter Having a Narrow Aperture
  • FIG. 22 is a perspective view of another nanowire filter 2200 having a narrow aperture 2208. FIGS. 23 and 24 illustrate a cross-sectional view and a top view of the nanowire filter 2200, respectively. The nanowire filter 2200 may comprise a top plate 2202 and a bottom plate 2204 disposed adjacent the top plate 2202. The top plate 2202 and the bottom plate 2204 may at least partially define a passage 2216 extending through the nanowire filter 2200. In one embodiment, the passage 2216 defines at least one aperture 2208 having a width less than at least one dimension of a set of contaminant particles.
  • The top plate 2202 may further include an entrance 2212 therethrough. The entrance 2212 may define an opening through which a primary flow (designated by the arrows 2201) of the solution may be directed. A conduit 2214 for the solution may be coupled to the entrance 2212 in order to guide a primary flow 2201 of the solution from the source container 12 into the nanowire filter 2200.
  • The nanowire filter 2200, like the nanowire filter 1700, may be formed from a variety of different materials. In one embodiment, the nanowire filter 2200 may comprise a molded plastic. In another embodiment, the nanowire filter 2200 may be formed from stainless steel.
  • In the illustrated embodiment, the top plate 2202 and the bottom plate 2204 are substantially parallel and define a separation distance between them of less than at least one dimension of a set of contaminant particles. The aperture 2208 having a width W may coincide with the entrance 2212 of the nanowire filter 2200 and may have a generally cylindrical shape, as illustrated by the dashed lines of FIG. 23. As described above, the size and configuration of the aperture 2208 and the position of the plates 2202, 2204 may be varied to filter out particular contaminant particles from the solution.
  • In operation, as best illustrated in FIG. 23, the solution containing nanowires may flow outwards from the entrance 2212 between the two plates 2202, 2204. In a manner similar to that described above with reference to FIG. 17, nanowires in the solution may align with the primary flow 2201 through the nanowire filter 2200, while large, low aspect ratio, contaminant particles may be prevented from passing radially outwards between the top and bottom plates 2202, 2204. Thus, the nanowire filter 2200 may build up filtrate at the aperture 2208. As described above with reference to FIG. 17, the nanowire filter 2200 may be occasionally de-clogged to maintain its filtering efficiency.
  • Description of Another Exemplary Nanowire Filter Having a Narrow Aperture
  • FIG. 25 is a perspective view, and FIG. 26 is a side view of another nanowire filter 2500 having a narrow aperture 2508. The nanowire filter 2500 may comprise a first plate 2502 and a second plate 2504 disposed adjacent the first plate 2502. The first and second plates 2502, 2504 may converge, such that a passage 2506 extending through the nanowire filter 2500 may narrow between an entrance 2510 and an exit 2512. In one embodiment, the aperture 2508 may be defined at the exit 2512 and may have a width less than at least one dimension of a set of contaminant particles.
  • The nanowire filter 2500 may be configured and may function similarly to the nanowire filter 1700. In addition, the size and configuration of the components of the nanowire filter 2500 may be varied depending on the desired filtering characteristics.
  • In operation, as large contaminant particles travel along the passage 2506 between the entrance 2510 and the exit 2512, each particle may be captured at that portion of the passage 2506 having a width approximately equal to that particle's diameter. Thus, for example, if the entrance 2510 of the nanowire filter 2500 has a width of 10 μm and the exit 2512 has a width of 1 μm, then 5 μm particles may be captured somewhere near the middle of the passage 2506, and 1.1 μm particles may be captured very close to the exit 2512.
  • As a result, unlike the nanowire filter 1700, which may capture all filtered particles at the entrance 1710, the nanowire filter 2500 may filter out contaminant particles along its entire length. Thus, it may take longer for the nanowire filter 2500 to become clogged.
  • Description of Another Exemplary Nanowire Filter Having a Narrow Aperture
  • FIG. 27 is a perspective view, and FIG. 28 is a side view of another nanowire filter 2700 having a narrow aperture 2708. The nanowire filter 2700 may comprise a first plate 2702, a second plate 2704 disposed adjacent the first plate 2702, and a passage 2706 defined between the two plates 2702, 2704. The passage 2706 may define at least one aperture 2708 approximately halfway through having a width less than at least one dimension of a set of contaminant particles.
  • The nanowire filter 2700 may have an aperture 2708 arranged substantially anywhere along the passage 2706 defined between the two plates 2702, 2704, and the plates 2702, 2704 may have a variety of different shapes and configurations. The nanowire filter 2700 may function generally similarly to the nanowire filter 2500 described above.
  • Description of an Exemplary Nanowire Filter Having Narrow Apertures
  • FIG. 29 is a perspective view, and FIG. 30 is a side view of another nanowire filter 2900 having a plurality of narrow apertures 2908, 2928 and 2938.
  • In one embodiment, the nanowire filter 2900 may comprise a first plate 2902 and a second plate 2904 disposed adjacent the first plate 2902. The two plates 2902, 2904 may at least partially define a passage having an entrance 2910 and an exit 2912, and may at least partially define an aperture 2908 having a width less than at least one dimension of a first set of contaminant particles (e.g., 2 μm).
  • The nanowire filter 2900 may further comprise a third plate 2922 and a fourth plate 2924 disposed adjacent the third plate 2922. The two plates 2922, 2924 may at least partially define a second passage having a second entrance 2926 and a second exit 2927, and may at least partially define a second aperture 2928 having a width less than at least one dimension of a second set of contaminant particles (e.g., 1 μm). As illustrated, the second set of contaminant particles may have at least one dimension smaller than the at least one dimension of the first set of contaminant particles.
  • Finally, the nanowire filter 2900 may comprise a fifth plate 2932 and a sixth plate 2934 disposed adjacent the fifth plate 2932. The two plates 2932, 2934 may at least partially define a third passage having a third entrance 2936 and a third exit 2937, and may at least partially define a third aperture 2938 having a width less than at least one dimension of a third set of contaminant particles (e.g., 0.5 μm). As illustrated, the third set of contaminant particles may have at least one dimension smaller than the at least one dimension of the second set of contaminant particles.
  • In other embodiments, more or fewer apertures of various sizes may be used to filter out particular sets of contaminant particles.
  • In operation, the nanowire filter 2900 may function generally similarly to the nanowire filter 2500 described above. For example, the nanowire filter 2900 may filter out contaminant particles having diameters larger than 2 μm at the first aperture 2908, other contaminant particles having diameters between 1 and 2 μm at the second aperture 2928 and still more contaminant particles having diameters between 0.5 and 1 μm at the third aperture 2938.
  • Description of an Exemplary Method of Filtering a Solution Containing Nanowires
  • FIG. 31 illustrates a flow diagram for a method 3100 of filtering a solution containing nanowires using a micro-structured nanowire filter, according to one embodiment. This method 3100 will be discussed primarily in the context of the nanowire filter 300 incorporated into the nanowire filtering system 10. However, it may be understood that the acts disclosed herein may also be executed using a variety of other micro-structured nanowire filters (e.g., nanowire filters 600, 800, 1100, 1400, and 2000), in accordance with the described method.
  • The method begins at 3102, when a solution containing nanowires is provided. As discussed above, in one embodiment, the solution containing nanowires may comprise the solution within which the nanowires were formed. In other embodiments, the solution within which the nanowires were formed may have already undergone a variety of processing and/or filtering acts.
  • The solution containing nanowires may comprise a polydisperse solution including a variety of particles and nano-structures in addition to the desired nanowires. A variety of different solutions may be filtered in different embodiments, including different percentages of nanowires, different solvents and additives, different shapes and types of low aspect ratio particles, etc. In one embodiment, based on these variable characteristics of the solution, the nanowire filtering system 10 and, in particular, the nanowire filter 300 may be configured differently.
  • At 3104, a primary flow of the solution is generated. The primary flow of the solution may be generated by any of a variety of mechanisms. In one embodiment, a pump 14, as illustrated in FIG. 1, may be used to generate the primary flow of the solution. In another embodiment, the primary flow of the solution may be generated by gravity from the source container 12. In yet another embodiment, a pressure differential (e.g., a source pressurized tank) may be used to generate the primary flow of the solution. A flow rate of this primary flow may also be varied in different embodiments, depending on the configuration of the nanowire filter 300, the source container 12, a pump 14, tubes and conduits connecting these components, a target filtration rate, etc.
  • At 3106, the solution is filtered by directing the primary flow over a micro-structured surface configured to filter the solution. The primary flow may be directed over the micro-structured surface in a variety of ways. In one embodiment, a plurality of tubes, connectors, valves and other fluid conduits may direct the primary flow towards, and subsequently over the micro-structured surface. In one embodiment, the primary flow may be directed over the micro-structured surface, at least in part, by structures (such as the interior walls of the elongate channel 302) within the nanowire filter 300 itself. The flow rate of the primary flow may also be varied in order to control an average height of the solution above the micro-structured surface.
  • The micro-structured surface may comprise any of a variety of microstructures. As illustrated in FIG. 3, the nanowire filter 300 may include a plurality of openings 306. As illustrated in FIG. 8, the nanowire filter 800 may include a micro-structured surface 808 having a plurality of microscopic protrusions and pores. As illustrated in FIG. 14, the nanowire filter 1400 may comprise a plurality of parallel ridges. As described above, micro-structures may include any small structures formed in, on or through a surface that may interfere with a fluid flow. The micro-structures are preferably configured to filter the solution by removing undesirable contaminant particles. Examples of suitable configurations are described above in greater detail with reference to the exemplary micro-structured nanowire filters.
  • In one embodiment, after passing over the micro-structured surface, the retentate 18 emerging from the nanowire filter 300 may comprise a more uniform solution of nanowires. Meanwhile, the filtrate from the solution may flow away from the micro-structured surface and thereby away from the nanowire filter 300. In other embodiment, the filtrate may be captured and held by the micro-structured surface (e.g., as illustrated in FIGS. 8-10).
  • In one embodiment, directing the primary flow over the micro-structured surface may further comprise creating a secondary flow through the plurality of openings 306. As described in greater detail above, as the primary flow travels over the plurality of openings 306, at least a portion of that primary flow may be diverted as a secondary flow through the plurality of openings 306. In one embodiment, the secondary flow through the plurality of openings 306 may include both solvent and low aspect ratio contaminant particles. A flow rate of the primary flow may be selected to be at least 10 times greater than a flow rate of the secondary flow. In another embodiment, a flow rate of the primary flow may be at least 100 times greater than a flow rate of the secondary flow. By increasing the ratio of the primary flow rate to the secondary flow rate, it may become less likely that the nanowires (which may align with a flow of the solution due to their higher aspect ratios) will be diverted through the plurality of openings 306 with the filtrate.
  • In another embodiment, as illustrated in FIGS. 14-16, directing the primary flow over the micro-structured surface may further comprise creating a secondary flow directed away from the primary flow of the solution via a plurality of fluid passages defined by a plurality of parallel ridges. A flow rate of the primary flow may be selected to be at least 10 times greater than a flow rate of the secondary flow. In another embodiment, a flow rate of the primary flow may be at least 100 times greater than a flow rate of the secondary flow.
  • The primary flow of the solution may also be occasionally stopped, and a cleaning solution may be passed over the micro-structured surface. For example, when micro-structures are implemented that capture and hold filtrate, this act of passing the cleaning solution over the micro-structured surface may be desirable to mitigate or prevent the build-up of filtrate and any resulting degradation in filtering efficiency. In one embodiment, the primary flow may be stopped and the cleaning solution applied periodically, according to some time interval. In another embodiment, these acts may be performed after a certain amount of solution has been filtered. In yet another embodiment, these acts may be performed when the performance of the nanowire filter has degraded by a certain amount.
  • In another embodiment, the retentate 18 may be collected, liquid may be added, and the retentate 18 may be recirculated over the micro-structured surface. An exemplary nanowire filtering system 22 for performing such acts is illustrated in FIG. 2. The retentate 18 may be collected in a variety of ways. In one embodiment, a second pump (not illustrated) may generate a flow of the retentate 18 from the nanowire filter 16 back to the source container 12, where it may be collected. At any stage in the recirculation of the retentate 18, replacement solvent may be added. In one embodiment, for example, an inlet (not shown) may combine additional solvent with the retentate 18 before the retentate 18 is collected at the source container 12. In another embodiment, the additional solvent may be added directly to the source container 12 (e.g., at a rate generally corresponding to the loss of filtrate from the solution).
  • The retentate 18 may be recirculated over the micro-structured surface a number of times. In one embodiment, for example, the retentate 18 may be recirculated a pre-determined number of times calibrated to approximately filter the solution to a desired purity. In another embodiment, a purity of the retentate 18 (corresponding, for example, to the percentage weight of nanowires in the retentate 18 or to a percentage concentration of replacement solvent) may be tested periodically or continuously, in order to determine whether or not to continue recirculating the retentate 18 over the micro-structured surface. Once a desired purity is reached, the recirculation of the retentate 18 may be stopped, and the solution collected in the source container 12.
  • Description of Another Exemplary Method of Filtering a Solution Containing Nanowires
  • FIG. 32 illustrates a flow diagram for an alternative method 3200 of filtering a solution containing nanowires using a nanowire filter having a narrow aperture, according to one embodiment. This method 3200 will be discussed in the context of the nanowire filter 1700 incorporated into the nanowire filtering system 10. However, it may be understood that the acts disclosed herein may also be executed using a variety of other nanowire filters having narrow apertures (e.g., nanowire filters 2000, 2200, 2500, 2700, and 2900), in accordance with the described method.
  • The method begins at 3202, when a solution containing nanowires and a first set of contaminant particles is provided. As discussed above, in one embodiment, the solution containing nanowires may comprise the solution within which the nanowires were formed. In other embodiments, the solution within which the nanowires were formed may have already undergone a variety of processing and/or filtering acts.
  • At 3204, a flow of the solution is generated. The flow of the solution may be generated by any of a variety of mechanisms, as described above with respect to act 3104.
  • At 3206, the solution is filtered by directing the flow through a passage defining an aperture having a width less than at least one dimension of the first set of contaminant particles. The flow may be directed through the passage in any of a variety of ways. In one embodiment, a plurality of tubes, connectors, valves and other fluid conduits may direct the flow towards and through the passage.
  • The passage and the aperture defined thereby may comprise any of a variety of shapes and configurations. In one embodiment, as illustrated in FIG. 17, a pair of parallel plates 1702, 1704 may at least partially define a passage having a generally rectangular cross-section. In other embodiments, the passage may define circular, elliptical, triangular or irregularly shaped apertures.
  • In one embodiment, as described in detail above, the nanowire filter 1700 may eventually become clogged by filtrate collecting at the entrance 1710 to the passage. The flow of the solution may therefore occasionally be stopped, a reverse flow of a liquid generated, and the reverse flow directed through the passage in a direction opposite to the flow of the solution. In one embodiment, a cleaning solution (e.g., water) may be periodically passed through the nanowire filter 1700 from the exit 1712 to the entrance 1720 in order to keep the nanowire filter 1700 running efficiently. In another embodiment, a reverse flow of the solution itself may occasionally be generated. For example, the pump 14 may be configured to pump in both a forward and reverse direction and may periodically switch direction in order to drive the solution back and forth through the nanowire filter 1700. A flow rate of the forward flow of the solution, and a flow rate of the reverse flow may be chosen such that there is a net flow of the solution towards the exit 1712 of the passage (i.e., in the forward direction). Thus, potential clogging of the nanowire filter 1700, as described above, may be avoided or at least delayed by the periodic flushing of the entrance 1710.
  • The reverse flow may be generated periodically, according to some time interval, or may be generated after a certain amount of solution has been filtered. In another embodiment, the reverse flow may be generated when the performance of the nanowire filter 1700 has degraded by a certain amount. For example, the reverse flow may be generated based on a reduction in a forward flow rate of the solution.
  • In another embodiment, the nanowire filter 16 may further include a tortuous path filter (not illustrated) located upstream from the aperture 1708. The tortuous path filter may comprise any type of tortuous path filter. In one embodiment, for example, the tortuous path filter may be configured similarly to a beta pure depth filter, manufactured by 3M, with a nominal pore size of 125 μm.
  • The flow of the solution may be further directed to a second passage defining a second aperture having a width less than at least one dimension of a second set of contaminant particles (e.g., 1 μm), and may then be directed to a third passage defining a third aperture having a width less than at least one dimension of a third set of contaminant particles (e.g., 0.5 μm) (as illustrated in FIG. 29). In one embodiment, the flow of the solution may be directed first through the first passage, then through the second passage, and then through the third passage.
  • Various embodiments described above can be combined to provide further embodiments. From the foregoing it will be appreciated that, although specific embodiments have been described herein for purposes of illustration, various modifications may be made without deviating from the spirit and scope of the teachings. Accordingly, the claims are not limited by the disclosed embodiments.

Claims (27)

1. A method, comprising:
providing a solution containing nanowires and a first set of contaminant particles;
generating a flow of the solution; and
filtering the solution by directing the flow through a passage defining an aperture having a width less than at least one dimension of the first set of contaminant particles.
2. The method of claim 1, wherein the passage is formed at least in part by two substantially parallel plates separated by less than the at least one dimension of the first set of contaminant particles.
3. The method of claim 2, wherein at least one of the plates includes an opening therethrough, through which the flow is directed.
4. The method of claim 3, wherein the solution flows radially outward between the pair of plates from the opening.
5. The method of claim 1, further comprising:
stopping the flow of the solution;
generating a reverse flow of a liquid; and
directing the reverse flow through the passage in a direction opposite to the flow of the solution.
6. The method of claim 5, wherein the reverse flow is generated in response to a reduction in a flow rate of the flow of the solution through the passage.
7. The method of claim 5, wherein the reverse flow is generated periodically.
8. The method of claim 1, wherein the solution further contains a second set of contaminant particles, the second set of contaminant particles having at least one dimension smaller than the at least one dimension of the first set of contaminant particles, the method further comprising:
directing the flow through a second passage defining a second aperture having a width less than the at least one dimension of the second set of contaminant particles.
9. The method of claim 8, wherein the solution further contains a third set of contaminant particles, the third set of contaminant particles having at least one dimension smaller than the at least one dimension of the second set of contaminant particles, the method further comprising:
directing the flow through a third passage defining a third aperture having a width less than the at least one dimension of the third set of contaminant particles.
10. The method of claim 9, wherein the flow is directed through the passage, then the second passage, and then the third passage.
11. The method of claim 1, wherein the passage is formed at least in part by two converging plates, and wherein the passage narrows from an entrance of the passage to an exit of the passage.
12. The method of claim 11, wherein the aperture comprises the exit of the passage.
13. The method of claim 1, further comprising:
generating a reverse flow of the solution; and
directing the reverse flow through the passage in a direction opposite to the flow of the solution;
wherein a flow rate of the flow and a flow rate of the reverse flow are chosen such that there is a net flow of the solution towards an exit of the passage.
14. A nanowire filtering system comprising:
a source container for holding a solution containing nanowires and a first set of contaminant particles; and
a nanowire filter passage communicatively coupled to the source container for receiving the solution, the nanowire filter passage defined at least in part by:
a first plate; and
a second plate disposed adjacent the first plate with a minimum separation distance between the first plate and the second plate of less than at least one dimension of the first set of contaminant particles.
15. The nanowire filtering system of claim 14, wherein the first plate defines an opening therethrough, the opening disposed opposite the second plate.
16. The nanowire filtering system of claim 15, wherein the opening is substantially circular.
17. The nanowire filtering system of claim 14, wherein the first plate and the second plate are substantially parallel.
18. The nanowire filtering system of claim 14, wherein the solution further contains a second set of contaminant particles, the second set of contaminant particles having at least one dimension smaller than the at least one dimension of the first set of contaminant particles, the nanowire filtering system further comprising:
a second nanowire filter passage communicatively coupled to the nanowire filter passage, the second nanowire filter passage defined at least in part by:
a third plate; and
a fourth plate disposed adjacent the third plate with a minimum separation distance between the third plate and the fourth plate of less than the at least one dimension of the second set of contaminant particles.
19. The nanowire filtering system of claim 18, wherein the solution further contains a third set of contaminant particles, the third set of contaminant particles having at least one dimension smaller than the at least one dimension of the second set of contaminant particles, the nanowire filtering system further comprising:
a third nanowire filter passage communicatively coupled to the second nanowire filter passage, the third nanowire filter passage defined at least in part by:
a fifth plate; and
a sixth plate disposed adjacent the fifth plate with a minimum separation distance between the fifth plate and the sixth plate of less than the at least one dimension of the third set of contaminant particles.
20. The nanowire filtering system of claim 14, wherein the first plate and the second plate converge, and wherein the nanowire filter passage narrows.
21. The nanowire filtering system of claim 14, further comprising a pump for generating a flow of the solution from the source container through the nanowire filter passage.
22. A method, comprising:
providing a solution containing nanowires;
generating a primary flow of the solution; and
filtering the solution by directing the primary flow over a micro-structured surface configured to filter the solution.
23. The method of claim 22, wherein the micro-structured surface includes a plurality of openings through the surface.
24. The method of claim 22, wherein the plurality of openings have an average diameter of greater than 5 μm.
25. A nanowire filtering system comprising:
a source container for holding a solution containing nanowires; and
a nanowire filter communicatively coupled to the source container for receiving the solution, the nanowire filter including:
a rotatable tube defining a passage for the solution;
a micro-structured surface lining an inside of the rotatable tube;
a substantially helical element adjacent the micro-structured surface and extending at least partially into the passage; and
a drive member adapted to turn the rotatable tube.
26. A nanowire filtering system comprising:
a source container for holding a solution containing nanowires; and
a nanowire filter communicatively coupled to the source container for receiving the solution, the nanowire filter including:
an elongate channel defining a passage for the solution flowing along a long axis, the elongate channel having a lower surface including a plurality of parallel ridges disposed at an angle to the long axis;
wherein the plurality of parallel ridges at least partially define a plurality of openings from the elongate channel.
27. A nanowire filtering system comprising:
a source container for holding a solution containing nanowires; and
a nanowire filter communicatively coupled to the source container for receiving the solution, the nanowire filter including:
an elongate channel defining a passage for the solution; and
a collection chamber defined in part by an outer surface of the elongate channel, the collection chamber communicatively coupled to the elongate channel via a plurality of openings having an average diameter of greater than 5 μm.
US12/105,525 2007-04-20 2008-04-18 Systems and methods for filtering nanowires Abandoned US20090321364A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US12/105,525 US20090321364A1 (en) 2007-04-20 2008-04-18 Systems and methods for filtering nanowires

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US91323107P 2007-04-20 2007-04-20
US12/105,525 US20090321364A1 (en) 2007-04-20 2008-04-18 Systems and methods for filtering nanowires

Publications (1)

Publication Number Publication Date
US20090321364A1 true US20090321364A1 (en) 2009-12-31

Family

ID=39620244

Family Applications (4)

Application Number Title Priority Date Filing Date
US12/106,193 Active 2029-08-13 US8018563B2 (en) 2007-04-20 2008-04-18 Composite transparent conductors and methods of forming the same
US12/105,525 Abandoned US20090321364A1 (en) 2007-04-20 2008-04-18 Systems and methods for filtering nanowires
US13/206,279 Active US10244637B2 (en) 2007-04-20 2011-08-09 Composite transparent conductors and methods of forming the same
US16/283,808 Active US11224130B2 (en) 2007-04-20 2019-02-24 Composite transparent conductors and methods of forming the same

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US12/106,193 Active 2029-08-13 US8018563B2 (en) 2007-04-20 2008-04-18 Composite transparent conductors and methods of forming the same

Family Applications After (2)

Application Number Title Priority Date Filing Date
US13/206,279 Active US10244637B2 (en) 2007-04-20 2011-08-09 Composite transparent conductors and methods of forming the same
US16/283,808 Active US11224130B2 (en) 2007-04-20 2019-02-24 Composite transparent conductors and methods of forming the same

Country Status (9)

Country Link
US (4) US8018563B2 (en)
EP (2) EP2477229B1 (en)
JP (2) JP6098860B2 (en)
KR (1) KR101456838B1 (en)
CN (2) CN103777417B (en)
HK (1) HK1134860A1 (en)
SG (1) SG156218A1 (en)
TW (2) TWI556456B (en)
WO (1) WO2008131304A1 (en)

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100078197A1 (en) * 2008-09-30 2010-04-01 Fujifilm Corporation Metal nanowires, method for producing the same, and transparent conductor
US20130039806A1 (en) * 2011-08-12 2013-02-14 Jeffrey Blinn Nanowire purification methods, compositions, and articles
US8454859B2 (en) 2011-02-28 2013-06-04 Nthdegree Technologies Worldwide Inc Metallic nanofiber ink, substantially transparent conductor, and fabrication method
US20140001418A1 (en) * 2009-08-24 2014-01-02 Cambrios Technologies Corporation Purification of metal nanostructures for improved haze in transparent conductors made from the same
WO2014004712A1 (en) * 2012-06-28 2014-01-03 Nthdegree Technologies Worldwide Inc. Systems and methods for fabrication of nanostructures
US8927855B2 (en) 2011-06-14 2015-01-06 Panasonic Intellectual Property Management Co., Ltd. Solar cell and method for fabricating the same
US9150746B1 (en) 2014-07-31 2015-10-06 C3Nano Inc. Metal nanowire inks for the formation of transparent conductive films with fused networks
US9645454B2 (en) 2013-04-01 2017-05-09 Kabushiki Kaisha Toshiba Transparent conductive film and electric device
US9802397B2 (en) 2014-11-27 2017-10-31 Panasonic Intellectual Property Management Co., Ltd. Structural member for electronic devices
US9920207B2 (en) 2012-06-22 2018-03-20 C3Nano Inc. Metal nanostructured networks and transparent conductive material
US10020807B2 (en) 2013-02-26 2018-07-10 C3Nano Inc. Fused metal nanostructured networks, fusing solutions with reducing agents and methods for forming metal networks
US10029916B2 (en) 2012-06-22 2018-07-24 C3Nano Inc. Metal nanowire networks and transparent conductive material
US10081020B2 (en) 2015-06-12 2018-09-25 Dow Global Technologies Llc Hydrothermal method for manufacturing filtered silver nanowires
US10376898B2 (en) 2015-06-12 2019-08-13 Dow Global Technologies Llc Method for manufacturing high aspect ratio silver nanowires
CN110201440A (en) * 2019-05-23 2019-09-06 中色科技股份有限公司 A kind of plate filter changes paper expansion shaft harmomegathus method
US10564780B2 (en) 2015-08-21 2020-02-18 3M Innovative Properties Company Transparent conductors including metal traces and methods of making same
US11274223B2 (en) 2013-11-22 2022-03-15 C3 Nano, Inc. Transparent conductive coatings based on metal nanowires and polymer binders, solution processing thereof, and patterning approaches
US11343911B1 (en) 2014-04-11 2022-05-24 C3 Nano, Inc. Formable transparent conductive films with metal nanowires
US11515058B2 (en) 2018-05-30 2022-11-29 Hefei Boe Display Technology Co., Ltd. Conductive film, production method thereof, and display apparatus
US11866827B2 (en) 2011-02-28 2024-01-09 Nthdegree Technologies Worldwide Inc Metallic nanofiber ink, substantially transparent conductor, and fabrication method
US11968787B2 (en) 2018-06-26 2024-04-23 C3 Nano, Inc. Metal nanowire networks and transparent conductive material

Families Citing this family (241)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2251389B8 (en) 2005-08-12 2012-09-19 Cambrios Technologies Corporation Nanowire ink
WO2008073143A2 (en) * 2006-06-21 2008-06-19 Cambrios Technologies Corporation Methods of controlling nanostructure formations and shapes
US8018568B2 (en) 2006-10-12 2011-09-13 Cambrios Technologies Corporation Nanowire-based transparent conductors and applications thereof
KR101545219B1 (en) 2006-10-12 2015-08-18 캄브리오스 테크놀로지즈 코포레이션 Nanowire-based transparent conductors and applications thereof
JP6017110B2 (en) 2007-05-29 2016-11-09 ティーピーケイ ホールディング カンパニー リミテッド Particle-containing surfaces and related methods
KR20090023803A (en) * 2007-09-03 2009-03-06 삼성전자주식회사 Liquid crystal display panel and method of manufacturing the same
JP5221088B2 (en) * 2007-09-12 2013-06-26 株式会社クラレ Transparent conductive film and method for producing the same
CN102015922A (en) 2008-02-26 2011-04-13 凯博瑞奥斯技术公司 Methods and compositions for ink jet deposition of conductive features
US10105875B2 (en) 2008-08-21 2018-10-23 Cam Holding Corporation Enhanced surfaces, coatings, and related methods
US20110281070A1 (en) * 2008-08-21 2011-11-17 Innova Dynamics, Inc. Structures with surface-embedded additives and related manufacturing methods
KR20100029633A (en) * 2008-09-08 2010-03-17 삼성전자주식회사 Display apparatus having an active transflective device
JP2010087105A (en) * 2008-09-30 2010-04-15 Fujifilm Corp Solar battery
JP5189449B2 (en) * 2008-09-30 2013-04-24 富士フイルム株式会社 Metal nanowire-containing composition and transparent conductor
US20100101829A1 (en) * 2008-10-24 2010-04-29 Steven Verhaverbeke Magnetic nanowires for tco replacement
KR20100045675A (en) * 2008-10-24 2010-05-04 삼성전자주식회사 Display apparatus
US20110180133A1 (en) * 2008-10-24 2011-07-28 Applied Materials, Inc. Enhanced Silicon-TCO Interface in Thin Film Silicon Solar Cells Using Nickel Nanowires
US20100101830A1 (en) * 2008-10-24 2010-04-29 Applied Materials, Inc. Magnetic nanoparticles for tco replacement
US20100101832A1 (en) * 2008-10-24 2010-04-29 Applied Materials, Inc. Compound magnetic nanowires for tco replacement
WO2010082429A1 (en) 2009-01-16 2010-07-22 コニカミノルタホールディングス株式会社 Method of manufacturing pattern electrode and pattern electrode
JP2012521566A (en) * 2009-03-18 2012-09-13 バイヤー・マテリアルサイエンス・アーゲー Wafer level optical system
JP5584991B2 (en) * 2009-04-02 2014-09-10 コニカミノルタ株式会社 Transparent electrode, method for producing transparent electrode, and organic electroluminescence element
JP5625256B2 (en) * 2009-04-02 2014-11-19 コニカミノルタ株式会社 Transparent electrode, method for producing transparent electrode, and organic electroluminescence element
KR20120102489A (en) * 2009-04-10 2012-09-18 스미또모 가가꾸 가부시키가이샤 Metal complex and composition containing same
WO2010117075A1 (en) * 2009-04-10 2010-10-14 住友化学株式会社 Metal complex and composition containing same
KR101009442B1 (en) * 2009-04-15 2011-01-19 한국과학기술연구원 Method for fabrication of conductive film using conductive frame and conductive film
GB0908300D0 (en) 2009-05-14 2009-06-24 Dupont Teijin Films Us Ltd Polyester films
CN101963681B (en) * 2009-07-24 2012-06-20 清华大学 Polarizing element
SG186652A1 (en) * 2009-08-25 2013-01-30 Cambrios Technologies Corp Methods for controlling metal nanostructures morphology
JP5391932B2 (en) * 2009-08-31 2014-01-15 コニカミノルタ株式会社 Transparent electrode, method for producing transparent electrode, and organic electroluminescence element
TWI420540B (en) 2009-09-14 2013-12-21 Ind Tech Res Inst Conductive material formed using light or thermal energy and method for manufacturing the same, and nano-scale composition
KR101587124B1 (en) * 2009-09-23 2016-01-21 삼성디스플레이 주식회사 Liquid crystal display including the same
US8917377B2 (en) 2009-10-22 2014-12-23 Samsung Electronics Co., Ltd. Active lenses, stereoscopic image display apparatuses including active lenses and methods of operating the same
KR101632315B1 (en) * 2009-10-22 2016-06-21 삼성전자주식회사 Active lens and stereoscopic image display apparatus employing the same
KR101611422B1 (en) * 2009-11-17 2016-04-12 삼성전자주식회사 Composite structure of graphene and nanostructure and method of manufacturing the same
JPWO2011065213A1 (en) * 2009-11-27 2013-04-11 コニカミノルタホールディングス株式会社 Dispersion, transparent electrode, and organic electroluminescence device
CN102834923B (en) * 2009-12-04 2017-05-10 凯姆控股有限公司 Nanostructure-based transparent conductors having increased haze and devices comprising the same
WO2011088323A2 (en) 2010-01-15 2011-07-21 Cambrios Technologies Corporation Low-haze transparent conductors
EP2528855A1 (en) 2010-01-25 2012-12-05 The Board of Regents of the Leland Stanford Junior University Fullerene-doped nanostructures and methods therefor
WO2011091257A1 (en) * 2010-01-25 2011-07-28 The Board Of Trustees Of The Leland Stanford Junior University Joined nanostructures and methods therefor
CN102834472B (en) * 2010-02-05 2015-04-22 凯博瑞奥斯技术公司 Photosensitive ink compositions and transparent conductors and method of using the same
US8518472B2 (en) * 2010-03-04 2013-08-27 Guardian Industries Corp. Large-area transparent conductive coatings including doped carbon nanotubes and nanowire composites, and methods of making the same
JP5718449B2 (en) 2010-03-23 2015-05-13 カンブリオス テクノロジーズ コーポレイション Etching pattern formation of transparent conductor with metal nanowires
EP2580647A1 (en) 2010-06-11 2013-04-17 3M Innovative Properties Company Positional touch sensor with force measurement
TWI416544B (en) * 2010-06-23 2013-11-21 Nat Univ Tsing Hua Composite electrode and mathod for fabricating the same, electrode of a silicon solar cell and silicon solar cell thereof
US10306758B2 (en) * 2010-07-16 2019-05-28 Atmel Corporation Enhanced conductors
FR2962852A1 (en) * 2010-07-19 2012-01-20 Saint Gobain TRANSPARENT ELECTRODE FOR HIGH-PERFORMANCE PHOTOVOLTAIC CELL
KR101119269B1 (en) * 2010-07-26 2012-03-16 삼성전기주식회사 Transparent conductive film for touch panel and manufacturing method the same
EP2598942A4 (en) * 2010-07-30 2014-07-23 Univ Leland Stanford Junior Conductive films
KR101489161B1 (en) * 2010-07-30 2015-02-06 주식회사 잉크테크 Method for manufacturing transparent conductive layer and transparent conductive layer manufactured by the method
KR101658154B1 (en) * 2010-07-30 2016-10-04 엘지디스플레이 주식회사 PHOTOELECTRIC ELEMENT and MANUFACTURING METHOD OF THE SAME
JP5988974B2 (en) 2010-08-07 2016-09-07 ティーピーケイ ホールディング カンパニー リミテッド Device component having surface embedded additive and related manufacturing method
US20120061625A1 (en) * 2010-09-09 2012-03-15 Eckert Karissa L Transparent conductive films, compositions, articles, and methods
US9281415B2 (en) 2010-09-10 2016-03-08 The Board Of Trustees Of The Leland Stanford Junior University Pressure sensing apparatuses and methods
WO2012040637A2 (en) 2010-09-24 2012-03-29 The Regents Of The University Of California Nanowire-polymer composite electrodes
JP5664119B2 (en) * 2010-10-25 2015-02-04 ソニー株式会社 Transparent conductive film, method for manufacturing transparent conductive film, photoelectric conversion device, and electronic device
KR20120044545A (en) * 2010-10-28 2012-05-08 삼성엘이디 주식회사 Semiconductor light emitting device
US20120111614A1 (en) * 2010-11-10 2012-05-10 Free James J Integrated composite structure and electrical circuit utilizing carbon fiber as structural materials and as electric conductor
GB201019212D0 (en) 2010-11-12 2010-12-29 Dupont Teijin Films Us Ltd Polyester film
CN103338882B (en) * 2010-12-07 2017-03-08 罗地亚管理公司 Electrically conductive nanostructures, prepare the method for this nanostructure, include the conductive polymer membrane of this nanostructure and include the electronic installation of this film
US8763525B2 (en) * 2010-12-15 2014-07-01 Carestream Health, Inc. Gravure printing of transparent conductive films containing networks of metal nanoparticles
KR101892198B1 (en) * 2010-12-15 2018-08-27 콘달리그 에이에스 Method for forming uv-curable conductive compositions and a composition thus formed
WO2012083082A1 (en) 2010-12-15 2012-06-21 Sun Chemical Corporation Printable etchant compositions for etching silver nanoware-based transparent, conductive film
EP2465966A1 (en) * 2010-12-15 2012-06-20 Innovation & Infinity Global Corp. Transparent conductive structure and method of making the same
CN102569432B (en) * 2010-12-17 2014-12-10 国家纳米科学中心 Transparent electrode material and preparation method thereof
KR20120071149A (en) * 2010-12-22 2012-07-02 엘지전자 주식회사 Thin film solar cell module and manufacturing method thereof
US20120273455A1 (en) * 2011-04-29 2012-11-01 Clean Energy Labs, Llc Methods for aligned transfer of thin membranes to substrates
US9575598B2 (en) 2010-12-27 2017-02-21 Tsinghua University Inputting fingertip sleeve
JP2012146430A (en) * 2011-01-11 2012-08-02 Innovation & Infinity Global Corp Transparent conductive structure utilizing mixed nanoparticle and method for producing the same
KR101795419B1 (en) 2011-01-26 2017-11-13 주식회사 잉크테크 Method for manufacturing transparent conductive layer and transparent conductive layer manufactured by the method
US20120196053A1 (en) * 2011-01-28 2012-08-02 Coull Richard Methods for creating an electrically conductive transparent structure
WO2012112818A2 (en) * 2011-02-16 2012-08-23 The Regents Of The University Of California Interpenetrating networks of crystalline carbon and nano-scale electroactive materials
CN108762575A (en) * 2011-02-23 2018-11-06 迪睿合电子材料有限公司 Dispersion liquid
US20140008747A1 (en) * 2011-03-29 2014-01-09 Sumitomo Chemical Company, Limited Method of producing organic photoelectric conversion device
WO2012137923A1 (en) * 2011-04-07 2012-10-11 日本写真印刷株式会社 Transfer sheet provided with transparent conductive film mainly composed of graphene, method for manufacturing same, and transparent conductor
CN103460123B (en) * 2011-04-15 2016-02-10 3M创新有限公司 For the transparency electrode of electronic console
CN102208547B (en) * 2011-04-18 2013-11-20 电子科技大学 Substrate for flexible photoelectronic device and preparation method thereof
CN102201549B (en) * 2011-04-18 2013-08-14 电子科技大学 Substrate for flexible light emitting device and fabrication method thereof
CN102195006A (en) * 2011-04-26 2011-09-21 福州大学 Flexible electrode based on AZO/graphene/AZO structure and preparation method thereof
US9175183B2 (en) * 2011-05-23 2015-11-03 Carestream Health, Inc. Transparent conductive films, methods, and articles
US8974900B2 (en) * 2011-05-23 2015-03-10 Carestream Health, Inc. Transparent conductive film with hardcoat layer
TWI427644B (en) * 2011-06-13 2014-02-21 Univ Nat Yunlin Sci & Tech Method for making transparent conductive film
EP2727165A4 (en) * 2011-06-28 2015-08-05 Innova Dynamics Inc Transparent conductors incorporating additives and related manufacturing methods
US9573163B2 (en) * 2011-07-01 2017-02-21 Cam Holding Corporation Anisotropy reduction in coating of conductive films
KR101327069B1 (en) * 2011-07-28 2013-11-07 엘지이노텍 주식회사 Electrode structure and method for producing electrode
EP2748827A4 (en) 2011-08-24 2015-05-27 Innova Dynamics Inc Patterned transparent conductors and related manufacturing methods
JP2014525607A (en) * 2011-08-26 2014-09-29 ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア Transparent conductive oxide electrochromic devices with nanostructures
KR20130030903A (en) * 2011-09-20 2013-03-28 엘지이노텍 주식회사 Solar cell and method of fabricating the same
JP5583097B2 (en) * 2011-09-27 2014-09-03 株式会社東芝 Transparent electrode laminate
JP5646424B2 (en) * 2011-09-27 2014-12-24 株式会社東芝 Transparent electrode laminate
KR101331112B1 (en) * 2011-09-28 2013-11-19 (주)바이오니아 Nanocomposites consisting of carbon nanotube and metal oxide and a process for preparing the same
EP2800994A4 (en) 2011-10-13 2015-10-07 Univ California Solution processed nanoparticle-nanowire composite film as a transparent conductor for opto-electronic devices
EP2766939B1 (en) * 2011-10-13 2019-04-24 Cambrios Film Solutions Corporation Oled with electrode incorporating metal nanowires
EP2788676B1 (en) * 2011-12-05 2016-06-08 Koninklijke Philips N.V. A lighting system
CN104040641A (en) * 2011-12-07 2014-09-10 杜克大学 Synthesis of cupronickel nanowires and their application in transparent conducting films
KR20130070729A (en) * 2011-12-20 2013-06-28 제일모직주식회사 Transparent conductive films including metal nanowires and carbon nanotubes
WO2013095971A1 (en) 2011-12-21 2013-06-27 3M Innovative Properties Company Laser patterning of silver nanowire - based transparent electrically conducting coatings
EP2795628B1 (en) 2011-12-22 2020-02-19 3M Innovative Properties Company Electrically conductive article with high optical transmission
JP2015507560A (en) 2011-12-22 2015-03-12 スリーエム イノベイティブ プロパティズ カンパニー Carbon coated article and method for producing the same
CN103213350B (en) * 2012-01-18 2015-07-08 国家纳米科学中心 Transparent conductive film and preparation method thereof
US9917255B2 (en) * 2012-02-03 2018-03-13 Northwestern University Methods of making composite of graphene oxide and nanostructures
US9524806B2 (en) * 2012-02-07 2016-12-20 Purdue Research Foundation Hybrid transparent conducting materials
GB201203511D0 (en) * 2012-02-29 2012-04-11 Ibm Position sensing apparatus
KR101324281B1 (en) * 2012-03-15 2013-11-01 인하대학교 산학협력단 Transparent conductive films by graphene oxide/silver nanowire having high flexibilities
DE102012102319A1 (en) 2012-03-20 2013-09-26 Rent A Scientist Gmbh Nonlinear nano-wire useful e.g. for producing transparent electrodes e.g. in the fields of display, touch screen and in the field of printed electronics, comprises two linear portions and curved portion arranged between the linear portions
US9490048B2 (en) 2012-03-29 2016-11-08 Cam Holding Corporation Electrical contacts in layered structures
US10483104B2 (en) 2012-03-30 2019-11-19 Kabushiki Kaisha Toshiba Method for producing stacked electrode and method for producing photoelectric conversion device
JP2013211212A (en) * 2012-03-30 2013-10-10 Toshiba Corp Laminated electrode, manufacturing method therefor and photoelectric conversion element
JP5836866B2 (en) * 2012-03-30 2015-12-24 株式会社東芝 Carbon electrode, method for producing the same, and photoelectric conversion element using the same
TW201342102A (en) * 2012-04-06 2013-10-16 Cambrios Technologies Corp System and methods of reducing diffuse reflection of an optical stack
FR2989485B1 (en) * 2012-04-11 2016-02-05 Commissariat Energie Atomique TOUCH SENSOR AND METHOD FOR MANUFACTURING SUCH SENSOR
CN102616033A (en) * 2012-04-13 2012-08-01 中国科学院苏州纳米技术与纳米仿生研究所 Method for quickly manufacturing high-light-transmission conductive patterns
TWI499647B (en) 2012-04-26 2015-09-11 Univ Osaka Transparent conductive ink and production method of transparent conductive pattern
KR101388682B1 (en) * 2012-04-30 2014-04-24 한국교통대학교산학협력단 HYBRID ELECTRODE USING Ag NANOWIRE AND GRAPHENE AND MANUFACTURING METHOD OF THE SAME
TWI450821B (en) * 2012-05-03 2014-09-01 Taiwan Textile Res Inst Transparent electrode with flexibility and method for manufacturing the same
US20130309613A1 (en) * 2012-05-16 2013-11-21 Corning Incorporated Liquid Based Films
US9086523B2 (en) * 2012-05-29 2015-07-21 The Boeing Company Nanotube signal transmission system
US20130323411A1 (en) * 2012-06-01 2013-12-05 Nuovo Film Inc. Low Haze Transparent Conductive Electrodes and Method of Making the Same
US20140014171A1 (en) 2012-06-15 2014-01-16 Purdue Research Foundation High optical transparent two-dimensional electronic conducting system and process for generating same
WO2014015284A1 (en) * 2012-07-20 2014-01-23 The Regents Of The University Of California High efficiency organic light emitting devices
KR101431705B1 (en) * 2012-08-29 2014-08-20 (주)탑나노시스 Nanowire-carbon nano tube hybrid film and method for manufacturing the same
US20140060726A1 (en) * 2012-09-05 2014-03-06 Bluestone Global Tech Limited Methods for transferring graphene films and the like between substrates
EP2900409B1 (en) 2012-09-27 2019-05-22 Rhodia Operations Process for making silver nanostructures and copolymer useful in such process
KR20140046923A (en) * 2012-10-11 2014-04-21 제일모직주식회사 Transparent conductor, composition for manufacturing the same and optical display apparatus comprising the same
KR20140058895A (en) * 2012-11-07 2014-05-15 삼성정밀화학 주식회사 Laminated electrodes including conducting polymers and method of the same
KR101991964B1 (en) * 2012-11-07 2019-06-21 삼성에스디아이 주식회사 Method for Preparing Nanowire having Core-Shell Structure
KR101714286B1 (en) * 2012-11-08 2017-03-08 알프스 덴키 가부시키가이샤 Conductor and method for producing same
KR101486636B1 (en) * 2012-12-06 2015-01-29 세종대학교산학협력단 Light transmittance composite film and method for fabricating the same
CN104838449B (en) 2012-12-07 2018-06-15 3M创新有限公司 Conductive articles
CN103151394A (en) * 2012-12-14 2013-06-12 广东志成冠军集团有限公司 Thin-film solar cell and manufacture method thereof
CN103078036B (en) * 2013-01-17 2015-11-18 北京工业大学 Based on the preparation method of the transparency electrode of graphene film
KR101364531B1 (en) * 2013-01-21 2014-02-19 덕산하이메탈(주) Transparent electrode having nano material layer and method of manufacturing the same
KR20150113050A (en) 2013-01-22 2015-10-07 캄브리오스 테크놀로지즈 코포레이션 Nanostructure transparent conductors having high thermal stability for esd protection
DE102013002855A1 (en) 2013-02-20 2014-08-21 Heraeus Precious Metals Gmbh & Co. Kg Formulations of washed silver wires and PEDOT
CN105283927B (en) 2013-02-20 2018-02-13 国立大学法人东京工业大学 The conductive board of conductive nanometer gauze network and the use network and transparency electrode and preparation method thereof
US9530531B2 (en) * 2013-02-21 2016-12-27 Nanotek Instruments, Inc. Process for producing highly conducting and transparent films from graphene oxide-metal nanowire hybrid materials
US10468152B2 (en) * 2013-02-21 2019-11-05 Global Graphene Group, Inc. Highly conducting and transparent film and process for producing same
JP2014165094A (en) * 2013-02-27 2014-09-08 Nippon Zeon Co Ltd Conductive film, touch panel, electrode for solar cell, and solar cell
US8871296B2 (en) * 2013-03-14 2014-10-28 Nanotek Instruments, Inc. Method for producing conducting and transparent films from combined graphene and conductive nano filaments
US20140262443A1 (en) * 2013-03-14 2014-09-18 Cambrios Technologies Corporation Hybrid patterned nanostructure transparent conductors
US20140272199A1 (en) * 2013-03-14 2014-09-18 Yi-Jun Lin Ultrasonic spray coating of conducting and transparent films from combined graphene and conductive nano filaments
WO2014150577A1 (en) 2013-03-15 2014-09-25 Sinovia Technologies Photoactive transparent conductive films, method of making them and touch sensitive device comprising said films
JP5450863B2 (en) * 2013-03-27 2014-03-26 富士フイルム株式会社 Dispersion for forming conductive layer and transparent conductor
US9368248B2 (en) 2013-04-05 2016-06-14 Nuovo Film, Inc. Transparent conductive electrodes comprising metal nanowires, their structure design, and method of making such structures
US9477128B2 (en) * 2013-04-19 2016-10-25 Board Of Regents, The University Of Texas System Graphene/metal nanowire hybrid transparent conductive films
CN104168009B (en) * 2013-05-17 2018-03-23 光宝电子(广州)有限公司 Light emitting-type touch switch device and light emitting-type touch switch module
CN103242630B (en) * 2013-05-20 2015-05-06 嘉兴学院 PET (polyethylene terephthalate)-based electromagnetic shielding composite and preparation method thereof
JP6319085B2 (en) * 2013-07-08 2018-05-09 東洋紡株式会社 Conductive paste
TW201502653A (en) * 2013-07-10 2015-01-16 Hon Hai Prec Ind Co Ltd Liquid crystal display device
KR20150019820A (en) * 2013-08-16 2015-02-25 일진엘이디(주) Nitride semiconductor light emitting device using nanowires
CN103426991A (en) * 2013-08-23 2013-12-04 厦门大学 Coining method for metal nanowire transparent ohmic electrode
JP6308737B2 (en) 2013-08-26 2018-04-11 デクセリアルズ株式会社 Metal nanowire, dispersion, transparent conductive film, information input device, and electronic device
KR101524069B1 (en) * 2013-09-16 2015-06-10 덕산하이메탈(주) Stacking type transparent electrode having nano material layer
US9663400B2 (en) * 2013-11-08 2017-05-30 Corning Incorporated Scratch-resistant liquid based coatings for glass
KR102065110B1 (en) 2013-11-12 2020-02-11 삼성전자주식회사 Flexible graphene switching devece
US9674947B2 (en) * 2013-12-04 2017-06-06 Samsung Sdi Co., Ltd. Transparent conductor, method for preparing the same, and optical display including the same
KR101514325B1 (en) * 2013-12-10 2015-04-22 국립대학법인 울산과학기술대학교 산학협력단 Method of manufacturing a transparent electrode using electro spinning method
KR102162426B1 (en) * 2013-12-11 2020-10-07 삼성디스플레이 주식회사 Touch panel and manufacturing method thereof
EP3084776B1 (en) * 2013-12-19 2018-06-20 Fraunhofer Gesellschaft zur Förderung der Angewand Transparent nanowire electrode with functional organic layer
EP3907368A1 (en) * 2013-12-24 2021-11-10 View, Inc. Obscuring bus bars in electrochromic glass structures
US10884311B2 (en) 2013-12-24 2021-01-05 View, Inc. Obscuring bus bars in electrochromic glass structures
US11906868B2 (en) 2013-12-24 2024-02-20 View, Inc. Obscuring bus bars in electrochromic glass structures
JP6327870B2 (en) 2014-01-29 2018-05-23 デクセリアルズ株式会社 Metal nanowire, transparent conductive film and manufacturing method thereof, dispersion, information input device, and electronic device
CN107078151B (en) * 2014-01-31 2021-05-25 英属维尔京群岛商天材创新材料科技股份有限公司 Tandem organic photovoltaic devices including metal nanostructured composite layers
CN105900182B (en) * 2014-01-31 2017-10-27 日本瑞翁株式会社 Nesa coating, dye-sensitized solar cell optoelectronic pole and touch panel and dye-sensitized solar cell
JP6441576B2 (en) 2014-02-03 2018-12-19 デクセリアルズ株式会社 Transparent conductive film, method for manufacturing the same, information input device, and electronic device
KR101586902B1 (en) * 2014-04-09 2016-01-19 인트리 주식회사 Light transmitting conductor comprising pattern of nanostructure and method of manufacturing the same
GB2526311B (en) * 2014-05-20 2019-06-19 M Solv Ltd Manufacturing a conductive nanowire layer
CN104009141B (en) * 2014-05-24 2017-10-13 北京工业大学 CNT nano silver wire recombination current extension layer light emitting diode and preparation method thereof
JP2016027464A (en) * 2014-05-30 2016-02-18 株式会社半導体エネルギー研究所 Input device and information processing device
CN104020887A (en) * 2014-05-30 2014-09-03 南昌欧菲光科技有限公司 Touch screen
TWI486969B (en) * 2014-06-11 2015-06-01 Nat Univ Tsing Hua A method for fabricating hybrid conductive materials and a conductive thin film made thereof
KR101536526B1 (en) * 2014-06-17 2015-07-15 한양대학교 산학협력단 Substrate comprising micro/nano structure and method of fabricating the same
US9801287B2 (en) 2014-07-09 2017-10-24 Cam Holding Corporation Electrical contacts in layered structures
EP2977993A1 (en) 2014-07-25 2016-01-27 Heraeus Deutschland GmbH & Co. KG Formulations comprising metal nanowires and pedot
EP3195342A4 (en) * 2014-08-07 2018-04-04 Flinders Partners Pty Ltd. Transparent electrode materials and methods for forming same
US9927667B2 (en) * 2014-08-11 2018-03-27 Sci Engineered Materials, Inc. Display having a transparent conductive oxide layer comprising metal doped zinc oxide applied by sputtering
US11111396B2 (en) * 2014-10-17 2021-09-07 C3 Nano, Inc. Transparent films with control of light hue using nanoscale colorants
CN104505149A (en) * 2014-11-19 2015-04-08 东北师范大学 Laminated transparent electrode and preparation method thereof
CN105304209B (en) * 2014-11-27 2017-02-22 中国科学院金属研究所 Method of manufacturing transparent conductive film on color filter
CN104393194A (en) * 2014-12-10 2015-03-04 京东方科技集团股份有限公司 Flexible electrode, fabrication method of flexible electrode, electronic skin and flexible display device
EP3234951A1 (en) * 2014-12-16 2017-10-25 Solvay SA Transparent conductor comprising metal nanowires, and method for forming the same
CN104503162A (en) * 2014-12-24 2015-04-08 深圳市华星光电技术有限公司 Touch display panel, manufacturing method of touch display panel and combined electrode
KR20160084715A (en) * 2015-01-06 2016-07-14 연세대학교 산학협력단 Transparent electrode and manufacturing method thereof
TWI684999B (en) * 2015-01-14 2020-02-11 日商東洋紡股份有限公司 Conductive film
CN104681645B (en) * 2015-01-23 2016-09-21 华南师范大学 A kind of method preparing composite transparent conductive electrode based on metal grill and metal nanometer line
KR102320382B1 (en) 2015-01-28 2021-11-02 삼성디스플레이 주식회사 Electronic device
KR102347960B1 (en) * 2015-02-03 2022-01-05 삼성전자주식회사 Conductor and method of manufacturing the same
TWI564071B (en) * 2015-02-09 2017-01-01 國立中山大學 A method of photochemically mounting a material particle on a surface of a graphene-semiconductor substrate and a semiconductor structure
KR101881195B1 (en) * 2015-04-01 2018-07-23 성균관대학교산학협력단 Strain sensor using nanocomposite and method for manufacturing thereof
KR101676760B1 (en) * 2015-04-09 2016-11-16 울산과학기술원 Electro-spinning apparatus using electric field and method of manufacturing a transparent electrode using the same
KR101689740B1 (en) * 2015-04-09 2016-12-26 울산과학기술원 Electro-spinning apparatus using drum collector and method of manufacturing a transparent electrode using the same
KR101701603B1 (en) * 2015-04-09 2017-02-02 희성전자 주식회사 Electro-spinning apparatus and method of manufacturing a transparent electrode using the same
KR101701601B1 (en) * 2015-04-09 2017-02-02 희성전자 주식회사 Electro-spinning apparatus using magnetic field and method of manufacturing a transparent electrode using the same
KR102335116B1 (en) * 2015-04-13 2021-12-03 삼성디스플레이 주식회사 Touch screen pannel and manufacturing method thereof
CN107615399A (en) * 2015-04-21 2018-01-19 峡谷科技股份有限公司 Nesa coating
EP3294543B1 (en) * 2015-05-05 2023-10-18 Nano-C, Inc. Carbon nanotube based hybrid films for mechanical reinforcement of multilayered, transparent-conductive, laminar stacks
CN105118836B (en) * 2015-07-29 2019-04-05 京东方科技集团股份有限公司 Array substrate and preparation method thereof with conductive flatness layer
KR20170018718A (en) * 2015-08-10 2017-02-20 삼성전자주식회사 Transparent electrode using amorphous alloy and method for manufacturing the same
CN105093638A (en) * 2015-09-02 2015-11-25 深圳市华科创智技术有限公司 Method for preparing PDLC intelligent film and PDLC intelligent film
EP3159897A1 (en) 2015-10-20 2017-04-26 Solvay SA Composition for forming transparent conductor and transparentconductor made therefrom
CN106611627A (en) * 2015-10-23 2017-05-03 苏州汉纳材料科技有限公司 High-quality carbon nanotube transparent conductive film, preparation method thereof and applications
CN105810305B (en) * 2015-10-23 2017-11-24 苏州汉纳材料科技有限公司 Flexible CNTs/ metal nanometer lines composite transparent conductive film, its preparation method and application
KR102581899B1 (en) * 2015-11-04 2023-09-21 삼성전자주식회사 Transparent electrodes and electronic devices including the same
US10147512B2 (en) 2015-12-09 2018-12-04 C3Nano Inc. Methods for synthesizing silver nanoplates and noble metal coated silver nanoplates and their use in transparent films for control of light hue
US9857930B2 (en) 2015-12-16 2018-01-02 3M Innovative Properties Company Transparent conductive component with interconnect circuit tab comprising cured organic polymeric material
CN105575477B (en) * 2016-01-27 2017-11-28 深圳先进技术研究院 A kind of method for improving nano silver wire flexible transparent conducting film electric conductivity
ES2632247B1 (en) * 2016-03-11 2020-06-03 Garcia Guerrero Jorge Smart fiber optic cable and carbon nanotube fibers
KR102277621B1 (en) * 2016-03-14 2021-07-15 유니티카 가부시끼가이샤 Nanowires and manufacturing method thereof, nanowire dispersion, and transparent conductive film
KR102004025B1 (en) * 2016-03-15 2019-07-25 삼성에스디아이 주식회사 Transparent conductor and display apparatus comprising the same
CN107293591B (en) * 2016-04-11 2020-03-31 华邦电子股份有限公司 Printed circuit, thin film transistor and manufacturing method thereof
US20180004318A1 (en) * 2016-07-01 2018-01-04 Khaled Ahmed Flexible sensor
CN106205876A (en) * 2016-08-31 2016-12-07 福建农林大学 A kind of preparation method of flexible fiber element base transparent conductive material
KR20180044618A (en) * 2016-10-24 2018-05-03 현대자동차주식회사 Transparent electrodes and touch panel comprising the same
CN106526991A (en) * 2016-12-02 2017-03-22 深圳市华星光电技术有限公司 Electrode manufacturing method and liquid crystal display panel
EP3340252A1 (en) 2016-12-22 2018-06-27 Solvay SA Electrode assembly
EP3340253A1 (en) 2016-12-22 2018-06-27 Solvay SA Uv-resistant electrode assembly
CN108630708A (en) 2017-03-15 2018-10-09 京东方科技集团股份有限公司 Electrically-conductive backing plate and preparation method thereof, display device
CN108621753A (en) * 2017-03-24 2018-10-09 凯姆控股有限公司 Planar heating structure
JP6978227B2 (en) * 2017-05-31 2021-12-08 日東電工株式会社 Dimming film
US11491327B2 (en) 2017-09-05 2022-11-08 Seoul National University R&Db Foundation Bio electrode and method of forming the same
JP6782211B2 (en) * 2017-09-08 2020-11-11 株式会社東芝 Transparent electrodes, devices using them, and methods for manufacturing devices
KR101987387B1 (en) * 2017-09-27 2019-06-10 한국화학연구원 Light sintering conductive electrode, and method of manufacturing the same
CN109822996A (en) * 2017-11-23 2019-05-31 宸美(厦门)光电有限公司 Electrocontrolled color change vehicle glass
CN108336191B (en) * 2017-12-08 2019-08-02 华灿光电(苏州)有限公司 A kind of light-emitting diode chip for backlight unit and preparation method
DE102018200659B4 (en) * 2018-01-16 2020-11-05 Continental Automotive Gmbh Multi-layer arrangement for a two-dimensional switchable glazing, glazing and vehicle
CN112088410B (en) * 2018-03-09 2023-08-08 大日本印刷株式会社 Conductive film, sensor, touch panel, and image display device
KR102003427B1 (en) * 2018-03-28 2019-07-24 전북대학교산학협력단 Flexible liquid crystal film using fiber-based foldable transparent electrode and fabrication method thereof
CN110676341B (en) * 2018-07-03 2021-06-25 清华大学 Semiconductor structure, photoelectric device, photodetector and photodetector
CN108598288A (en) * 2018-07-10 2018-09-28 上海大学 A kind of composite multifunction OLED electrodes and preparation method thereof
CN108693597A (en) * 2018-08-01 2018-10-23 京东方科技集团股份有限公司 Light guide structure and its manufacturing method, backlight module, liquid crystal display device
TWI684519B (en) * 2018-08-20 2020-02-11 郭明智 Composite conductive material
KR101996833B1 (en) * 2018-09-21 2019-10-01 현대자동차 주식회사 Transparent electrodes and touch panel comprising the same
CN110083279A (en) * 2019-05-07 2019-08-02 业成科技(成都)有限公司 Transparent conductive material, touch-control structure and touch device
CN110333793B (en) * 2019-05-09 2022-12-09 业成科技(成都)有限公司 Flexible touch control structure
CN110429202A (en) 2019-07-18 2019-11-08 武汉华星光电半导体显示技术有限公司 A kind of flexibility OLED display panel, production method and intelligent wearable device
CN111112862A (en) * 2019-12-16 2020-05-08 顾氏纳米科技(浙江)有限公司 Method for chemically welding silver nanowires
US11947233B2 (en) 2019-12-30 2024-04-02 Sage Electrochromics, Inc. Controlled randomization of electrochromic ablation patterns
CN113650373B (en) * 2020-05-12 2023-09-08 京东方科技集团股份有限公司 Touch layer, preparation method thereof and touch device
CN115699220A (en) * 2020-08-19 2023-02-03 东洋纺株式会社 Transparent conductive film
CN114694877A (en) * 2020-12-28 2022-07-01 乐凯华光印刷科技有限公司 Nano-silver wire composite transparent conductive film
JP2022122545A (en) * 2021-02-10 2022-08-23 日東電工株式会社 transparent conductive film

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040256318A1 (en) * 2001-10-26 2004-12-23 Kazuhiro Iida Separating device, analysis system separation method and method of manufacture of separating device

Family Cites Families (224)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2426318A (en) * 1945-11-15 1947-08-26 Stanolind Oil & Gas Co Inhibiting corrosion
US3164308A (en) 1961-02-28 1965-01-05 Marcovitch Isaac Containers for liquified fuel gas
DE3368092D1 (en) 1982-07-30 1987-01-15 Mishima Paper Co Ltd Conductive film for packaging
FR2537898A1 (en) * 1982-12-21 1984-06-22 Univ Paris METHOD FOR REDUCING METAL COMPOUNDS BY THE POLYOLS, AND METAL POWDERS OBTAINED BY THIS PROCESS
DE3479793D1 (en) 1983-08-01 1989-10-26 Allied Signal Inc Oriented film laminates of polyamides and ethylene vinyl alcohol
US4523976A (en) * 1984-07-02 1985-06-18 Motorola, Inc. Method for forming semiconductor devices
US4780371A (en) 1986-02-24 1988-10-25 International Business Machines Corporation Electrically conductive composition and use thereof
JPS63229061A (en) * 1987-03-18 1988-09-22 テルモ株式会社 Membrane type artificial lung and its production
DE3870012D1 (en) * 1987-04-03 1992-05-21 Ciba Geigy Ag ANTISTATIC AND ELECTRICALLY CONDUCTING POLYMERS AND MOLDS.
JP2547765B2 (en) * 1987-04-07 1996-10-23 株式会社日立製作所 Electromagnetic wave shield structure for electronic devices
US5292784A (en) 1989-05-23 1994-03-08 Ganns Financial Group, Inc., Dba Glare Tech Industries Incorporated Anti-glare coating for reflective-transmissive surfaces and method
US5063125A (en) 1989-12-29 1991-11-05 Xerox Corporation Electrically conductive layer for electrical devices
US5716663A (en) 1990-02-09 1998-02-10 Toranaga Technologies Multilayer printed circuit
CA2038785C (en) 1990-03-27 1998-09-29 Atsushi Oyamatsu Magneto-optical recording medium
US5225244A (en) * 1990-12-17 1993-07-06 Allied-Signal Inc. Polymeric anti-reflection coatings and coated articles
US5165985A (en) * 1991-06-28 1992-11-24 Minnesota Mining And Manufacturing Company Method of making a flexible, transparent film for electrostatic shielding
US5198267A (en) * 1991-09-20 1993-03-30 Allied-Signal Inc. Fluoropolymer blend anti-reflection coatings and coated articles
US5270364A (en) 1991-09-24 1993-12-14 Chomerics, Inc. Corrosion resistant metallic fillers and compositions containing same
WO1993012186A1 (en) * 1991-12-16 1993-06-24 Peter Graham Ibbotson Antiglare and/or reflection formulation
EP0554220A1 (en) 1992-01-29 1993-08-04 Ciba-Geigy Ag Charge-transfer complexes containing ferrocenes, their preparation and their use
EP0583220B1 (en) 1992-07-15 1996-11-20 Ciba-Geigy Ag Coated material, its production and use
EP0588759A1 (en) * 1992-08-20 1994-03-23 Ciba-Geigy Ag Dithiopentacene derivatives, their preparation and their use in charge-transfer complexes
KR100214428B1 (en) * 1993-06-30 1999-08-02 후지무라 마사지카, 아키모토 유미 Infrared ray cutoff material and infrared cutoff powder used for the same
US5415815A (en) 1993-07-14 1995-05-16 Bruno; Art Film for glare reduction
US5460701A (en) 1993-07-27 1995-10-24 Nanophase Technologies Corporation Method of making nanostructured materials
EP0653763A1 (en) 1993-11-17 1995-05-17 SOPHIA SYSTEMS Co., Ltd. Ultraviolet hardenable, solventless conductive polymeric material
US5759230A (en) 1995-11-30 1998-06-02 The United States Of America As Represented By The Secretary Of The Navy Nanostructured metallic powders and films via an alcoholic solvent process
US5897945A (en) 1996-02-26 1999-04-27 President And Fellows Of Harvard College Metal oxide nanorods
JP2984595B2 (en) 1996-03-01 1999-11-29 キヤノン株式会社 Photovoltaic element
IT1282387B1 (en) 1996-04-30 1998-03-20 Videocolor Spa ANTI-STATIC, ANTI-GLARE COATING FOR A REFLECTION-TRANSMISSION SURFACE
US5820957A (en) 1996-05-06 1998-10-13 Minnesota Mining And Manufacturing Company Anti-reflective films and methods
JPH1017325A (en) 1996-07-03 1998-01-20 Sumitomo Metal Mining Co Ltd Indium oxide powder and its production
JPH1046382A (en) 1996-07-26 1998-02-17 Mitsubishi Materials Corp Production of fine metallic fiber and conductive paint using the fiber
US6344271B1 (en) 1998-11-06 2002-02-05 Nanoenergy Corporation Materials and products using nanostructured non-stoichiometric substances
US6202471B1 (en) 1997-10-10 2001-03-20 Nanomaterials Research Corporation Low-cost multilaminate sensors
US5952040A (en) 1996-10-11 1999-09-14 Nanomaterials Research Corporation Passive electronic components from nano-precision engineered materials
US6933331B2 (en) 1998-05-22 2005-08-23 Nanoproducts Corporation Nanotechnology for drug delivery, contrast agents and biomedical implants
US5788738A (en) 1996-09-03 1998-08-04 Nanomaterials Research Corporation Method of producing nanoscale powders by quenching of vapors
US5905000A (en) 1996-09-03 1999-05-18 Nanomaterials Research Corporation Nanostructured ion conducting solid electrolytes
US5851507A (en) 1996-09-03 1998-12-22 Nanomaterials Research Corporation Integrated thermal process for the continuous synthesis of nanoscale powders
US5731119A (en) 1996-11-12 1998-03-24 Eastman Kodak Company Imaging element comprising an electrically conductive layer containing acicular metal oxide particles and a transparent magnetic recording layer
US5719016A (en) 1996-11-12 1998-02-17 Eastman Kodak Company Imaging elements comprising an electrically conductive layer containing acicular metal-containing particles
JP3398587B2 (en) 1996-12-10 2003-04-21 タキロン株式会社 Moldable antistatic resin molded product
US6379745B1 (en) 1997-02-20 2002-04-30 Parelec, Inc. Low temperature method and compositions for producing electrical conductors
US6001163A (en) 1997-04-17 1999-12-14 Sdc Coatings, Inc. Composition for providing an abrasion resistant coating on a substrate
US6045925A (en) 1997-08-05 2000-04-04 Kansas State University Research Foundation Encapsulated nanometer magnetic particles
TW505685B (en) 1997-09-05 2002-10-11 Mitsubishi Materials Corp Transparent conductive film and composition for forming same
US6514453B2 (en) 1997-10-21 2003-02-04 Nanoproducts Corporation Thermal sensors prepared from nanostructureed powders
JP2972702B2 (en) 1998-03-17 1999-11-08 静岡日本電気株式会社 Pen input type portable information terminal
US5867945A (en) 1998-06-04 1999-02-09 Scafidi; Stephen J. Self-cleaning gutter
US6416818B1 (en) 1998-08-17 2002-07-09 Nanophase Technologies Corporation Compositions for forming transparent conductive nanoparticle coatings and process of preparation therefor
US6294401B1 (en) 1998-08-19 2001-09-25 Massachusetts Institute Of Technology Nanoparticle-based electrical, chemical, and mechanical structures and methods of making same
US6241451B1 (en) 1998-09-08 2001-06-05 Knight Manufacturing Corp. Distributor apparatus for spreading materials
US6541539B1 (en) 1998-11-04 2003-04-01 President And Fellows Of Harvard College Hierarchically ordered porous oxides
US6855202B2 (en) 2001-11-30 2005-02-15 The Regents Of The University Of California Shaped nanocrystal particles and methods for making the same
US6274412B1 (en) 1998-12-21 2001-08-14 Parelec, Inc. Material and method for printing high conductivity electrical conductors and other components on thin film transistor arrays
US6265466B1 (en) 1999-02-12 2001-07-24 Eikos, Inc. Electromagnetic shielding composite comprising nanotubes
JP3909791B2 (en) 1999-04-19 2007-04-25 共同印刷株式会社 Transfer method of transparent conductive film
US6342097B1 (en) 1999-04-23 2002-01-29 Sdc Coatings, Inc. Composition for providing an abrasion resistant coating on a substrate with a matched refractive index and controlled tintability
US6881604B2 (en) 1999-05-25 2005-04-19 Forskarpatent I Uppsala Ab Method for manufacturing nanostructured thin film electrodes
WO2001001475A1 (en) 1999-06-30 2001-01-04 The Penn State Research Foundation Electrofluidic assembly of devices and components for micro- and nano-scale integration
EP2239794A3 (en) 1999-07-02 2011-03-23 President and Fellows of Harvard College Nanoscopic wire-based devices, arrays, and methods of their manufacture
JP4358936B2 (en) * 1999-07-15 2009-11-04 株式会社半導体エネルギー研究所 Display device, goggle type display device, method for manufacturing display device, and method for manufacturing goggle type display device
JP3882419B2 (en) 1999-09-20 2007-02-14 旭硝子株式会社 Coating liquid for forming conductive film and use thereof
EP1089113B1 (en) 1999-09-28 2010-03-03 Kyodo Printing Co., Ltd. Transfer body and method using the same
SK286855B6 (en) 1999-10-20 2009-06-05 Ciba Specialty Chemicals Holding Inc. Photoinitiator formulations, method for their preparation and their use
JP2002083518A (en) 1999-11-25 2002-03-22 Sumitomo Metal Mining Co Ltd Transparent conductive substrate, its manufacturing method, display device using this transparent conductive substrate, coating solution for forming transparent conductive layer, and its manufacturing method
NL1016815C2 (en) 1999-12-15 2002-05-14 Ciba Sc Holding Ag Oximester photo initiators.
WO2001044132A1 (en) 1999-12-17 2001-06-21 Asahi Glass Company, Limited Dispersion composition of ultrafine particles, composition for interlayer for laminated glass, interlayer, and laminated glass
JP2001205600A (en) 2000-01-27 2001-07-31 Canon Inc Fine structure and its manufacture
JP2004502554A (en) 2000-03-22 2004-01-29 ユニバーシティー オブ マサチューセッツ Nano cylinder array
FR2807052B1 (en) 2000-04-03 2003-08-15 Clariant France Sa SILICO-ACRYLIC COMPOSITIONS, PROCESS FOR THEIR PREPARATION AND THEIR USE
US6773823B2 (en) 2000-04-07 2004-08-10 University Of New Orleans Research And Technology Foundation, Inc. Sequential synthesis of core-shell nanoparticles using reverse micelles
JP2001291431A (en) 2000-04-10 2001-10-19 Jsr Corp Composition for anisotropic conductive sheet, anisotropic conductive sheet, its production and contact structure using anisotropic conductive sheet
JP4077596B2 (en) 2000-05-31 2008-04-16 中島工業株式会社 Transfer material having low reflective layer and method for producing molded product using the same
US6939576B2 (en) 2000-06-30 2005-09-06 Ngimat Co. Polymer coatings
JP4788852B2 (en) 2000-07-25 2011-10-05 住友金属鉱山株式会社 Transparent conductive substrate, manufacturing method thereof, transparent coating layer forming coating solution used in the manufacturing method, and display device to which transparent conductive substrate is applied
JP4759215B2 (en) 2000-08-15 2011-08-31 ハマヘッド デザイン アンド ディベラップメント、インコーポレイテッド Stomach access port
AU2002220566B8 (en) 2000-09-25 2007-09-13 Chemetall Gmbh Method for pretreating and coating metal surfaces, prior to forming, with a paint-like coating and use of substrates so coated
GB0025016D0 (en) 2000-10-12 2000-11-29 Micromass Ltd Method nad apparatus for mass spectrometry
DE60129524T2 (en) 2000-11-21 2007-11-22 Nissan Chemical Industries, Ltd. Electrically conductive oxide particles and process for their preparation
MXPA03004958A (en) 2000-12-04 2003-09-05 Ciba Sc Holding Ag Onium salts and the use therof as latent acids.
KR100815038B1 (en) 2000-12-12 2008-03-18 코니카 미놀타 홀딩스 가부시키가이샤 Method for Forming Thin Film, Article Having Thin Film, Optical Film, Dielectric Coated Electrode, and Plasma Discharge Processor
US6744425B2 (en) 2000-12-26 2004-06-01 Bridgestone Corporation Transparent electroconductive film
US6444495B1 (en) 2001-01-11 2002-09-03 Honeywell International, Inc. Dielectric films for narrow gap-fill applications
JP3560333B2 (en) 2001-03-08 2004-09-02 独立行政法人 科学技術振興機構 Metal nanowire and method for producing the same
AU2002254367B2 (en) 2001-03-26 2007-12-06 Eikos, Inc. Coatings containing carbon nanotubes
EP1374309A1 (en) 2001-03-30 2004-01-02 The Regents Of The University Of California Methods of fabricating nanostructures and nanowires and devices fabricated therefrom
JP2002322558A (en) 2001-04-25 2002-11-08 Konica Corp Thin film forming method, optical film, polarizing plate and image display device
WO2002096262A2 (en) 2001-05-25 2002-12-05 Northwestern University Non-alloying core shell nanoparticles
US7147687B2 (en) 2001-05-25 2006-12-12 Nanosphere, Inc. Non-alloying core shell nanoparticles
US6697881B2 (en) 2001-05-29 2004-02-24 Hewlett-Packard Development Company, L.P. Method and system for efficient format, read, write, and initial copy processing involving sparse logical units
US20050164515A9 (en) 2001-06-05 2005-07-28 Belcher Angela M. Biological control of nanoparticle nucleation, shape and crystal phase
US20030148380A1 (en) 2001-06-05 2003-08-07 Belcher Angela M. Molecular recognition of materials
CA2450014A1 (en) 2001-06-08 2002-12-19 Eikos, Inc. Nanocomposite dielectrics
US6835591B2 (en) 2001-07-25 2004-12-28 Nantero, Inc. Methods of nanotube films and articles
US6706402B2 (en) 2001-07-25 2004-03-16 Nantero, Inc. Nanotube films and articles
CA2471842A1 (en) 2001-07-27 2003-02-13 Eikos, Inc. Conformal coatings comprising carbon nanotubes
US6934001B2 (en) 2001-08-13 2005-08-23 Sharp Laboratories Of America, Inc. Structure and method for supporting a flexible substrate
KR100438408B1 (en) 2001-08-16 2004-07-02 한국과학기술원 Method for Synthesis of Core-Shell type and Solid Solution type Metallic Alloy Nanoparticles via Transmetalation Reactions and Their Applications
ITTO20020033A1 (en) 2002-01-11 2003-07-11 Fiat Ricerche ELECTRO-LUMINESCENT DEVICE.
WO2003068674A1 (en) 2002-02-15 2003-08-21 Japan Science And Technology Agency Noble-metal nanowire structure and process for producing the same
EP1339082A1 (en) 2002-02-25 2003-08-27 Asahi Glass Company Ltd. Impact-resistant film for flat display panel, and flat display panel
JP4556204B2 (en) 2003-02-06 2010-10-06 三菱マテリアル株式会社 Metal nanofiber-containing composition and use thereof
US6872645B2 (en) 2002-04-02 2005-03-29 Nanosys, Inc. Methods of positioning and/or orienting nanostructures
US6946410B2 (en) 2002-04-05 2005-09-20 E. I. Du Pont De Nemours And Company Method for providing nano-structures of uniform length
JP4130655B2 (en) 2002-05-10 2008-08-06 ザ トラスティーズ オブ コロンビア ユニヴァーシティ イン ザ シティ オブ ニューヨーク Field-assisted deposition method of nanoparticle films
TWI360098B (en) * 2002-05-17 2012-03-11 Semiconductor Energy Lab Display apparatus and driving method thereof
WO2003099709A2 (en) * 2002-05-21 2003-12-04 Eikos, Inc. Method for patterning carbon nanotube coating and carbon nanotube wiring
EP1521811B1 (en) 2002-06-13 2009-12-02 Nanopowders Industries Ltd. A method for the production of conductive and transparent nano-coatings and nano-powder coatings
JP3606855B2 (en) * 2002-06-28 2005-01-05 ドン ウン インターナショナル カンパニー リミテッド Method for producing carbon nanoparticles
JP3842177B2 (en) 2002-07-03 2006-11-08 独立行政法人科学技術振興機構 Noble metal nanotube and method for producing the same
JP2004035962A (en) 2002-07-04 2004-02-05 Toyota Motor Corp Method of producing metal nanotube
JP2004055298A (en) 2002-07-18 2004-02-19 Catalysts & Chem Ind Co Ltd Coating solution for forming transparent conductive film and substrate with transparent conductive coat, and display device
JP4134313B2 (en) 2002-07-24 2008-08-20 Dowaエレクトロニクス株式会社 Method for producing conductive powder
JP4266732B2 (en) 2002-08-30 2009-05-20 キヤノン株式会社 Multilayer diffractive optical element
WO2004035612A2 (en) 2002-09-04 2004-04-29 Board Of Regents, University Of Texas System Composition, method and use of bi-functional biomaterials
EP1540741B1 (en) * 2002-09-05 2014-10-29 Nanosys, Inc. Nanostructure and nanocomposite based compositions and photovoltaic devices
EP2399970A3 (en) 2002-09-05 2012-04-18 Nanosys, Inc. Nanocomposites
US7572393B2 (en) * 2002-09-05 2009-08-11 Nanosys Inc. Organic species that facilitate charge transfer to or from nanostructures
JP4134314B2 (en) 2002-09-13 2008-08-20 Dowaエレクトロニクス株式会社 Method for producing conductive powder
US20050064508A1 (en) 2003-09-22 2005-03-24 Semzyme Peptide mediated synthesis of metallic and magnetic materials
US7067867B2 (en) 2002-09-30 2006-06-27 Nanosys, Inc. Large-area nonenabled macroelectronic substrates and uses therefor
US7051945B2 (en) 2002-09-30 2006-05-30 Nanosys, Inc Applications of nano-enabled large area macroelectronic substrates incorporating nanowires and nanowire composites
US7135728B2 (en) 2002-09-30 2006-11-14 Nanosys, Inc. Large-area nanoenabled macroelectronic substrates and uses therefor
US7560160B2 (en) 2002-11-25 2009-07-14 Materials Modification, Inc. Multifunctional particulate material, fluid, and composition
US6949931B2 (en) 2002-11-26 2005-09-27 Honeywell International Inc. Nanotube sensor
JP3972093B2 (en) 2002-12-04 2007-09-05 独立行政法人物質・材料研究機構 β-Ga2O3 nano whisker and method for producing the same
EP1583715A2 (en) * 2002-12-06 2005-10-12 Eikos, Inc. Optically transparent nanostructured electrical conductors
JP4341005B2 (en) 2002-12-17 2009-10-07 三菱マテリアル株式会社 Metal nanowire-containing composition and electromagnetic wave shielding filter
JP2004196981A (en) 2002-12-19 2004-07-15 Toyobo Co Ltd Resin molded article having conductive surface
US6975067B2 (en) 2002-12-19 2005-12-13 3M Innovative Properties Company Organic electroluminescent device and encapsulation method
KR100502821B1 (en) 2002-12-26 2005-07-22 이호영 Low temperature formation method for emitter tip including copper oxide nanowire or copper nanowire and display device or light source having emitter tip manufactured by using the same method
JP2007112133A (en) 2003-01-30 2007-05-10 Takiron Co Ltd Electroconductive shaped article
US20060257638A1 (en) 2003-01-30 2006-11-16 Glatkowski Paul J Articles with dispersed conductive coatings
JP2004230690A (en) 2003-01-30 2004-08-19 Takiron Co Ltd Antistatic transparent resin sheet
JP4471346B2 (en) 2003-01-31 2010-06-02 タキロン株式会社 Electromagnetic shield
JP2004241228A (en) * 2003-02-05 2004-08-26 Toin Gakuen Plastic film electrode and photoelectric cell using it
JP2004253326A (en) 2003-02-21 2004-09-09 Toyobo Co Ltd Conductive film
JP2004256702A (en) 2003-02-26 2004-09-16 Toyobo Co Ltd Conductive coating
WO2004083290A2 (en) 2003-03-17 2004-09-30 University Of Rochester Core-shell magnetic nanoparticles and nanocomposite materials formed therefrom
US6916842B2 (en) 2003-03-24 2005-07-12 E. I. Du Pont De Nemours And Company Production of 5-methyl-n-(methyl aryl)-2-pyrrolidone, 5-methyl-n-(methyl cycloalkyl)-2-pyrrolidone and 5-methyl-n-alkyl-2-pyrrolidone by reductive amination of levulinic acid esters with cyano compounds
US20070003472A1 (en) * 2003-03-24 2007-01-04 Tolt Zhidan L Electron emitting composite based on regulated nano-structures and a cold electron source using the composite
US6936761B2 (en) 2003-03-29 2005-08-30 Nanosolar, Inc. Transparent electrode, optoelectronic apparatus and devices
CN1442872A (en) * 2003-04-17 2003-09-17 上海交通大学 Multilayer nano transparent conductive membrane and its preparation method
KR101097028B1 (en) 2003-04-28 2011-12-22 타키론 가부시기가이샤 Electromagnetic-shielding light diffusion sheet
TWI250202B (en) 2003-05-13 2006-03-01 Eternal Chemical Co Ltd Process and slurry for chemical mechanical polishing
US7033416B2 (en) 2003-05-22 2006-04-25 The United States Of America As Represented By The Secretary Of The Navy Low temperature synthesis of metallic nanoparticles
WO2004112151A2 (en) * 2003-06-12 2004-12-23 Patterning Technologies Limited Transparent conducting structures and methods of production thereof
CN100395283C (en) 2003-07-04 2008-06-18 日东电工株式会社 Electroconductive cellulose-based film
WO2005017962A2 (en) 2003-08-04 2005-02-24 Nanosys, Inc. System and process for producing nanowire composites and electronic substrates therefrom
EP1661648A4 (en) 2003-09-05 2008-06-11 Mitsubishi Materials Corp Metal microparticle, composition containing the same and process for producing metal microparticle
US7416993B2 (en) 2003-09-08 2008-08-26 Nantero, Inc. Patterned nanowire articles on a substrate and methods of making the same
US7062848B2 (en) 2003-09-18 2006-06-20 Hewlett-Packard Development Company, L.P. Printable compositions having anisometric nanostructures for use in printed electronics
US7067328B2 (en) 2003-09-25 2006-06-27 Nanosys, Inc. Methods, devices and compositions for depositing and orienting nanostructures
JP2005103723A (en) 2003-10-01 2005-04-21 National Institute Of Advanced Industrial & Technology Single crystallization method and device of metal nanowire
US6982206B1 (en) 2003-10-02 2006-01-03 Lsi Logic Corporation Mechanism for improving the structural integrity of low-k films
JP2007517500A (en) 2003-10-15 2007-07-05 ボード・オブ・リージエンツ,ザ・ユニバーシテイ・オブ・テキサス・システム Multifunctional biological materials as scaffolds for electronic, optical, magnetic, semiconductor, and biotechnology applications
KR100570206B1 (en) 2003-10-15 2006-04-12 주식회사 하이닉스반도체 Organic anti-reflective coating polymer, its preparation method and organic anti-reflective coating composition comprising the same
KR100570634B1 (en) 2003-10-16 2006-04-12 한국전자통신연구원 Electromagnetic shielding materials manufactured by filling carbon tube and metallic powder as electrical conductor
JP4374439B2 (en) 2003-10-24 2009-12-02 国立大学法人京都大学 Metal nanotube manufacturing apparatus and metal nanotube manufacturing method
US6896739B1 (en) 2003-12-03 2005-05-24 For Your Ease Only, Inc. Anti-tarnish aqueous treatment
EP1541528A1 (en) * 2003-12-08 2005-06-15 Institut Jozef Stefan Quasi-one-dimensional polymers based on the metal-chalcogen-halogen system
JP2005181392A (en) 2003-12-16 2005-07-07 Canon Inc Optical system
JP4807933B2 (en) * 2003-12-17 2011-11-02 株式会社アルバック Method for forming transparent conductive film and transparent electrode
US20070158642A1 (en) 2003-12-19 2007-07-12 Regents Of The University Of California Active electronic devices with nanowire composite components
TWI243004B (en) 2003-12-31 2005-11-01 Ind Tech Res Inst Method for manufacturing low-temperature highly conductive layer and its structure
US7923109B2 (en) 2004-01-05 2011-04-12 Board Of Regents, The University Of Texas System Inorganic nanowires
US20050165120A1 (en) 2004-01-22 2005-07-28 Ashavani Kumar Process for phase transfer of hydrophobic nanoparticles
JP2005239481A (en) 2004-02-26 2005-09-08 Nagoya Institute Of Technology Metal occlusion carbon nanotube aggregate, its manufacturing method, metal occlusion carbon nanotube, metal nanowire, and its manufacturing method
KR100708644B1 (en) 2004-02-26 2007-04-17 삼성에스디아이 주식회사 TFT, flat panel display device therewith, manufacturing method of TFT, manufacturing method of flat panel display, and manufacturing method of donor sheet
US7381579B2 (en) * 2004-02-26 2008-06-03 Samsung Sdi Co., Ltd. Donor sheet, method of manufacturing the same, method of manufacturing TFT using the donor sheet, and method of manufacturing flat panel display device using the donor sheet
JP2005277405A (en) 2004-02-27 2005-10-06 Takiron Co Ltd Optically transparent antinoise formed body for image display device
JP2005302695A (en) * 2004-03-18 2005-10-27 Toyota Central Res & Dev Lab Inc Photoelectrode and dye-sensitized solar cell equipped with above
JP2005311330A (en) 2004-03-22 2005-11-04 Takiron Co Ltd Radio wave absorber
JP2005281357A (en) 2004-03-29 2005-10-13 Koyo Sangyo Co Ltd Conductive coating
JP2005335054A (en) 2004-04-27 2005-12-08 Japan Science & Technology Agency Metallic nano wire, and its manufacturing method
JP4491776B2 (en) 2004-04-28 2010-06-30 三菱マテリアル株式会社 Method for producing conductive paste, etc.
JP4524745B2 (en) 2004-04-28 2010-08-18 三菱マテリアル株式会社 Metal nanowire-containing conductive material and use thereof
JP2006049843A (en) 2004-06-29 2006-02-16 Takiron Co Ltd Antistatic molding for image display apparatus
WO2006006462A1 (en) 2004-07-08 2006-01-19 Mitsubishi Materials Corporation Method for producing metal fine particle, metal fine particle produced thereby, composition containing same, light absorbing material, and application thereof
US7255796B2 (en) 2004-07-08 2007-08-14 General Electric Company Method of preventing hydrogen sulfide odor generation in an aqueous medium
JP2006035771A (en) 2004-07-29 2006-02-09 Takiron Co Ltd Conductive layer transfer sheet
JP2006035773A (en) 2004-07-29 2006-02-09 Takiron Co Ltd Self-adhesive conductive molding
JP4257429B2 (en) 2004-09-13 2009-04-22 国立大学法人東北大学 Method for producing metal nanowire by controlling atom diffusion and metal nanowire produced by this method
WO2006030762A1 (en) * 2004-09-13 2006-03-23 Sumitomo Metal Mining Co., Ltd. Transparent conductive film, process for producing the same, transparent conductive base material and luminescent device
US20060070559A1 (en) 2004-09-30 2006-04-06 Incredible Technologies, Inc. Unitary currency/credit card unit
JP4372654B2 (en) 2004-09-30 2009-11-25 住友大阪セメント株式会社 Method for producing rod-shaped conductive tin-containing indium oxide fine powder
JP4372653B2 (en) 2004-09-30 2009-11-25 住友大阪セメント株式会社 Method for producing rod-shaped conductive tin-containing indium oxide fine powder
US7270694B2 (en) 2004-10-05 2007-09-18 Xerox Corporation Stabilized silver nanoparticles and their use
US7345307B2 (en) 2004-10-12 2008-03-18 Nanosys, Inc. Fully integrated organic layered processes for making plastic electronics based on conductive polymers and semiconductor nanowires
JP2006111675A (en) 2004-10-13 2006-04-27 Mitsubishi Materials Corp Metal nanorod alignment composition and its application
JP2006128233A (en) * 2004-10-27 2006-05-18 Hitachi Ltd Semiconductor material, field effect transistor, and manufacturing method thereof
JP2006133528A (en) 2004-11-05 2006-05-25 Takiron Co Ltd Anti-static light diffusion sheet
KR100661116B1 (en) * 2004-11-22 2006-12-22 가부시키가이샤후지쿠라 Electrode, photoelectric conversion element, and dye-sensitized solar cell
US7349045B2 (en) 2004-11-24 2008-03-25 Chunghwa Picture Tubes, Ltd. Displacement-designed color filter structure and method of forming the same
EP2202579A3 (en) 2004-12-03 2010-10-27 Tokyo Ohka Kogyo Co., Ltd. Chemically amplified photoresist composition, photoresist laminated product, manufacturing method for photoresist composition, manufacturing method for photoresist pattern, and manufacturing method for connection element
JP4665499B2 (en) 2004-12-10 2011-04-06 三菱マテリアル株式会社 Metal fine particles, production method thereof, composition containing the same, and use thereof
JP2006171336A (en) 2004-12-15 2006-06-29 Takiron Co Ltd Transparent electrode member for image display, and the image display device
TWI246103B (en) * 2004-12-22 2005-12-21 Powertip Technology Corp Carbon nanotube substrate structure and the manufacturing method thereof
US20070153362A1 (en) 2004-12-27 2007-07-05 Regents Of The University Of California Fabric having nanostructured thin-film networks
JP2008076416A (en) 2004-12-27 2008-04-03 Sharp Corp Driving device for display panel, display panel, display device with the same, and driving method for display panel
US20060172282A1 (en) * 2005-01-31 2006-08-03 Naik Rajesh R Peptide templates for nanoparticle synthesis obtained through PCR-driven phage display method
JP4821951B2 (en) 2005-02-23 2011-11-24 三菱マテリアル株式会社 Wire-shaped gold fine particles, production method thereof, containing composition and use
US20100127241A1 (en) * 2005-02-25 2010-05-27 The Regents Of The University Of California Electronic Devices with Carbon Nanotube Components
JP2006239790A (en) 2005-03-01 2006-09-14 Tohoku Univ Metal nano-wire producing method and metal nano-wire
US7489432B2 (en) 2005-03-25 2009-02-10 Ricoh Company, Ltd. Electrochromic display device and display apparatus
JP2006272876A (en) 2005-03-30 2006-10-12 Takiron Co Ltd Electroconductive element
JP2006310353A (en) 2005-04-26 2006-11-09 Takiron Co Ltd Radio wave absorber
US7902639B2 (en) 2005-05-13 2011-03-08 Siluria Technologies, Inc. Printable electric circuits, electronic components and method of forming the same
KR100686796B1 (en) 2005-05-17 2007-02-26 삼성에스디아이 주식회사 Battery case having electromagnetic wave shielding layer and Pouch type secondary battery using it
KR100720101B1 (en) * 2005-08-09 2007-05-18 삼성전자주식회사 Top-emitting Light Emitting Devices Using Nano-structured Multifunctional Ohmic Contact Layer And Method Of Manufacturing Thereof
EP2251389B8 (en) * 2005-08-12 2012-09-19 Cambrios Technologies Corporation Nanowire ink
JP4974332B2 (en) 2005-09-07 2012-07-11 一般財団法人電力中央研究所 Nanostructure and manufacturing method thereof
US7341944B2 (en) 2005-09-15 2008-03-11 Honda Motor Co., Ltd Methods for synthesis of metal nanowires
JP2007091859A (en) 2005-09-28 2007-04-12 Koyo Sangyo Co Ltd Conductive paint
JP2007105822A (en) 2005-10-12 2007-04-26 National Institute For Materials Science Atomic scale metal wire or metal nanocluster, and method for manufacturing same
GB2434692A (en) * 2005-12-29 2007-08-01 Univ Surrey Photovoltaic or electroluminescent devices with active region comprising a composite polymer and carbon nanotube material.
US7507449B2 (en) * 2006-05-30 2009-03-24 Industrial Technology Research Institute Displays with low driving voltage and anisotropic particles
US8372685B2 (en) * 2006-06-12 2013-02-12 Nanosolar, Inc. Bandgap grading in thin-film devices via solid group IIIA particles
US7630041B2 (en) * 2006-06-23 2009-12-08 Tsinghua University Liquid crystal cell assembly for liquid crystal display
WO2008127313A2 (en) * 2006-11-17 2008-10-23 The Regents Of The University Of California Electrically conducting and optically transparent nanowire networks
JP2009057518A (en) * 2007-09-03 2009-03-19 Institute Of Physical & Chemical Research Anisotropic film and manufacturing method of it
CN102365753A (en) * 2008-10-30 2012-02-29 纳米太阳能公司 Hybrid transparent conductive electrodes

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040256318A1 (en) * 2001-10-26 2004-12-23 Kazuhiro Iida Separating device, analysis system separation method and method of manufacture of separating device

Cited By (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100078197A1 (en) * 2008-09-30 2010-04-01 Fujifilm Corporation Metal nanowires, method for producing the same, and transparent conductor
US20140001418A1 (en) * 2009-08-24 2014-01-02 Cambrios Technologies Corporation Purification of metal nanostructures for improved haze in transparent conductors made from the same
US8454859B2 (en) 2011-02-28 2013-06-04 Nthdegree Technologies Worldwide Inc Metallic nanofiber ink, substantially transparent conductor, and fabrication method
US11866827B2 (en) 2011-02-28 2024-01-09 Nthdegree Technologies Worldwide Inc Metallic nanofiber ink, substantially transparent conductor, and fabrication method
US8927855B2 (en) 2011-06-14 2015-01-06 Panasonic Intellectual Property Management Co., Ltd. Solar cell and method for fabricating the same
US20130039806A1 (en) * 2011-08-12 2013-02-14 Jeffrey Blinn Nanowire purification methods, compositions, and articles
US9993875B2 (en) 2012-01-30 2018-06-12 Nthdegree Technologies Worldwide, Inc. Methods for fabrication of nanostructures
US9920207B2 (en) 2012-06-22 2018-03-20 C3Nano Inc. Metal nanostructured networks and transparent conductive material
US10781324B2 (en) 2012-06-22 2020-09-22 C3Nano Inc. Metal nanostructured networks and transparent conductive material
US10029916B2 (en) 2012-06-22 2018-07-24 C3Nano Inc. Metal nanowire networks and transparent conductive material
WO2014004712A1 (en) * 2012-06-28 2014-01-03 Nthdegree Technologies Worldwide Inc. Systems and methods for fabrication of nanostructures
TWI585032B (en) * 2012-06-28 2017-06-01 無限科技全球公司 Methods for fabricating nanostructures
US10020807B2 (en) 2013-02-26 2018-07-10 C3Nano Inc. Fused metal nanostructured networks, fusing solutions with reducing agents and methods for forming metal networks
US9645454B2 (en) 2013-04-01 2017-05-09 Kabushiki Kaisha Toshiba Transparent conductive film and electric device
US11274223B2 (en) 2013-11-22 2022-03-15 C3 Nano, Inc. Transparent conductive coatings based on metal nanowires and polymer binders, solution processing thereof, and patterning approaches
US11343911B1 (en) 2014-04-11 2022-05-24 C3 Nano, Inc. Formable transparent conductive films with metal nanowires
US9183968B1 (en) 2014-07-31 2015-11-10 C3Nano Inc. Metal nanowire inks for the formation of transparent conductive films with fused networks
US11814531B2 (en) 2014-07-31 2023-11-14 C3Nano Inc. Metal nanowire ink for the formation of transparent conductive films with fused networks
US9150746B1 (en) 2014-07-31 2015-10-06 C3Nano Inc. Metal nanowire inks for the formation of transparent conductive films with fused networks
US10100213B2 (en) 2014-07-31 2018-10-16 C3Nano Inc. Metal nanowire inks for the formation of transparent conductive films with fused networks
US10870772B2 (en) 2014-07-31 2020-12-22 C3Nano Inc. Transparent conductive films with fused networks
US9447301B2 (en) 2014-07-31 2016-09-20 C3Nano Inc. Metal nanowire inks for the formation of transparent conductive films with fused networks
US11512215B2 (en) 2014-07-31 2022-11-29 C3 Nano, Inc. Metal nanowire ink and method for forming conductive film
US9802397B2 (en) 2014-11-27 2017-10-31 Panasonic Intellectual Property Management Co., Ltd. Structural member for electronic devices
US10376898B2 (en) 2015-06-12 2019-08-13 Dow Global Technologies Llc Method for manufacturing high aspect ratio silver nanowires
US10081020B2 (en) 2015-06-12 2018-09-25 Dow Global Technologies Llc Hydrothermal method for manufacturing filtered silver nanowires
US10564780B2 (en) 2015-08-21 2020-02-18 3M Innovative Properties Company Transparent conductors including metal traces and methods of making same
US11515058B2 (en) 2018-05-30 2022-11-29 Hefei Boe Display Technology Co., Ltd. Conductive film, production method thereof, and display apparatus
US11968787B2 (en) 2018-06-26 2024-04-23 C3 Nano, Inc. Metal nanowire networks and transparent conductive material
CN110201440A (en) * 2019-05-23 2019-09-06 中色科技股份有限公司 A kind of plate filter changes paper expansion shaft harmomegathus method

Also Published As

Publication number Publication date
CN101689568A (en) 2010-03-31
EP2477229A2 (en) 2012-07-18
US11224130B2 (en) 2022-01-11
JP2010525526A (en) 2010-07-22
US20080259262A1 (en) 2008-10-23
CN101689568B (en) 2014-02-26
TW201543701A (en) 2015-11-16
JP2015135831A (en) 2015-07-27
HK1134860A1 (en) 2010-05-14
EP2477229B1 (en) 2021-06-23
US20120033367A1 (en) 2012-02-09
CN103777417A (en) 2014-05-07
EP2147466A1 (en) 2010-01-27
KR101456838B1 (en) 2014-11-04
TW200924203A (en) 2009-06-01
JP6098860B2 (en) 2017-03-22
US8018563B2 (en) 2011-09-13
SG156218A1 (en) 2009-11-26
CN103777417B (en) 2017-01-18
EP2477229A3 (en) 2012-09-19
JP6181698B2 (en) 2017-08-16
EP2147466B1 (en) 2014-03-12
EP2147466B9 (en) 2014-07-16
US20190191569A1 (en) 2019-06-20
TWI556456B (en) 2016-11-01
WO2008131304A1 (en) 2008-10-30
TWI487125B (en) 2015-06-01
KR20100017128A (en) 2010-02-16
US10244637B2 (en) 2019-03-26

Similar Documents

Publication Publication Date Title
US20090321364A1 (en) Systems and methods for filtering nanowires
US9375790B2 (en) Continuous flow reactor and method for nanoparticle synthesis
Pradel et al. Cross‐flow purification of nanowires
WO2016035856A1 (en) Method for manufacturing metal nanowire having improved length distribution uniformity
TWI710400B (en) Methods of purifying nanostructures
CN103842530B (en) Solid yellow gold
JP5252843B2 (en) Silver ink and its manufacturing method
KR20140005969A (en) Nanowire preparation methods, compositions, and articles
TW201643259A (en) Hydrothermal method for manufacturing filtered silver nanowires
TWI665037B (en) Silver nanowire and manufacturing method thereof and silver nanowire ink
US9050655B2 (en) Continuous reactor and method for manufacturing nanoparticles
US10376898B2 (en) Method for manufacturing high aspect ratio silver nanowires
US20080245184A1 (en) Preparation method of metal nano particle using micro mixer
JP5950476B2 (en) Method for producing fine particles
Shiau et al. The characteristics and mechanisms of Au nanoparticles processed by functional centrifugal procedures
CN114178542A (en) Preparation method of silver nanowires
JP7011835B2 (en) Method for manufacturing high crystalline silver fine particles
CN107442132A (en) A kind of Ag@Cu2O core-shell nanos and preparation method thereof
JP5062506B2 (en) Extraction method of metal fine particles
WO2020045336A1 (en) Silver nano wire aggregate, silver nano wire dispersion liquid, silver nano wire ink, and production method therefor
Hosseini et al. Synthesis of different copper nanostructures by the use of polyol technique
CN108404676A (en) A kind of monodimension nanometer material separating-purifying device and method
CN115415518B (en) Purification system and purification method of metal nanowire
JP2019214782A (en) Alcoholic silver-nanowire fluid dispersion and method for producing the same
US20140234220A1 (en) Method and composition for dispersions of gold nanoparticles

Legal Events

Date Code Title Description
AS Assignment

Owner name: CAMBRIOS TECHNOLOGIES CORPORATION, CALIFORNIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SPAID, MICHAEL A.;HEIDECKER, MANFRED;ALLEMAND, PIERRE-MARC;AND OTHERS;REEL/FRAME:021457/0349;SIGNING DATES FROM 20080711 TO 20080714

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION

AS Assignment

Owner name: CAM HOLDING CORPORATION, VIRGIN ISLANDS, BRITISH

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:CHAMP GREAT INTERNATIONAL CORPORATION;REEL/FRAME:040322/0944

Effective date: 20160909