US20140267107A1 - Photoactive Transparent Conductive Films - Google Patents
Photoactive Transparent Conductive Films Download PDFInfo
- Publication number
- US20140267107A1 US20140267107A1 US14/205,001 US201414205001A US2014267107A1 US 20140267107 A1 US20140267107 A1 US 20140267107A1 US 201414205001 A US201414205001 A US 201414205001A US 2014267107 A1 US2014267107 A1 US 2014267107A1
- Authority
- US
- United States
- Prior art keywords
- layer
- conductive film
- photoresist material
- particles
- composite conductive
- 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
Links
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Images
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- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/80—Constructional details
- H10K50/805—Electrodes
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- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24355—Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
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- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/10—Scrim [e.g., open net or mesh, gauze, loose or open weave or knit, etc.]
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- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/10—Scrim [e.g., open net or mesh, gauze, loose or open weave or knit, etc.]
- Y10T442/184—Nonwoven scrim
- Y10T442/188—Metal or metal-coated fiber-containing scrim
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- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/10—Scrim [e.g., open net or mesh, gauze, loose or open weave or knit, etc.]
- Y10T442/184—Nonwoven scrim
- Y10T442/191—Inorganic fiber-containing scrim
Definitions
- the disclosed embodiments relate generally to transparent conductive films and, more particularly, to composite transparent conductive films that are imparted with the properties of a matrix material employed therein (e.g., photoactivity and/or scratch resistance).
- a matrix material employed therein e.g., photoactivity and/or scratch resistance
- ITO indium oxide
- Most conventional transparent conductive films used in such devices are composed of sputtered metal oxides, the most common of which is tin-doped indium oxide (ITO).
- ITO is inconvenient for several reasons. First, the price of ITO is restrictive in raw material and formation. Second, many applications require patterning of transparent conductive films on length-scales ranging from microns to meters. Optical lithography is currently used to pattern ITO, but this process is time-consuming and expensive, further adding to the cost of ITO-based devices.
- ITO tends to have properties that are unsuitable for certain types of devices. For example, ITO tends to be brittle after formation, making it unsuitable for flexible electronics (e.g., flexible displays, touch screens, and the like). As another example, ITO has a high index of refraction, which means that ITO films have to be coated with expensive anti-reflective coatings for many applications (e.g., display devices).
- Photoactive transparent conductive films Disclosed are photoactive transparent conductive films, methods of fabricating photoactive transparent conductive films, and devices that incorporate photoactive transparent conductive films that overcome the abovementioned limitations in conventional transparent conductive materials, their corresponding methods of manufacture, and their uses.
- the disclosed embodiments provide a composite conductive film.
- the composite conductive film includes a layer of photoresist material and an inorganic mesh comprising a plurality of particles of an inorganic material.
- the plurality of particles of the inorganic mesh is embedded within the layer of photoresist material.
- the layer of photoresist material and the inorganic mesh are arranged to form the composite conductive film.
- the composite conductive film is substantially transparent to optical light.
- composite conductive film is characterized by an optical transparency to optical light in one or more of the following ranges: 60%-100%, 60%-99%, 60%-90%, and greater than 50%.
- optical light refers to light that is in the visible spectrum (e.g., 380 nm to 700 nm).
- optical light refers to light that is in the visible spectrum, the longwave ultraviolet spectrum (e.g., 350 nm to 380 nm), midrange ultraviolet (e.g., 300 nm to 350 nm), shortwave ultraviolet (e.g., 200 nm to 300 nm), and/or infrared spectrum (e.g., 700 nm to 1 mm).
- the longwave ultraviolet spectrum e.g., 350 nm to 380 nm
- midrange ultraviolet e.g., 300 nm to 350 nm
- shortwave ultraviolet e.g., 200 nm to 300 nm
- infrared spectrum e.g., 700 nm to 1 mm
- the respective particles of the plurality of particles of the inorganic mesh comprise a conductive material.
- the conductive material is a metallic material.
- the respective particles of the plurality of particles comprise one of nanowires or nanotubes.
- the respective particles of the plurality of particles are fused to form a substantially continuous network of the conductive material over a continuous portion of the composite conductive film.
- the substantially continuous network of the conductive material is confined to a surface region of the layer of photoresist material, thereby forming a substantially two-dimensional continuous network of the conductive material proximal to a surface of the layer of photoresist material.
- the plurality of particles are metallic particles characterized by a density within the surface region that is above a two-dimensional percolation threshold and less than a bulk percolation threshold of the conductive material suspended throughout the layer of photoresist material.
- the surface region has a thickness and the composite conductive film is characterized by a first surface roughness that is less than a second surface roughness of a stand-alone film consisting of the same thickness of the inorganic mesh. In some embodiments, the first surface roughness is about fifty percent less than the second surface roughness.
- the thickness of the surface region is selected in accordance with a target conductivity value.
- the composite conductive film is bendable to a bending radius of at least 0.5 millimeters (mm).
- the layer of photoresist material comprises a polymer that undergoes cross-linking when exposed to ultraviolet (UV) radiation.
- UV radiation ultraviolet
- a plurality of instances of the composite conductive film is patterned upon a substrate. Each instance of the plurality of instances comprises a region of the composite conductive film. The polymer within each of the regions is substantially cross-linked.
- the disclosed embodiments provide a method of fabricating a composite conductive film.
- the method includes providing, as a matrix, a layer of photoresist material, introducing a plurality of inorganic particles upon a surface of the layer of photoresist material, and embedding at least some of the plurality of inorganic particles into the layer of photoresist material to form an inorganic mesh within the layer of photoresist material, thereby forming the composite conductive film.
- the method further includes, prior to embedding the inorganic particles into the layer of photoresist material, heating the layer of photoresist material from a first temperature (e.g., room temperature) to a second temperature greater than the first temperature.
- a first temperature e.g., room temperature
- the layer of photoresist material is softer at the second temperature than at the first temperature.
- introducing the plurality of inorganic particles upon the surface of the layer of photoresist material includes spraying a nanowire suspension onto the surface of the layer of photoresist material.
- introducing the plurality of inorganic particles upon the surface of the layer of photoresist material includes transferring said plurality of inorganic particles from a stamp in a stamp transfer process.
- embedding the at least some of the plurality of inorganic particles into the layer of photoresist material to form the inorganic mesh within the layer of photoresist material includes pressing the nanowire suspension into the surface of the layer of photoresist material.
- the method further includes patterning the composite conductive film by exposing at least a first region of the composite conductive film to light having a wavelength.
- the photoresist material is cross-linked by exposure to light having the wavelength.
- Patterning the composite conductive film further includes removing at least a second region of the composite conductive film using a chemical developer. The second region of the composite conductive film has not been exposed to light having the wavelength and the photoresist material is soluble in the chemical developer when the photoresist material is in a noncross-linked state.
- the method further includes patterning the composite conductive film by exposing at least a first region of the composite conductive film to light having a wavelength.
- the photoresist material is characterized by cross-linking of polymers and the cross-linking of polymers is broken to form a noncross-linked state by exposure to light having the wavelength.
- Patterning the composite conductive film further includes removing the first region of the composite conductive film using a chemical developer. The photoresist material is soluble in the chemical developer when the photoresist material is in the noncross-linked state.
- the wavelength is in a range of ultraviolet wavelengths.
- the disclosed embodiments provide a touch-sensitive device.
- the touch-sensitive device includes a driving panel, a sensing panel electrically coupled with the driving panel by an electrical characteristic having a value, and a plurality of conductive lines patterned upon a surface of at least one of the driving panel and the sensing panel.
- Each of the plurality of conductive lines includes a layer of photoresist material and an inorganic mesh that includes a plurality of particles embedded within the layer of photoresist material.
- the touch-sensitive device further includes electronic circuitry to detect, using the plurality of conductive lines, a touch input by sensing a change in the value of the electrical characteristic between the driving panel and the sensing panel.
- the layer of photoresist material and the inorganic mesh are arranged to form a composite conductive film.
- FIG. 1 illustrates a perspective view of a device that includes a transparent conductive film, in accordance with some embodiments.
- FIGS. 2A-2C illustrate a method of fabricating (e.g., manufacturing) a photoactive transparent conductive film, in accordance with some embodiments.
- FIGS. 3A-3C illustrate a method of patterning a photoactive transparent conductive film using an abbreviated lithographic process, in accordance with some embodiments.
- FIGS. 4A-4C illustrate various embodiments of a transparent conductive film.
- FIG. 5 illustrates a touch-sensitive device having conductive lines made of a transparent conductive film, in accordance with some embodiments.
- FIGS. 6A-6C illustrate examples of conductive line shapes, in accordance with some embodiments.
- FIGS. 7A-7B are a flowchart illustrating a method of fabricating a composite conductive film, in accordance with some embodiments.
- the embodiments described herein provide photoactive transparent conductive films that may be implemented in connection with many different types of devices, in accordance with various embodiments.
- thin film solar cells displays such as liquid crystal displays (LCDs), organic light-emitting displays, electrophoretic displays, touch screens (e.g., capacitive or resistive), anti-fog devices such as in automotive and aeronautic windshields, flexible flat-panel lighting (e.g., using evaporated and/or printed white organic light-emitting diodes), or photodetectors can be formed and patterned using materials and/or approaches as described herein.
- LCDs liquid crystal displays
- organic light-emitting displays organic light-emitting displays
- electrophoretic displays e.g., electrophoretic displays
- touch screens e.g., capacitive or resistive
- anti-fog devices such as in automotive and aeronautic windshields
- flexible flat-panel lighting e.g., using evaporated and/or printed white organic light-emitting diodes
- Conductivity is to improve the electrical conductivity (hereinafter “conductivity”) of a conventional photoresist. This can be done, for example, by dissolving the conductive particles in a solution along with the photoresist prior to application of the photoresist (e.g., onto a wafer or a chip). Above a so-called “percolation threshold” (e.g., a percolation threshold density of the conductive particles), an electrically coupled network is formed by the conductive particles through which electrical currents can move, resulting in a low sheet resistance.
- percolation threshold e.g., a percolation threshold density of the conductive particles
- An exact cutoff sheet resistance between electrically conducting and electrically insulating films is somewhat subjective and application specific but, generally speaking, a film with a sheet resistance less than 100 ⁇ ⁇ 1 (“ohms per square”) may be considered conducting.
- the embodiments described herein provide photoactive transparent conductive films that are inexpensive and easy to pattern using abbreviated lithographic processes.
- the photoactive transparent conductive film is a composite conductive film that includes at least two parts: (1) a layer of photoresist material (e.g., forming a matrix material) and (2) an inorganic mesh made of a plurality of particles of an inorganic material.
- the plurality of particles of the inorganic mesh is embedded, for example, within the very surface of the layer of photoresist material to form a conductive film that is photoactive by virtue of the matrix material being a photoactive photoresist.
- the composite conductive films described herein are bendable to a bending radius of at least 0.5 millimeters (mm).
- FIG. 1 illustrates a perspective view of a device 100 , in accordance with some embodiments.
- Device 100 includes a substrate 102 that provides underlying support for the device 100 .
- the substrate 102 comprises glass or polyethylene terephthalate (PET).
- Device 100 further includes distinct instances of a transparent conductive film 104 (e.g., transparent conductive films 104 - a and 104 - b ) that are patterned upon the substrate 102 .
- the distinct instances of the transparent conductive film 104 form wires, conductive lines, or other electrical components of the device 100 that are permanently and/or functionally incorporated into the device 100 (e.g., in its end- or product-ready-state).
- the distinct instances of the transparent conductive film 104 form conductive lines for a touch screen device or electrical contacts for a solar cell.
- the transparent conductive film 104 comprises a layer of photoresist material 106 (distinct instances of which are 106 - a and 106 - b ).
- photoresist may be construed to mean any material that undergoes a structural or chemical change when exposed to a predetermined wavelength of light (or light within a predetermined range of wavelengths, such as optical light, ultraviolet light, etc.).
- the layer of photoresist material 106 can comprise either a positive photoresist or a negative photoresist.
- Selectively exposing the photoresist material to light thus enables one to fashion the transparent conductive film 104 according to a complex pattern (e.g., create distinct instances of the transparent conductive film 104 ) with high resolution (e.g., micron resolution or sub-micron resolution).
- a complex pattern e.g., create distinct instances of the transparent conductive film 104
- high resolution e.g., micron resolution or sub-micron resolution
- the photoresist is an electrically insulating material (e.g., the layer of photoresist material 106 has a sheet resistance above 5000 ⁇ ⁇ 1 ).
- the photoresist material comprises an organic material.
- the photoresist is a negative photoresist.
- the layer of photoresist material 106 comprises poly(methyl methacrylate) (PMMA, sometimes called “acrylic glass”).
- PMMA poly(methyl methacrylate)
- Poly(methyl methacrylate) is photosensitive to deep ultraviolet (UV) light (e.g., light having a wavelength in a range of 200-270 nanometers (nm)). Exposure to deep UV light creates chain scissions that de-crosslink chains of PMMA, making the photoresist soluble in certain developers (thus, PMMA is a positive photoresist).
- the layer of photoresist material 106 comprises a photoresist provided by Kayaku Microchem, such as SU-8, which is a negative photoresist that is photosensitive to near ultraviolet light (e.g., light having a wavelength in a range of 300-400 nm).
- a photoresist provided by Kayaku Microchem, such as SU-8, which is a negative photoresist that is photosensitive to near ultraviolet light (e.g., light having a wavelength in a range of 300-400 nm).
- negative resists examples include, but are not limited to, azidelisoprene negative resists, polymethylisopropyl ketone (PMIPK), poly-butene-1-sulfone (PBS), poly-(trifluoroethyl chloroacrylate) TFECA, copolymer-(V-cyano ethyl acrylate-V-amido ethyl acrylate) (COP), poly-(2-methyl pentene-1-sulfone) (PMPS) and the like.
- PMIPK polymethylisopropyl ketone
- PBS poly-butene-1-sulfone
- COP poly-(trifluoroethyl chloroacrylate
- COP copolymer-(V-cyano ethyl acrylate-V-amido ethyl acrylate)
- PMPS poly-(2-methyl pentene-1-sulfone)
- the photoresist is a positive photoresist.
- the positive resist is relatively insoluble. After exposure to the proper light energy, the resist converts to a more soluble state. This reaction is called photosobulization.
- One positive photoresist in accordance with the present disclosure is the phenol-formaldehyde polymer, also called phenol-formaldehyde novolak resin. See, for example, DeForest, Photoresist: Materials and Processes, McGraw-Hill, New York, 1975, which is hereby incorporated by reference herein in its entirety.
- the resist layer is LOR OSA, LOR 5 0.7 A, LOR 1 A, LOR 3 A, or LOR 5 A (MICROCHEM, Newton, Mass.). LOR lift-off resists use polydimethylglutarimide.
- the layer of photoresist material 106 has a controllable thickness (e.g., a thickness that is controlled by process parameters during fabrication).
- the substrate 102 is a chip or a wafer and the layer of photoresist material 106 is applied to the chip or wafer by spin coating the photoresist onto the substrate 102 and subsequently baking the photoresist (e.g., to evaporate solvent).
- the resulting thickness of the layer of photoresist material 106 depends on an angular speed of the spin coater (e.g., as measured in revolutions per minute) as well as the composition and viscosity of the photoresist in dissolved form.
- the thickness of the layer of photoresist material 106 is in a range of 100-500 nm, 400-1000 nm, 900-1500 nm, or 1-10 microns.
- the layer of photoresist material 106 is deposited onto the substrate using another deposition technique such as the Spin-On-Glass method (SOG). More information on SOG can be found, for example, in Nguyen Nhu Toan, Spin - On Glass Materials and Applications in Advanced IC Technologies, 1999, which is hereby incorporated herein by reference in its entirety.
- SOG Spin-On-Glass method
- the layer of photoresist material 106 is deposited onto the substrate using ink-jet printing
- Ink-jet printing is based on the same principles of commercial ink-jet printing.
- the ink-jet nozzle is connected to a reservoir filled with the chemical solution and placed above a computer-controlled x-y stage.
- the target object is placed on the x-y stage and, under computer control, liquid drops (e.g., 50 microns in diameter) are expelled through the nozzle onto a well-defined place on the object. Different nozzles print different spots in parallel.
- a bubble jet with drops as small as a few picoliters, is used to form a layer of the photoresist material 106 .
- a thermal ink jet (Hewlett Packard, Palo Alto, Calif.) is used to form a layer of a deposit material.
- resistors are used to rapidly heat a thin layer of liquid ink.
- a superheated vapor explosion vaporizes a tiny fraction of the ink to form an expanding bubble that ejects a drop of ink from the ink cartridge onto the substrate.
- a piezoelectric ink jet head is used for ink jet printing.
- a piezoelectric ink jet head includes a reservoir with an inlet port and a nozzle at the other end.
- One wall of the reservoir consists of a thin diaphragm with an attached piezoelectric crystal.
- an epoxy delivery system is used to deposit photoresist material 106 .
- An example of an epoxy delivery system is the Ivek Digispense 2000 (Ivek Corporation, North Springfield, Vt.). For more information on jet spraying, see, for example, Madou, Fundamentals of Microfabrication , Second Edition, 2002, pp. 164-167, CRC Press, which is hereby incorporated by reference herein in its entirety.
- the layer of photoresist material 106 is deposited onto the substrate by a screen printing (also known as silk-screening) process.
- a paste or ink is pressed onto portions of the substrate through openings in the emulsion on a screen. See, for example, Lambrechts and Sansen, Biosensors: Microelectrochemical Devices , The Institute of Physics Publishing, Philadelphia, 1992, which is hereby incorporated by reference in its entirety.
- the paste consists of a mixture of the material of interest, an organic binder, and a solvent.
- the organic binder determines the flow properties of the paste.
- the bonding agent provides adhesion of particles to one another and to the substrate.
- the active particles make the ink a conductor, a resistor, or an insulator.
- the lithographic pattern in the screen emulsion is transferred onto portions of the underlying structure by forcing the paste through the mask openings with a squeegee.
- paste is put down on the screen.
- the squeegee lowers and pushes the screen onto the substrate, forcing the paste through openings in the screen during its horizontal motion.
- the screen snaps back, the thick film paste that adheres between the screening frame and the substrate shears, and the printed pattern is formed on the substrate.
- the resolution of the process depends on the openings in the screen and the nature of the paste. With a 325-mesh screen (i.e., 325 wires per inch or 40 ⁇ M holes) and a typical paste, a lateral resolution of 100 ⁇ M can be obtained.
- a shadow mask such as a thin metal foil with openings
- the resolution of this method is inferior (>500 ⁇ M).
- the wet films are allowed to settle for a period of time (e.g., fifteen minutes) to flatten the surface while drying. This removes the solvents from the paste.
- Subsequent firing burns off the organic binder, metallic particles are reduced or oxidized, and glass particles are sintered. Typical temperatures range from 500° C. to 1000° C.
- the thickness of the resulting layer ranges from 10 ⁇ M to 50 ⁇ M.
- One silk-screening setup is the DEK 4265 (Universal Instrument Corporation, Binghamton, N.Y.).
- conductive e.g., Au, Pt, Ag/Pd, etc.
- resistive e.g., RuO 2 , IrO 2
- dielectric e.g., Al 2 O 3 , ZrO 2
- the conductive pastes are based on metal particles, such as Ag, Pd, Au, or Pt, or a mixture of these combined with glass.
- Resistive pastes are based on RuO 2 or Bi 2 Ru 2 O 7 mixed with glass (e.g., 65% PBO, 25% SiO 2 , 10% Bi 2 O 3 ).
- the resistivity is determined by the mixing ratio. Overglaze and dielectric pastes are based on glass mixtures. Different melting temperatures can be achieved by adjusting the paste composition. See, for example, Madou, Fundamentals of Microfabrication , Second Edition, CRC Press, Boca Raton, Fla., 2002, pp. 154-156, which is hereby incorporated by reference herein in its entirety.
- the transparent conductive film 104 is characterized by a low index of refraction (e.g., in a range of 1.5-2), obviating the need for anti-reflective coatings in certain applications (i.e., as compared to ITO when used in the same applications).
- the transparent conductive film 104 includes an inorganic mesh 108 embedded within the layer of photoresist material 106 .
- the inorganic mesh 108 includes a plurality of particles 110 of an inorganic material.
- particle 110 - a and particle 110 - b are respective particles of the plurality of particles.
- the respective particles of the plurality of particles 110 comprise a conductive material.
- the plurality of particles 110 comprises nanowires (as shown in FIG. 1 ), nanotubes, nanospheres, graphene, or a heterogeneous mixture thereof.
- the nanowires are silver (Ag) nanowires.
- the nanowires are metallic nanowires.
- the nanotubes comprise carbon nanotubes (CNT).
- the inorganic mesh 108 comprises a heterogeneous mixture of particles (e.g., a mixture of carbon nanotubes and graphene particles).
- each nanowire or nanotube is characterized by a major axis and one or more minor axes. The major axes are aligned substantially parallel to a surface 114 of the layer of photoresist material 106 .
- a typical width of a nanowire (i.e., along a respective minor axis of the nanowire) will be on the order of tens of nanometers, while the length (i.e., along the major axis of the nanowire) is often on the order of hundreds of nanometers or microns.
- the respective particles of the plurality of particles 110 are fused (e.g., electrically coupled) to form a substantially continuous network of the conductive material over a continuous portion of the composite conductive film (e.g., the respective particles of the plurality of particles 110 are fused to form a substantially continuous network over the conductive material over each instance of the transparent conductive film 104 ).
- the respective particles of the plurality of particles 110 are fused in the sense that they form a continuous network of the conductive material.
- the respective particles of the plurality of particles 110 may still be considered fused if the network includes dead-ends or if there are some particles or groups of particles that are not continuous with the network (e.g., islands of particles).
- the substantially continuous network of the conductive material is confined to a surface region 112 of the layer of photoresist material 106 (e.g., the surface region 112 has a thickness that is thin compared to the thickness of the layer of photoresist material 106 ), thereby forming a substantially two-dimensional continuous network of the conductive material proximal to the surface 114 of the layer of photoresist material 106 .
- the thickness of the surface region 112 is 10, 20, 50, or 100 times thinner than the overall thickness the layer of photoresist material 106 (e.g., the thickness of the surface region 112 is 25 nm while the overall thickness of the layer of photoresist material 106 is 1 micron, giving a ratio of the thickness of the surface region 112 to the overall thickness of the layer of photoresist material 106 of 40).
- some embodiments take advantage of the fact that the conductive transparent film 104 can confer conductivity to surface region 112 using far fewer particles than would be otherwise required to make the photoresist material 106 as a whole conductive through dispersement of the particles throughout the bulk of the photoresist material.
- the plurality of particles 110 is characterized by a density within the surface region 112 that is above the two-dimensional percolation threshold (corresponding to a 2D network of particles) and less than the bulk percolation threshold of the conductive material suspended throughout the layer of photoresist material 106 . This is particularly advantageous in certain circumstances (e.g., when a high-degree of transparency is needed) because, in some embodiments, the respective particles of the plurality of particles 110 comprise metallic particles which tend to absorb and/or scatter optical light.
- the layer of photoresist material 106 is substantially transparent to optical light (e.g., light having a wavelength within a range of 400-700 nm).
- optical light e.g., light having a wavelength within a range of 400-700 nm.
- the term “transparent” may be understood to refer to characteristics relating to the passage of at least some light as measured with respect to light from a light source having a predetermined spectral density.
- the light source is the sun.
- the light source is a light source that emits a narrow band of light (e.g., a laser or light that has passed through a band pass filter).
- the light source is a common household light source, such as an incandescent light bulb or a compact fluorescent lamp (CFL).
- the composite conductive film is characterized by a transparency to optical light in one or more of the following ranges: 60%-100%, 60%-99%, 60%-90%, and greater than 50%.
- the transparent conductive films pass between about 60% and 90% of incident light, as dictated by the application.
- FIGS. 2A-2C illustrate a method 200 of fabricating (e.g., manufacturing) a photoactive transparent conductive film, in accordance with some embodiments.
- the method 200 is described with reference to a nanowire mesh (e.g., inorganic mesh 108 , FIG. 1 ) comprising a plurality of nanowires made of a conductive material. It should be understood, however, that the method 200 can be implemented using a variety of conductive materials, including but not limited to conductive nanowires, nanotubes, nanospheres, graphene, and/or a heterogeneous mixture thereof.
- FIG. 2A illustrates an operation in which a nanowire suspension 202 (e.g., comprising a solution of nanowires suspended in a solvent) is applied to (e.g., drop-cast onto) a surface 204 of a glass transfer block 206 .
- the nanowire suspension 208 is applied, for example, in some embodiments, by mixing nanowires in the solution and coating or depositing the solution on the surface 204 of the glass transfer block 206 .
- the transfer block may comprise a material other than glass.
- the nanowire suspension 202 is dispersed on the surface 204 to form a nanowire mesh 208 .
- the nanowire suspension 202 is dispersed by spin coating the nanowire suspension 202 onto the glass transfer block 206 .
- the nanowire suspension 202 is dispersed by any of the deposition techniques disclosed or referenced herein.
- the nanowire suspension 202 is subsequently dried to evaporate the solvent leaving behind the nanowire mesh 208 .
- the nanowire suspension 202 is dried slowly (e.g., at room temperature) while the glass transfer block 206 is shaken (e.g., moved laterally and/or angularly at a frequency between 1-60 Hz).
- the nanowire mesh 208 is optionally annealed (e.g., by raising the temperature of the glass transfer block 206 to about 180° C. for a period of about 1 hour) to further fuse (e.g., electrically couple) the nanowires and form a substantially continuous network of the conductive material, thereby reducing sheet resistance of the final transparent conductive film.
- FIG. 2C illustrates an operation in which the surface 204 of the glass transfer block 206 is pressed onto a surface 114 of a layer of photoresist material 106 , which is disposed upon an underlying substrate 102 (e.g., glass or PET).
- the surface 204 of the glass transfer block 206 is pressed onto the surface 114 of the layer of photoresist material 106 with a predetermined (e.g., calibrated) pressure (e.g., a pressure of 2.4 ⁇ 10 4 psi).
- the method 200 results in a device 210 that includes a nanowire mesh 108 embedded in the layer of photoresist material 106 , thus forming the transparent conductive film 104 .
- the photoresist is an electrically insulating material (e.g., the layer of photoresist material 106 has a sheet resistance above 5000 ⁇ ⁇ 1 ).
- the composite film becomes conducting (e.g., with a sheet resistance less than 100 ⁇ ⁇ 1 or 200 ⁇ ⁇ 1 ).
- the application of pressure serves to improve electrical conductivity and reduce surface roughness for the resulting device 210 .
- This affects both optical and electrical properties of the device 210 .
- the haze of a transparent conductive film e.g., transparent conductive film 104 , FIG. 1
- the electrical resistance of the transparent conductive film 104 substantially decreases.
- the nanowires in the nanowire suspension 202 have varying diameters (e.g., ranging between 50-100 nm). Accordingly, diameters of nanowires in the nanowire mesh 208 (e.g., prior to embedding the nanowire mesh 208 in the layer of photoresist material 106 ) may vary from one another, with differences upwards of 50 nanometers.
- a conductive transparent film 104 having a surface roughness that is less than 40 nanometers root-mean-square (RMS) is achieved.
- the surface roughness is less than about 20 nanometers RMS. More generally, in some embodiments, the transparent conductive film 104 is characterized by a first surface roughness that is less than a second surface roughness of a stand-alone film (e.g., nanowire mesh 208 ) consisting of the same thickness of the inorganic mesh. For example, the first surface roughness is about fifty percent less than the second surface roughness.
- one or more parameters can be varied to deliberately alter (e.g., tune) the transparency and haze of the device 210 for specific applications (e.g., by varying the thickness of surface region 112 , FIG. 1 or the surface roughness).
- the thickness of the surface region 112 is selected in accordance with a target conductivity value.
- FIGS. 3A-3C illustrate a method 300 of patterning a transparent conductive film 104 using an abbreviated lithographic process, in accordance with some embodiments.
- a photomask 302 is positioned with respect to the conductive surface of a photoactive transparent conductive film 104 (e.g., the photomask 302 is either in contact with the photoactive transparent conductive film 104 or separated from the photoactive transparent conductive film 104 by a predetermined distance).
- the photomask is a stepper reticle and, when in use, one or more optical elements (not shown) are disposed between photomask 302 and the transparent conductive film 104 .
- the photomask 302 is a contact printing photomask and, when in use, photomask 302 is in contact with or very close to (e.g., 1 micron, or 2 microns away from) the transparent conductive film 104 .
- Transparent conductive film 104 is described here as a “photoactive” transparent conductive film because, prior to outset of method 300 , the photoresist included in the transparent conductive film 104 has not been exposed to light to which the photoresist is sensitive.
- the photomask 302 has one or more opaque regions 304 which block light and one or more transparent region 306 which allow light to pass onto the surface 114 of the photoactive transparent conductive film 104 .
- the photomask 302 is illuminated with light 308 having a predetermined wavelength or range of wavelengths.
- the photoactive transparent conductive film 104 is sensitive to light of the predetermined wavelength or range of wavelengths.
- the photomask 302 is illuminated in this manner with a predetermined intensity for a predetermined amount of time in accordance with process requirements and recipes.
- the predetermined wavelength is in a range of ultraviolet (UV) wavelengths (e.g., 200-270 nm for deep-UV, or 300-400 nm for near-UV).
- the predetermined wavelength is distinct from (e.g., outside a range of) wavelengths for which the transparent conductive film 104 is intended to be transparent.
- the transparent regions 306 result in the exposure of selected regions 310 (e.g., regions 310 - a , 310 - b , 310 - c , and 310 - d ) of the photoactive transparent conductive film 104 to light having the predetermined wavelength.
- the photoresist material is a positive photoresist.
- the positive resist is relatively insoluble. After exposure to the proper light energy, the resist converts to a more soluble state. This reaction is called photosobulization.
- the photoresist material is a positive photoresist that is degraded by exposure of light having the predetermined wavelength.
- the photoresist prior to exposure to light, is characterized by cross-linking of polymers. The cross-linking of polymers is broken in the first region (e.g., scissions are formed and the polymers are de-crosslinked) to form a noncross-linked state by exposure to light having the predetermined wavelength.
- FIG. 3B illustrates the result of the method 300 when a positive photoresist is used.
- the selected regions 310 are removed upon application of a developer to form, for example, trenches 312 (e.g., trenches 312 - a , 312 - b , 312 - c , and 312 - d ), while the unexposed regions are not removed.
- trenches 312 e.g., trenches 312 - a , 312 - b , 312 - c , and 312 - d
- the photoresist is a negative photoresist in which polymers in the resist form a cross-linked material that is etch resistant upon exposure to light.
- the photoresist is a negative photoresist comprising a polymer and exposing the selected regions 310 of the photoactive transparent conductive film 104 to light having the predetermined wavelength results in crosslinking of the polymer.
- the selected regions 310 remain upon application of a developer, while unexposed regions are removed.
- FIG. 3C illustrates the result of the method 300 when a negative photoresist is used.
- the selected regions 310 remain (i.e., are not removed) upon application of a developer to form, for example, pillars 314 (e.g., pillars 314 - a , 314 - b , 314 - c , and 314 - d ), while the unexposed regions are removed.
- the cross-linking of the polymer is driven by thermal processes activated by the UV radiation (e.g., the UV radiation locally increases the temperature of the photoresist, which drives the cross-linking process).
- the transparent conductive film 104 does not include a photoresist, but is nonetheless a layer of a material that undergoes cross-linking when exposed to elevated temperature (e.g., thermal cross-linking). Such materials can be beneficial when mechanical robustness is desired (e.g., without the need for patterning).
- the transparent conductive film 104 includes an electron-beam (e-beam) sensitive resist in lieu of a photoresist (however, PMMA is considered both an e-beam resist and a photoresist sensitive to UV light).
- the transparent conductive film 104 is deposited using monomers or oligomers in solution, and a catalyst is added to the solution to facilitate cross-linking (e.g., prior to depositing the solution onto the substrate, drying the solution to form the layer, and embedding the wires into the surface of the layer).
- some embodiments utilize a mechanical approach to removing such regions.
- Such mechanical approaches can include an applied force or blasting with a fluid such as air or water.
- FIGS. 4A-4C illustrate alternate embodiments of a transparent conductive film.
- the layers of photoresist material 106 shown in FIGS. 4A-4C are disposed upon a substrate (e.g., substrate 102 , FIG. 1 ), although the substrate is not shown here for visual clarity.
- the transparent conductive films illustrated in FIG. 4A-4C are intended to be only exemplary and are not intended to limit the claims that follow.
- FIG. 4A illustrates a transparent conductive film 402 .
- the transparent conductive film 402 is a composite conductive film that includes a layer of photoresist material 106 and an inorganic mesh comprising a plurality of nanospheres 404 (e.g., metallic nanospheres).
- the inorganic mesh is confined to a surface region 406 of the transparent conductive film 402 , which is advantageous in that fewer nanospheres 404 are required to achieve a suitable sheet resistance, resulting in improved transparency characteristics.
- FIG. 4B illustrates a transparent conductive film 408 .
- the transparent conductive film 408 is a composite conductive film that includes a layer of photoresist material 106 and an inorganic mesh comprising a plurality of nanospheres 404 (e.g., metallic nanospheres).
- the inorganic mesh is not confined to a surface region of the transparent conductive film 408 and is instead suspended throughout the bulk of the layer of photoresist material 106 .
- the transparent conductive film 408 can be used when a high degree of transparency is not needed (or a hazy film is desired) or when a high degree of conductivity is not needed.
- FIG. 4C illustrates a transparent conductive film 410 .
- FIG. 4C is analogous to FIG. 4B but for the fact that transparent conductive film 410 includes an inorganic mesh comprising a plurality of nanowires 110 suspended throughout the bulk of the layer of photoresist material 106 .
- FIG. 5 illustrates a touch-sensitive device 500 having conductive lines of a transparent conductive film, in accordance with some embodiments.
- FIG. 5 illustrates several layers, panels, and/or components of the touch-sensitive device 500 . For visual clarity, these layers are illustrated as separated in the vertical direction. More typically, these layers will be connected to one another or, alternatively, coupled with one another (e.g., with spacer layers in between).
- the touch-sensitive device 500 includes a driving panel 502 which has a plurality of conductive driving lines 504 patterned upon a surface of the driving panel 502 (e.g., a top surface).
- Each of the plurality of conducting driving lines 504 can have any of the properties or features of the distinct instances of the transparent conductive film 104 described with reference to any of the other figures (e.g., FIG. 1 ).
- the device 100 illustrated in FIG. 1 is a partial cross-section of driving panel 502 .
- each of the plurality of driving lines 504 comprises a layer of photoresist material and an inorganic mesh that includes a plurality of particles embedded within the layer of photoresist material.
- the touch-sensitive device 500 further includes a sensing panel 506 electrically coupled with the driving panel 502 by an electrical characteristic (e.g., capacitance, resistance) having a value.
- the sensing panel 506 includes a plurality of sensing lines 508 disposed upon a surface of the sensing panel.
- the sensing lines 508 are analogous to the driving lines 504 , except that the sensing lines 508 run in a different direction (e.g., substantially perpendicularly) to the driving lines 504 such that the two sets of lines form a grid.
- the touch-sensitive device 500 further includes electronic circuitry to detect, using the plurality of driving lines 504 and the plurality of sensing lines 508 , a touch input by sensing a change in the value of the electrical characteristic (e.g., capacitance or resistance) between the driving panel 502 and the sensing panel 506 .
- the electrical characteristic e.g., capacitance or resistance
- the touch-sensitive device 500 includes a display 510 (e.g., an LCD display).
- the display 510 produces light that is shone upwards through the driving panel 502 and sensing panel 506 .
- the conductive lines are straight lines.
- the conductive lines e.g., driving lines 504 or sensing lines 508
- the conductive lines can have an arbitrary shape.
- FIGS. 6A-6C illustrate examples of conductive line shapes, in accordance with some embodiments.
- FIG. 6A illustrates conductive lines 602 comprising a plurality of rectangles 604 separated by straight segments 606 of the transparent conductive film.
- FIG. 6B illustrates conductive lines 608 comprising a plurality of diamonds 610 separated by straight segments 606 of the transparent conductive film.
- FIG. 6C illustrates conductive lines 612 comprising a plurality of circles 614 separated by straight segments 606 of the transparent conductive film.
- FIGS. 7A-7B are a flowchart illustrating a method 700 of fabricating a composite conductive film.
- the method 700 can be used to fabricate the composite conductive film shown, for example, in FIG. 1 , and/or the conductive driving lines/conductive sensing lines shown in FIG. 5 and FIG. 6 .
- the method 700 includes providing ( 702 ), as a matrix, a layer of photoresist material.
- the layer of photoresist material is spin-coated onto a glass substrate (e.g., substrate 102 , FIG. 1 ).
- the photoresist material is an electrically insulating material (e.g., with a sheet resistance above 5000 ⁇ ⁇ 1 ).
- the method 700 further includes introducing ( 704 ) a plurality of inorganic particles upon a surface (e.g., a top surface) of the layer of photoresist material.
- the plurality of inorganic particles comprise one of nanowires (as shown in FIG. 1 ), nanotubes, nanospheres, graphene, or a combination (e.g., heterogeneous mixture) thereof.
- introducing the plurality of inorganic particles upon the surface of the layer of photoresist material comprises spraying ( 706 ) a nanowire suspension onto the surface of the layer of photoresist material.
- introducing the plurality of inorganic particles upon the surface of the layer of photoresist material comprises transferring ( 708 ) said plurality of inorganic particles from a stamp (e.g., glass transfer block 206 , FIG. 2 ) in a stamp transfer process (e.g., by the process shown in FIGS. 2A-2C ).
- the method 700 includes annealing ( 710 ) the plurality of inorganic particles on the stamp to form a substantially continuous conductive network of the inorganic particles.
- the stamp can be raised to an elevated temperature of 180° C. for a predetermined period of time (e.g., 1 hour) to anneal the plurality of particles.
- the method 700 includes heating ( 712 ) the layer of photoresist material from a first temperature (e.g., room temperature, or 25° C.) to a second temperature (e.g., 90° C.) greater than the first temperature.
- a first temperature e.g., room temperature, or 25° C.
- a second temperature e.g., 90° C.
- the layer of photoresist material is softer at the second temperature than at the first temperature, thereby facilitating the embedding operation 714 ).
- the method 700 includes embedding ( 714 ) at least some of the plurality of inorganic particles into the layer of photoresist material to form an inorganic mesh within the layer of photoresist material, thereby forming the composite conductive film.
- embedding the at least some of the plurality of inorganic particles into the layer of photoresist material to form the inorganic mesh within the layer of photoresist material comprises pressing ( 716 ) the nanowire suspension into the surface of the layer of photoresist material (e.g., by pressing the stamp into the surface of the layer of photoresist material with a pressure of 2.4 ⁇ 10 4 psi).
- the method 700 includes patterning ( 718 ) the composite conductive film by exposing ( 720 ) at least a first region of the composite conductive film to light having a wavelength.
- the photoresist material is cross-linked by exposure to light having the wavelength (e.g., the photoresist material is a negative photoresist).
- patterning the composite conductive film further comprises removing ( 722 ) at least a second region of the composite conductive film using a chemical developer. The second region of the composite conductive film has not been exposed to light having the wavelength and the photoresist material is soluble in the chemical developer when the photoresist material is in a noncross-linked state.
- the wavelength is in a range of ultraviolet wavelengths (e.g., in a range of 200-270 nm for deep-UV or 300-400 for near-UV).
- the method further includes patterning ( 726 ) the composite conductive film by exposing ( 728 ) at least a first region of the composite conductive film to light having a wavelength.
- the photoresist material is characterized by cross-linking of polymers and said cross-linking of polymers is broken to form a noncross-linked state by exposure to light having the wavelength (e.g., the photoresist material is a positive photoresist).
- patterning the composite conductive film further comprises removing ( 730 ) the first region of the composite conductive film using a chemical developer.
- the photoresist material is soluble in the chemical developer when the photoresist material is in the noncross-linked state.
- the wavelength is in a range of ultraviolet wavelengths (e.g., in a range of 200-270 nm for deep-UV or 300-400 for near-UV).
- first, second, etc. may be used herein to describe various elements, these elements should not be limited by these terms. These terms are only used to distinguish one element from another.
- a first instance of a layer of material could be termed a second instance of the layer of material, and, similarly, a second first instance of the layer of material could be termed a first instance of the layer of material, without changing the meaning of the description, so long as all occurrences of the “first instance of the layer of material” are renamed consistently and all occurrences of the “second instance of the layer of material” are renamed consistently.
- the first instance of the layer of material and the second first instance of the layer of material are both instances of the layer of material, but they are not the same instance of the layer of material.
- the term “if” may be construed to mean “when” or “upon” or “in response to determining” or “in accordance with a determination” or “in response to detecting,” that a stated condition precedent is true, depending on the context.
- the phrase “if it is determined [that a stated condition precedent is true]” or “if [a stated condition precedent is true]” or “when [a stated condition precedent is true]” may be construed to mean “upon determining” or “upon a determination that” or “in response to determining” or “in accordance with a determination” or “upon detecting” or “in response to detecting” that the stated condition precedent is true, depending on the context.
Abstract
A composite conductive film is provided that includes a layer of photoresist material and an inorganic mesh comprising a plurality of particles of an inorganic material. The plurality of particles of the inorganic mesh is embedded within the layer of photoresist material and the layer of photoresist material and the inorganic mesh are arranged to form the composite conductive film. Furthermore, a method of making a composite conductive film is provided that includes providing, as a matrix, a layer of photoresist material, introducing a plurality of inorganic particles upon a surface of the layer of photoresist material and embedding at least some of the plurality of inorganic particles into the layer of photoresist material to form an inorganic mesh within the layer of photoresist material, thereby forming the composite conductive film.
Description
- This application claims priority to U.S. Provisional Patent Application No. 61/792,924, filed Mar. 15, 2013, and entitled “Photoactive Transparent Conductive Films Patterned Via Abbreviated Photolithography,” and United State Provisional Patent Application No. 61/949,727, filed Mar. 7, 2014, and entitled “Photoactive Transparent Conductive Films,” both of which are hereby incorporated by reference in their entirety. This application is also related to U.S. patent application Ser. No. 13/194,134, filed Jul. 29, 2011, and entitled “Conductive Films,” which is hereby incorporated by reference in its entirety.
- The disclosed embodiments relate generally to transparent conductive films and, more particularly, to composite transparent conductive films that are imparted with the properties of a matrix material employed therein (e.g., photoactivity and/or scratch resistance).
- A variety of materials are used as transparent conductors (conductors which pass at least some incident light). These materials are used, for example, in optoelectronic devices, touch screen displays, and solar cells. Most conventional transparent conductive films used in such devices are composed of sputtered metal oxides, the most common of which is tin-doped indium oxide (ITO). However, ITO is inconvenient for several reasons. First, the price of ITO is restrictive in raw material and formation. Second, many applications require patterning of transparent conductive films on length-scales ranging from microns to meters. Optical lithography is currently used to pattern ITO, but this process is time-consuming and expensive, further adding to the cost of ITO-based devices. Lastly, ITO tends to have properties that are unsuitable for certain types of devices. For example, ITO tends to be brittle after formation, making it unsuitable for flexible electronics (e.g., flexible displays, touch screens, and the like). As another example, ITO has a high index of refraction, which means that ITO films have to be coated with expensive anti-reflective coatings for many applications (e.g., display devices).
- Thus, there is a need for transparent conductive films that are more cost effective than ITO with improved properties (e.g., flexibility) while still maintaining sufficient performance for transparency and conductivity. There is also a need for methods of fabricating such conductive films.
- Disclosed are photoactive transparent conductive films, methods of fabricating photoactive transparent conductive films, and devices that incorporate photoactive transparent conductive films that overcome the abovementioned limitations in conventional transparent conductive materials, their corresponding methods of manufacture, and their uses.
- In particular, to address the aforementioned problems with conventional transparent conductive films, the disclosed embodiments provide a composite conductive film. The composite conductive film includes a layer of photoresist material and an inorganic mesh comprising a plurality of particles of an inorganic material. The plurality of particles of the inorganic mesh is embedded within the layer of photoresist material. The layer of photoresist material and the inorganic mesh are arranged to form the composite conductive film.
- In some embodiments, the composite conductive film is substantially transparent to optical light. In some embodiments, composite conductive film is characterized by an optical transparency to optical light in one or more of the following ranges: 60%-100%, 60%-99%, 60%-90%, and greater than 50%. As used herein, in some specific embodiments, the term “optical light” refers to light that is in the visible spectrum (e.g., 380 nm to 700 nm). In other embodiments the term “optical light” refers to light that is in the visible spectrum, the longwave ultraviolet spectrum (e.g., 350 nm to 380 nm), midrange ultraviolet (e.g., 300 nm to 350 nm), shortwave ultraviolet (e.g., 200 nm to 300 nm), and/or infrared spectrum (e.g., 700 nm to 1 mm).
- In some embodiments, the respective particles of the plurality of particles of the inorganic mesh comprise a conductive material. In some embodiments, the conductive material is a metallic material. In some embodiments, the respective particles of the plurality of particles comprise one of nanowires or nanotubes.
- In some embodiments, the respective particles of the plurality of particles are fused to form a substantially continuous network of the conductive material over a continuous portion of the composite conductive film.
- In some embodiments, the substantially continuous network of the conductive material is confined to a surface region of the layer of photoresist material, thereby forming a substantially two-dimensional continuous network of the conductive material proximal to a surface of the layer of photoresist material.
- In some embodiments, the plurality of particles are metallic particles characterized by a density within the surface region that is above a two-dimensional percolation threshold and less than a bulk percolation threshold of the conductive material suspended throughout the layer of photoresist material.
- In some embodiments, the surface region has a thickness and the composite conductive film is characterized by a first surface roughness that is less than a second surface roughness of a stand-alone film consisting of the same thickness of the inorganic mesh. In some embodiments, the first surface roughness is about fifty percent less than the second surface roughness.
- In some embodiments, the thickness of the surface region is selected in accordance with a target conductivity value.
- In some embodiments, the composite conductive film is bendable to a bending radius of at least 0.5 millimeters (mm).
- In some embodiments, the layer of photoresist material comprises a polymer that undergoes cross-linking when exposed to ultraviolet (UV) radiation. In some embodiments, a plurality of instances of the composite conductive film is patterned upon a substrate. Each instance of the plurality of instances comprises a region of the composite conductive film. The polymer within each of the regions is substantially cross-linked.
- In another aspect of the present disclosure, the disclosed embodiments provide a method of fabricating a composite conductive film. The method includes providing, as a matrix, a layer of photoresist material, introducing a plurality of inorganic particles upon a surface of the layer of photoresist material, and embedding at least some of the plurality of inorganic particles into the layer of photoresist material to form an inorganic mesh within the layer of photoresist material, thereby forming the composite conductive film.
- In some embodiments, the method further includes, prior to embedding the inorganic particles into the layer of photoresist material, heating the layer of photoresist material from a first temperature (e.g., room temperature) to a second temperature greater than the first temperature. The layer of photoresist material is softer at the second temperature than at the first temperature.
- In some embodiments, introducing the plurality of inorganic particles upon the surface of the layer of photoresist material includes spraying a nanowire suspension onto the surface of the layer of photoresist material.
- In some embodiments, introducing the plurality of inorganic particles upon the surface of the layer of photoresist material includes transferring said plurality of inorganic particles from a stamp in a stamp transfer process.
- In some embodiments, embedding the at least some of the plurality of inorganic particles into the layer of photoresist material to form the inorganic mesh within the layer of photoresist material includes pressing the nanowire suspension into the surface of the layer of photoresist material.
- In some embodiments, the method further includes patterning the composite conductive film by exposing at least a first region of the composite conductive film to light having a wavelength. The photoresist material is cross-linked by exposure to light having the wavelength. Patterning the composite conductive film further includes removing at least a second region of the composite conductive film using a chemical developer. The second region of the composite conductive film has not been exposed to light having the wavelength and the photoresist material is soluble in the chemical developer when the photoresist material is in a noncross-linked state.
- In some embodiments, the method further includes patterning the composite conductive film by exposing at least a first region of the composite conductive film to light having a wavelength. The photoresist material is characterized by cross-linking of polymers and the cross-linking of polymers is broken to form a noncross-linked state by exposure to light having the wavelength. Patterning the composite conductive film further includes removing the first region of the composite conductive film using a chemical developer. The photoresist material is soluble in the chemical developer when the photoresist material is in the noncross-linked state.
- In some embodiments, the wavelength is in a range of ultraviolet wavelengths.
- In yet another aspect of the present disclosure, the disclosed embodiments provide a touch-sensitive device. The touch-sensitive device includes a driving panel, a sensing panel electrically coupled with the driving panel by an electrical characteristic having a value, and a plurality of conductive lines patterned upon a surface of at least one of the driving panel and the sensing panel. Each of the plurality of conductive lines includes a layer of photoresist material and an inorganic mesh that includes a plurality of particles embedded within the layer of photoresist material. The touch-sensitive device further includes electronic circuitry to detect, using the plurality of conductive lines, a touch input by sensing a change in the value of the electrical characteristic between the driving panel and the sensing panel. The layer of photoresist material and the inorganic mesh are arranged to form a composite conductive film.
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FIG. 1 illustrates a perspective view of a device that includes a transparent conductive film, in accordance with some embodiments. -
FIGS. 2A-2C illustrate a method of fabricating (e.g., manufacturing) a photoactive transparent conductive film, in accordance with some embodiments. -
FIGS. 3A-3C illustrate a method of patterning a photoactive transparent conductive film using an abbreviated lithographic process, in accordance with some embodiments. -
FIGS. 4A-4C illustrate various embodiments of a transparent conductive film. -
FIG. 5 illustrates a touch-sensitive device having conductive lines made of a transparent conductive film, in accordance with some embodiments. -
FIGS. 6A-6C illustrate examples of conductive line shapes, in accordance with some embodiments. -
FIGS. 7A-7B are a flowchart illustrating a method of fabricating a composite conductive film, in accordance with some embodiments. - Like reference numerals refer to corresponding parts throughout the drawings.
- The embodiments described herein provide photoactive transparent conductive films that may be implemented in connection with many different types of devices, in accordance with various embodiments. For example, thin film solar cells, displays such as liquid crystal displays (LCDs), organic light-emitting displays, electrophoretic displays, touch screens (e.g., capacitive or resistive), anti-fog devices such as in automotive and aeronautic windshields, flexible flat-panel lighting (e.g., using evaporated and/or printed white organic light-emitting diodes), or photodetectors can be formed and patterned using materials and/or approaches as described herein.
- Conventional photoresists are poor conductors of electricity. One way to improve the electrical conductivity (hereinafter “conductivity”) of a conventional photoresist is to disperse conductive particles throughout the photoresist. This can be done, for example, by dissolving the conductive particles in a solution along with the photoresist prior to application of the photoresist (e.g., onto a wafer or a chip). Above a so-called “percolation threshold” (e.g., a percolation threshold density of the conductive particles), an electrically coupled network is formed by the conductive particles through which electrical currents can move, resulting in a low sheet resistance. An exact cutoff sheet resistance between electrically conducting and electrically insulating films is somewhat subjective and application specific but, generally speaking, a film with a sheet resistance less than 100Ω□−1 (“ohms per square”) may be considered conducting.
- The problem with this approach (essentially loading a photoresist with so much conductive material that it becomes electrically conducting) is that appropriate conductive materials tend to absorb and/or scatter optical light, making such photoresist opaque and thus unsuitable for applications that require transparent conductive films. This is a primary reason that, despite the expensive nature of tin-doped indium oxide (ITO) and the difficulty in patterning ITO, ITO remains an industry standard for conductive transparent films. To be sure, the fact that ITO remains prevalent speaks to the elusive nature of suitable alternatives.
- The embodiments described herein, however, provide photoactive transparent conductive films that are inexpensive and easy to pattern using abbreviated lithographic processes. The photoactive transparent conductive film is a composite conductive film that includes at least two parts: (1) a layer of photoresist material (e.g., forming a matrix material) and (2) an inorganic mesh made of a plurality of particles of an inorganic material. The plurality of particles of the inorganic mesh is embedded, for example, within the very surface of the layer of photoresist material to form a conductive film that is photoactive by virtue of the matrix material being a photoactive photoresist. By restricting the inorganic mesh to a surface region of the layer of photoresist material, absorption of light is greatly reduced. This is due to the fact that absorption by the conductive material occurs over a lesser extent of the film than if the conductive material was dispersed throughout the bulk of the film, as well as the fact that the percolation threshold for a substantially two-dimensional (2D) mesh of conductive material is less than the percolation threshold for a bulk, or three-dimensional (3D), mesh of conductive material. The latter effect reduces the density of conductive material needed in the surface region.
- Since they are made using a photoresist matrix, these films can be patterned quite easily. Nearly any arbitrary shape down to sub-micron length-scales can be realized simply by exposing the film to light of an appropriate wavelength and developing the film in an appropriate developer. The resulting structure can be permanently or functionally incorporated as electrical components (e.g., wires or conductive lines) into devices such as displays, solar cells, and others. As an added benefit, photoresists tend not to be brittle, making the films disclosed herein suitable for flexible electronics. For example, in some embodiments, the composite conductive films described herein are bendable to a bending radius of at least 0.5 millimeters (mm).
- Reference will now be made in detail to various implementations, examples of which are illustrated in the accompanying drawings. In the following detailed description, numerous specific details are set forth in order to provide a thorough understanding of the present disclosure and the described implementations herein. However, implementations described herein may be practiced without these specific details. In other instances, well-known methods, procedures, components, and mechanical apparatus have not been described in detail so as not to unnecessarily obscure aspects of the implementations.
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FIG. 1 illustrates a perspective view of adevice 100, in accordance with some embodiments.Device 100 includes asubstrate 102 that provides underlying support for thedevice 100. In some embodiments, thesubstrate 102 comprises glass or polyethylene terephthalate (PET).Device 100 further includes distinct instances of a transparent conductive film 104 (e.g., transparent conductive films 104-a and 104-b) that are patterned upon thesubstrate 102. In some embodiments, the distinct instances of the transparentconductive film 104 form wires, conductive lines, or other electrical components of thedevice 100 that are permanently and/or functionally incorporated into the device 100 (e.g., in its end- or product-ready-state). For example, in some embodiments, the distinct instances of the transparentconductive film 104 form conductive lines for a touch screen device or electrical contacts for a solar cell. - The transparent
conductive film 104 comprises a layer of photoresist material 106 (distinct instances of which are 106-a and 106-b). The term photoresist, as used herein, may be construed to mean any material that undergoes a structural or chemical change when exposed to a predetermined wavelength of light (or light within a predetermined range of wavelengths, such as optical light, ultraviolet light, etc.). These changes can facilitate the removal of undesired portions of the photoresist material by either (1) making exposed portions insoluble to removing agents (said removing agents are sometimes called “developers”), in which case the photoresist is considered a negative photoresist, or (2) making an insoluble portion of the photoresist soluble when exposed to light, in which case the photoresist is considered a positive photoresist. As described in greater detail later, the layer ofphotoresist material 106 can comprise either a positive photoresist or a negative photoresist. Selectively exposing the photoresist material to light thus enables one to fashion the transparentconductive film 104 according to a complex pattern (e.g., create distinct instances of the transparent conductive film 104) with high resolution (e.g., micron resolution or sub-micron resolution). - In some embodiments, the photoresist is an electrically insulating material (e.g., the layer of
photoresist material 106 has a sheet resistance above 5000Ω□−1). - In some embodiments, the photoresist material comprises an organic material. In some embodiments the photoresist is a negative photoresist. For example, in some embodiments, the layer of
photoresist material 106 comprises poly(methyl methacrylate) (PMMA, sometimes called “acrylic glass”). Poly(methyl methacrylate) is photosensitive to deep ultraviolet (UV) light (e.g., light having a wavelength in a range of 200-270 nanometers (nm)). Exposure to deep UV light creates chain scissions that de-crosslink chains of PMMA, making the photoresist soluble in certain developers (thus, PMMA is a positive photoresist). In another example, in some embodiments the layer ofphotoresist material 106 comprises a photoresist provided by Kayaku Microchem, such as SU-8, which is a negative photoresist that is photosensitive to near ultraviolet light (e.g., light having a wavelength in a range of 300-400 nm). Other examples of negative resists that can be used include, but are not limited to, azidelisoprene negative resists, polymethylisopropyl ketone (PMIPK), poly-butene-1-sulfone (PBS), poly-(trifluoroethyl chloroacrylate) TFECA, copolymer-(V-cyano ethyl acrylate-V-amido ethyl acrylate) (COP), poly-(2-methyl pentene-1-sulfone) (PMPS) and the like. It should be understood, however, that the exact nature or chemical composition of the photoresist is not intended to limit the claims that follow. In fact, since photoresist are oftentimes proprietary in nature, the exact chemical composition or nature of the photoresist may not be known when practicing the present disclosure. - In some embodiments the photoresist is a positive photoresist. The positive resist is relatively insoluble. After exposure to the proper light energy, the resist converts to a more soluble state. This reaction is called photosobulization. One positive photoresist in accordance with the present disclosure is the phenol-formaldehyde polymer, also called phenol-formaldehyde novolak resin. See, for example, DeForest, Photoresist: Materials and Processes, McGraw-Hill, New York, 1975, which is hereby incorporated by reference herein in its entirety. In some embodiments, the resist layer is LOR OSA, LOR 5 0.7 A, LOR 1 A, LOR 3 A, or LOR 5 A (MICROCHEM, Newton, Mass.). LOR lift-off resists use polydimethylglutarimide.
- In some embodiments, the layer of
photoresist material 106 has a controllable thickness (e.g., a thickness that is controlled by process parameters during fabrication). For example, in some embodiments, thesubstrate 102 is a chip or a wafer and the layer ofphotoresist material 106 is applied to the chip or wafer by spin coating the photoresist onto thesubstrate 102 and subsequently baking the photoresist (e.g., to evaporate solvent). In such embodiments, the resulting thickness of the layer ofphotoresist material 106 depends on an angular speed of the spin coater (e.g., as measured in revolutions per minute) as well as the composition and viscosity of the photoresist in dissolved form. In some embodiments, the thickness of the layer ofphotoresist material 106 is in a range of 100-500 nm, 400-1000 nm, 900-1500 nm, or 1-10 microns. In some embodiments, the layer ofphotoresist material 106 is deposited onto the substrate using another deposition technique such as the Spin-On-Glass method (SOG). More information on SOG can be found, for example, in Nguyen Nhu Toan, Spin-On Glass Materials and Applications in Advanced IC Technologies, 1999, which is hereby incorporated herein by reference in its entirety. - In some embodiments, the layer of
photoresist material 106 is deposited onto the substrate using ink-jet printing Ink-jet printing is based on the same principles of commercial ink-jet printing. The ink-jet nozzle is connected to a reservoir filled with the chemical solution and placed above a computer-controlled x-y stage. The target object is placed on the x-y stage and, under computer control, liquid drops (e.g., 50 microns in diameter) are expelled through the nozzle onto a well-defined place on the object. Different nozzles print different spots in parallel. In one embodiment of the present disclosure, a bubble jet, with drops as small as a few picoliters, is used to form a layer of thephotoresist material 106. In another embodiment, a thermal ink jet (Hewlett Packard, Palo Alto, Calif.) is used to form a layer of a deposit material. In a thermal ink jet, resistors are used to rapidly heat a thin layer of liquid ink. A superheated vapor explosion vaporizes a tiny fraction of the ink to form an expanding bubble that ejects a drop of ink from the ink cartridge onto the substrate. In still another embodiment of the present disclosure, a piezoelectric ink jet head is used for ink jet printing. A piezoelectric ink jet head includes a reservoir with an inlet port and a nozzle at the other end. One wall of the reservoir consists of a thin diaphragm with an attached piezoelectric crystal. When voltage is applied to the crystal, it contracts laterally, thus deflecting the diaphragm and ejecting a small drop of fluid from the nozzle. The reservoir then refills via capillary action through the inlet. One, and only one, drop is ejected for each voltage pulse applied to the crystal, thus allowing complete control over the when a drop is ejected. In yet another embodiment of the present disclosure, an epoxy delivery system is used to depositphotoresist material 106. An example of an epoxy delivery system is the Ivek Digispense 2000 (Ivek Corporation, North Springfield, Vt.). For more information on jet spraying, see, for example, Madou, Fundamentals of Microfabrication, Second Edition, 2002, pp. 164-167, CRC Press, which is hereby incorporated by reference herein in its entirety. - In another embodiment of the present disclosure, the layer of
photoresist material 106 is deposited onto the substrate by a screen printing (also known as silk-screening) process. A paste or ink is pressed onto portions of the substrate through openings in the emulsion on a screen. See, for example, Lambrechts and Sansen, Biosensors: Microelectrochemical Devices, The Institute of Physics Publishing, Philadelphia, 1992, which is hereby incorporated by reference in its entirety. The paste consists of a mixture of the material of interest, an organic binder, and a solvent. The organic binder determines the flow properties of the paste. The bonding agent provides adhesion of particles to one another and to the substrate. The active particles make the ink a conductor, a resistor, or an insulator. The lithographic pattern in the screen emulsion is transferred onto portions of the underlying structure by forcing the paste through the mask openings with a squeegee. In a first step, paste is put down on the screen. Then the squeegee lowers and pushes the screen onto the substrate, forcing the paste through openings in the screen during its horizontal motion. During the last step, the screen snaps back, the thick film paste that adheres between the screening frame and the substrate shears, and the printed pattern is formed on the substrate. The resolution of the process depends on the openings in the screen and the nature of the paste. With a 325-mesh screen (i.e., 325 wires per inch or 40 μM holes) and a typical paste, a lateral resolution of 100 μM can be obtained. - For difficult-to-print pastes, a shadow mask, such as a thin metal foil with openings, complements the process. However, the resolution of this method is inferior (>500 μM). After printing, the wet films are allowed to settle for a period of time (e.g., fifteen minutes) to flatten the surface while drying. This removes the solvents from the paste. Subsequent firing burns off the organic binder, metallic particles are reduced or oxidized, and glass particles are sintered. Typical temperatures range from 500° C. to 1000° C. After firing, the thickness of the resulting layer ranges from 10 μM to 50 μM. One silk-screening setup is the DEK 4265 (Universal Instrument Corporation, Binghamton, N.Y.). Commercially available inks (pastes) that can be used in the screen printing include conductive (e.g., Au, Pt, Ag/Pd, etc.), resistive (e.g., RuO2, IrO2), overglaze, and dielectric (e.g., Al2O3, ZrO2). The conductive pastes are based on metal particles, such as Ag, Pd, Au, or Pt, or a mixture of these combined with glass. Resistive pastes are based on RuO2 or Bi2Ru2O7 mixed with glass (e.g., 65% PBO, 25% SiO2, 10% Bi2O3).
- The resistivity is determined by the mixing ratio. Overglaze and dielectric pastes are based on glass mixtures. Different melting temperatures can be achieved by adjusting the paste composition. See, for example, Madou, Fundamentals of Microfabrication, Second Edition, CRC Press, Boca Raton, Fla., 2002, pp. 154-156, which is hereby incorporated by reference herein in its entirety.
- In some embodiments, the transparent
conductive film 104 is characterized by a low index of refraction (e.g., in a range of 1.5-2), obviating the need for anti-reflective coatings in certain applications (i.e., as compared to ITO when used in the same applications). - The transparent
conductive film 104 includes aninorganic mesh 108 embedded within the layer ofphotoresist material 106. Theinorganic mesh 108 includes a plurality ofparticles 110 of an inorganic material. As shown inFIG. 1 , particle 110-a and particle 110-b are respective particles of the plurality of particles. For visual clarity, the remaining particles are not labeled. In some embodiments, the respective particles of the plurality ofparticles 110 comprise a conductive material. For example, in various embodiments, the plurality ofparticles 110 comprises nanowires (as shown inFIG. 1 ), nanotubes, nanospheres, graphene, or a heterogeneous mixture thereof. In some embodiments, the nanowires are silver (Ag) nanowires. More generally, in some embodiments, the nanowires are metallic nanowires. In some embodiments, the nanotubes comprise carbon nanotubes (CNT). In some embodiments, theinorganic mesh 108 comprises a heterogeneous mixture of particles (e.g., a mixture of carbon nanotubes and graphene particles). In some embodiments, each nanowire or nanotube is characterized by a major axis and one or more minor axes. The major axes are aligned substantially parallel to asurface 114 of the layer ofphotoresist material 106. A typical width of a nanowire (i.e., along a respective minor axis of the nanowire) will be on the order of tens of nanometers, while the length (i.e., along the major axis of the nanowire) is often on the order of hundreds of nanometers or microns. - In some embodiments, the respective particles of the plurality of
particles 110 are fused (e.g., electrically coupled) to form a substantially continuous network of the conductive material over a continuous portion of the composite conductive film (e.g., the respective particles of the plurality ofparticles 110 are fused to form a substantially continuous network over the conductive material over each instance of the transparent conductive film 104). In other words, the respective particles of the plurality ofparticles 110 are fused in the sense that they form a continuous network of the conductive material. For example, the respective particles of the plurality ofparticles 110 may still be considered fused if the network includes dead-ends or if there are some particles or groups of particles that are not continuous with the network (e.g., islands of particles). - In some embodiments, the substantially continuous network of the conductive material is confined to a
surface region 112 of the layer of photoresist material 106 (e.g., thesurface region 112 has a thickness that is thin compared to the thickness of the layer of photoresist material 106), thereby forming a substantially two-dimensional continuous network of the conductive material proximal to thesurface 114 of the layer ofphotoresist material 106. For example, in some circumstances, the thickness of thesurface region 112 is 10, 20, 50, or 100 times thinner than the overall thickness the layer of photoresist material 106 (e.g., the thickness of thesurface region 112 is 25 nm while the overall thickness of the layer ofphotoresist material 106 is 1 micron, giving a ratio of the thickness of thesurface region 112 to the overall thickness of the layer ofphotoresist material 106 of 40). - By confining the plurality of
particles 110 to the surface region 112 (e.g., proximal to surface 114), some embodiments take advantage of the fact that the conductivetransparent film 104 can confer conductivity to surfaceregion 112 using far fewer particles than would be otherwise required to make thephotoresist material 106 as a whole conductive through dispersement of the particles throughout the bulk of the photoresist material. The reason for this is two-fold: (1) even if particles had the same density in both cases, fewer particles would be needed to achieve that density in a smaller region (e.g., thesurface region 112 as compared to the bulk) and (2) the percolation threshold is lower for a two-dimensional (2D) network of particles than it is for a bulk, or three-dimensional (3D), network of particles. Thus, in some embodiments, the plurality ofparticles 110 is characterized by a density within thesurface region 112 that is above the two-dimensional percolation threshold (corresponding to a 2D network of particles) and less than the bulk percolation threshold of the conductive material suspended throughout the layer ofphotoresist material 106. This is particularly advantageous in certain circumstances (e.g., when a high-degree of transparency is needed) because, in some embodiments, the respective particles of the plurality ofparticles 110 comprise metallic particles which tend to absorb and/or scatter optical light. - In some embodiments, the layer of
photoresist material 106 is substantially transparent to optical light (e.g., light having a wavelength within a range of 400-700 nm). As used herein, the term “transparent” may be understood to refer to characteristics relating to the passage of at least some light as measured with respect to light from a light source having a predetermined spectral density. In some embodiments, the light source is the sun. Alternatively, the light source is a light source that emits a narrow band of light (e.g., a laser or light that has passed through a band pass filter). Alternatively, the light source is a common household light source, such as an incandescent light bulb or a compact fluorescent lamp (CFL). Regardless of the type of light source that is used to define transparency, different transparent materials (in accordance with different embodiments) exhibit different levels of transparency. For example, in some embodiments, the composite conductive film is characterized by a transparency to optical light in one or more of the following ranges: 60%-100%, 60%-99%, 60%-90%, and greater than 50%. In many optoelectronic implementations, the transparent conductive films pass between about 60% and 90% of incident light, as dictated by the application. -
FIGS. 2A-2C illustrate amethod 200 of fabricating (e.g., manufacturing) a photoactive transparent conductive film, in accordance with some embodiments. For ease of explanation, themethod 200 is described with reference to a nanowire mesh (e.g.,inorganic mesh 108,FIG. 1 ) comprising a plurality of nanowires made of a conductive material. It should be understood, however, that themethod 200 can be implemented using a variety of conductive materials, including but not limited to conductive nanowires, nanotubes, nanospheres, graphene, and/or a heterogeneous mixture thereof. -
FIG. 2A illustrates an operation in which a nanowire suspension 202 (e.g., comprising a solution of nanowires suspended in a solvent) is applied to (e.g., drop-cast onto) asurface 204 of aglass transfer block 206. Thenanowire suspension 208 is applied, for example, in some embodiments, by mixing nanowires in the solution and coating or depositing the solution on thesurface 204 of theglass transfer block 206. In alternate embodiments, the transfer block may comprise a material other than glass. - In
FIG. 2B , thenanowire suspension 202 is dispersed on thesurface 204 to form ananowire mesh 208. In some embodiments, thenanowire suspension 202 is dispersed by spin coating thenanowire suspension 202 onto theglass transfer block 206. In some embodiments, thenanowire suspension 202 is dispersed by any of the deposition techniques disclosed or referenced herein. Thenanowire suspension 202 is subsequently dried to evaporate the solvent leaving behind thenanowire mesh 208. In some embodiments, to prevent nanowire aggregation, thenanowire suspension 202 is dried slowly (e.g., at room temperature) while theglass transfer block 206 is shaken (e.g., moved laterally and/or angularly at a frequency between 1-60 Hz). Thenanowire mesh 208 is optionally annealed (e.g., by raising the temperature of theglass transfer block 206 to about 180° C. for a period of about 1 hour) to further fuse (e.g., electrically couple) the nanowires and form a substantially continuous network of the conductive material, thereby reducing sheet resistance of the final transparent conductive film. -
FIG. 2C illustrates an operation in which thesurface 204 of theglass transfer block 206 is pressed onto asurface 114 of a layer ofphotoresist material 106, which is disposed upon an underlying substrate 102 (e.g., glass or PET). In some embodiments, thesurface 204 of theglass transfer block 206 is pressed onto thesurface 114 of the layer ofphotoresist material 106 with a predetermined (e.g., calibrated) pressure (e.g., a pressure of 2.4×104 psi). Themethod 200 results in adevice 210 that includes ananowire mesh 108 embedded in the layer ofphotoresist material 106, thus forming the transparentconductive film 104. - In some embodiments, the photoresist is an electrically insulating material (e.g., the layer of
photoresist material 106 has a sheet resistance above 5000Ω□−1). Upon embedding thenanowire mesh 108 in the layer ofphotoresist material 106, the composite film becomes conducting (e.g., with a sheet resistance less than 100Ω□−1 or 200 Ω□−1). - By applying pressure to the
nanowire mesh 108 in this manner, a mechanical force is applied to the nanowires. The mechanical force fuses the nanowires together (e.g., where they are in contact with one another) and fills in the spaces between nanowires with photoresist. Thus, the application of pressure serves to improve electrical conductivity and reduce surface roughness for the resultingdevice 210. This, in turn, affects both optical and electrical properties of thedevice 210. For example, the haze of a transparent conductive film (e.g., transparentconductive film 104,FIG. 1 ) is proportional to the transparent conductive film's surface roughness because the stacking and projection of the nanowires increases the transparent conductive film's tendency to absorb and/or scatter light. In addition, when the nanowires become fused, the electrical resistance of the transparentconductive film 104 substantially decreases. - As a more detailed example, in some implementations, the nanowires in the
nanowire suspension 202 have varying diameters (e.g., ranging between 50-100 nm). Accordingly, diameters of nanowires in the nanowire mesh 208 (e.g., prior to embedding thenanowire mesh 208 in the layer of photoresist material 106) may vary from one another, with differences upwards of 50 nanometers. In some embodiments, after thesurface 204 of theglass transfer block 206 is pressed onto the layer ofphotoresist material 106, a conductivetransparent film 104 having a surface roughness that is less than 40 nanometers root-mean-square (RMS) is achieved. In other implementations, the surface roughness is less than about 20 nanometers RMS. More generally, in some embodiments, the transparentconductive film 104 is characterized by a first surface roughness that is less than a second surface roughness of a stand-alone film (e.g., nanowire mesh 208) consisting of the same thickness of the inorganic mesh. For example, the first surface roughness is about fifty percent less than the second surface roughness. - In some embodiments, one or more parameters (e.g., the applied pressure and/or the composition, length, and/or density of the nanowires) can be varied to deliberately alter (e.g., tune) the transparency and haze of the
device 210 for specific applications (e.g., by varying the thickness ofsurface region 112,FIG. 1 or the surface roughness). Alternatively, or in addition to, in some embodiments, the thickness of the surface region 112 (FIG. 1 ) is selected in accordance with a target conductivity value. -
FIGS. 3A-3C illustrate amethod 300 of patterning a transparentconductive film 104 using an abbreviated lithographic process, in accordance with some embodiments. - In
FIG. 3A , aphotomask 302 is positioned with respect to the conductive surface of a photoactive transparent conductive film 104 (e.g., thephotomask 302 is either in contact with the photoactive transparentconductive film 104 or separated from the photoactive transparentconductive film 104 by a predetermined distance). In some embodiments, the photomask is a stepper reticle and, when in use, one or more optical elements (not shown) are disposed betweenphotomask 302 and the transparentconductive film 104. In other embodiments, thephotomask 302 is a contact printing photomask and, when in use,photomask 302 is in contact with or very close to (e.g., 1 micron, or 2 microns away from) the transparentconductive film 104. Transparentconductive film 104 is described here as a “photoactive” transparent conductive film because, prior to outset ofmethod 300, the photoresist included in the transparentconductive film 104 has not been exposed to light to which the photoresist is sensitive. Thephotomask 302 has one or moreopaque regions 304 which block light and one or moretransparent region 306 which allow light to pass onto thesurface 114 of the photoactive transparentconductive film 104. - The
photomask 302 is illuminated with light 308 having a predetermined wavelength or range of wavelengths. The photoactive transparentconductive film 104 is sensitive to light of the predetermined wavelength or range of wavelengths. Thephotomask 302 is illuminated in this manner with a predetermined intensity for a predetermined amount of time in accordance with process requirements and recipes. In some embodiments, the predetermined wavelength is in a range of ultraviolet (UV) wavelengths (e.g., 200-270 nm for deep-UV, or 300-400 nm for near-UV). In some embodiments, the predetermined wavelength is distinct from (e.g., outside a range of) wavelengths for which the transparentconductive film 104 is intended to be transparent. - The
transparent regions 306 result in the exposure of selected regions 310 (e.g., regions 310-a, 310-b, 310-c, and 310-d) of the photoactive transparentconductive film 104 to light having the predetermined wavelength. In some embodiments, the photoresist material is a positive photoresist. The positive resist is relatively insoluble. After exposure to the proper light energy, the resist converts to a more soluble state. This reaction is called photosobulization. In some embodiments, the photoresist material is a positive photoresist that is degraded by exposure of light having the predetermined wavelength. For example, the photoresist, prior to exposure to light, is characterized by cross-linking of polymers. The cross-linking of polymers is broken in the first region (e.g., scissions are formed and the polymers are de-crosslinked) to form a noncross-linked state by exposure to light having the predetermined wavelength. -
FIG. 3B illustrates the result of themethod 300 when a positive photoresist is used. When a positive photoresist is used, the selectedregions 310 are removed upon application of a developer to form, for example, trenches 312 (e.g., trenches 312-a, 312-b, 312-c, and 312-d), while the unexposed regions are not removed. - In some embodiments, the photoresist is a negative photoresist in which polymers in the resist form a cross-linked material that is etch resistant upon exposure to light. In some embodiments, the photoresist is a negative photoresist comprising a polymer and exposing the selected
regions 310 of the photoactive transparentconductive film 104 to light having the predetermined wavelength results in crosslinking of the polymer. When a negative photoresist is used, the selectedregions 310 remain upon application of a developer, while unexposed regions are removed. -
FIG. 3C illustrates the result of themethod 300 when a negative photoresist is used. When a negative photoresist is used, the selectedregions 310 remain (i.e., are not removed) upon application of a developer to form, for example, pillars 314 (e.g., pillars 314-a, 314-b, 314-c, and 314-d), while the unexposed regions are removed. - In some circumstances (e.g., for some photoresists), the cross-linking of the polymer is driven by thermal processes activated by the UV radiation (e.g., the UV radiation locally increases the temperature of the photoresist, which drives the cross-linking process). In some circumstances, the transparent
conductive film 104 does not include a photoresist, but is nonetheless a layer of a material that undergoes cross-linking when exposed to elevated temperature (e.g., thermal cross-linking). Such materials can be beneficial when mechanical robustness is desired (e.g., without the need for patterning). In some embodiments, the transparentconductive film 104 includes an electron-beam (e-beam) sensitive resist in lieu of a photoresist (however, PMMA is considered both an e-beam resist and a photoresist sensitive to UV light). In some embodiments, the transparentconductive film 104 is deposited using monomers or oligomers in solution, and a catalyst is added to the solution to facilitate cross-linking (e.g., prior to depositing the solution onto the substrate, drying the solution to form the layer, and embedding the wires into the surface of the layer). - Although removal of the unwanted regions of the photoresist (e.g., the unexposed regions or, alternatively, the exposed regions, depending on the nature of the photoresist) has been described with reference to use of a developer, some embodiments utilize a mechanical approach to removing such regions. Such mechanical approaches can include an applied force or blasting with a fluid such as air or water.
-
FIGS. 4A-4C illustrate alternate embodiments of a transparent conductive film. In some embodiments, the layers ofphotoresist material 106 shown inFIGS. 4A-4C are disposed upon a substrate (e.g.,substrate 102,FIG. 1 ), although the substrate is not shown here for visual clarity. The transparent conductive films illustrated inFIG. 4A-4C are intended to be only exemplary and are not intended to limit the claims that follow. -
FIG. 4A illustrates a transparentconductive film 402. The transparentconductive film 402 is a composite conductive film that includes a layer ofphotoresist material 106 and an inorganic mesh comprising a plurality of nanospheres 404 (e.g., metallic nanospheres). The inorganic mesh is confined to asurface region 406 of the transparentconductive film 402, which is advantageous in thatfewer nanospheres 404 are required to achieve a suitable sheet resistance, resulting in improved transparency characteristics. -
FIG. 4B illustrates a transparentconductive film 408. In an analogous manner toFIG. 4A , the transparentconductive film 408 is a composite conductive film that includes a layer ofphotoresist material 106 and an inorganic mesh comprising a plurality of nanospheres 404 (e.g., metallic nanospheres). Unlike inFIG. 4A , however, the inorganic mesh is not confined to a surface region of the transparentconductive film 408 and is instead suspended throughout the bulk of the layer ofphotoresist material 106. The transparentconductive film 408 can be used when a high degree of transparency is not needed (or a hazy film is desired) or when a high degree of conductivity is not needed. -
FIG. 4C illustrates a transparentconductive film 410.FIG. 4C is analogous toFIG. 4B but for the fact that transparentconductive film 410 includes an inorganic mesh comprising a plurality ofnanowires 110 suspended throughout the bulk of the layer ofphotoresist material 106. -
FIG. 5 illustrates a touch-sensitive device 500 having conductive lines of a transparent conductive film, in accordance with some embodiments.FIG. 5 illustrates several layers, panels, and/or components of the touch-sensitive device 500. For visual clarity, these layers are illustrated as separated in the vertical direction. More typically, these layers will be connected to one another or, alternatively, coupled with one another (e.g., with spacer layers in between). - The touch-
sensitive device 500 includes a drivingpanel 502 which has a plurality ofconductive driving lines 504 patterned upon a surface of the driving panel 502 (e.g., a top surface). Each of the plurality of conducting drivinglines 504 can have any of the properties or features of the distinct instances of the transparentconductive film 104 described with reference to any of the other figures (e.g.,FIG. 1 ). In some embodiments, thedevice 100 illustrated inFIG. 1 is a partial cross-section of drivingpanel 502. In particular, each of the plurality of drivinglines 504 comprises a layer of photoresist material and an inorganic mesh that includes a plurality of particles embedded within the layer of photoresist material. - The touch-
sensitive device 500 further includes asensing panel 506 electrically coupled with the drivingpanel 502 by an electrical characteristic (e.g., capacitance, resistance) having a value. Thesensing panel 506 includes a plurality ofsensing lines 508 disposed upon a surface of the sensing panel. In some embodiments, thesensing lines 508 are analogous to the drivinglines 504, except that thesensing lines 508 run in a different direction (e.g., substantially perpendicularly) to the drivinglines 504 such that the two sets of lines form a grid. - The touch-
sensitive device 500 further includes electronic circuitry to detect, using the plurality of drivinglines 504 and the plurality ofsensing lines 508, a touch input by sensing a change in the value of the electrical characteristic (e.g., capacitance or resistance) between the drivingpanel 502 and thesensing panel 506. - Finally, the touch-
sensitive device 500 includes a display 510 (e.g., an LCD display). Thedisplay 510 produces light that is shone upwards through the drivingpanel 502 andsensing panel 506. - In some embodiments, the conductive lines are straight lines. Alternatively, the conductive lines (e.g., driving
lines 504 or sensing lines 508) can have an arbitrary shape. -
FIGS. 6A-6C illustrate examples of conductive line shapes, in accordance with some embodiments.FIG. 6A illustratesconductive lines 602 comprising a plurality ofrectangles 604 separated bystraight segments 606 of the transparent conductive film.FIG. 6B illustratesconductive lines 608 comprising a plurality ofdiamonds 610 separated bystraight segments 606 of the transparent conductive film.FIG. 6C illustratesconductive lines 612 comprising a plurality ofcircles 614 separated bystraight segments 606 of the transparent conductive film. -
FIGS. 7A-7B are a flowchart illustrating amethod 700 of fabricating a composite conductive film. Themethod 700 can be used to fabricate the composite conductive film shown, for example, inFIG. 1 , and/or the conductive driving lines/conductive sensing lines shown inFIG. 5 andFIG. 6 . - The
method 700 includes providing (702), as a matrix, a layer of photoresist material. For example, in some embodiments, the layer of photoresist material is spin-coated onto a glass substrate (e.g.,substrate 102,FIG. 1 ). In some embodiments, the photoresist material is an electrically insulating material (e.g., with a sheet resistance above 5000Ω□−1). - The
method 700 further includes introducing (704) a plurality of inorganic particles upon a surface (e.g., a top surface) of the layer of photoresist material. In some embodiments, the plurality of inorganic particles comprise one of nanowires (as shown inFIG. 1 ), nanotubes, nanospheres, graphene, or a combination (e.g., heterogeneous mixture) thereof. In some embodiments, introducing the plurality of inorganic particles upon the surface of the layer of photoresist material comprises spraying (706) a nanowire suspension onto the surface of the layer of photoresist material. In some embodiments, introducing the plurality of inorganic particles upon the surface of the layer of photoresist material comprises transferring (708) said plurality of inorganic particles from a stamp (e.g.,glass transfer block 206,FIG. 2 ) in a stamp transfer process (e.g., by the process shown inFIGS. 2A-2C ). In some embodiments, prior to introducing the plurality of inorganic particles upon the surface of the layer of photoresist material, themethod 700 includes annealing (710) the plurality of inorganic particles on the stamp to form a substantially continuous conductive network of the inorganic particles. For example, the stamp can be raised to an elevated temperature of 180° C. for a predetermined period of time (e.g., 1 hour) to anneal the plurality of particles. - In some embodiments, prior to embedding the inorganic particles into the layer of photoresist material (see operation 714), the
method 700 includes heating (712) the layer of photoresist material from a first temperature (e.g., room temperature, or 25° C.) to a second temperature (e.g., 90° C.) greater than the first temperature. The layer of photoresist material is softer at the second temperature than at the first temperature, thereby facilitating the embedding operation 714). - The
method 700 includes embedding (714) at least some of the plurality of inorganic particles into the layer of photoresist material to form an inorganic mesh within the layer of photoresist material, thereby forming the composite conductive film. In some embodiments, embedding the at least some of the plurality of inorganic particles into the layer of photoresist material to form the inorganic mesh within the layer of photoresist material comprises pressing (716) the nanowire suspension into the surface of the layer of photoresist material (e.g., by pressing the stamp into the surface of the layer of photoresist material with a pressure of 2.4×104 psi). - In some embodiments, the
method 700 includes patterning (718) the composite conductive film by exposing (720) at least a first region of the composite conductive film to light having a wavelength. The photoresist material is cross-linked by exposure to light having the wavelength (e.g., the photoresist material is a negative photoresist). In some embodiments, patterning the composite conductive film further comprises removing (722) at least a second region of the composite conductive film using a chemical developer. The second region of the composite conductive film has not been exposed to light having the wavelength and the photoresist material is soluble in the chemical developer when the photoresist material is in a noncross-linked state. In some embodiments (724), the wavelength is in a range of ultraviolet wavelengths (e.g., in a range of 200-270 nm for deep-UV or 300-400 for near-UV). - In some embodiments, the method further includes patterning (726) the composite conductive film by exposing (728) at least a first region of the composite conductive film to light having a wavelength. The photoresist material is characterized by cross-linking of polymers and said cross-linking of polymers is broken to form a noncross-linked state by exposure to light having the wavelength (e.g., the photoresist material is a positive photoresist). In some embodiments, patterning the composite conductive film further comprises removing (730) the first region of the composite conductive film using a chemical developer. The photoresist material is soluble in the chemical developer when the photoresist material is in the noncross-linked state. In some embodiments (732), the wavelength is in a range of ultraviolet wavelengths (e.g., in a range of 200-270 nm for deep-UV or 300-400 for near-UV).
- The foregoing description, for purpose of explanation, has been described with reference to specific embodiments. However, the illustrative discussions above are not intended to be exhaustive or to limit the invention to the precise forms disclosed. Many modifications and variations are possible in view of the above teachings. The embodiments were chosen and described in order to best explain the principles of the invention and its practical applications, to thereby enable others skilled in the art to best utilize the invention and various embodiments with various modifications as are suited to the particular use contemplated.
- It will be understood that, although the terms “first,” “second,” etc. may be used herein to describe various elements, these elements should not be limited by these terms. These terms are only used to distinguish one element from another. For example, a first instance of a layer of material could be termed a second instance of the layer of material, and, similarly, a second first instance of the layer of material could be termed a first instance of the layer of material, without changing the meaning of the description, so long as all occurrences of the “first instance of the layer of material” are renamed consistently and all occurrences of the “second instance of the layer of material” are renamed consistently. The first instance of the layer of material and the second first instance of the layer of material are both instances of the layer of material, but they are not the same instance of the layer of material.
- The terminology used herein is for the purpose of describing particular implementations only and is not intended to be limiting of the claims. As used in the description of the implementations and the appended claims, the singular forms “a,” “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will also be understood that the term “and/or” as used herein refers to and encompasses any and all possible combinations of one or more of the associated listed items. It will be further understood that the terms “comprises” and/or “comprising,” when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof.
- As used herein, the term “if” may be construed to mean “when” or “upon” or “in response to determining” or “in accordance with a determination” or “in response to detecting,” that a stated condition precedent is true, depending on the context. Similarly, the phrase “if it is determined [that a stated condition precedent is true]” or “if [a stated condition precedent is true]” or “when [a stated condition precedent is true]” may be construed to mean “upon determining” or “upon a determination that” or “in response to determining” or “in accordance with a determination” or “upon detecting” or “in response to detecting” that the stated condition precedent is true, depending on the context.
Claims (20)
1. A composite conductive film, comprising:
a layer of photoresist material; and
an inorganic mesh comprising a plurality of particles of an inorganic material;
wherein
the plurality of particles of the inorganic mesh is embedded within the layer of photoresist material; and
the layer of photoresist material and the inorganic mesh are arranged to form the composite conductive film, wherein the composite conductive film is substantially transparent to optical light.
2. The composite conductive film of claim 1 , wherein composite conductive film is characterized by a transparency in that is greater than 50%.
3. The composite conductive film of claim 1 , wherein the respective particles of the plurality of particles of the inorganic mesh comprise a conductive material.
4. The composite conductive film of claim 3 , wherein the respective particles of the plurality of particles are fused to form a substantially continuous network of the conductive material over a continuous portion of the composite conductive film.
5. The composite conductive film of claim 4 , wherein the substantially continuous network of the conductive material is confined to a surface region of the layer of photoresist material, thereby forming a substantially two-dimensional continuous network of the conductive material proximal to a surface of the layer of photoresist material.
6. The composite conductive film of claim 5 , wherein the conductive material is a metallic material.
7. The composite conductive film of claim 6 , wherein the respective particles of the plurality of particle are metallic particles and the plurality of particles is characterized by a density within the surface region that is above a two-dimensional percolation threshold and less than a bulk percolation threshold of the conductive material suspended throughout the layer of photoresist material.
8. The composite conductive film of claim 1 , wherein:
the surface region has a thickness; and
the composite conductive film is characterized by a first surface roughness that is less than a second surface roughness of a stand-alone film consisting of the same thickness of the inorganic mesh.
9. The composite conductive film of claim 8 , wherein the first surface roughness is about fifty percent less than the second surface roughness.
10. The composite conductive film of claim 1 , wherein the thickness of the surface region is selected in accordance with a target conductivity value.
11. The composite conductive film of claim 1 , wherein the respective particles of the plurality of particles comprise one of nanowires or nanotubes.
12. The composite conductive film of claim 1 , wherein the layer of photoresist material comprises a polymer that undergoes cross-linking when exposed to ultraviolet (UV) radiation.
13. The composite conductive film of claim 12 , further comprising a plurality of instances of the composite conductive film patterned upon a substrate, each instance of the plurality of instances comprising a region of the composite conductive film, wherein the polymer within each of the regions is substantially cross-linked.
14. A method of fabricating a transparent composite conductive film, comprising:
providing, as a matrix, a layer of photoresist material;
introducing a plurality of inorganic particles upon a surface of the layer of photoresist material; and
embedding at least some of the plurality of inorganic particles into the layer of photoresist material to form an inorganic mesh within the layer of photoresist material, thereby forming the composite conductive film,
wherein embedding at least some of the plurality of inorganic particles into the layer of photoresist material results in the composite conductive film that is substantially transparent to optical light.
15. The method of claim 14 , further comprising, prior to embedding the inorganic particles into the layer of photoresist material, heating the layer of photoresist material from a first temperature to a second temperature, greater than the first temperature, wherein the layer of photoresist material is softer at the second temperature than at first temperature.
16. The method of claim 14 , wherein introducing the plurality of inorganic particles upon the surface of the layer of photoresist material comprises spraying a nanowire suspension onto the surface of the layer of photoresist material.
17. The method of claim 14 , wherein introducing the plurality of inorganic particles upon the surface of the layer of photoresist material comprises transferring said plurality of inorganic particles from a stamp in a stamp transfer process.
18. The method of claim 17 , wherein embedding the at least some of the plurality of inorganic particles into the layer of photoresist material to form the inorganic mesh within the layer of photoresist material comprises pressing the nanowire suspension into the surface of the layer of photoresist material.
19. The method of claim 14 , wherein the photoresist is photosensitive to light having an ultraviolet wavelength or a range of wavelengths in an ultraviolet range of wavelengths.
20. A touch-sensitive device, comprising:
a driving panel;
a sensing panel electrically coupled with the driving panel by an electrical characteristic having a value;
a plurality of conductive lines patterned upon a surface of at least one of the driving panel and the sensing panel, each of the plurality of conductive lines comprising:
a layer of photoresist material; and
an inorganic mesh that includes a plurality of particles embedded within the layer of photoresist material; and
electronic circuitry to detect, using the plurality of conductive lines, a touch input by sensing a change in the value of the electrical characteristic between the driving panel and the sensing panel;
wherein the layer of photoresist material and the inorganic mesh are arranged to form a composite conductive film that is substantially transparent to optical light.
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US14/486,775 US9666337B2 (en) | 2011-07-29 | 2014-09-15 | Composite conductive films with enhanced thermal stability |
US15/494,800 US10234969B2 (en) | 2011-07-29 | 2017-04-24 | Method of forming a composite conductive film |
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US16/992,750 US20200371615A1 (en) | 2013-03-15 | 2020-08-13 | Method of Forming a Composite Conductive Film |
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US16/267,126 Active US10782804B2 (en) | 2013-03-15 | 2019-02-04 | Method of forming a composite conductive film |
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Also Published As
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US20190171311A1 (en) | 2019-06-06 |
US20170228055A1 (en) | 2017-08-10 |
US20200371615A1 (en) | 2020-11-26 |
WO2014150577A1 (en) | 2014-09-25 |
US9666337B2 (en) | 2017-05-30 |
US20150038033A1 (en) | 2015-02-05 |
US20150000960A1 (en) | 2015-01-01 |
US10782804B2 (en) | 2020-09-22 |
US9491853B2 (en) | 2016-11-08 |
US10234969B2 (en) | 2019-03-19 |
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