WO2011124039A1 - 一种燃料电池用膜-催化剂涂层膜电极的集成化制备方法 - Google Patents
一种燃料电池用膜-催化剂涂层膜电极的集成化制备方法 Download PDFInfo
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- WO2011124039A1 WO2011124039A1 PCT/CN2010/073485 CN2010073485W WO2011124039A1 WO 2011124039 A1 WO2011124039 A1 WO 2011124039A1 CN 2010073485 W CN2010073485 W CN 2010073485W WO 2011124039 A1 WO2011124039 A1 WO 2011124039A1
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- proton exchange
- membrane
- ccm
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/10—Fuel cells with solid electrolytes
- H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
- H01M8/1018—Polymeric electrolyte materials
- H01M8/1069—Polymeric electrolyte materials characterised by the manufacturing processes
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/86—Inert electrodes with catalytic activity, e.g. for fuel cells
- H01M4/88—Processes of manufacture
- H01M4/8825—Methods for deposition of the catalytic active composition
- H01M4/8828—Coating with slurry or ink
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/86—Inert electrodes with catalytic activity, e.g. for fuel cells
- H01M4/88—Processes of manufacture
- H01M4/8825—Methods for deposition of the catalytic active composition
- H01M4/8828—Coating with slurry or ink
- H01M4/8835—Screen printing
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/86—Inert electrodes with catalytic activity, e.g. for fuel cells
- H01M4/88—Processes of manufacture
- H01M4/8825—Methods for deposition of the catalytic active composition
- H01M4/8828—Coating with slurry or ink
- H01M4/8839—Painting
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/86—Inert electrodes with catalytic activity, e.g. for fuel cells
- H01M4/88—Processes of manufacture
- H01M4/8825—Methods for deposition of the catalytic active composition
- H01M4/886—Powder spraying, e.g. wet or dry powder spraying, plasma spraying
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/86—Inert electrodes with catalytic activity, e.g. for fuel cells
- H01M4/88—Processes of manufacture
- H01M4/8878—Treatment steps after deposition of the catalytic active composition or after shaping of the electrode being free-standing body
- H01M4/8882—Heat treatment, e.g. drying, baking
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/10—Fuel cells with solid electrolytes
- H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
- H01M8/1018—Polymeric electrolyte materials
- H01M8/1069—Polymeric electrolyte materials characterised by the manufacturing processes
- H01M8/1081—Polymeric electrolyte materials characterised by the manufacturing processes starting from solutions, dispersions or slurries exclusively of polymers
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/10—Fuel cells with solid electrolytes
- H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
- H01M8/1018—Polymeric electrolyte materials
- H01M8/1069—Polymeric electrolyte materials characterised by the manufacturing processes
- H01M8/1086—After-treatment of the membrane other than by polymerisation
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- 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
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Definitions
- the present invention relates to the field of fuel cells, and more particularly to a method for preparing a catalyst coated membrane electrode for a fuel cell, and more particularly to a method for integrating the preparation of a proton exchange membrane with the preparation of a catalyst coated membrane electrode.
- Membrane-electrodes assembly is mainly composed of a cathode electrode, an anode electrode and a proton exchange membrane, wherein the anode and cathode electrodes are respectively composed of a gas diffusion layer (GDL) and a catalytic layer (CL).
- GDL gas diffusion layer
- CL catalytic layer
- the MEA provides a place for fuel cells to convert chemical energy to electrical energy, so it undertakes tasks such as fuel and oxidant supply, electronics and water export.
- membrane electrode assemblies of various structures have been developed. Their main difference lies in the structure of the electrodes, which can be roughly divided into thick gas diffusion electrodes (GDE) and thin hydrophilic groups. electrode.
- the conventional MEA first prepares a catalytic layer on a porous gas diffusion layer to form a gas diffusion electrode (GDE), and then heat-presses the two electrodes together with the proton exchange membrane to form a MEA.
- the catalytic layer of this MEA is relatively thick, and the catalyst is required to have a high load, and the catalytic layer has poor adhesion to the membrane.
- Wilson et al. Thin film catalyst layers for polymer electrolyte fuel cell electrode
- a catalytic layer on a proton exchange membrane Proposed to prepare a catalytic layer on a proton exchange membrane, and then to The gas diffusion layers are combined to form an MEA, which is called a Catalyst coated membrane (CCM) from the viewpoint of preparation process, and is a thin hydrophilic electrode in terms of electrode structure characteristics.
- CCM Catalyst coated membrane
- the thin layer of hydrophilic electrode mainly contains two components: one is a catalyst, such as Pt/C, which acts to provide electrochemical reactivity and conduct electrons, and the other is an ionomer such as perfluorosulfonate. Acid resin, the network formed by it acts to conduct protons.
- a dispersant, a binder, a pore former or a water repellent may be added to the electrode slurry for preparing the electrode as needed.
- the electrode paste as used in US 5,330,860 contains a catalyst (Pt/C), an ionomer (perfluorosulfonic acid polymer) and a dispersant (ethylene glycol monomethyl ether).
- the viscosity of the slurry is adjusted using ethylene glycol or NaOH in US 5,211,984.
- the dense catalytic layer prepared from these slurries is completely hydrophilic, has a continuous proton transfer channel, and it also has a good combination with the proton exchange membrane, which is very advantageous for proton and water transfer. It is precisely because of this, in order to ensure that there is enough gas (fuel and oxidant) It is necessary to achieve an electrochemical reaction on the surface of the catalyst, and it is required that the hydrophilic catalytic layer must be very thin, and therefore, it is important to ensure uniform dispersion of the catalyst particles.
- the existing preparation techniques of CCM are mainly divided into direct method and indirect method.
- the direct method is to disperse a catalyst slurry on a proton exchange membrane to form a CCM.
- CN200, 410, 012, 745.6 discloses a method in which a catalyst, a proton exchange resin, a hydrophobic agent, a dispersant and a surfactant are mixed to prepare an electrode powder, which is laser printed.
- Technology and xerographic techniques disperse it onto the proton exchange membrane to form CCM.
- the method disclosed in U.S. Patent No. 6,074,692 is to first pre-swell the proton exchange membrane and fix it with equipment to limit shrinkage.
- the electrode slurry is dispersed on both sides of the proton exchange membrane by spraying, and dried to form CCM.
- the method disclosed in US 7,041,191 is to fix a proton exchange membrane on a substrate, and then place the substrate on which the membrane is fixed on a screen printing machine, screen the electrode paste on both sides of the film, and dry and heat-press to form CCM.
- US 7,285,307 discloses a method of laminating a proton exchange membrane on a plastic backing film, dispersing the electrode slurry on one side of the proton exchange membrane by screen printing or stencil printing, and removing the back film after the electrode slurry is completely dried. The electrode slurry was then dispersed to the other side of the proton exchange membrane by the method described above.
- the indirect method is to first apply an electrode slurry to a substrate medium to form a catalyst layer, and then transfer the catalyst layer to a proton exchange membrane by a hot press method.
- the method disclosed in US Pat. No. 5,211,984 is a catalyst/ionomer having a suitable viscosity.
- the slurry is applied to a base medium-Teflon film, and after drying, a catalytic layer is formed, and then it is bonded to the proton exchange membrane, and the catalytic layer is firmly bonded to the film by hot pressing, and finally the special layer is removed. Fluorine film.
- the method disclosed in US 5,211,984 is to first pretreat the PTFE microporous membrane with a diluted Nafion solution, followed by coating the electrode slurry thereon, and after the solvent is completely dried, the catalytic layer is attached to the proton exchange membrane. Together, the catalytic layer is firmly bonded to the membrane by hot pressing, and then the PTFE microporous membrane is removed.
- CN200, 410, 012, 744.1 first applies an electrode paste to a substrate medium by screen printing techniques to form a catalyst layer, and then transfers the catalyst layer to the proton exchange membrane by hot pressing.
- the prior art methods use the existing proton exchange membrane to prepare CCM, that is, the preparation of the proton exchange membrane and the preparation of the electrode are performed separately, and the preparation process and the route are relatively cumbersome, which is disadvantageous to Reducing costs is especially detrimental to mass production.
- the present invention proposes a method for preparing a catalyst coated membrane electrode (CCM) by integrating the preparation of a proton exchange membrane with the preparation of an electrode.
- CCM catalyst coated membrane electrode
- An integrated preparation method of a membrane-catalyst coated membrane electrode (CCM) for a fuel cell comprising the steps of preparing a proton exchange membrane and the step of preparing a CCM, wherein the preparation of the proton exchange membrane is performed by using a proton exchange resin solution
- a method of casting, impregnating or spraying is applied to a proton exchange resin solution film, which is dried to form a proton exchange membrane body, and the prepared proton exchange membrane body is not subjected to subsequent treatment; Applying the electrode slurry to both sides of the proton exchange membrane blank by any one of screen printing, spraying or painting on the proton exchange membrane body without subsequent treatment, and drying to form a stable morphology
- the CCM body; the CCM body is then subjected to ion transformation, heat treatment and activation treatment.
- the film of the proton exchange resin solution is dried in the process of coating the proton exchange resin solution into a film, and simultaneously heating and drying the proton exchange resin solution film to remove the solvent to obtain a proton exchange film body, and the heating temperature is at Between 50 and 150 ° C.
- the method of heating and drying the membrane of the proton exchange resin solution is heated by a hot plate.
- the drying of the electrode slurry is performed by heating and drying the electrode slurry on both sides of the proton exchange membrane body, and removing the reagent in the electrode slurry to obtain a stable morphology.
- the CCM body has a heating temperature between 50 and 150 °C.
- the method of removing the reagent in the electrode slurry is heated by a hot plate.
- the prepared proton exchange membrane body is any one of a homogeneous structure proton exchange membrane body and a composite structure proton exchange membrane body.
- the homogeneous structure proton exchange membrane body is prepared by casting or spraying a proton exchange resin solution onto a substrate sheet while heating and drying to remove the solvent in the proton exchange resin solution to form a continuous proton exchange membrane body.
- the base sheet is a stainless steel strip or a plastic film;
- the proton exchange membrane body of the composite structure is prepared by: using a developed microporous membrane or fiber fabric as a composite matrix, applying a proton exchange resin solution to the substrate by dipping or spraying, while heating and drying, removing the solvent A proton exchange membrane body having a stable morphology is obtained; the composite matrix is a microporous membrane or a fiber fabric.
- the method for preparing a CCM body by using a homogeneous structure proton exchange membrane blank is to first apply an electrode slurry on one side of a homogeneous structure proton exchange membrane blank and dry it, then peel off the base membrane and apply an electrode slurry on one side.
- the homogenous structure proton exchange membrane body of the material is inverted, and the electrode slurry is coated on the other side and dried;
- the preparation of a CCM body by using a proton exchange membrane body of a composite structure is a separate coating method in which an electrode slurry is coated on one side of a proton exchange membrane body and dried, and then the electrode slurry is coated on the other side and dried. Or a method in which an electrode slurry is simultaneously coated on both sides of a proton exchange membrane body and dried.
- the CCM body ion transformation treatment comprises: immersing the CCM body in an alkaline solution or a salt solution for 0.5 to 2 hours to make the electrode layer
- the ion exchange resin is converted to a non-H + type
- the alkaline solution is a NaOH or KOH solution
- the salt solution is a saturated NaCl, KC1 solution
- the ion transformation treatment temperature is between room temperature and 10 CTC;
- the heat treatment of the CCM body is: under the protection of an inert gas, the ion-converted CCM body is placed in an oven at 100-250 ° C for 3-5 hours;
- the activation treatment is: immersing in a 0.1 to 1 M sulfuric acid solution, followed by water washing to convert the proton exchange membrane and the resin in the CCM body into H + type.
- the preparation of the CCM is any one of preparing a CCM process using a homogeneous structure proton exchange membrane body and preparing a CCM using a composite structure proton exchange membrane body;
- the roller conveying device drives the stainless steel crawler to rotate cyclically.
- the proton exchange resin solution in the proton exchange resin solution tank is poured onto the stainless steel crawler through the pouring trough, and the solution is evenly distributed by the baffle scraper.
- the baffle scraper On stainless steel tracks,
- a stainless steel crawler coated with a proton exchange resin solution enters the heating channel to volatilize the solvent to obtain a homogeneous structure proton exchange membrane body.
- the homogenous structure proton exchange membrane blank is peeled off from the stainless steel crawler, and the stainless steel crawler belt continues to circulate. After the stripping, the homogeneous structure proton exchange membrane blank is sent to the spraying equipment by another transmission line, and the spraying equipment sprays the electrode slurry onto the membrane. Both sides of the blank,
- the support frame with the microporous membrane fixed is placed in a dilute solution of proton exchange resin, and then placed on a hot plate to be dried.
- the CCM preform is soaked in sulfuric acid, immersed and rinsed with deionized water to remove the surface liquid to obtain a composite CCM.
- the invention has a total of five figures, wherein
- Embodiment 1 is a schematic view showing a preparation process of Embodiment 1 of the present invention
- FIG. 2 is a schematic structural view of a CCM prepared in Embodiment 1 of the present invention.
- Figure 3 is a graph showing the performance of a fuel cell assembled using the CCM prepared in Example 1,
- Embodiment 2 of the present invention is a schematic view showing a preparation process of Embodiment 2 of the present invention
- Figure 5 is a schematic view showing the structure of a CCM prepared in Example 2 of the present invention. In the picture,
- the integrated preparation method of the membrane-catalyst-coated membrane electrode for a fuel cell of the present invention comprises preparation of a proton exchange membrane blank, preparation of a catalyst coated membrane electrode (CCM) body, and ion transformation, heat treatment and activation treatment of a CCM body.
- CCM catalyst coated membrane electrode
- the proton exchange membrane body is prepared by applying a proton exchange resin solution to a substrate membrane by casting, dipping or spraying, drying by heating, and removing the solvent to obtain a proton exchange membrane body.
- the proton exchange resin solution used was a proton exchange resin and a solvent.
- the content of the proton exchange resin in the proton exchange resin solution is 3% to 20% by weight.
- the proton exchange resin may be one of a perfluoro or partially fluorinated sulfonic acid resin or a non-fluorine sulfonic acid resin;
- the solvent may be a single solvent or a mixed solvent, including an alcohol, water and a high boiling polar solvent, and the alcohol may be It is one or several of methanol, ethanol, n-propanol, isopropanol and n-butanol;
- the high boiling polar solvent may be hydrazine, hydrazine-dimethylformamide, hydrazine, hydrazine-dimethylacetamide.
- dimethyl sulfoxide and 1-methyl-2-pyrrolidone One or more of dimethyl sulfoxide and 1-methyl-2-pyrrolidone.
- the proton exchange membrane body may be of a homogeneous structure or a composite structure.
- the base sheet used to prepare the homogeneous structure of the proton exchange membrane blank is a stainless steel belt or a plastic film.
- the matrix of the proton exchange membrane blank used to prepare the composite structure is a microporous membrane or a fibrous web which can be transported using a roller or support frame with fastening means.
- the drying of the proton exchange membrane body is carried out simultaneously in the process of coating the proton exchange resin, and is heated by a hot plate at a temperature of 50 to 150 °C.
- the process of preparing the CCM blank is: applying the electrode slurry to both sides of the proton exchange membrane blank by screen printing, spraying or painting, and simultaneously drying and removing the reagent in the electrode slurry to form a CCM having a stable morphology.
- Blank body The electrode slurry is an electrocatalyst, a proton exchange resin, and a dispersant.
- the electrocatalyst is a supported catalyst, and the catalyst carrier is one or more of carbon black, carbon nanotubes, carbon whiskers, Ti0 2, etc., and the active component of the catalyst is one of Pt, Pt-Pd, Pt-Ru, and the like. Kind or several, the active component loading is 20% ⁇ 70%wt.
- the proton exchange resin in the electrode slurry is one of a perfluoro or partially fluorinated sulfonic acid resin or a non-fluorine sulfonic acid resin.
- the dispersing agent in the electrode slurry is one or more of water, alcohol, ester or ether.
- the drying of the CCM body is carried out simultaneously during the application of the electrode paste, and is heated by a hot plate at a temperature of 50 to 150 °C.
- the electrode slurry is first coated on one side of the homogeneous structure of the proton exchange membrane body and dried, and then the substrate membrane is peeled off, inverted, and coated on the other side.
- the electrode slurry was overlaid and dried.
- protons can be used.
- the electrode layer may be separately coated on both sides of the exchange film body, or the electrode layer may be prepared by simultaneously coating the electrode paste on both sides of the proton exchange film body.
- the CCM is prepared by using a proton exchange membrane body with a composite structure, and the specific preparation steps are as follows:
- Preparation of proton exchange resin solution 105 A certain amount of hydrazine, hydrazine-dimethylacetamide was added to a 5% wt. perfluorosulfonic acid resin solution, and the mixture was ultrasonically shaken for use.
- the solvent system of the perfluorosulfonic acid resin solution is composed of n-propanol and water, and the mass ratio of hydrazine, hydrazine-dimethylacetamide to the proton exchange resin solution is 1:1.
- Electrode slurry 106 Weigh Pt/C catalyst with 70% mass content, perfluorosulfonic acid solution with 5% wt. and dispersing agent of isopropanol in weighing bottle, where catalyst and perfluorocarbon The mass ratio of the sulfonic acid resin was 2:1, and the mass ratio of the catalyst to the dispersing agent was 1:300. The above materials were ultrasonically stirred in an ultrasonic generator for 30 minutes to form an electrode slurry.
- the support frame to which the microporous membrane is fixed is placed in the dilute solution 103 for 15 minutes, and then removed and placed on a hot plate 109 at 90 ° C for drying.
- the spraying device 107 is activated to uniformly spray the proton exchange resin solution 105 on both sides of the microporous film 110 fixed on the support frame, while maintaining the temperature of the hot plate 109 at 90 to 120 ° C, so that the coating is repeatedly applied until the film is applied.
- the thickness of the film reaches a predetermined requirement to form a film body.
- the Na + -type CCM blank 114 was placed in an oven 115 at 140 ° C and dried under nitrogen for 4 hours to obtain a CCM preform 116.
- the CCM preform 116 was immersed in 0.5 M sulfuric acid 117 at 80 ° C for 1 hour, washed repeatedly with deionized water, and the surface liquid was removed to obtain a composite CCM 118.
- the composite CCM structure prepared in the above steps is as shown in Fig. 2, the film body is a composite film body 202+203, the thickness is 10-100 ⁇ m, and the electrode layers 201a and 201b are respectively 3-10 ⁇ m thick, the electrode The layer catalyst loading is 0.4-0.05 mg Pt/cm 2 .
- the CCM electrode is pressed together with two gas diffusion layers to form a CCM assembly, and the assembled fuel cell has the performance as shown in Fig. 3.
- the test conditions are as follows: the active area of the battery is 35 cm 2 , and the working gas is H Air. Atmospheric pressure, relative humidity 100%, battery temperature 60 °C.
- the CCM is prepared by using a proton exchange membrane body of homogeneous structure, and the specific preparation steps are as follows:
- Preparation of proton exchange resin solution 401 The sulfonated polyphenylene ether sulfone is dissolved in a mixed solvent of hydrazine, hydrazine-dimethylacetamide and tetrahydrofuran, and the content of the sulfonated polyphenylene ether sulfone is 15% by weight.
- the mass ratio of hydrazine-dimethylacetamide to tetrahydrofuran is 2:1.
- Electrode slurry 406 Weigh 40% Pt/C catalyst, 5% wt. perfluorosulfonic acid solution, ethylene glycol and isopropanol dispersant in a weighing bottle, wherein the catalyst and perfluorocarbon
- the mass ratio of the sulfonic acid resin is 3.5:1
- the mass ratio of the catalyst to the dispersing agent is 1:300
- the mass ratio of ethylene glycol to isopropanol in the dispersing agent is 1:5.
- the above materials are placed in an ultrasonic generator for ultrasonication. Stir for 30 min to form an electrode slurry.
- the stainless steel crawler 402 is transferred to the working area of the coating machine by a roller, and the proton exchange resin solution 401 prepared in the step 1 is poured onto the stainless steel crawler through the pouring trough, and then the solution is evenly distributed by the baffle scraper 403.
- Stainless steel track
- the stainless steel crawler covered with the proton exchange resin solution is fed into the heating passage 404, and the temperature is controlled at 60 to 130 ° C to volatilize the solvent to obtain a homogeneous membrane body 405.
- the homogenized film body 405 and the stainless steel track are peeled off and sent to the spraying device 407, and the spraying device 407 is started.
- the electrode slurry 406 prepared in the step 2 is uniformly sprayed to one side of the film body, and the temperature of the hot plate 408 is maintained. 90 ⁇ 120 ° C, the electrode slurry is dried to form a single-sided CCM body.
- the single-sided CCM blank is transferred to the spraying device 410 through another transfer, and the electrode slurry 406 prepared in the step 2 is uniformly sprayed onto the other side of the single-sided CCM blank, and the temperature of the hot plate 408 is maintained at 90-120. °C, the electrode slurry is dried to form a double-sided CCM body 411. 7.
- the CCM body 411 is poured into a tank 412 containing a 30% by weight NaCl solution at 60 ° C, and then washed in a deionized water tank 413, and the liquid on the surface of the CCM body is removed by a suction drum 414.
- the CCM blank is fed to a drying tunnel 415 at 180 ° C and dried under nitrogen to obtain a CCM preform 416.
- CCM preform 416 was immersed in 0.5 M sulfuric acid at 80 ° C for 1 hour, rinsed repeatedly with deionized water, and the surface liquid was removed to obtain a homogeneous CCM.
- the CCM structure prepared by the above process is as shown in Fig. 5.
- the thickness of the homogeneous film body 502 is 10 to 100 m
- the thickness of the electrode layers 501a and 501b is 3 to 15 ⁇ m
- the amount of the electrode catalyst is 0.4 ⁇ . 0.05 mg Pt/cm 2 .
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Description
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Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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DE112010002921T DE112010002921T5 (de) | 2010-04-09 | 2010-06-03 | Verfahren zur einheitlichen Anfertigung einer Membrankatalysator beschichtetenMembranelektrode für eine Brennstoffzelle |
US13/394,142 US20120279648A1 (en) | 2010-04-09 | 2010-06-03 | Preparing method for integrated membrane-catalyst coated layer membrane electrode for a fuel cell |
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CN201010144010.4 | 2010-04-09 | ||
CN2010101440104A CN101887975B (zh) | 2010-04-09 | 2010-04-09 | 一种燃料电池用膜-膜电极的集成化制备方法 |
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US (1) | US20120279648A1 (zh) |
CN (1) | CN101887975B (zh) |
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WO (1) | WO2011124039A1 (zh) |
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CN101887975A (zh) | 2010-11-17 |
CN101887975B (zh) | 2012-07-18 |
US20120279648A1 (en) | 2012-11-08 |
DE112010002921T5 (de) | 2012-05-31 |
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