CN1862855A - Mehtod for preparing core assembly for proton exchange membrane fuel cell with adjustable hydrophilicity and hydrophobicity - Google Patents
Mehtod for preparing core assembly for proton exchange membrane fuel cell with adjustable hydrophilicity and hydrophobicity Download PDFInfo
- Publication number
- CN1862855A CN1862855A CNA2006100186330A CN200610018633A CN1862855A CN 1862855 A CN1862855 A CN 1862855A CN A2006100186330 A CNA2006100186330 A CN A2006100186330A CN 200610018633 A CN200610018633 A CN 200610018633A CN 1862855 A CN1862855 A CN 1862855A
- Authority
- CN
- China
- Prior art keywords
- exchange membrane
- proton exchange
- fuel cell
- core component
- polytetrafluoroethylene
- 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
Links
Images
Classifications
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
Landscapes
- Fuel Cell (AREA)
- Inert Electrodes (AREA)
Abstract
This invention relates to preparation method of core components used in proton exchanging film fuel battery. It is preparation method of core components used in philic hydrophobicity adjustable proton exchanging film fuel battery. The procedures are that 1) slime making, weight ratio 0.1:1 to 1:0.1 of proton conduction polymer and polytetrafluoroethylene are selected, 3-40 percent weight concentration proton conduction polymer solution and 60-70 percent weight concentration polytetrafluoroethylene are also selected, then they are used to make into slime. 2) The slime is silk-screen printed, cast, coated or sprayed on the medium, en solution is heated eliminated, and catalyst layer is formed on the medium. Then the proton exchanging film is set between the catalyst layers on the two media, the material of the catalyst layer is transferred printed onto the proton exchanging film through heating to get the core component used in the proton exchanging film fuel battery. The feature is that wetting angle of the component to water can be adjusted through making process, so water managing when the core component is practical applied in the fuel battery will has good adaptability.
Description
Technical field
The present invention relates to a kind of preparation method of core component of used in proton exchange membrane fuel cell.
Background technology
Proton Exchange Membrane Fuel Cells (PEMFC) has high power density; high-energy conversion efficiency; cold-starting; advantages of environment protection; promise to be most the power source of zero disposal of pollutants electric car; make it in today that global energy crisis and environment go from bad to worse, become one of focus of international new and high technology competition.The core component of used in proton exchange membrane fuel cell (catalyst coated membrane, CCM) then be that development in recent years gets up to be different from conventional film electrode (membraneelectrode assembly, MEA) core components of PEMFC of structure.Traditional membrane electrode (MEA) manufacture method mainly is catalyst to be transferred to form Catalytic Layer on the diffusion layer, then with proton exchange membrane hot pressing, floods on its Catalytic Layer or spraying proton conductive resin solution again.The kind electrode structure, Catalytic Layer combines relatively poor with proton exchange membrane, and a very important shortcoming is that the proton conductive resin of dipping or spraying is merely able to enter Catalytic Layer surface and does not arrive Catalytic Layer inside, and proton-conducting is subjected to very big the influence.And employing CCM technology (catalyst is directly transferred on the proton exchange membrane), Catalytic Layer combines with film closely, and Catalytic Layer and film can be done very thinly, and proton-conducting is very good, not only improve the electrochemical reaction activity of Catalytic Layer, but also can reduce the manufacturing cost of membrane electrode.
[US6074692, US5330860, US5316871, US5211984, US5234777, JP2002280003l have described a kind of catalyst pulp with configuration and have directly printed, are coated with and be sprayed on the method for preparing CCM on the proton exchange membrane.[JP5538934, JP5847471l have described a kind of method that Pt directly is deposited on the film surface.These above-mentioned method technologies are simple, and catalyst loss is little, but the swelling set of film is bigger in the catalyst transfer process.[US6749892, EPll37090A2] described a kind of method of electric arc sputter that adopts catalyst metals or carbon supported catalyst has been splashed to the method that the proton exchange membrane surface forms CCM.Catalyst metals is directly transferred to the CCM on the proton exchange membrane, because the very high surface activity of nano metal particles, catalyst generally exists with the form of reunion or film, and this has just reduced the surface activity area of catalyst.CN1269428A has introduced a kind of powder direct heat with catalyst and protonically conductive polymer and has been pressed onto the method for preparing CCM on the proton exchange membrane.The CCM of this method preparation, its Catalytic Layer is comparatively fine and close, but continuity and uniformity are bad, and the fuel cell output performance is also bad.
[US5415888, US5702755, US4272353, US3134697, US6391486B1] introduced a kind of with the configuration catalyst slurry at first print, cast or be sprayed on the materials such as polyester film, PTFE film, porous dielectric film, sheet metal, glass plate, solvent is removed in heating, catalyst is transferred to the method for preparing CCM on the proton exchange membrane by hot pressing then.Because just removing, so proton exchange membrane do not have the swelling phenomenon to solvent before Catalytic Layer is transferred to proton exchange membrane, Catalytic Layer has good uniformity.[US5211984, US5234777] adopts Nafion is proton conductive substance and binding agent, uses transfer printing to prepare CCM.The CCM of this method preparation, Catalytic Layer contacts with the proton exchange film close, and uniformity is better, but the hydrophilic and hydrophobic of its Catalytic Layer is unadjustable.For improving the hydrophobicity of Catalytic Layer, US5272017 adds PTFE (polytetrafluoroethylene) in catalyst pulp.Though this method can be improved the hydrophobicity of Catalytic Layer, PTFE can not disperse in Catalytic Layer continuously uniformly, thereby lacks the modulability in fuel cells applications upper hose reason.
The employed core component of existing Proton Exchange Membrane Fuel Cells (CCM), Catalytic Layer generally use hydrophilic proton conductive resin or hydrophobic polytetrafluoroethylene (PTFE) as binding agent; When only adopting proton conductive resin as binding agent, the Catalytic Layer that makes combines with film closely, and Catalytic Layer can be done very thinly, and proton-conducting is very good, but this CCM hydrophily is too strong, is difficult to water management regulated make the Catalytic Layer water blockoff easily and battery performance sharply descends; When only adopting polytetrafluoroethylene (PTFE is generally emulsion) as binding agent, Catalytic Layer has excellent hydrophobic property, but the proton conductivity of Catalytic Layer is significantly less than the Catalytic Layer of employing protonically conductive polymer as binding agent.
Summary of the invention
The preparation method who the purpose of this invention is to provide the core component of the used in proton exchange membrane fuel cell that a kind of hydrophilic and hydrophobic is adjustable, the fuel cell output performance is good, be characterized in that this core component can regulate by preparation process the angle of wetting of water, thereby make core component in fuel cell, have excellent adaptability to water management during practical application.
To achieve these goals, technical scheme of the present invention is: the preparation method of the used in proton exchange membrane fuel cell core component that a kind of hydrophilic and hydrophobic is adjustable, it comprises the steps:
1) preparation slip: by protonically conductive polymer and polytetrafluoroethylene weight ratio is 0.1: 1-1: 0.1 to choose protonically conductive polymer solution and the weight concentration that weight concentration is 3-40% be the ptfe emulsion of 60-70%, under 3000 rev/mins-20000 rev/mins high-speed stirred, be prepared into polytetrafluoroethylene/protonically conductive polymer mixing material, again with catalyst by protonically conductive polymer: the catalyst weight ratio is 1: 3-3: drop in polytetrafluoroethylene/protonically conductive polymer mixing material in 1 the scope and be prepared into slip; Big as the need angle of wetting, then the polytetrafluoroethylene in protonically conductive polymer and the polytetrafluoroethylene weight ratio is got big value;
2) with at first silk screen printing, casting of slip, be coated with or be sprayed on the medium, the heating remove solvent, on medium, form catalyst layer; Then proton exchange membrane is placed between two catalyst layers on the medium, be transferred on the proton exchange membrane, get the core component (CCM) of used in proton exchange membrane fuel cell by the material of hot pressing with catalyst layer.
The need preliminary treatment of described proton exchange membrane: it is 3-10wt%H that proton exchange membrane is immersed weight concentration
2O
2In, 70-90 ℃ of following heat treatment 0.5-2h uses deionized water rinsing 3-5 time; Immerse the H of 0.3-2mol/L again
2SO
470-90 ℃ of following heat treatment 0.5-2h in the solution; 70-90 ℃ of following heat treatment 0.5-2h in deionized water changes deionized water therebetween 3-5 time then.By above-mentioned preprocessing process, can remove the organic and inorganic impurity of bringing in the proton exchange membrane production process.
Described protonically conductive polymer is meant the perfluorinated sulfonic resin with proton exchange ability that contains sulfonic acid group, Nafion resin or Nafion solution as DuPont company, the Kraton G1650 resin of Dias company, or the Flemion protonically conductive polymer etc.; Also can be partly sulfonated sulfonic fluoropolymer resin, or have proton exchange function sulfonation thermal stability polymer, as sulfonation trifluorostyrene, sulfonated polyether-ether-ketone etc.
Described catalyst is meant Pt, Pd, Ru, Rh, Ir, Os noble metal or its carbon loading Pt/C, Pd/C, Ru/C, Rh/C, Ir/C, Os/C, bianry alloy PtPd, the PtRu of Pt and Pd, Ru, Rh, Ir, Os, PtRh, PtIr, PtOs or its carbon loading, bianry alloy, ternary alloy three-partalloy or its carbon that Pt, Pd, Ru, Rh, Ir, Os noble metal and Fe, Cr, Ni, Co form carry bianry alloy, ternary alloy three-partalloy.Above-mentioned carrier carbon is generally conductive carbon black or carbon nano-tube, carbon nano-fiber.
Described proton exchange membrane is a perfluoro sulfonic acid membrane, as Nafion film, Dow film, Flemion film, Aciplex film, partly sulfonated proton exchange membrane, BAM3G film as Ballard company, the proton exchange membrane of nonfluorinated, as the sulfonated polyether-ether-ketone film, be the composite membrane of substrate with the PTFE perforated membrane, as Gore-select
TM
Described medium is polyester film, PTFE film, porous dielectric film, sheet metal or glass plate etc.
The present invention directly adopts step 1) and step 2) flow process, Catalytic Layer can be regulated in 40 ° of-100 ° of scopes the angle of wetting (hydrophilic and hydrophobic) of water; Protonically conductive polymer and polytetrafluoroethylene weight ratio are 0.1: 1-1: 0.1, and when the polytetrafluoroethylene in protonically conductive polymer and the polytetrafluoroethylene weight ratio was got big value, its angle of wetting was big value.
In order further to increase the hydrophobic scope of Catalytic Layer, particularly improve the stability of Catalytic Layer, need heat-treat the core component of used in proton exchange membrane fuel cell.Its concrete steps are: (1) puts into the core component of used in proton exchange membrane fuel cell NaCl, the Na of 0.5-2mol/L
2SO
4Perhaps NaNO
3Soak 0.5-2h in the solution, after the washed with de-ionized water at N
2Or in the reducing gas atmosphere, 340-350 ℃ of high temperature is handled 20-40min down and is made polytetrafluoroethylene (PTFE) vitrifying and crystallization in the Catalytic Layer, and the core component of the used in proton exchange membrane fuel cell after (2) heat treatment is put into 0.3-2mol/L H
2SO
4Soak in the solution, soak 0.5-2h and washed with de-ionized water remove in proton exchange membrane and the Catalytic Layer inner proton conducting polymer Na ion and protonated.Prepared like this CCM is in step 1) and step 2) flow process under, Catalytic Layer can be regulated in 50 ° of-130 ° of scopes the angle of wetting of water, sees Table 1.
Adjusting to the wet angle of Catalytic Layer water among the present invention is by the dosage ratio of change protonically conductive polymer with polytetrafluoroethylene (PTFE), and the Catalytic Layer post-processing temperature is realized.Protonically conductive polymer and polytetrafluoroethylene mass ratio are 0.1: 1-1: regulate in 0.1 scope, Catalytic Layer is not heat-treated, angle of wetting is respective change in 40 ° of-100 ° of scopes; If 340-350 ℃ of heat treatment, angle of wetting is respective change in 50 ° of-130 ° of scopes to Catalytic Layer.At 340-350 ℃ heat treated the time, Catalytic Layer and proton exchange membrane must adopt NaCl, Na to Catalytic Layer
2SO
4Perhaps NaNO
3The processing of solution Naization, thereby so that in proton exchange membrane and the Catalytic Layer protonically conductive polymer change the Na type into and have vitrification point more than 340 ℃.
Characteristics of the present invention are that this Catalytic Layer can be regulated by preparation process the angle of wetting of water, thereby the core component that makes used in proton exchange membrane fuel cell has excellent adaptability to water management during practical application in fuel cell.The present invention adopts protonically conductive polymer to mix by certain proportioning with polytetrafluoroethylene, and the PTFE/ protonically conductive polymer has good dispersiveness in the prepared Catalytic Layer, makes the present invention have the good characteristics of fuel cell output performance.
Description of drawings
Fig. 1 is the monocell polarization curve of the embodiment of the invention 1 and comparative example 1
Embodiment
In order to understand the present invention better, further illustrate content of the present invention below in conjunction with embodiment, but content of the present invention not only is confined to the following examples.
Embodiment 1:
Getting the 20g weight concentration is Nafion solution (the Du Pont company production of 5wt%, 5wt% is a Nafion resin, and 95wt% is low-boiling point alcohol compositions such as water and ethanol, isopropyl alcohol), adding weight concentration is the PTFE emulsion 1g of 60wt%, electronic stirring 30min, 3000 rev/mins of rotating speeds.Add 3gPt/C catalyst (Johnson Matthey company produces, and the average grain diameter of formed by catalytic active particles Pt is 3nm, and the Pt carrying capacity is 40wt%), ultrasonic agitation 20min makes slip.The preliminary treatment of proton exchange membrane: getting Nafion 212 films is proton exchange membrane, thickness 51 μ m; The immersion weight concentration is 5wt%H
2O
2In, 70 ℃ of following heat treatment 1h (hour), with deionized water rinsing 3 times; Immerse the H of 0.5mol/L again
2SO
470 ℃ of following heat treatment 1h in the solution; 70 ℃ of following heat treatment 1h in deionized water change deionized water therebetween 3 times then.
Getting thickness is 100 μ m, and film is wide to be the non-directional PTFE film of 8cm, and cleans with absolute ethyl alcohol; Adopt coating apparatus that slip is coated on the transfer medium (being the PTFE film), and send into drying tunnel, with N by conveyer
2Be protective atmosphere, under 100-130 ℃ of condition, carry out drying, the long 1-20m of drying tunnel wherein, the film walking speed is 0.3-2m/min, solvent is removed in heating, forms catalyst layer on the PTFE film; Coating machine scraper gap is 60 μ m, and coating width is 5cm.Nafion 212 films are placed between the catalyst layer of two PTFE films, send into hot-pressing processing in the calender by conveyer, the roll-in temperature is 130 ℃, pressure is 0.6MPa, the film walking speed is 0.3-2m/min, adopt automatic stripping machine to divest the PTFE film of Nafion 212 film both sides, Nafion 212 films that obtain having Catalytic Layer.Nafion 212 films that will have Catalytic Layer are put into the Na of 2mol/L
2SO
4Soak 0.5h in the solution, at N
2Or make PTFE sintering in the Catalytic Layer under the inert gas atmosphere protection, 345 ℃ of conditions; Immerse the H of 0.5mol/L again
2SO
470 ℃ of following heat treatment 1h in the solution; 70 ℃ of following heat treatment 1h in deionized water change deionized water therebetween 3 times then; Obtain CCM of the present invention at last.The CCM thickness of preparation is 61 μ m, error≤10%, and Catalytic Layer has good uniformity.Catalytic Layer thickness 5 ± 1 μ m, Pt carrying capacity 0.53mg/cm
2, anode 0.26mg/cm wherein
2, negative electrode 0.27mg/cm
2The angle of wetting of Catalytic Layer is 68 °, and the proton conductivity of CCM is 0.048s/cm.
As a comparative example 1, adopting the Nafion resin is binding agent, does not add the PTFE emulsion in the catalyst precursor mixed emulsion, and Catalytic Layer is without 340-350 ℃ of heat treatment step, and other process is the same.The CCM thickness of preparation is 62 μ m, error≤10%, and Catalytic Layer has good uniformity.Catalytic Layer thickness 5.5+1 μ m, Pt carrying capacity 0.54mg/cm
2, anode 0.27mg/cm wherein
2, negative electrode 0.27mg/cm
2The angle of wetting of Catalytic Layer is 41 °, and the proton conductivity of CCM is 0.053s/cm.
Assembling of CCM monocell and performance test.The carbon paper that adopts E-TEK company to produce is a diffusion layer, and carbon paper passes through 30wt%PTFE hydrophobic treatment and thickness 100 μ m in advance.Employing a side have parallel slot to graphite cake be collector plate, end plate is gold-plated corrosion resistant plate.Operating condition is: P
CO2=P
H2=OMPa, battery temperature are 60 ℃, and anode 100% humidification, humidification temperature are 70 ℃.The monocell polarization curve of embodiment 1 and comparative example 1 is seen Fig. 1, illustrates that fuel cell output performance of the present invention is good.
The relation of Nafion/PTFE ratio and angle of wetting and conductivity in the table 1.CCM Catalytic Layer
| Nafion:PTFE (weight ratio) | 1∶0.1 | 1∶0.5 | 1∶0.8 | 1∶1 | 1∶3 | 1∶5 | 1∶10 |
| Angle of wetting (°) conductivity (s/cmm) | 50 0.051 | 65 0.049 | 87 0.045 | 102 0.045 | 114 0.043 | 123 0.042 | 130 0.040 |
Embodiment 2:
Get the sulfonation trifluorostyrene solution 40g of 3wt%, add the PTFE emulsion 2g of 60wt%, electronic stirring 10min, 10000 rev/mins of rotating speeds; Add pure platinum black catalyst 1.2g, ultrasonic agitation 15min.The preprocess method of Nafion 212 films, PTFE film is identical in embodiment 1.Adopt screen printing apparatus that slip is coated on the transfer medium (PTFE film).And send into drying tunnel by conveyer, with N
2For protection gas, under 100-130 ℃ of condition, carry out drying, the coated film rolling of preparation is standby, and solvent is removed in heating, forms catalyst layer on the PTFE film; Silk screen specification 40-200 order nylon wire, the one way printing area is 15cm * 30cm, coated film is 0.3-2m/min at the drying tunnel walking speed.Nafion 212 films are placed between the catalyst layer of two PTFE films, send into hot-pressing processing in the calender by conveyer, the roll-in temperature is 120 ℃, pressure is 0.6MPa, the film walking speed is 0.3-2m/min, adopt automatic stripping machine to divest the PTFE film of Nafion 212 film both sides, Nafion 212 films that obtain having Catalytic Layer.Nafion 212 films that will have Catalytic Layer immerse the H of 0.5mol/L again
2SO
480 ℃ of following heat treatment 1h in the solution; 80 ℃ of following heat treatment 1h in deionized water change deionized water therebetween 3 times then, obtain CCM of the present invention at last.The CCM thickness of preparation is 62 μ m, error≤10%, and Catalytic Layer has good uniformity.Catalytic Layer thickness 5.5+1 μ m, Pt carrying capacity 0.51mg/cm
2, anode 0.26mg/cm wherein
2, negative electrode 0.25mg/cm
2, the angle of wetting of Catalytic Layer is 85 °, the proton conductivity of CCM is 0.045s/cm.
Claims (4)
1. the preparation method of the adjustable used in proton exchange membrane fuel cell core component of a hydrophilic and hydrophobic is characterized in that it comprises the steps:
1) preparation slip: by protonically conductive polymer and polytetrafluoroethylene weight ratio is 0.1: 1-1: 0.1 to choose protonically conductive polymer solution and the weight concentration that weight concentration is 3-40% be the ptfe emulsion of 60-70%, under 3000 rev/mins-20000 rev/mins high-speed stirred, be prepared into polytetrafluoroethylene/protonically conductive polymer mixing material, again with catalyst by protonically conductive polymer: the catalyst weight ratio is 1: 3-3: drop in polytetrafluoroethylene/protonically conductive polymer mixing material in 1 the scope and be prepared into slip; Big as the need angle of wetting, then the polytetrafluoroethylene in protonically conductive polymer and the polytetrafluoroethylene weight ratio is got big value;
2) with at first silk screen printing, casting of slip, be coated with or be sprayed on the medium, the heating remove solvent, on medium, form catalyst layer; Then proton exchange membrane is placed between two catalyst layers on the medium, be transferred on the proton exchange membrane, get the core component of used in proton exchange membrane fuel cell by the material of hot pressing with catalyst layer.
2. the preparation method of the used in proton exchange membrane fuel cell core component that a kind of hydrophilic and hydrophobic according to claim 1 is adjustable is characterized in that: the need preliminary treatment of described proton exchange membrane: it is 3-10wt%H that proton exchange membrane is immersed weight concentration
2O
2In, 70-90 ℃ of following heat treatment 0.5-2h uses deionized water rinsing 3-5 time; Immerse the H of 0.3-2mol/L again
2SO
470-90 ℃ of following heat treatment 0.5-2h in the solution; 70-90 ℃ of following heat treatment 0.5-2h in deionized water changes deionized water therebetween 3-5 time then.
3. the preparation method of the used in proton exchange membrane fuel cell core component that a kind of hydrophilic and hydrophobic according to claim 1 is adjustable is characterized in that: described medium is polyester film, PTFE film, porous dielectric film, sheet metal or glass plate.
4. the preparation method of the used in proton exchange membrane fuel cell core component that a kind of hydrophilic and hydrophobic according to claim 1 is adjustable, it is characterized in that: the core component of described used in proton exchange membrane fuel cell need be heat-treated, and its concrete steps are: (1) puts into the core component of used in proton exchange membrane fuel cell NaCl, the Na of 0.5-2mol/L
2SO
4Perhaps NaNO
3Soak 0.5-2h in the solution, after the washed with de-ionized water at N
2Or in the reducing gas atmosphere, 340-350 ℃ of high temperature is handled 20-40min down and is made polytetrafluoroethylene vitrifying and crystallization in the Catalytic Layer, and the core component of the used in proton exchange membrane fuel cell after (2) heat treatment is put into 0.3-2mol/L H
2SO
4Soak in the solution, soak 0.5-2h and washed with de-ionized water remove in proton exchange membrane and the Catalytic Layer inner proton conducting polymer Na ion and protonated.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100186330A CN100392896C (en) | 2006-03-23 | 2006-03-23 | Mehtod for preparing core assembly for proton exchange membrane fuel cell with adjustable hydrophilicity and hydrophobicity |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100186330A CN100392896C (en) | 2006-03-23 | 2006-03-23 | Mehtod for preparing core assembly for proton exchange membrane fuel cell with adjustable hydrophilicity and hydrophobicity |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1862855A true CN1862855A (en) | 2006-11-15 |
| CN100392896C CN100392896C (en) | 2008-06-04 |
Family
ID=37390222
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2006100186330A Expired - Fee Related CN100392896C (en) | 2006-03-23 | 2006-03-23 | Mehtod for preparing core assembly for proton exchange membrane fuel cell with adjustable hydrophilicity and hydrophobicity |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100392896C (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101800321A (en) * | 2010-03-31 | 2010-08-11 | 武汉理工新能源有限公司 | Method for preparing membrane electrode for hydrophilicity and hydrophobicity-adjustable proton exchange membrane fuel battery on the basis of catalyst/membrane technology |
| CN101728542B (en) * | 2008-10-10 | 2012-06-20 | 中国科学院大连化学物理研究所 | Method for preparing thin hydrophobisation layer |
| CN107658485A (en) * | 2017-09-22 | 2018-02-02 | 深圳先进储能材料国家工程研究中心有限公司 | Membrane electrode of fuel batter with proton exchange film and preparation method thereof |
| CN111370739A (en) * | 2020-03-02 | 2020-07-03 | 成都新柯力化工科技有限公司 | Method for preparing fuel cell membrane electrode by transfer polymerization |
| CN111740118A (en) * | 2020-06-03 | 2020-10-02 | 武汉大学 | Hydrophobicity regulation and control method for catalyst layer of alkaline polyelectrolyte fuel cell |
| CN113793962A (en) * | 2021-08-11 | 2021-12-14 | 广州市乐基智能科技有限公司 | High-performance fuel cell binder and preparation method and application thereof |
| CN114188555A (en) * | 2021-12-03 | 2022-03-15 | 中国科学院大连化学物理研究所 | Continuous preparation process of enhanced proton exchange membrane |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102088092B (en) * | 2011-01-10 | 2013-04-03 | 北京科技大学 | Preparation method for three-dimensional network structure membrane electrode for direct methanol fuel cell |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5272017A (en) * | 1992-04-03 | 1993-12-21 | General Motors Corporation | Membrane-electrode assemblies for electrochemical cells |
| US5399184A (en) * | 1992-05-01 | 1995-03-21 | Chlorine Engineers Corp., Ltd. | Method for fabricating gas diffusion electrode assembly for fuel cells |
| US5945231A (en) * | 1996-03-26 | 1999-08-31 | California Institute Of Technology | Direct liquid-feed fuel cell with membrane electrolyte and manufacturing thereof |
| CN1263189C (en) * | 2004-02-20 | 2006-07-05 | 武汉理工大学 | Catalyst coated membrane fuel cell by indirect method ultrathin core assembly for synthetising |
| CN1274046C (en) * | 2004-10-11 | 2006-09-06 | 武汉理工大学 | Method for producing proton exchange film fuel cell core module |
-
2006
- 2006-03-23 CN CNB2006100186330A patent/CN100392896C/en not_active Expired - Fee Related
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101728542B (en) * | 2008-10-10 | 2012-06-20 | 中国科学院大连化学物理研究所 | Method for preparing thin hydrophobisation layer |
| CN101800321A (en) * | 2010-03-31 | 2010-08-11 | 武汉理工新能源有限公司 | Method for preparing membrane electrode for hydrophilicity and hydrophobicity-adjustable proton exchange membrane fuel battery on the basis of catalyst/membrane technology |
| CN101800321B (en) * | 2010-03-31 | 2012-07-18 | 武汉理工新能源有限公司 | Method for preparing membrane electrode for hydrophilicity and hydrophobicity-adjustable proton exchange membrane fuel battery on the basis of catalyst/membrane technology |
| CN107658485A (en) * | 2017-09-22 | 2018-02-02 | 深圳先进储能材料国家工程研究中心有限公司 | Membrane electrode of fuel batter with proton exchange film and preparation method thereof |
| CN111370739A (en) * | 2020-03-02 | 2020-07-03 | 成都新柯力化工科技有限公司 | Method for preparing fuel cell membrane electrode by transfer polymerization |
| CN111370739B (en) * | 2020-03-02 | 2020-11-10 | 成都新柯力化工科技有限公司 | Method for preparing fuel cell membrane electrode by transfer polymerization |
| CN111740118A (en) * | 2020-06-03 | 2020-10-02 | 武汉大学 | Hydrophobicity regulation and control method for catalyst layer of alkaline polyelectrolyte fuel cell |
| CN113793962A (en) * | 2021-08-11 | 2021-12-14 | 广州市乐基智能科技有限公司 | High-performance fuel cell binder and preparation method and application thereof |
| CN113793962B (en) * | 2021-08-11 | 2023-09-19 | 广州市乐基智能科技有限公司 | Fuel cell adhesive and preparation method and application thereof |
| CN114188555A (en) * | 2021-12-03 | 2022-03-15 | 中国科学院大连化学物理研究所 | Continuous preparation process of enhanced proton exchange membrane |
| CN114188555B (en) * | 2021-12-03 | 2023-11-10 | 中国科学院大连化学物理研究所 | Continuous preparation process of enhanced proton exchange membrane |
Also Published As
| Publication number | Publication date |
|---|---|
| CN100392896C (en) | 2008-06-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101800321B (en) | Method for preparing membrane electrode for hydrophilicity and hydrophobicity-adjustable proton exchange membrane fuel battery on the basis of catalyst/membrane technology | |
| CA2591870C (en) | Highly durable electrode catalyst layer | |
| CN100392896C (en) | Mehtod for preparing core assembly for proton exchange membrane fuel cell with adjustable hydrophilicity and hydrophobicity | |
| CN1263189C (en) | Catalyst coated membrane fuel cell by indirect method ultrathin core assembly for synthetising | |
| EP1648047B1 (en) | Polymer electrolyte for a direct oxidation fuel cell, method of preparing the same, and direct oxidation fuell cell comprising the same | |
| CN100345332C (en) | Process for preparing proton exchange film full cell chips with water retaining function | |
| US20060105226A1 (en) | Metal catalyst and fuel cell with electrode including the same | |
| CN1764001B (en) | Polymer electrolyte for a direct oxidation fuel cell, method of preparing the same, and direct oxidation fuel cell comprising the same | |
| CN110459774A (en) | A kind of preparation method of fuel cell membrane electrode | |
| CN101557001B (en) | Fuel cell film electrode and preparation method thereof | |
| CN100392897C (en) | Method for preparing film electrode for hydrophilic and hydrophobic adjustable proton exchange film fuel cell | |
| CN113517449B (en) | Membrane electrode assembly and preparation method thereof | |
| EP1520310B1 (en) | Production of catalyst coated membranes | |
| EP2774203A1 (en) | Method for the preparation of catalyst-coated membranes | |
| US9034134B2 (en) | Manufacturability of ePTFE laminated membranes | |
| CN1492531A (en) | Film electrode module of fuel cell and its preparing method and fuel cell using it | |
| US20110097651A1 (en) | Membrane Electrode Assembly (MEA) Fabrication Procedure on Polymer Electrolyte Membrane Fuel Cell | |
| CN111261878B (en) | Catalyst slurry containing aqueous gel, catalyst layer and fuel cell electrode produced therefrom | |
| CN104701552A (en) | Preparation method of membrane electrode for proton exchange membrane fuel battery with high performance | |
| JPH1140172A (en) | Method for producing film-electrode joined body for fuel cell | |
| EP1378952A1 (en) | Treated gas diffusion backings and their use in fuel cells | |
| CN1315221C (en) | Full cross-linked proton exchange film fuel cell chip and preparing process | |
| CN1180249A (en) | Gas diffusion electrodes based on polyethersulfone carbon blends | |
| CN115149006A (en) | Preparation method of membrane electrode with multi-layer catalyst layer structure | |
| CN114094124A (en) | Gas diffusion layer and preparation method and application thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20080604 Termination date: 20140323 |