CN108486544A - A kind of preparation method and applications of the graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic - Google Patents

A kind of preparation method and applications of the graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic Download PDF

Info

Publication number
CN108486544A
CN108486544A CN201810125540.0A CN201810125540A CN108486544A CN 108486544 A CN108486544 A CN 108486544A CN 201810125540 A CN201810125540 A CN 201810125540A CN 108486544 A CN108486544 A CN 108486544A
Authority
CN
China
Prior art keywords
graphene
zinc oxide
nano
oxide micro
grading function
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.)
Granted
Application number
CN201810125540.0A
Other languages
Chinese (zh)
Other versions
CN108486544B (en
Inventor
肖帅
陈惠琄
杨伯儒
柳成林
林迪安
杭天
杨成端
谢曦
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sun Yat Sen University
SYSU CMU Shunde International Joint Research Institute
Research Institute of Zhongshan University Shunde District Foshan
National Sun Yat Sen University
Original Assignee
SYSU CMU Shunde International Joint Research Institute
Research Institute of Zhongshan University Shunde District Foshan
National Sun Yat Sen University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SYSU CMU Shunde International Joint Research Institute, Research Institute of Zhongshan University Shunde District Foshan, National Sun Yat Sen University filed Critical SYSU CMU Shunde International Joint Research Institute
Priority to CN201810125540.0A priority Critical patent/CN108486544B/en
Publication of CN108486544A publication Critical patent/CN108486544A/en
Application granted granted Critical
Publication of CN108486544B publication Critical patent/CN108486544B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/22Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
    • C23C16/26Deposition of carbon only
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/22Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
    • C23C16/30Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
    • C23C16/40Oxides
    • C23C16/407Oxides of zinc, germanium, cadmium, indium, tin, thallium or bismuth
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/455Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
    • C23C16/45523Pulsed gas flow or change of composition over time
    • C23C16/45525Atomic layer deposition [ALD]
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C18/00Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
    • C23C18/02Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
    • C23C18/12Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
    • C23C18/1204Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material inorganic material, e.g. non-oxide and non-metallic such as sulfides, nitrides based compounds
    • C23C18/1208Oxides, e.g. ceramics
    • C23C18/1216Metal oxides
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C18/00Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
    • C23C18/02Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
    • C23C18/12Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
    • C23C18/125Process of deposition of the inorganic material
    • C23C18/1295Process of deposition of the inorganic material with after-treatment of the deposited inorganic material
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/04Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material
    • C23C28/048Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material with layers graded in composition or physical properties

Abstract

The preparation method and applications of the invention discloses a kind of graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic.The preparation method of this graphene zinc oxide micro-nano grading function material includes the following steps:S1:Vertical graphene is generated on substrate;S2:By atomic layer deposition method, dip-coating adsorption and oxidation zinc nanoparticles crystal seed on the surface of graphene;S3:By hydro-thermal method, the growth of zinc oxide nano line on graphene forms graphene zinc oxide micro-nano structure material;S4:Graphene zinc oxide micro-nano structure material is modified processing, you can.The application of this graphene zinc oxide micro-nano grading function material is also disclosed that simultaneously.Graphene zinc oxide micro-nano grading function material produced by the present invention has the superperformance of super-hydrophobic, superoleophobic, super thin blood, is a kind of functional self-cleaning material.This material can be used as electrode or modified electrode, as a sensor to detection substance, has broad application prospects.

Description

A kind of graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic The preparation method and applications of material
Technical field
The system of the present invention relates to a kind of graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic Preparation Method and its application.
Background technology
Super lyophoby (having both super-hydrophobic, superoleophobic, super thin blood characteristic) material is because its unique reprimand liquid characteristic is in automatically cleaning, anti- National defence, the daily life fields such as dirty anti-corrosion, liquid transporting, draft reduction material, miniflow management and control design, which are gathered around, to have broad application prospects.With Deepening continuously for material surface fundamental research, the fast development of new glass forming theory, the research of super lyophoby material increasingly by To concern.There are many example of super hydrophobic surface in nature, can such as tumble the lotus flower leaf of water droplet like a dream.It need not set It doubts, the super-hydrophobic biomimetic material based on " lotus leaf effect " confirms that it is extensive in industrial applications such as coating, films Application value.By fluorine-containing multi-level nanometer titanium dioxide silicon ball with it is carbon nano tube modified on the carbon cloth of micro-meter scale, can be right Common oil has stable superoleophobic characteristic.There is good antiplatelet to stick on fluorinated titania nanotube surface Property.
For coarse surface, wetting behavior can theoretically by two wetting models of Wenzel and Cassie models Description.Under Wenzel states, in micro-structure such as hole, recessed gap that rough surface can be completely penetrated due to liquid, therefore it can increase Contact area between liquid feeding body and solid substrate, to amplify wetting or the non wettability of solid material, at this time liquid with it is solid Adhesive attraction between body is stronger.And under Cassie states, air is trapped on the rough surface below liquid, forms energy Composite solid-liquid-gas interface that drop is supported, this makes drop have larger contact angle and lower roll angle.So being Allow material surface can be with the property of super lyophoby, it should liquid be allowed to be in stable Cassie states in material surface.Profit The wettability of lotus leaf can be explained with Cassie models, current research discloses the micro-nano hierarchical structure of lotus leaf surface to it Wettability has played key effect.By the Bionic Design of lotus leaf surface, can be prepared super with micro-nano hierarchical structure Hydrophobic surface.In general, the lyophobic surface with hierarchical structure can pass through the design table low with the surface of solids of surface roughness It is acted synergistically of both the modification of face energy to realize the repulsion to liquid.
Grapheme material is because of its good electricity, and optics, calorifics, mechanical characteristic has a wide range of applications field, and is based on The composite material of graphene is even more a highly important research direction, graphene and nanogold in the numerous application fields of graphene Belong to the compound of oxide and prepare lithium battery material, enhances its electric conductivity and increase specific surface area.Graphene and conductive polymer Son or the compound of metal oxide prepare ultracapacitor, and ultracapacitor has energy density high, and the charge and discharge time is short, cycle Service life is long, it is economic and environment-friendly the advantages that.
Application of the graphene in biosensor direction is more and more in recent years, and biosensor is one kind to biological object Matter is sensitive, and the instrument being detected to it using this sensitivity.Biosensor according to biomaterial sensitive material not Together, it is divided into immunosensor, enzyme sensor, electrochemical DNA biosensor, animal vegetable tissue sensor and microbiological sensor. And graphene is cheap, environmental-friendly, bio-compatibility and active group are evenly distributed, also a large amount of carboxyl, hydroxyl etc. Functional group and good dissolubility can allow graphene to become a kind of ideal biological sensing material.Due to graphene composite wood The introducing for expecting the electrode of modification, greatly reduces oxidizing potential, improves sensitivity, expand detection range.Small to biology In terms of Molecular Detection, the electrode of graphene composite material modification can to cigarette phthalein amine arteries and veins he two core former times of cry of certain animals it is sour (NADH), dopamine (DA) category pyrocatechol substance, paracetamol (APAP), the biological micromolecules such as ascorbic acid, uric acid, tyrosine and tryptophan Carry out more accurate detection.In terms of biomacromolecule detection, immunity biosensor can be used as to detect protein, disease Original, bacterium, virus type and cell etc..Meanwhile graphene also has wide application in terms of enzyme biologic sensor.
The unique two-dimensional structure of grapheme material, excellent mechanical property, good photoelectric property, larger specific surface area etc. All cause the concern of whole world scientist.Its energy storage, liquid crystal device, electronic device, biomaterial, sensing material and The fields such as catalyst carrier have shown excellent performance, have broad application prospects.But how to improve graphene-based compound The problems such as control of dispersibility, compatibility, nanostructure and size between material component and the selection of solvent, be worth after Continuous research and discussion.
Since biosensor is the instrument using biological substance sensitivity to be detected to it, life that can be to being detected Object molecule carries out fast track, so biosensor needs to have highly selective, high sensitivity, analysis fast, of low cost The features such as Miniaturized with instrument, grapheme material all extremely meet these conditions in all fields, but due to bio-sensing Device needs to touch various organic liquid when being detected substance, can inevitably stick some and be detected in liquid Water, dust, oil or dirt immune, once biosensor is polluted by these liquid, detection performance will decline, cannot Continue to use as biosensor, to limit the service life of biosensor, stability and durability, sensibility. Lead to this result be vertical graphene itself is super-hydrophobic, but it is very big to the adhesive force of water, even if by vertical Graphene inverts, and water droplet still adheres to vertical graphene surface.In general, the three of surface of solids viscosity and the surface of solids Phase line (solid-liquid-gas) is related, and continuously then tackness is high for triple line, and discontinuously then tackness is low for triple line.And vertical graphene Triple line is continuous, so its tackness is high.It is exactly to cause to allow when as biosensor because tackness is too high Liquid polluted biosensor.
Invention content
In order to overcome grapheme material when as biomaterial, sensor and catalyst carrier easily contaminated defect and Deficiency, the purpose of the present invention is to provide a kind of graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic The preparation method and applications of material.
The technical solution used in the present invention is:
A kind of preparation method of the graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic, including Following steps:
S1:Vertical graphene is generated on substrate;
S2:By atomic layer deposition method, dip-coating adsorption and oxidation zinc nanoparticles crystal seed on the surface of graphene;
S3:By hydro-thermal method, the growth of zinc oxide nano line on graphene forms graphene-zinc oxide micro-nano structure material Material;
S4:Graphene-zinc oxide micro-nano structure material is modified processing, obtains that there is automatically cleaning super lyophoby characteristic Graphene zinc oxide micro-nano grading function material.
In step S1, the method for generating vertical graphene is plasma enhanced chemical vapor deposition method.
In step S1, the control condition that plasma enhanced chemical vapor deposition method generates vertical graphene is:Substrate is Stainless steel lining bottom;It is CH to grow the sources C4And H2;Growth power 800W~1200W;800 DEG C~1000 DEG C of growth temperature;Growth time For 15min~20min;Cooling time is 20min~40min.
In step S2, the presoma of atomic layer deposition method is organic zinc compound and water;The temperature of deposition is 95 DEG C~105 ℃;The time deposited every time is 45s~55s;The number of cycle is 280 times~320 times.
In step S3, hydro-thermal method is specially:By the graphene of adsorption and oxidation zinc nanoparticles crystal seed, water, zinc nitrate and six Methenamine sealing carries out hydrothermal synthesis reaction.
In step S3, the temperature of hydro-thermal reaction is 80 DEG C~100 DEG C, and the time of reaction is 80min~100min.
In step S4, modification is specially:Graphene-zinc oxide micro-nano structure material is mixed with modifying agent, true Reciprocal of duty cycle is that 10h~14h is reacted under 0.05MPa~0.1MPa.
In step S4, the modifying agent used in modification is fluorochemical, carbon nanotube, organosilicon-modified acrylic tree At least one of fat.
This graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic is in preparing sensor Application.
The beneficial effects of the invention are as follows:
A kind of graphene zinc oxide micro-nano grading function material has been prepared in the present invention, this material has super-hydrophobic, super The superperformance of oleophobic, super thin blood is a kind of functional self-cleaning material.High contact angle due to super hydrophobic material and low rolling Angle can allow drop freely to be rolled on surface, reach automatically cleaning effect itself by the effect of water and taken away by the rolling of water droplet Dirt.The graphene zinc oxide micro-nano hierarchical structure of the present invention can be used as electrode or modified electrode, as a sensor to detection Some substances, such as the various biomolecule of hydrogen peroxide, glucose, urea, pH, amino acid, protein, DNA, have Wide application prospect.
Description of the drawings
Fig. 1 is the process schematic that the present invention prepares graphene zinc oxide micro-nano grading function material;
Fig. 2 is the scanning electron microscope (SEM) photograph of graphene zinc oxide micro-nano grading function material made from embodiment 1;
Fig. 3 is design sketch of the graphene zinc oxide micro-nano grading function material of the present invention when there is drop to drop in surface.
Specific implementation mode
A kind of preparation method of the graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic, including Following steps:
S1:Vertical graphene is generated on substrate;
S2:By atomic layer deposition method, dip-coating adsorption and oxidation zinc nanoparticles crystal seed on the surface of graphene;
S3:By hydro-thermal method, the growth of zinc oxide nano line on graphene forms graphene-zinc oxide micro-nano structure material Material;
S4:Graphene-zinc oxide micro-nano structure material is modified processing, obtains that there is automatically cleaning super lyophoby characteristic Graphene zinc oxide micro-nano grading function material.
Preferably, in step S1, the method for generating vertical graphene is plasma enhanced chemical vapor deposition method.
Preferably, in step S1, the control condition that plasma enhanced chemical vapor deposition method generates vertical graphene is: Substrate is stainless steel lining bottom;It is CH to grow the sources C4And H2;Growth power 800W~1200W;800 DEG C~1000 DEG C of growth temperature;It is raw It is 15min~20min for a long time;Cooling time is 20min~40min.
Preferably, in step S2, the presoma of atomic layer deposition method is organic zinc compound and water;The temperature of deposition is 95 DEG C~105 DEG C;The time deposited every time is 45s~55s;The number of cycle is 280 times~320 times;It is further preferred that step In S2, organic zinc compound is diethyl zinc;The temperature of deposition is 100 DEG C;The time deposited every time is 50s;The number of cycle It is 300 times.
Preferably, in step S3, hydro-thermal method is specially:By the graphene, water, nitric acid of adsorption and oxidation zinc nanoparticles crystal seed Zinc and hexa (HTMA) sealing carry out hydrothermal synthesis reaction.
Preferably, in step S3, a concentration of 0.2mol/L~0.3mol/L of zinc nitrate;Hexa it is a concentration of 0.2mol/L~0.3mol/L.
Preferably, in step S3, the temperature of hydro-thermal reaction is 80 DEG C~100 DEG C, time of reaction be 80min~ 100min。
Preferably, in step S4, modification is specially:Graphene-zinc oxide micro-nano structure material is mixed with modifying agent It closes, reacts 10h~14h in the case where vacuum degree is 0.05MPa~0.1MPa.
Preferably, in step S4, modifying agent used in modification is fluorochemical, carbon nanotube, organic-silicon-modified At least one of acrylic resin;It is further preferred that in step S4, the modifying agent used in modification is fluorine-containing chemical combination Object;Still further preferably, in step S4, the modifying agent used in modification is 1H, 1H, 2H, 2H- perfluoro capryl triethoxies Silane.
Further, in step S4, when the modifying agent used is fluorochemical, modification is fluorination treatment;Tool Body, the fluorination treatment is fluorinated for vacuum gas-phase.
The visible attached drawing of the preparation process schematic diagram of graphene zinc oxide micro-nano grading function material of the present invention 1.Fig. 1 is only indicated To the example of preparation method, method of the invention is not limited only to the related substances indicated in figure.
This graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic is in preparing sensor Application.
Preferably, in, sensor is electrochemical sensor and/or biosensor;The biosensor can To be field-effect transistor biosensor or optical biosensor.
Further, the graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic can be used for repairing Decorations electrode directly prepares electrode, is used as to glucose, urea, pH, amino acid, protein, DNA, hydrogen peroxide etc. The biosensor that various biomolecule are detected.
The graphene zinc oxide micro-nano grading function material that the present invention is prepared is that have self-cleaning functionalization material, Protection biosensor is can be very good, prevents it by the various complicated molecules in biological tissue's liquid or biological sample, such as egg In vain, the adherency of polypeptide, small molecule etc. can not be polluted by biological tissue's liquid or biological sample, can be extended it and be used the longevity Life, durability and its sensitivity of maintenance and stability.In addition, graphene zinc oxide micro-nano grading function material prepared by the present invention Material, moreover it is possible to can detect H when electrode as electrochemical sensor2O2, H2S, NO, ascorbic acid etc.;As field-effect transistor Biosensor detects pH;Utilize the characteristic of graphene fluorescent quenching in DNA bio-sensings, moreover it is possible to optical bio sensing be made Device detects DNA.
The invention thinking that the present invention is further illustrated below is as follows:
By the present invention in that manufacturing the piece with vertical orientation with the vapour deposition process (PECVD) of plasma enhanced chemical Shape graphene, by changing temperature, power, the time controls the density of graphene growth, controllable preparation vertical orientation Graphene.By atom deposition method, the series of steps such as hydro-thermal method prepare graphene zinc oxide micro-nano hierarchical structure, hydro-thermal method By controlling growth agents concentration, growth temperature, the time grows number to control the growth length of zinc oxide nanowire, diameter. Graphene zinc oxide micro-nano hierarchical structure makes its air when contacting drop be trapped within due to the distribution of zinc oxide nanowire On rough surface below liquid, the composite solid-liquid-gas interface that drop can be supported is formed, liquid is in steady in material surface Fixed Cassie states, this makes drop have larger contact angle and lower roll angle.And by fluorinated processing, it can Further decrease the surface energy of material surface so that the lyophoby performance of material is improved.In terms of hydrophobic oleophobic performance, make it With super-hydrophobicity, superoleophobic property, water droplet or oil droplet can be easy to slide from functional surface.In thin blood aspect of performance, Sticking experiment by antiplatelet and can obtaining the functional surface of graphene zinc oxide micro-nano hierarchical structure can make blood light Pine slides, and has achieved the effect that super thin blood.
Graphene zinc oxide micro-nano grading structure material can obtain outstanding waterproof, anti-blood and the performances such as grease proofing, provide The method for creating the graphene zinc oxide micro-nano hierarchical structure with self-cleaning performance, this answers protection as electrode with other Graphene is extremely important from polluting.As detection sensor, use graphene zinc oxide micro-nano hierarchical structure as electrode Or modified electrode, it can be as a sensor to some substances be detected, such as hydrogen peroxide, glucose, urea, pH, amino acid, egg The various biomolecule such as white matter, DNA.
Present disclosure is described in further detail below by way of specific embodiment, but embodiment is not to this Invention limits in any form.Unless stated otherwise, the present invention uses reagent, method and apparatus is the art routines Reagent, method and apparatus.
Embodiment 1:
One, preparation method
The preparation of the graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic of embodiment 1 includes Following steps:
The growth of S1, vertical graphene
(1) deionized water, ethyl alcohol is used to clean stainless steel lining bottom, then nitrogen removes moisture;
(2) stainless steel lining bottom is emitted in PECVD chamber inner foundation, is vacuumized;Control PECVD power is 1200W, raw Long temperature is 900 DEG C, and the sources growth C are CH4And H2, growth time is 15 minutes, is cooled to the time 30 minutes, goes out after growth Vertical graphene is made in stove;
S2, by atomic layer deposition method step 1 graphene surface dip-coating adsorption and oxidation zinc nanoparticles crystal seed
The sample of step S1 is arranged to the inside cavity for being put into ALD instruments, controlled at 100 DEG C, presoma two Zinc ethyl and oxygen, oxygen source are water, and time 50s repeats 300 cycles, on the surface of graphene dip-coating with argon cleaning sample surfaces Adsorption and oxidation zinc nanoparticles crystal seed, so as in next step being capable of growth of zinc oxide nano line on the surface of graphene;
S3, hydrothermal synthesis method the growth of zinc oxide nano line on graphene
Reagent needed for configuration growth first:0.25mol/L zinc nitrate hexahydrates and 0.25mol/L HTMA (hexa-methylenes four Amine);Then the graphene substrate of step 2 adsorption and oxidation zinc nanoparticles crystal seed is inverted in the beaker of appropriate volume size, Respectively plus 4mL deionized waters, 0.5mL zinc nitrates and 0.5mL HTMA, it is sealed with preservative film, is positioned in drying box 90 DEG C, water It thermally grown 90 minutes, is taken out after having grown and extra ZnO is rinsed out with deionized water.It repeats the above steps, makes flake graphite alkene Channel is filled up by zinc oxide nanowire between piece, forms secondary oxidative zinc nano wire branch, that is, it is micro- that graphene zinc oxide is prepared Receive grading function material;
The fluorination of S4, graphene zinc oxide micro-nano grading function material
Vacuum gas-phase fluoride process is fluorinated:The graphene zinc oxide micro-nano grading function material that step 3 is prepared is taken to place In vacuum desiccator, 100 μ L 1H, 1H, 2H, 2H- perfluoro capryl triethoxysilanes are added, vacuumize, vacuum degree reaches 0.08MPa vacuumizes 2min, and the fluorination time is 12 hours or so, after fluorination is completed, rinses sample with acetone or alcohol, goes Except extra fluorination reagent, the graphene zinc oxide micro-nano grading function material of embodiment 1 is obtained.
Two, performance test
Graphene zinc oxide micro-nano grading function material made from embodiment 1 is subjected to phenetic analysis, SEM figures are shown in attached drawing 2。
Graphene zinc oxide micro-nano grading function material made from embodiment 1 is subjected to hydrophobicity, oleophobic property, dredges courageous and upright survey Examination:
(1) hydrophobicity is tested
A drop water is added dropwise on graphene zinc oxide micro-nano grading material surface by contact angle measurement and drips (4 microlitres), sees Examine the motion conditions of water droplet.As a result as shown in Fig. 3, drop drops in the function wetting table of graphene zinc oxide micro-nano hierarchical structure Face, and due to the low-surface-energy after sample fluorination, drop is made to form the contact angle more than 150 ° on function wetting surface, and Angle of lag very little, drop freely slide on graphene zinc oxide micro-nano grading structure material surface, have hydrophobicity and automatically cleaning Performance.
(2) oleophobic property is tested
It is identical as step (1), change water droplet into oil droplet.The results show that oil droplet is in graphene zinc oxide micro-nano hierarchical structure Material liquid surface freely slides, and has oleophobic property.
(3) courageous and upright test is dredged
It is identical as step (1), change water droplet into drop of blood.The results show that drop of blood is in graphene zinc oxide micro-nano hierarchical structure Material liquid surface freely slides, and has achieved the effect that super thin blood.
Embodiment 2:
One, preparation method
The preparation of the graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic of embodiment 2 includes Following steps:
The growth of S1, vertical graphene
(1) deionized water, ethyl alcohol is used to clean stainless steel lining bottom, then nitrogen removes moisture;
(2) stainless steel lining bottom is emitted in PECVD chamber inner foundation, is vacuumized;Control PECVD power is 1000W, raw Long temperature is 800 DEG C, and the sources growth C are CH4And H2, growth time is 20 minutes, is cooled to the time 30 minutes, goes out after growth Vertical graphene is made in stove;
S2, by atomic layer deposition method step 1 graphene surface dip-coating adsorption and oxidation zinc nanoparticles crystal seed
It is same as Example 1;
S3, hydrothermal synthesis method the growth of zinc oxide nano line on graphene
Reagent needed for configuration growth first:0.25mol/L zinc nitrate hexahydrates and 0.25mol/L HTMA (hexa-methylenes four Amine);Then the graphene substrate of step 2 adsorption and oxidation zinc nanoparticles crystal seed is inverted in the beaker of appropriate volume size, Respectively plus 4mL deionized waters, 0.5mL zinc nitrates and 0.5mL HTMA, it is sealed with preservative film, is positioned in drying box 80 DEG C, water It thermally grown 100 minutes, is taken out after having grown and extra ZnO is rinsed out with deionized water.It repeats the above steps, makes flake graphite alkene Channel is filled up by zinc oxide nanowire between piece, forms secondary oxidative zinc nano wire branch, that is, it is micro- that graphene zinc oxide is prepared Receive grading function material;
The fluorination of S4, graphene zinc oxide micro-nano grading function material
Vacuum gas-phase fluoride process is fluorinated:The graphene zinc oxide micro-nano grading function material that step 3 is prepared is taken to place In vacuum desiccator, 100 μ L 1H, 1H, 2H, 2H- perfluoro capryl triethoxysilanes are added, vacuumize, vacuum degree reaches 0.08MPa vacuumizes 2min, and the fluorination time is 14 hours or so, after fluorination is completed, rinses sample with acetone or alcohol, goes Except extra fluorination reagent, the graphene zinc oxide micro-nano grading function material of embodiment 2 is obtained.
Two, performance test
The carry out hydrophobicity for the graphene zinc oxide micro-nano grading function material that embodiment 2 is prepared, is dredged oleophobic property Courage and uprightness test;The results show that the graphene zinc oxide micro-nano grading function material of embodiment 2 have it is super-hydrophobic, it is superoleophobic, it is super thin The superperformance of blood has automatically cleaning super lyophoby characteristic.
Embodiment 3:
One, preparation method
The preparation of the graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic of embodiment 3 includes Following steps:
The growth of S1, vertical graphene
(1) deionized water, ethyl alcohol is used to clean stainless steel lining bottom, then nitrogen removes moisture;
(2) stainless steel lining bottom is emitted in PECVD chamber inner foundation, is vacuumized;Control PECVD power is 800W, raw Long temperature is 1000 DEG C, and the sources growth C are CH4And H2, growth time is 18 minutes, is cooled to the time 30 minutes, goes out after growth Vertical graphene is made in stove;
S2, by atomic layer deposition method step 1 graphene surface dip-coating adsorption and oxidation zinc nanoparticles crystal seed
It is same as Example 1;
S3, hydrothermal synthesis method the growth of zinc oxide nano line on graphene
Reagent needed for configuration growth first:0.25mol/L zinc nitrate hexahydrates and 0.25mol/L HTMA (hexa-methylenes four Amine);Then the graphene substrate of step 2 adsorption and oxidation zinc nanoparticles crystal seed is inverted in the beaker of appropriate volume size, Respectively plus 4mL deionized waters, 0.5mL zinc nitrates and 0.5mL HTMA, it is sealed with preservative film, is positioned in drying box 100 DEG C, water It thermally grown 80 minutes, is taken out after having grown and extra ZnO is rinsed out with deionized water.It repeats the above steps, makes flake graphite alkene Channel is filled up by zinc oxide nanowire between piece, forms secondary oxidative zinc nano wire branch, that is, it is micro- that graphene zinc oxide is prepared Receive grading function material;
The fluorination of S4, graphene zinc oxide micro-nano grading function material
Vacuum gas-phase fluoride process is fluorinated:The graphene zinc oxide micro-nano grading function material that step 3 is prepared is taken to place In vacuum desiccator, 100 μ L 1H, 1H, 2H, 2H- perfluoro capryl triethoxysilanes are added, vacuumize, vacuum degree reaches 0.08MPa vacuumizes 2min, and the fluorination time is 10 hours or so, after fluorination is completed, rinses sample with acetone or alcohol, goes Except extra fluorination reagent, the graphene zinc oxide micro-nano grading function material of embodiment 3 is obtained.
Two, performance test
The graphene zinc oxide micro-nano grading function material that embodiment 3 is prepared carries out hydrophobicity, oleophobic property, dredges blood Property test;The results show that the graphene zinc oxide micro-nano grading function material of embodiment 3 has super-hydrophobic, superoleophobic, super thin blood Superperformance, have automatically cleaning super lyophoby characteristic.
Comparative example 1:
One, preparation method
The preparation of the graphene zinc oxide micro-nano grading function material of comparative example 1 includes the following steps:
The growth of S1, vertical graphene
It is same as Example 1;
S2, graphene surface dip-coating adsorption and oxidation zinc nanoparticles crystal seed
The vertical graphene sample of step 1 is gently stained with to the methanol solution of 0.005mol/L zinc acetates, weight is evaporated at 60 DEG C It plural time, then under 300 DEG C of vacuum states, is reacted, plates crystal seed on the surface of graphene;
S3, hydrothermal synthesis method the growth of zinc oxide nano line on graphene
It is same as Example 1;
The fluorination of S4, graphene zinc oxide micro-nano grading function material
It is same as Example 1, the graphene zinc oxide micro-nano grading function material of comparative example 1 is made.
Two, performance test
By above-mentioned steps 2 prepare to crystal seed be unevenly distributed, so as to cause subsequent growth oxidation nanometer line not It is enough uniform, hydrophobicity, oleophobic property and the thin courageous and upright all poor (leaching of the graphene zinc oxide micro-nano grading function material being prepared Profit, does not fall off), it can not be applied to practical.
In summary:
The preparation of graphene zinc oxide micro-nano compound structure of the present invention, passes through the vapour deposition process of plasma enhanced chemical Graphene is grown, by controlling temperature, power, the conditions such as time control the stand density length of graphene.In graphene table Face dip-coating adsorption and oxidation zinc nanoparticles crystal seed, is prepared step by step using hydro-thermal method, ensures that micro-structure controllably adds level by several times, Prepared dendroid graphene zinc oxide micro-nano hierarchical structure surface further uses the fluorochemical with low-surface-energy Surface modification is carried out, hydrophobic, oleophobic is made it have, dredges blood or lyophoby performance.The principle of super-hydrophobic automatic cleaning material is to pass through water Effect reach automatically cleaning effect itself, due to the high contact angle of super hydrophobic material, low roll angle can allow water droplet on surface It freely rolls, it is possible to which dirt is taken away by the rolling of water droplet.
It, can since the graphene zinc oxide micro-nano grading function material prepared is that have self-cleaning functionalization material To protect biosensor well, prevent it by the various complicated molecules in biological tissue's liquid or biological sample, such as albumen, The adherency of polypeptide, small molecule etc. can not be polluted by biological tissue's liquid or biological sample, can extend its service life, Durability and its sensitivity of maintenance and stability.

Claims (9)

1. a kind of preparation method of the graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic, feature It is:
Include the following steps:
S1:Vertical graphene is generated on substrate;
S2:By atomic layer deposition method, dip-coating adsorption and oxidation zinc nanoparticles crystal seed on the surface of graphene;
S3:By hydro-thermal method, the growth of zinc oxide nano line on graphene forms graphene-zinc oxide micro-nano structure material;
S4:Graphene-zinc oxide micro-nano structure material is modified processing, obtains the graphite with automatically cleaning super lyophoby characteristic Alkene zinc oxide micro-nano grading function material.
2. a kind of graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic according to claim 1 The preparation method of material, it is characterised in that:In step S1, it is heavy for plasma enhanced chemical vapor to generate the method for vertical graphene Area method.
3. a kind of graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic according to claim 2 The preparation method of material, it is characterised in that:In step S1, plasma enhanced chemical vapor deposition method generates the control of vertical graphene Condition processed is:Substrate is stainless steel lining bottom;It is CH to grow the sources C4And H2;Growth power 800W~1200W;800 DEG C of growth temperature~ 1000℃;Growth time is 15min~20min;Cooling time is 20min~40min.
4. a kind of graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic according to claim 1 The preparation method of material, it is characterised in that:In step S2, the presoma of atomic layer deposition method is organic zinc compound and water;Deposition Temperature be 95 DEG C~105 DEG C;The time deposited every time is 45s~55s;The number of cycle is 280 times~320 times.
5. a kind of graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic according to claim 1 The preparation method of material, it is characterised in that:In step S3, hydro-thermal method is specially:By the graphite of adsorption and oxidation zinc nanoparticles crystal seed Alkene, water, zinc nitrate and hexa sealing carry out hydrothermal synthesis reaction.
6. a kind of graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic according to claim 5 The preparation method of material, it is characterised in that:In step S3, the temperature of hydro-thermal reaction is 80 DEG C~100 DEG C, and the time of reaction is 80min~100min.
7. a kind of graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic according to claim 1 The preparation method of material, it is characterised in that:In step S4, modification is specially:By graphene-zinc oxide micro-nano structure material with Modifying agent mixes, and reacts 10h~14h in the case where vacuum degree is 0.05MPa~0.1MPa.
8. a kind of graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic according to claim 7 The preparation method of material, it is characterised in that:In step S4, the modifying agent used in modification is fluorochemical, carbon nanotube, has At least one of machine fluorine-silicon modified acrylic resin.
9. any one of claim 1~8 prepares the graphene zinc oxide micro-nano grading function material of gained in preparing sensor Application.
CN201810125540.0A 2018-02-08 2018-02-08 Preparation method and application of graphene zinc oxide micro-nano grading functional material with self-cleaning and super-lyophobic characteristics Active CN108486544B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810125540.0A CN108486544B (en) 2018-02-08 2018-02-08 Preparation method and application of graphene zinc oxide micro-nano grading functional material with self-cleaning and super-lyophobic characteristics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810125540.0A CN108486544B (en) 2018-02-08 2018-02-08 Preparation method and application of graphene zinc oxide micro-nano grading functional material with self-cleaning and super-lyophobic characteristics

Publications (2)

Publication Number Publication Date
CN108486544A true CN108486544A (en) 2018-09-04
CN108486544B CN108486544B (en) 2020-06-05

Family

ID=63339896

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810125540.0A Active CN108486544B (en) 2018-02-08 2018-02-08 Preparation method and application of graphene zinc oxide micro-nano grading functional material with self-cleaning and super-lyophobic characteristics

Country Status (1)

Country Link
CN (1) CN108486544B (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109713050A (en) * 2018-12-24 2019-05-03 香港中文大学(深圳) A kind of graphene-ZnO composite material and preparation method and ultraviolet detector
CN110308188A (en) * 2019-01-11 2019-10-08 天津理工大学 Golden co-modified Graphene electrodes of platinum and its preparation method and application
CN110721599A (en) * 2019-09-24 2020-01-24 江苏大学 Preparation method and application of SGO-ZnO-PSF composite ultrafiltration membrane
CN111153430A (en) * 2019-11-20 2020-05-15 广州钰芯瀚吉科技有限公司 Zinc oxide spine array with anti-pollution function and preparation method and application thereof
CN111497365A (en) * 2020-04-03 2020-08-07 武汉大学 Hydrophobic material based on two-dimensional material modified micro-nano structure and preparation method and application thereof
CN114717533A (en) * 2022-02-25 2022-07-08 中国地质大学(北京) Method for preparing sensor electrode protection film by utilizing bionic structure and application
CN116695091A (en) * 2023-08-01 2023-09-05 南京原磊纳米材料有限公司 Hydrophobic conductive film and preparation method and application thereof

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103346199A (en) * 2013-07-10 2013-10-09 合肥工业大学 Ultraviolet photoelectric detector and preparation method thereof based on single-layer graphene/zinc oxide nano-rod array schottky junction
CN104781305A (en) * 2012-11-26 2015-07-15 麻省理工学院 Nanowire-modified graphene and methods of making and using same
CN105271361A (en) * 2015-10-28 2016-01-27 中国科学院上海微***与信息技术研究所 Preparation method of dendritic zinc oxide nanowire array
CN106442642A (en) * 2016-08-30 2017-02-22 安徽师范大学 Preparation method of zinc oxide/graphene composite material and resistance type gas sensor
CN106629817A (en) * 2016-11-18 2017-05-10 哈尔滨理工大学 Preparation and application of graphene/zinc oxide nanowire array/three-dimensional foam graphene composite material
CN206244402U (en) * 2016-10-09 2017-06-13 全普光电科技(上海)有限公司 A kind of graphene-based nanowire composite structures
CN106847667A (en) * 2016-12-27 2017-06-13 苏州大学 Modified nitride-based semiconductor in a kind of surface and preparation method thereof
CN107315045A (en) * 2017-07-05 2017-11-03 哈尔滨理工大学 The preparation and application of a kind of graphene/zinc oxide nano popped rice/ITO electrode
CN107403853A (en) * 2017-06-16 2017-11-28 河南大学 A kind of ZTO ZnO/CBS GSs flexible thin-film solar cells and preparation method thereof

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104781305A (en) * 2012-11-26 2015-07-15 麻省理工学院 Nanowire-modified graphene and methods of making and using same
CN103346199A (en) * 2013-07-10 2013-10-09 合肥工业大学 Ultraviolet photoelectric detector and preparation method thereof based on single-layer graphene/zinc oxide nano-rod array schottky junction
CN105271361A (en) * 2015-10-28 2016-01-27 中国科学院上海微***与信息技术研究所 Preparation method of dendritic zinc oxide nanowire array
CN106442642A (en) * 2016-08-30 2017-02-22 安徽师范大学 Preparation method of zinc oxide/graphene composite material and resistance type gas sensor
CN206244402U (en) * 2016-10-09 2017-06-13 全普光电科技(上海)有限公司 A kind of graphene-based nanowire composite structures
CN106629817A (en) * 2016-11-18 2017-05-10 哈尔滨理工大学 Preparation and application of graphene/zinc oxide nanowire array/three-dimensional foam graphene composite material
CN106847667A (en) * 2016-12-27 2017-06-13 苏州大学 Modified nitride-based semiconductor in a kind of surface and preparation method thereof
CN107403853A (en) * 2017-06-16 2017-11-28 河南大学 A kind of ZTO ZnO/CBS GSs flexible thin-film solar cells and preparation method thereof
CN107315045A (en) * 2017-07-05 2017-11-03 哈尔滨理工大学 The preparation and application of a kind of graphene/zinc oxide nano popped rice/ITO electrode

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109713050B (en) * 2018-12-24 2021-06-29 香港中文大学(深圳) graphene-ZnO composite material, preparation method thereof and ultraviolet detector
CN109713050A (en) * 2018-12-24 2019-05-03 香港中文大学(深圳) A kind of graphene-ZnO composite material and preparation method and ultraviolet detector
CN110308188A (en) * 2019-01-11 2019-10-08 天津理工大学 Golden co-modified Graphene electrodes of platinum and its preparation method and application
CN110308188B (en) * 2019-01-11 2021-04-13 天津理工大学 Gold-platinum co-modified graphene electrode and preparation method and application thereof
CN110721599A (en) * 2019-09-24 2020-01-24 江苏大学 Preparation method and application of SGO-ZnO-PSF composite ultrafiltration membrane
CN110721599B (en) * 2019-09-24 2022-01-11 江苏大学 Preparation method and application of SGO-ZnO-PSF composite ultrafiltration membrane
CN111153430A (en) * 2019-11-20 2020-05-15 广州钰芯瀚吉科技有限公司 Zinc oxide spine array with anti-pollution function and preparation method and application thereof
CN111497365B (en) * 2020-04-03 2021-07-06 武汉大学 Hydrophobic material based on two-dimensional material modified micro-nano structure and preparation method and application thereof
CN111497365A (en) * 2020-04-03 2020-08-07 武汉大学 Hydrophobic material based on two-dimensional material modified micro-nano structure and preparation method and application thereof
CN114717533A (en) * 2022-02-25 2022-07-08 中国地质大学(北京) Method for preparing sensor electrode protection film by utilizing bionic structure and application
CN114717533B (en) * 2022-02-25 2023-03-10 中国地质大学(北京) Method for preparing sensor electrode protection film by utilizing bionic structure and application
CN116695091A (en) * 2023-08-01 2023-09-05 南京原磊纳米材料有限公司 Hydrophobic conductive film and preparation method and application thereof
CN116695091B (en) * 2023-08-01 2023-09-29 南京原磊纳米材料有限公司 Hydrophobic conductive film and preparation method and application thereof

Also Published As

Publication number Publication date
CN108486544B (en) 2020-06-05

Similar Documents

Publication Publication Date Title
CN108486544A (en) A kind of preparation method and applications of the graphene zinc oxide micro-nano grading function material with automatically cleaning super lyophoby characteristic
Kahoush et al. Surface modification of carbon felt by cold remote plasma for glucose oxidase enzyme immobilization
Sartori et al. Laser-induced periodic surface structures (LIPSS) on heavily boron-doped diamond for electrode applications
Kang et al. Sensitive detection of ascorbic acid and alkaline phosphatase activity by double-channel photoelectrochemical detection design based on g-C3N4/TiO2 nanotubes hybrid film
Li et al. Toward smart sensing by MXene
Ortiz-Ortega et al. Aging of plasma-activated carbon surfaces: Challenges and opportunities
Jung et al. Commercial silk-based electronic textiles for NO2 sensing
CN112240898B (en) Photoelectrochemical aptamer sensor and preparation method and application thereof
CN105842312A (en) Nano flower-shaped ultramicro gold electrode and preparation and application thereof
US11350858B2 (en) Ultra-sensitive glucose sensor based on graphene and carbon fiber substrate and preparation method thereof
CN104020204A (en) Electrochemical sensor for detecting lead as well as preparation method and application thereof
Wei et al. Fe3O4/SiO2/CS surface ion-imprinted polymer modified glassy carbon electrode for highly sensitivity and selectivity detection of toxic metal ions
Lu et al. A novel and disposable enzyme-labeled amperometric immunosensor based on MWCNT fibers for Listeria monocytogenes detection
US20220348468A1 (en) Procedure for the doping of graphene oxide by the use of microorganisms, nitrogen- and sulfur-dual doped graphene thus obtained and its use
CN106841344B (en) The preparation and application of a kind of poroid single-walled carbon nanotube and its modified electrode
Messina et al. Simultaneous detection and photocatalysis performed on a 3D graphene/ZnO hybrid platform
Hu et al. Fabrication and potential applications of highly durable superhydrophobic polyethylene terephthalate fabrics produced by in-situ zinc oxide (ZnO) nanowires deposition and polydimethylsiloxane (PDMS) packaging
CN103412020B (en) Preparation method and application of acetylcholin esterase electrochemical biosensor
CN103207222B (en) Method for preparing graphene nano-material electrochemical sensor by atomic layer deposition process
CN108802121B (en) Photocurrent dissolved oxygen sensor
Wang et al. Aligned open-ended carbon nanotube membranes for direct electrochemistry applications
Cheng et al. Enhanced microorganism attachment and flavin excretion in microbial fuel cells via an N, S-codoped carbon microflower anode
Jeykumari et al. Covalent modification of multiwalled carbon nanotubes with neutral red for the fabrication of an amperometric hydrogen peroxide sensor
CN104237351A (en) Preparation method and application of glucose sensor
Cogal et al. Plasma-assisted synthesis of MnO2–polyaniline composite for electrochemical sensing of dopamine

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant