WO2024004856A1 - 電解質膜、触媒層付電解質膜およびその作製に用いられる転写シート、膜電極接合体、水電解装置並びに触媒層付電解質膜の製造方法 - Google Patents

電解質膜、触媒層付電解質膜およびその作製に用いられる転写シート、膜電極接合体、水電解装置並びに触媒層付電解質膜の製造方法 Download PDF

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WO2024004856A1
WO2024004856A1 PCT/JP2023/023320 JP2023023320W WO2024004856A1 WO 2024004856 A1 WO2024004856 A1 WO 2024004856A1 JP 2023023320 W JP2023023320 W JP 2023023320W WO 2024004856 A1 WO2024004856 A1 WO 2024004856A1
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layer
electrolyte membrane
catalyst
catalyst layer
porosity
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PCT/JP2023/023320
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English (en)
French (fr)
Japanese (ja)
Inventor
孝哉 伊神
健太 南林
友之 國田
一直 松井
大輔 出原
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Toray Industries Inc
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Toray Industries Inc
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Priority to JP2023544501A priority Critical patent/JPWO2024004856A1/ja
Priority to AU2023300508A priority patent/AU2023300508A1/en
Priority to EP23831298.7A priority patent/EP4545687A1/en
Priority to CN202380036365.7A priority patent/CN119110859A/zh
Priority to KR1020247037951A priority patent/KR20250027503A/ko
Publication of WO2024004856A1 publication Critical patent/WO2024004856A1/ja
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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
    • H01M8/1041—Polymer electrolyte composites, mixtures or blends
    • H01M8/1053—Polymer electrolyte composites, mixtures or blends consisting of layers of polymers with at least one layer being ionically conductive
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00—Electrolytic production of inorganic compounds or non-metals
    • C25B1/01—Products
    • C25B1/02—Hydrogen or oxygen
    • C25B1/04—Hydrogen or oxygen by electrolysis of water
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B13/00—Diaphragms; Spacing elements
    • C25B13/02—Diaphragms; Spacing elements characterised by shape or form
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B13/00—Diaphragms; Spacing elements
    • C25B13/04—Diaphragms; Spacing elements characterised by the material
    • C25B13/05—Diaphragms; Spacing elements characterised by the material based on inorganic materials
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B13/00—Diaphragms; Spacing elements
    • C25B13/04—Diaphragms; Spacing elements characterised by the material
    • C25B13/08—Diaphragms; Spacing elements characterised by the material based on organic materials
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B9/00—Cells or assemblies of cells; Constructional parts of cells; Assemblies of constructional parts, e.g. electrode-diaphragm assemblies; Process-related cell features
    • C25B9/17—Cells comprising dimensionally-stable non-movable electrodes; Assemblies of constructional parts thereof
    • C25B9/19—Cells comprising dimensionally-stable non-movable electrodes; Assemblies of constructional parts thereof with diaphragms
    • C25B9/23—Cells comprising dimensionally-stable non-movable electrodes; Assemblies of constructional parts thereof with diaphragms comprising ion-exchange membranes in or on which electrode material is embedded
    • 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
    • H01M4/8803—Supports for the deposition of the catalytic active composition
    • H01M4/881—Electrolytic membranes
    • 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
    • H01M8/1004—Fuel cells with solid electrolytes characterised by membrane-electrode assemblies [MEA]
    • 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
    • H01M8/1039—Polymeric electrolyte materials halogenated, e.g. sulfonated polyvinylidene fluorides
    • 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
    • H01M8/1041—Polymer electrolyte composites, mixtures or blends
    • H01M8/1046—Mixtures of at least one polymer and at least one additive
    • 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
    • H01M8/1041—Polymer electrolyte composites, mixtures or blends
    • H01M8/1046—Mixtures of at least one polymer and at least one additive
    • H01M8/1051—Non-ion-conducting additives, e.g. stabilisers, SiO2 or ZrO2
    • 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
    • H01M8/1067—Polymeric electrolyte materials characterised by their physical properties, e.g. porosity, ionic conductivity or thickness
    • 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
    • H01M8/18—Regenerative fuel cells, e.g. redox flow batteries or secondary fuel cells
    • H01M8/184—Regeneration by electrochemical means
    • H01M8/188—Regeneration by electrochemical means by recharging of redox couples containing fluids; Redox flow type batteries
    • 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
    • H01M2008/1095—Fuel cells with polymeric electrolytes
    • 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
    • Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
    • 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

Definitions

  • the present invention relates to an electrolyte membrane, an electrolyte membrane with a catalyst layer, a transfer sheet used for producing the same, a membrane electrode assembly, a water electrolysis device, and a method for manufacturing the electrolyte membrane with a catalyst layer.
  • hydrogen energy has been attracting attention as a next-generation means of energy storage and transportation.
  • hydrogen can be converted into electricity with theoretically higher energy efficiency than power generation using heat engines, and has relatively low emissions of harmful substances, making it a highly efficient and clean energy source. It can be a source of energy.
  • One of the hydrogen production methods is water electrolysis.
  • water electrolysis By electrolyzing water using surplus electricity from renewable energy, it is possible to convert electricity into hydrogen energy without emitting carbon dioxide.
  • hydrogen can be transported by tanker or tanker, and can be supplied when and where it is needed, so water electrolysis has great potential as a tool for power storage.
  • Hydrogen production methods using water electrolysis include alkaline water electrolysis and solid polymer electrolyte membrane (PEM) type water electrolysis.
  • PEM water electrolysis has the advantage of being able to operate at high current density and being able to flexibly respond to fluctuations in the output of renewable energy.
  • a PEM type water electrolysis device is usually configured as a unit of a cell in which a membrane electrode assembly (MEA) is sandwiched between separators.
  • MEA is composed of a catalyst coated membrane (CCM) in which catalyst layers are formed on both sides of a polymer electrolyte membrane, one of which is an anode catalyst layer and the other is a cathode catalyst layer.
  • CCM catalyst coated membrane
  • Water is supplied to the anode catalyst layer of the PEM water electrolysis cell to which a current is applied, and protons are generated by an electrochemical reaction. Subsequently, protons diffuse in the polymer electrolyte membrane from the anode electrode layer side to the cathode electrode layer side, and hydrogen is produced from the protons by an electrochemical reaction in the cathode layer.
  • the bondability of the interface between the catalyst layer and the polymer electrolyte membrane may decrease during water electrolysis operation.
  • an object of the present invention is to provide an electrolyte membrane that has good bonding properties with a catalyst layer.
  • the electrolyte membrane of the present invention has the following configuration. That is, an electrolyte membrane comprising a (A) layer containing a polymer electrolyte and a (B) layer on at least one surface of the (A) layer, wherein the (A) layer of the (B) layer.
  • This is an electrolyte membrane in which the porosity (X1) in the interface region with the (B) layer is higher than the porosity (X2) in the interface region of the (B) layer on the opposite side of the (A) layer.
  • an electrolyte membrane that has excellent bonding properties between the electrolyte membrane and the catalyst layer and has good durability.
  • FIG. 1 is a schematic cross-sectional view of an electrolyte membrane according to Embodiment 1 of the present invention.
  • FIG. 1 is a schematic cross-sectional view of an electrolyte membrane with a catalyst layer using the electrolyte membrane according to Embodiment 1 of the present invention.
  • FIG. 2 is a schematic cross-sectional view of an electrolyte membrane according to Embodiment 2 of the present invention.
  • FIG. 2 is a schematic cross-sectional view of an electrolyte membrane with a catalyst layer using an electrolyte membrane according to Embodiment 2 of the present invention.
  • An electrolyte membrane according to an embodiment of the present invention is an electrolyte membrane comprising a (A) layer containing a polymer electrolyte and a (B) layer on at least one surface of this (A) layer, It is important that the porosity (X1) in the interface region of layer B) with layer (A) is higher than the porosity (X2) in the interface region of layer (B) on the opposite side from layer (A). .
  • the interfacial region refers to a region in the (B) layer from each interface between the (B) layer and another adjacent layer that has a thickness of 10% of the total thickness of the (B) layer.
  • the porosity (X1) and the porosity (X2) can be measured by observing a cross section of the electrolyte membrane with a field emission scanning electron microscope and performing image processing. Details are described in Examples.
  • FIG. 1 is a schematic cross-sectional view showing an example of an electrolyte membrane according to Embodiment 1 of the present invention.
  • the electrolyte membrane 1 has a structure in which the (B) layer 20 is laminated on one surface of the (A) layer 10.
  • the (B) layer 20 has an interface region 21 on the (A) layer side and an interface region 22 on the opposite side to the (A) layer.
  • the porosity in the interface region 21 is the porosity (X1)
  • the porosity in the interface region 22 is the porosity (X2).
  • FIG. 2 is a schematic cross-sectional view showing an example of an electrolyte membrane with a catalyst layer, in which catalyst layers are laminated on both sides of the electrolyte membrane of Embodiment 1, respectively.
  • a catalyst coated electrolyte membrane (Catalyst Coated Membrane) may be abbreviated as "CCM”.
  • the CCM 100 has a structure in which a catalyst layer 30 and a catalyst layer 40 are laminated on both sides of an electrolyte membrane 1, respectively.
  • the catalyst layers 30 and 40 are an anode catalyst layer and a cathode catalyst layer, respectively, in random order.
  • the porosity (X1) in the interface region 21 of the (B) layer 20 with the (A) layer 10 is on the opposite side of the (A) layer 10 of the (B) layer 20.
  • the porosity is higher than the porosity (X2) in the interface region 22 of .
  • the degree of porosity on the outermost surface of the layer affects the surface roughness (unevenness), and the higher the porosity, the larger the surface roughness (unevenness), and the lower the porosity, the smaller the surface roughness (unevenness). (higher smoothness). It is thought that the unevenness formed on the outermost surface of the layer functions as an anchor at the bonding interface with other layers.
  • the layer (A) 10 containing the polymer electrolyte has a relatively smooth surface, and the catalyst layers 30 and 40 have uneven surfaces because they contain catalyst particles. Therefore, the relatively high porosity interface region 21 (porosity (X1)) of the (B) layer 20 is placed opposite to the (A) layer 10 side having a smooth surface, and the (B) layer 20 is placed opposite to the catalyst layer 30 side having an uneven surface.
  • the present invention is particularly effective when the polymer electrolyte contained in the (A) layer 10 and the polymer electrolyte contained in the catalyst layer 30 are different from each other.
  • the polymer electrolytes are different from each other, for example, when one is a hydrocarbon-based polymer electrolyte and the other is a fluorine-based polymer electrolyte.
  • layer 10 contains a hydrocarbon polymer electrolyte and catalyst layer 30 contains a fluoropolymer electrolyte (Form 1)
  • (A) layer 10 contains a fluoropolymer electrolyte.
  • the catalyst layer 30 may include a hydrocarbon polymer electrolyte (form 2). Form 1 is preferred from the viewpoint of water electrolysis performance.
  • the (B) layer 20 preferably contains the same type of polymer as the catalyst layer 30.
  • the polymers are of the same type, it means that the main skeletons of the polymers are of the same type, such as fluorine-based polymers or hydrocarbon-based polymers, regardless of whether they are ionic or nonionic.
  • an ionic fluoropolymer (fluoropolymer electrolyte) and a nonionic fluoropolymer are the same type of polymer, and similarly an ionic hydrocarbon polymer (hydrocarbon polymer electrolyte) and a nonionic fluoropolymer are the same type of polymer.
  • the ionic hydrocarbon polymer is the same type of polymer.
  • the (B) layer 20 more preferably contains the same type of polymer electrolyte as the polymer electrolyte contained in the catalyst layer 30. (B) Details of the polymer contained in layer 20 will be described later.
  • a particularly preferable combination of the materials contained in the (A) layer, the catalyst layer, and the (B) layer is such that the (A) layer contains a hydrocarbon polymer electrolyte, the catalyst layer contains a fluoropolymer electrolyte, and ( B) A structure in which the layer contains a fluorine-based polymer is mentioned.
  • the porosity ratio (X2/X1) between the porosity (X1) and the porosity (X2) is preferably 0.90 or less, and 0.80.
  • the following is more preferable, and 0.70 or less is particularly preferable.
  • the lower limit of (X2/X1) is 0.00.
  • the porosity (X1) is preferably 20% or more, more preferably 22% or more, particularly preferably 25% or more, from the viewpoint of improving the bonding properties between the (A) layer 10 and the (B) layer 20. .
  • the porosity (X1) is preferably 60% or less, more preferably 50% or less, further preferably 40% or less, and particularly preferably 37% or less.
  • the porosity (X2) is preferably less than 20%, more preferably less than 19%, from the viewpoint of improving the bondability between the (B) layer 20 and the catalyst layer 30.
  • the lower limit is 0%.
  • the porosity (X1) is 20% or more and the porosity (X2) is less than 20%. Furthermore, within the range of the porosity ratio (X2/X1), it is more preferable that the porosity (X1) is 20% or more and the porosity (X2) is less than 20%.
  • the porosity (X2) depends on the mass ratio (C/I) of the content (C) of catalyst particles (including catalyst-supported particles) and the content (I) of the polymer electrolyte contained in the catalyst layer 30. It is preferable to adjust it accordingly. Generally, the surface roughness (unevenness) of a catalyst layer with a high C/I tends to increase, and the surface roughness (unevenness) of a catalyst layer with a low C/I tends to decrease. In order to improve the anchoring effect at the joint surface, (X2) is preferably low for a catalyst layer with a relatively high C/I, and (X2) is preferably high for a catalyst layer with a relatively low C/I.
  • the porosity (X2) is more preferably less than 12%, further preferably less than 8%, and particularly preferably less than 6%.
  • the porosity (X2) is preferably less than 20%.
  • the (B) layer 20 When the (B) layer 20 is arranged only on one side of the (A) layer 10, it may be arranged only on the anode catalyst layer side or only on the cathode catalyst layer side.
  • the electrolyte membrane according to the first embodiment is applied to a water electrolysis device, by arranging the (B) layer 20 on the anode catalyst layer side, in addition to improving the bonding property, electrochemical oxidation of the (A) layer It can be expected to have the effect of suppressing deterioration.
  • the (B) layer 20 on the cathode catalyst layer side in addition to improving bonding properties, it can be expected that the (A) layer is protected from peroxide radicals by-generated at the cathode.
  • the anode In a water electrolysis device, the anode is in a high potential environment, and in order to suppress electrochemical oxidative deterioration of the (A) layer 10, the (B) layer on the anode catalyst layer side preferably has a barrier function.
  • the catalyst layer 30 is an anode catalyst layer
  • the (B) layer 20 on the anode catalyst layer side has a relatively low porosity (X2).
  • the porosity (X2) is preferably less than 12%, more preferably less than 8%, even more preferably less than 6%, and most preferably 0%.
  • the (B) layer on the cathode catalyst layer side has a catalyst layer 30 from the viewpoint of suppressing interfacial peeling between the catalyst layer and the (B) layer due to hydrogen generated at the cathode (ensuring an escape route for hydrogen).
  • the porosity (X2) of layer (B) 20 on the cathode catalyst layer side is preferably relatively high. Specifically, the porosity (X2) is more preferably 3% or more, even more preferably 5% or more, and particularly preferably 7% or more. Further, the upper limit of the porosity (X2) is preferably less than 20%.
  • the content ratio of catalyst particles to polymer electrolyte in the anode catalyst layer is set to be relatively large, it is difficult to obtain bondability between the anode catalyst layer and the (A) layer. Therefore, it is more beneficial to arrange the layer (B) on the anode catalyst layer side from the viewpoint of improving bondability. Therefore, it is more preferable that the catalyst layer 30 is an anode catalyst layer.
  • FIG. 3 is a schematic cross-sectional view showing an example of an electrolyte membrane according to Embodiment 2 of the present invention.
  • the electrolyte membrane 2 has a structure in which a (B) layer 20a is laminated on one side of the (A) layer 10, and another (B) layer 20b is laminated on the opposite side. be.
  • the (B) layer 20a has an interface region 21a on the (A) layer 10 side and an interface region 22a on the opposite side to the (A) layer 10.
  • the (B) layer 20b has an interface region 21b on the (A) layer 10 side and an interface region 22b on the opposite side to the (A) layer 10.
  • the porosity in the interface regions 21a and 21b is the porosity (X1)
  • the porosity in the interface regions 22a and 22b is the porosity (X2).
  • the porosity in the interface regions 21a and 21b is (X1-1) and (X1-2), respectively
  • the porosity in the interface regions 22a and 22b is (X2-1) and (X2-2), respectively.
  • (X1-1) and (X1-2) and (X2-1) and (X2-2) may be the same or different.
  • the porosity (X1) is higher than the porosity (X2) if (X1-1)>(X2-1) and/or (X1-2)>(X2-2). means.
  • FIG. 4 shows an electrolyte membrane with a catalyst layer (CCM) in which an anode catalyst layer 50 is laminated on the (B) layer 20a side of the electrolyte membrane of Embodiment 2, and a cathode catalyst layer 60 is laminated on the (B) layer 20b side.
  • CCM catalyst layer
  • the CCM 200 has a structure in which an anode catalyst layer 50 and a cathode catalyst layer 60 are laminated on both sides of an electrolyte membrane 2, respectively.
  • the relationship (X1)>(X2) is preferably satisfied at least in the (B) layer 20a on the anode catalyst layer 50 side, and the (B) layer 20a on the anode catalyst layer 50 side and the cathode catalyst layer It is more preferable that both the layer (B) 20b on the 60 side and the layer (B) 20b are filled. That is, it is preferable that (X1-1)>(X2-1), and more preferably that (X1-1)>(X2-1) and (X1-2)>(X2-2).
  • the porosity (X2-1) in the (B) layer 20a on the anode catalyst layer 50 side is preferably smaller than the porosity (X2-2) in the (B) layer 20b on the cathode catalyst layer 60 side. Further, the porosity (X2-1) in the (B) layer 20a adjacent to the anode catalyst layer 50 is less than 12%, and the porosity (X2-2) in the (B) layer 20b adjacent to the cathode catalyst layer 60 is less than 12%. Particularly preferred is less than 20%.
  • (A) Layer contains a polymer electrolyte.
  • the polymer electrolyte include fluorine-based polymer electrolytes and hydrocarbon-based polymer electrolytes. From the viewpoint of water electrolysis performance, hydrocarbon polymer electrolytes are preferred.
  • the fluoropolymer electrolyte is a fluoropolymer having an ionic group.
  • a fluorine-based polymer means a polymer in which most or all of the hydrogen atoms in an alkyl group and/or an alkylene group have been replaced with fluorine atoms.
  • Representative examples of fluoropolymer electrolytes include commercial products such as Nafion (registered trademark) (manufactured by DuPont), Flemion (registered trademark) (manufactured by Asahi Glass Co., Ltd.), and Aciplex (registered trademark) (manufactured by Asahi Kasei Corporation). be able to.
  • a hydrocarbon polymer electrolyte is a hydrocarbon polymer having an ionic group.
  • the hydrocarbon polymer an aromatic hydrocarbon polymer having an aromatic ring in the main chain is preferable.
  • the aromatic ring may include not only a hydrocarbon aromatic ring but also a hetero ring.
  • some aliphatic units may constitute the polymer together with the aromatic ring units.
  • aromatic hydrocarbon polymers include polysulfone, polyether sulfone, polyphenylene oxide, polyarylene ether polymer, polyphenylene sulfide, polyphenylene sulfide sulfone, polyparaphenylene, polyarylene polymer, polyarylene ketone, and polyether ketone.
  • hydrocarbon skeleton may have multiple structures among these structures.
  • the most preferred aromatic hydrocarbon polymer is a polymer having a polyetherketone skeleton, that is, a polyetherketone polymer.
  • a block copolymer having at least one segment (A1) containing an ionic group and one or more segments (A2) not containing an ionic group is preferable.
  • segment refers to a partial structure in a copolymer chain consisting of repeating units exhibiting specific properties, and has a molecular weight of 2000 or more.
  • segment (A1) or polymer containing an ionic group may be referred to as an "ionic block", and the segment (A2) or polymer not containing an ionic group may be referred to as a "nonionic block".
  • ionic block the segment (A1) or polymer containing an ionic group
  • nonionic block the segment (A2) or polymer not containing an ionic group
  • the statement "contains no ionic group” does not exclude embodiments in which the segment or polymer contains a small amount of ionic group to the extent that the effects of the present invention are not impaired.
  • the ionic group that the polymer electrolyte has may be any ionic group that has proton exchange ability.
  • a functional group a functional group selected from a sulfonic acid group, a sulfonimide group, a sulfuric acid group, a phosphonic acid group, a phosphoric acid group, and a carboxylic acid group is preferably used. Two or more types of ionic groups can be included in the polymer.
  • the polymer has at least one selected from a sulfonic acid group, a sulfonimide group, and a sulfuric acid group, and from the viewpoint of raw material cost, it is most preferable that the polymer has a sulfonic acid group.
  • the ion exchange capacity (IEC) of the polymer electrolyte is preferably 0.1 meq/g or more and 5.0 meq/g or less in view of the balance between proton conductivity and water resistance.
  • IEC is more preferably 1.4 meq/g or more, and even more preferably 2.0 meq/g or more.
  • IEC is more preferably 3.5 meq/g or less, and even more preferably 3.0 meq/g or less. If IEC is less than 0.1 meq/g, proton conductivity may be insufficient, and if it is greater than 5.0 meq/g, water resistance may be insufficient.
  • IEC is the molar amount of ionic groups introduced per unit dry weight of the polymer electrolyte, and the larger the value, the greater the amount of ionic groups introduced.
  • IEC is defined as a value determined by neutralization titration method. Calculation of IEC by neutralization titration is performed by the method described in Example section (2).
  • an aromatic hydrocarbon block copolymer as the hydrocarbon polymer electrolyte, and more preferably a polyetherketone block copolymer.
  • a polyetherketone block copolymer containing a segment containing a structural unit (S1) containing an ionic group and a segment containing a structural unit (S2) not containing an ionic group as described below is particularly preferably used. be able to.
  • Ar 1 to Ar 4 represent any divalent arylene group, Ar 1 and/or Ar 2 contain an ionic group, and Ar 3 and Ar 4 contain an ionic group. However, it does not need to be included. Ar 1 to Ar 4 may be optionally substituted, and two or more types of arylene groups may be used independently of each other. * represents a bonding site with general formula (S1) or another structural unit.
  • Ar 5 to Ar 8 represent any divalent arylene group and may be optionally substituted, but do not contain an ionic group. Two or more types of arylene groups may be used independently of each other for Ar 5 to Ar 8 .
  • * represents a bonding site with general formula (S2) or another structural unit.
  • preferred divalent arylene groups as Ar 1 to Ar 8 include hydrocarbon arylene groups such as a phenylene group, naphthylene group, biphenylene group, and fluorenediyl group, and heteroarylene groups such as pyridinediyl, quinoxalinediyl, and thiophenediyl. Examples include, but are not limited to, groups.
  • the "phenylene group” can be of three types, o-phenylene group, m-phenylene group, and p-phenylene group, depending on the location where the benzene ring and the other structural unit are bonded, but in this specification, Unless otherwise specified, these terms are used collectively.
  • Ar 1 to Ar 8 are preferably phenylene groups containing a phenylene group and an ionic group, most preferably p-phenylene groups containing a p-phenylene group and an ionic group. Further, Ar 5 to Ar 8 may be substituted with a group other than an ionic group, but unsubstituted is more preferable in terms of proton conductivity, chemical stability, and physical durability.
  • the polymer electrolyte is preferably an aromatic hydrocarbon polymer having crystallinity.
  • “having crystallinity” means that the material has a crystallizable property that can be crystallized when the temperature is increased, or that it has already been crystallized.
  • the presence or absence of crystallizable properties that can be crystallized when the temperature is increased can be confirmed by checking that the crystallization heat amount measured by differential scanning calorimetry (DSC) after film formation is 0.1 J/g or more.
  • the crystallization heat amount measured by differential scanning calorimetry (DSC) after film formation is 0.1 J/g or more.
  • the heat of crystallization measured by differential scanning calorimetry (DSC) after film formation is 0.1 J/g or more, or the degree of crystallinity measured by wide-angle X-ray diffraction is It is preferably 0.5% or more.
  • Aromatic hydrocarbon polymers with crystallinity may have poor processability into electrolyte membranes.
  • a protecting group may be introduced into the aromatic hydrocarbon polymer to temporarily suppress crystallinity.
  • a crystalline aromatic hydrocarbon polymer can be used as a polymer electrolyte in the present invention by forming a film with a protective group introduced therein and then deprotecting it.
  • (A) Layer may be reinforced with a porous base material.
  • a porous base material examples include woven fabric, nonwoven fabric, porous film, mesh fabric, and the like.
  • known materials such as hydrocarbon-based porous base materials and fluorine-based porous base materials can be used.
  • the layer (A) may contain various additives such as surfactants, radical scavengers, hydrogen peroxide decomposers, non-electrolyte polymers, elastomers, fillers, etc., as long as they do not impede the effects of the present invention.
  • the thickness of layer (A) is preferably relatively large, specifically preferably 30 ⁇ m or more, more preferably 50 ⁇ m or more, and particularly preferably 70 ⁇ m or more. Further, the thickness is preferably 250 ⁇ m or less, more preferably 200 ⁇ m or less, and particularly preferably 175 ⁇ m or less.
  • the (B) layer has a function of increasing the bonding property between the (A) layer and the catalyst layer, that is, a function as a bonding layer.
  • the (B) layer has an interface region with the (A) layer and an interface region on the opposite side to the (A) layer, and the porosity in these two interface regions is different.
  • Such layer (B) may be composed of a single layer, or may have a laminated structure of two or more layers.
  • the voids in the interface region can be formed, for example, by containing particles.
  • the porosity can then be controlled, for example, by adjusting the particle density.
  • the layer (B) preferably contains at least particles and a polymer. That is, the porosity can be controlled by adjusting the ratio (P/F) between the mass (P) of the polymer and the mass (F) of the particles. Generally, as the ratio (P/F) increases, the porosity decreases.
  • the (B) layer is a single layer, for example, in the process of applying and drying one coating liquid containing particles and a polymer on the (A) layer that is horizontally placed or horizontally transported, the (A) layer By performing an operation to increase the particle density on the side, the porosity (X1) can be made higher than the porosity (X2).
  • the above operations include, for example, using particles whose specific gravity is sufficiently larger than that of the polymer, making the viscosity of the coating liquid relatively low, and slowing down the drying rate so that the particles tend to settle, or Examples include a method of phase-separating the two.
  • the above method for phase separation is, for example, by using particles and a polymer whose surface tension is sufficiently lower than that of the particles and which is incompatible with the particles, and by using a solvent that is relatively compatible with the particles.
  • Examples include a method of making it easier for the polymer to be unevenly distributed at the air interface during phase separation.
  • the layer (B) preferably has a laminated structure.
  • the porosity (X1) and the porosity (X2) can be easily controlled.
  • layer (B) having a laminated structure with different porosity depending on the layer is formed. Ru.
  • the (B) layer has a laminated structure consisting of n layers, they are called (B-1) layer, (B-2) layer, ... (Bn) layer in order from the (A) layer side.
  • the layer (B) has a laminated structure, it is preferable that the layer (B-1) adjacent to the layer (A) has the highest porosity.
  • the layer (B) has a laminated structure, a two-layer structure and a three-layer structure are preferable, and a two-layer structure is more preferable.
  • the (B) layer is composed of two layers, the layer adjacent to the (A) layer is the (B-1) layer, and the layer opposite to the (A) layer is the (B-2) layer.
  • the (B-1) layer in the two-layer configuration is a layer that includes an interface region with the (A) layer. That is, the (B-1) layer is a layer that provides a porosity (X1) in the interface region with the (A) layer.
  • Layer (B-2) is a layer that includes an interface region on the opposite side to layer (A). That is, the (B-2) layer is a layer that provides a porosity (X2) in the interface region on the opposite side to the (A) layer.
  • the ratio (P/ F) is preferably in the range of 0.2 to 1.6, more preferably in the range of 0.4 to 1.4, and particularly preferably in the range of 0.6 to 1.2.
  • the ratio (P/F) is preferably 1.2 or more, and 1.4 or more. is more preferable, and 1.6 or more is particularly preferable.
  • the porosity (X2) is 0%, it is preferable that the layer (B-2) in this case has a structure containing no particles, that is, a structure containing only polymer.
  • the (B-2) layer includes a form that does not contain particles as described above. Even if layer (B-2) does not contain particles, if layer (B-1) contains particles, this corresponds to the case that "layer (B) contains particles and a polymer.”
  • the layer (B) contains particles
  • examples of the particles include inorganic particles, organic particles, and organic/inorganic composite particles.
  • inorganic particles include carbon particles, silica, titanium oxide, aluminum oxide, zirconium oxide, cerium oxide, calcium carbonate, zeolite, mica, sericite, sericite, kaolin clay, kaolin, mica, talc, and montmorillonite. It will be done.
  • carbon particles are preferred because they are relatively stable against acids and alkalis.
  • examples of carbon particles include carbon black, graphite, activated carbon, carbon nanotubes, carbon nanofibers, and fullerene.
  • organic particles include various resin particles.
  • the resin constituting the resin particles include polyethylene resin, polypropylene resin, polyvinyl acetate resin, poly(meth)acrylic resin, polyvinyl chloride resin, polystyrene resin, polycarbonate resin, Polyester resin, polyphenylene sulfide resin, polyamide resin, polyimide resin, polyurethane resin, ethylene-(meth)acrylate copolymer, ABS resin, fluorine resin, epoxy resin, phenolic resin, melamine
  • thermoplastic resins and thermosetting resins such as guanamine resin, polyazole resin, polyether sulfone resin, and polyether ketone resin.
  • organic/inorganic composite particles include acrylic/silica composite particles, melamine/silica composite particles, benzoguanamine/silica composite particles, benzoguanamine/melamine/silica composite particles, polystyrene/silica composite particles, and silsesquioxane organic-inorganic hybrids. Examples include particles, organic substance-coated inorganic nanoparticles, and the like.
  • inorganic particles are preferred, carbon particles are more preferred, and carbon black is particularly preferred.
  • the average particle diameter of the particles is preferably 5 nm or more, more preferably 10 nm or more, particularly preferably 20 nm or more, from the viewpoints of void formation effective for bonding, dispersibility, and film formability. Further, the thickness is preferably 1,000 nm or less, more preferably 500 nm or less, and particularly preferably 200 nm or less.
  • the layer (B) contains a polymer
  • a nonionic polymer or an ionic polymer can be used as the polymer.
  • Each of these polymers may be used alone, or a plurality of polymers may be used in combination.
  • nonionic polymers include fluorine-based polymers and hydrocarbon-based polymers.
  • nonionic fluoropolymers include polytetrafluoroethylene, poly(vinylidene fluoride), a copolymer of vinylidene fluoride and hexafluoropropylene, a copolymer of vinylidene fluoride and trifluoroethylene, and a copolymer of vinylidene fluoride and tetrafluoroethylene. Examples include copolymers with fluoroethylene and poly(vinylidene fluoride).
  • nonionic hydrocarbon polymers include polysulfone, polyether sulfone, polyphenylene oxide, polyarylene ether, polyphenylene sulfide, polyphenylene sulfide sulfone, polyparaphenylene, polyarylene polymer, polyarylene ketone, polyether ketone, and polyphenylene sulfone.
  • examples include arylene phosphine oxide, polyether phosphine oxide, polybenzoxazole, polybenzthiazole, polybenzimidazole, polyamide, polyimide, polyetherimide, polyimide sulfone, and polyvinyl alcohol.
  • ionic polymers include ionic fluoropolymers and ionic hydrocarbon polymers, and examples of these polymers include the polymers mentioned above as examples of the fluoropolymer electrolyte and hydrocarbon polymer electrolyte. It will be done.
  • fluorine-based polymers are preferable from the viewpoint of imparting a barrier function in a high-potential environment to the layer (B), and from the viewpoint of increasing proton conductivity, hydrocarbon-based polymer electrolytes or fluorine-based polymer electrolytes are preferable. is preferred. That is, when the layer (B) contains a polymer, a fluoropolymer electrolyte is most preferable from the above viewpoint.
  • the particles and polymers contained in each layer may be of the same type or different types, but from the viewpoint of bondability within the layer (B), the particles and polymers contained in each layer are of the same type. It is preferable.
  • the layer (B) may contain various additives, such as surfactants, radical scavengers, hydrogen peroxide decomposers, non-electrolyte polymers, elastomers, etc., as long as they do not impede the effects of the present invention.
  • additives such as surfactants, radical scavengers, hydrogen peroxide decomposers, non-electrolyte polymers, elastomers, etc.
  • the thickness of the layer (B) is preferably 0.5 ⁇ m or more, more preferably 0.8 ⁇ m or more, and particularly preferably 1 ⁇ m or more from the viewpoint of enhancing the bonding function. Further, from the viewpoint of ensuring good proton conductivity, the thickness is preferably 20 ⁇ m or less, more preferably 15 ⁇ m or less, and particularly preferably 10 ⁇ m or less.
  • the thickness of the (A) layer is 30 ⁇ m or more and 250 ⁇ m or less, and the thickness of the (B) layer is 0.5 ⁇ m or more and 20 ⁇ m or less.
  • the thickness of each layer constituting the (B) layer may be the same or different.
  • the thickness of the (B-1) layer is preferably in the range of 0.25 ⁇ m to 10 ⁇ m, more preferably in the range of 0.4 ⁇ m to 7.5 ⁇ m, and more preferably in the range of 0.5 ⁇ m to A range of 5 ⁇ m is particularly preferred.
  • the thickness of the layer (B-2) is preferably in the range of 0.25 ⁇ m to 10 ⁇ m, more preferably in the range of 0.4 ⁇ m to 7.5 ⁇ m, and particularly preferably in the range of 0.5 ⁇ m to 5 ⁇ m.
  • the thickness of the (B-1) layer and the (B-2) layer is preferably at least 10% of the total thickness of the (B) layer.
  • the thickness of the layer can be measured by a contact film thickness measurement method or by SEM observation described in Examples.
  • the layer (A) can be formed by, for example, a coating method or a melt extrusion method. Among these, the coating method is preferred. The coating method will be described below as an example, but the present invention is not limited thereto.
  • Layer (A) can be produced, for example, by applying a polymer electrolyte solution onto a film-forming base material such as a polyethylene terephthalate (PET) film and drying it.
  • a film-forming base material such as a polyethylene terephthalate (PET) film
  • the layer (A) may be a so-called "composite membrane” reinforced with a porous base material.
  • This composite membrane preferably has a polymer electrolyte layer on one or both sides of a porous base material impregnated with a polymer electrolyte.
  • a porous base material is laminated onto a polymer electrolyte solution coated on a membrane forming base material and impregnated with the polymer electrolyte solution.
  • An example is a method of applying and drying.
  • the polymer electrolyte one in which the ionic group forms a salt with an alkali metal or alkaline earth metal cation can also be used.
  • acid treatment it is preferable to perform acid treatment to exchange the cations of the alkali metal or alkaline earth metal with protons.
  • a known method can be used for the acid treatment.
  • the electrolyte membrane according to the embodiment of the present invention is manufactured by laminating the (B) layer on the (A) layer manufactured as described above.
  • the lamination method is not particularly limited, but a coating method, a transfer method, and a combination of these methods can be employed.
  • the coating method is a method in which a coating liquid for layer (B) is applied to layer (A) formed on a film-forming base material, and then dried and laminated.
  • the transfer method heat-presses a transfer sheet in which the (B) layer is laminated on the transfer base material and the (A) layer formed on the film forming base material, and then the (B) layer is layered on the (A) layer. This is a method of transferring.
  • the coating liquid for the (B-1) layer is applied onto the (A) layer formed on the film-forming base material, and the coating liquid for the (B-2) layer is applied undried or after drying.
  • a method of applying and drying the coating liquid can be adopted.
  • we have adopted a method in which two coating liquids with different ratios of polymer to particles (P/F) are prepared, and the two coating liquids are simultaneously applied onto layer (A) using a multilayer die or multilayer slide coater and dried. can.
  • the transfer method includes a (B) layer transfer sheet in which layers (B-2) and (B-1) are sequentially laminated on a transfer base material, and (A) layer transfer sheet formed on a film forming base material.
  • a method can be adopted in which the layers (B-1) and (B-2) are transferred onto the layer (A) by hot pressing the layers.
  • the coating method is more preferable because it has high bonding properties with the layer (A) and can suppress interfacial resistance.
  • the coating method is not particularly limited as long as it can be applied to the desired shape, and for example, a die coating method, a screen printing method, a spray method, a gravure coating method, a slide coating method, etc. can be used.
  • the above-mentioned coating method, transfer method, or combination method of the coating method and the transfer method can be adopted.
  • the (B) layer laminated on one side of the (A) layer is called the first (B) layer
  • the (B) layer laminated on the other side of the (A) layer is called the first (B) layer. It is called the 2(B) layer.
  • An example of a manufacturing method includes a step (1-3) of applying a layer coating liquid, drying, and laminating.
  • a step of laminating a protective base material on the first (B) layer can be provided between the above steps (1-1) and (1-3).
  • the protective base material the same material as the film-forming base material or the transfer base material, or a resin film laminated with a slightly adhesive layer can be used.
  • a first (B layer) transfer sheet in which a first (B) layer is laminated on a transfer base material and a second (B) layer in a transfer base material are laminated.
  • a step (2-1) of obtaining a second (B) layer transfer sheet a step (2-2) of peeling off the film forming base material from the layer (A) formed on the film forming base material, and a step (2-2) of peeling off the film forming base material from the (A) layer formed on the film forming base material;
  • a manufacturing method including a step (2-3) of sandwiching the (A) layer between the B) layer transfer sheet and the second (B) layer transfer sheet and heat pressing.
  • a coating liquid for the first (B) layer is applied onto the (A) layer formed on the film forming base material, dried, and laminated.
  • Step (3-1) of obtaining a second (B) layer transfer sheet in which the second (B) layer is laminated on the transfer substrate (3-2)
  • a manufacturing method including a step (3-4) of bringing the layer transfer sheet into contact and hot pressing.
  • a step of laminating a protective base material on the first (B) layer can be provided between the above steps (3-1) and (3-4).
  • a modification of the manufacturing method using the above combination method includes a manufacturing method in which the first (B) layer is laminated by a transfer method, and the second (B) layer is laminated by a coating method.
  • either one of the first (B) layer and the second (B) layer may have a laminated structure of the (B-1) layer and the (B-2) layer, or both layers may have a laminated structure. Both may have a laminated structure.
  • the method for preparing the coating liquid for the layer is not particularly limited as long as the desired coating liquid can be obtained, and examples include stirring with a stirrer tip, crushing with a homogenizer, and homogenization with a rotation-revolution mixer. , dispersion using a bead mill or ball mill, etc. can be used.
  • the solvent contained in the layer coating liquid (B) is not particularly limited as long as it can disperse the particles and polymer, but a solvent that can be easily removed by evaporation by heating is preferred.
  • a solvent having a boiling point of 140°C or lower is preferable.
  • the solvent for the layer coating liquid include water, methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, isobutyl alcohol, Alcohols such as tert-butyl alcohol and pentanol, ketones such as acetone, methyl ethyl ketone, pentanone, hexanone, heptanone, cyclohexanone, methylcyclohexanone, acetonylacetone, and diisobutyl ketone, tetrahydrofuran, dioxane, diethylene glycol dimethyl ether, anisole, Ethers such as methoxytoluene and dibutyl ether, esters such as methyl acetate, ethyl acetate, n-propyl acetate, isopropyl acetate, butyl acetate, methyl lactate, ethyl lactate, butyl lac
  • the (B) layer can be formed by passing through a drying process as necessary.
  • the coating is heated to evaporate the solvent.
  • the heating means is not particularly limited as long as it can heat the fixed polymer electrolyte membrane, but for example, heating devices such as ovens and heaters, infrared rays, hot air, etc. A device or the like that controls the temperature in the vicinity can be used. Alternatively, heat may be conducted to the polymer electrolyte membrane via the fixing means.
  • the heating temperature range is preferably close to the boiling point of the solvent and below the glass transition temperature of the polymer electrolyte membrane.
  • the solvent can be removed without heating, only by reducing pressure or introducing an air flow, and furthermore, it is also possible to omit the drying step.
  • the (B) layer transfer sheet can be produced by applying the (B) layer coating liquid onto the transfer substrate and, if necessary, performing a drying process.
  • the drying process can use the method described above.
  • the layer (B) can be laminated on the layer (A) by overlapping and hot pressing the layer (A) and the layer (B) coated surface of the layer transfer sheet (B).
  • the temperature and pressure of the hot press may be appropriately selected depending on (A) layer thickness and moisture content, (B) layer thickness and type of transfer substrate, but may be determined depending on industrial productivity and the heat of the polymer electrolyte. From the viewpoint of suppressing decomposition, it is preferable to conduct the reaction at a temperature in the range of 120°C to 250°C.
  • the pressure applied during hot pressing is preferably as weak as possible from the viewpoint of protecting the electrolyte membrane, and for example, in the case of flat plate pressing, it is preferably in the range of 2 to 10 MPa.
  • the transfer base material resin films and substrates similar to those used in forming the layer (A) can be used, as well as polytetrafluoroethylene, ethylene-tetrafluoroethylene copolymer, ethylene-hexafluoropropylene.
  • a fluororesin film made of a fluororesin such as a copolymer, a tetrafluoroethylene-perfluoro(alkyl vinyl ether) copolymer, or polyvinylidene fluoride can be used.
  • the transfer base material may be one in which a mold release layer containing a known mold release agent such as a fluorine-based mold release agent is laminated on a base material such as a resin film in order to improve mold release properties.
  • a fluororesin film is preferable from the viewpoint of heat resistance and solvent resistance, as well as chemical stability and mold releasability.
  • the electrolyte membrane according to the embodiment of the present invention can be made into a CCM by disposing a catalyst layer on one or both sides thereof. That is, CCM includes a catalyst layer on one or both sides of an electrolyte membrane.
  • the catalyst layer is generally a layer containing catalyst particles and a polymer electrolyte.
  • the catalyst layer can be formed by laminating a coating liquid for a catalyst layer in which catalyst particles are added to a polymer electrolyte solution on the electrolyte membrane by a coating method or a transfer method.
  • a hydrocarbon polymer electrolyte or a fluorine polymer electrolyte as described above can be used as the polymer electrolyte. From the viewpoint of gas diffusibility and chemical durability, fluoropolymer electrolytes are preferred, and perfluorocarbon sulfonic acid polymers are more preferred.
  • Catalyst particles generally include platinum group elements (platinum, ruthenium, rhodium, palladium, osmium, iridium), iron, lead, gold, silver, copper, chromium, cobalt, nickel, manganese, vanadium, molybdenum, gallium, Metals such as aluminum, alloys thereof, oxides, double oxides, etc. are used, and carbon particles supporting the above metals (catalyst-supported carbon particles) are also generally used.
  • the above-mentioned carbon particles are not particularly limited as long as they are fine particles, have conductivity, and do not corrode or deteriorate due to reaction with a catalyst, but include carbon black, graphite, activated carbon, carbon fiber, carbon nanotubes, and fullerene particles can be preferably used.
  • the mass ratio (C/I) between the content (C) of catalyst particles (including catalyst-supported particles) and the content (I) of polymer electrolyte in the catalyst layer is in the range of 1.0 to 15.0. Generally, it is preferably in the range of 1.5 to 13.0.
  • the mass ratio (C/I) in the anode catalyst layer is preferably 4.0 or more, more preferably 5.0 or more, and particularly preferably 7.0 or more. Further, it is preferably 15.0 or less, more preferably 14.0 or less, and particularly preferably 13.0 or less.
  • the mass ratio (C/I) in the cathode catalyst layer is preferably less than 4.0, more preferably less than 3.5, and particularly preferably less than 3.0. Further, it is preferably 1.0 or more, more preferably 1.5 or more, and particularly preferably 1.7 or more.
  • the thickness of the catalyst layer is preferably 0.1 ⁇ m or more, more preferably 0.5 ⁇ m or more, and particularly preferably 1 ⁇ m or more from the viewpoint of gas diffusivity and durability. Moreover, it is preferably 500 ⁇ m or less, more preferably 100 ⁇ m or less, and particularly preferably 30 ⁇ m or less.
  • the anode catalyst layer and the cathode catalyst layer may be made of the same material or may be made of different materials.
  • the anode catalyst layer may be any catalyst that generates oxygen using water or hydroxide as a raw material as catalyst particles, and noble metals such as iridium, ruthenium, rhodium, and palladium or oxidation thereof. It is preferable to use a material.
  • the catalyst particles may be used in the form of individual particles, or may be used as catalyst-supported particles supported on titanium oxide or the like.
  • the cathode catalyst layer may be any catalyst that generates hydrogen using protons or water as catalyst particles, and it is preferable to use platinum-supported carbon particles in which platinum is supported on carbon particles.
  • a CCM according to an embodiment of the present invention is manufactured by laminating a catalyst layer on an electrolyte membrane.
  • the method for laminating the catalyst layer is not particularly limited, but a coating method, a transfer method, and a combination of these methods can be employed.
  • the coating method is a method in which a catalyst layer coating liquid is applied to the electrolyte membrane, dried, and then laminated.
  • the transfer method is a method in which a catalyst layer transfer sheet in which a catalyst layer is laminated on a transfer base material and an electrolyte membrane are laminated by hot pressing. Among these, the transfer method is preferred.
  • the transfer base material used in the catalyst layer transfer sheet the same resin film or substrate as described above can be used.
  • CCM manufacturing method (I) a step of obtaining an electrolyte membrane in which a layer (B) is laminated on a layer (A), a step of obtaining a catalyst layer transfer sheet in which a catalyst layer is laminated on a transfer base material, It is possible to employ a manufacturing method including a step of bringing the layer (B) of the electrolyte membrane and the catalyst layer of the transfer sheet into facing contact with each other and hot pressing them.
  • the CCM manufacturing method (II) includes a step of forming a layer (A), and a step of obtaining a catalyst layer/(B) layer transfer sheet in which a catalyst layer and a layer (B) are sequentially laminated on a transfer substrate. It is possible to employ a manufacturing method comprising the steps of: bringing the layer (A) and the layer (B) of the transfer sheet into facing contact with each other and hot-pressing the layer.
  • the catalyst layer/(B) layer transfer sheet used in the above CCM manufacturing method (II) is useful as one member for obtaining the CCM according to the embodiment of the present invention. That is, one member for obtaining a CCM according to an embodiment of the present invention is, for example, a catalyst layer/(B) layer transfer sheet in which a catalyst layer and a (B) layer are sequentially laminated on a transfer base material. Consisting of
  • the (B) layer is composed of two layers, of which the layer adjacent to the (A) layer is placed as the (B-1) layer on the opposite side to the (A) layer.
  • the catalyst layer, (B-2) layer and (B-1) layer are sequentially laminated on the transfer base material as a catalyst layer/(B) layer transfer sheet.
  • a catalyst layer/(B-2) layer/(B-1) layer transfer sheet can be used. This transfer sheet is useful as one member for obtaining the CCM according to the embodiment of the present invention.
  • one member for obtaining the CCM according to the embodiment of the present invention is, for example, a transfer base material in which a catalyst layer, a layer (B-2), and a layer (B-1) are sequentially laminated. It consists of a catalyst layer/(B-2) layer/(B-1) layer transfer sheet.
  • a step of obtaining a laminate in which the (B-1) layer is laminated on the (A) layer, and a transfer base material a step of obtaining a catalyst layer/(B-2) layer transfer sheet in which a catalyst layer and a (B-2) layer are sequentially laminated; 2) A manufacturing method including the step of hot pressing the layers in facing contact with each other can be adopted.
  • the catalyst layer/(B-2) layer transfer sheet used in the above CCM manufacturing method (III) is useful as one member for obtaining the CCM according to the embodiment of the present invention. That is, one member for obtaining the CCM according to the embodiment of the present invention is, for example, a catalyst layer/(B-2) in which a catalyst layer and a (B-2) layer are sequentially laminated on a transfer base material. Consists of a layer transfer sheet.
  • the transfer sheet used in the above CCM manufacturing methods (II) and (III), that is, the member for obtaining the CCM, is prepared by, for example, applying a catalyst layer coating liquid to a transfer base material, undried or after drying ( B) It can be manufactured by applying a layer coating liquid and drying it. Alternatively, a method may be adopted in which the coating liquid for the catalyst layer and the coating liquid for the (B) layer are simultaneously applied to the transfer substrate using a multilayer die or a multilayer slide coater and then dried.
  • the coating method is not particularly limited as long as it can be applied to the desired shape, and for example, a die coating method, a screen printing method, a spray method, a gravure coating method, a slide coating method, etc. can be used.
  • the temperature and pressure of the hot press may be appropriately selected depending on the thickness and moisture content of the (A) layer, the thickness of the (B) layer and catalyst layer, and the type of transfer substrate. It is preferable to conduct the reaction at a temperature in the range of 120° C. to 250° C. from the viewpoint of productivity and suppression of thermal decomposition of the polymer electrolyte. Specifically, it is more preferable to conduct the heating at a temperature higher than the glass transition temperature of the polymer contained in layer (B) and 200° C. or lower.
  • the pressure in hot pressing is preferably as low as possible from the viewpoint of protecting the electrolyte membrane, and for example, in the case of flat plate pressing, it is preferably in the range of 2 to 10 MPa.
  • the membrane electrode assembly includes the CCM and gas diffusion layers (gas diffusion electrodes) disposed on both sides of the CCM. Specifically, an anode gas diffusion layer is placed and bonded to the anode catalyst layer side of the CCM, and a cathode gas diffusion layer is placed to the cathode catalyst layer side.
  • the gas diffusion layer is generally made of a member having gas permeability and electron conductivity, such as a porous carbon material or a porous metal material.
  • a porous carbon material or a porous metal material examples include carbon paper, carbon cloth, carbon mesh, carbon nonwoven fabric, and the like.
  • the metal porous body examples include metal mesh, foam metal, metal fabric, metal sintered body, metal nonwoven fabric, and the like.
  • this metal include titanium, aluminum, copper, nickel, nickel-chromium alloy, copper and its alloys, silver, aluminum alloy, zinc alloy, lead alloy, titanium, niobium, tantalum, iron, stainless steel, gold, platinum, etc. can be mentioned.
  • the gas diffusion layer is treated with water repellent treatment to prevent gas diffusion and permeability from decreasing due to water retention, partial water repellent treatment and partial hydrophilic treatment to form water drainage channels, and lower resistance. It is also possible to add carbon powder for this purpose. Further, the gas diffusion layer can also be provided with a conductive intermediate layer containing at least an inorganic conductive substance and a hydrophobic polymer on the CCM side. In particular, when the gas diffusion layer is made of a carbon fiber fabric or nonwoven fabric with a high porosity, providing a conductive intermediate layer can suppress performance degradation due to the catalyst solution seeping into the gas diffusion layer.
  • the thickness of the gas diffusion layer is preferably 50 ⁇ m or more, more preferably 100 ⁇ m or more, and particularly preferably 150 ⁇ m or more. Further, the thickness is preferably 1,000 ⁇ m or less, more preferably 700 ⁇ m or less, and particularly preferably 500 ⁇ m or less.
  • the anode gas diffusion layer and the cathode gas diffusion layer may be made of the same material, or may be made of different materials.
  • the anode gas diffusion layer and the cathode gas diffusion layer are made of different materials.
  • the anode gas diffusion layer is made of a porous metal material
  • the cathode gas diffusion layer is made of a porous carbon material.
  • the electrolyte membrane, the CCM using the electrolyte membrane, and the membrane electrode assembly according to the embodiments of the present invention can be applied to, for example, electrochemical applications.
  • electrochemical applications include fuel cells, redox flow batteries, water electrolysis devices, electrochemical hydrogen compression devices, and the like. Among these, it is preferably applied to a water electrolysis type hydrogen device, and particularly preferably applied to a water electrolysis device.
  • Molecular weight of polymer The number average molecular weight and weight average molecular weight of the polymer solution were measured by gel permeation chromatography (GPC). HLC-8022GPC manufactured by Tosoh Corporation was used as a device. An ultraviolet detector and a differential refractometer were used as detectors. Furthermore, two TSK gel SuperHM-H (inner diameter 6.0 mm, length 15 cm) manufactured by Tosoh Corporation were used as GPC columns. Measurements were made using N-methyl-2-pyrrolidone solvent (N-methyl-2-pyrrolidone solvent containing 10 mmol/L of lithium bromide) as a developing solvent at a flow rate of 0.2 mL/min, and the number was calculated by standard polystyrene conversion. The average molecular weight and weight average molecular weight were determined.
  • the sodium sulfate aqueous solution after ion exchange was titrated using a 0.01 mol/L sodium hydroxide aqueous solution.
  • 0.1 w/v % of a commercially available phenolphthalein solution for titration was added as an indicator, and the point at which the color turned pale reddish-purple was defined as the end point.
  • the ion exchange capacity (IEC) was determined using the following formula.
  • IEC (meq/g) [concentration of aqueous sodium hydroxide solution (mmol/mL) x dropping amount (mL)]/dry weight of sample (g).
  • an image analysis method was applied to images taken at a magnification of 50,000 times. After performing image noise reduction processing, background brightness unevenness reduction, and contrast enhancement using image analysis software ImageJ, binary values of particle components and void components in the image are determined by machine learning using Trainable Weka Segmentation. .
  • the same classifier was applied and each sample was binarized based on the same criteria. From the obtained binarized image, determine the total area of void components (void area) in each 10% thick region from both interfaces of layer (B), and calculate the ratio of the void area to the total area of the region. Then, the porosity was obtained.
  • the porosity in the interface region with the (A) layer was defined as the porosity (X1), and the porosity in the interface region on the opposite side to the (A) layer was defined as the porosity (X2).
  • a commercially available gas diffusion electrode 24BCH manufactured by SGL was used as a cathode gas diffusion layer on the cathode catalyst layer side of the CCM in which catalyst layers were laminated on both sides of the electrolyte membranes prepared in Examples and Comparative Examples.
  • Commercially available porous titanium sintered plates were laminated as an anode gas diffusion layer on the anode catalyst layer side to prepare a membrane electrode assembly.
  • the membrane electrode assembly prepared above was set in a JARI standard cell "Ex-1" (electrode area 25 cm 2 ) manufactured by Eiwa Co., Ltd., the cell was tightened so that the average CCM pressure was 4 MPa, and the cell temperature was set at 80°C. And so.
  • Deionized water with an electrical conductivity of 1 ⁇ S/cm or less is supplied to both the cathode electrode and the anode electrode at atmospheric pressure at a flow rate of 0.2 L/min, and a current of 2.0 A/cm 2 is applied to cause a water electrolysis reaction. Hydrogen gas and oxygen gas were produced.
  • V 1 the rate of increase in voltage
  • V 0 the initial applied voltage
  • NMP N-methylpyrrolidone
  • toluene 100 mL
  • polymerization was carried out at 170°C for 3 hours.
  • Reprecipitation purification was performed using a large amount of methanol to obtain a terminal hydroxyl form of nonionic oligomer a1.
  • the number average molecular weight of the terminal hydroxyl form of this nonionic oligomer a1 was 10,000.
  • Coating solutions p1 to p4 containing various polymer electrolytes were prepared in the following manner.
  • Coating liquid p1 Coating liquid containing polyetherketone block copolymer P1 16 g of ionic oligomer a2 and 11 g of nonionic oligomer a1 was added, NMP was added so that the total amount of oligomers was 7 wt%, and the reaction was carried out at 105° C. for 24 hours.
  • Coating liquid p2 Coating liquid containing polyetherketone random copolymer P2
  • the 2,2-bis synthesized in Synthesis Example 1 was placed in a 5 L reaction vessel equipped with a stirrer, a nitrogen inlet tube, and a Dean-Stark trap.
  • NMP was added to dilute the polymerization stock solution so that the viscosity was 500 mPa ⁇ s.
  • An angle rotor RA-800 was set in an inverter compact high-speed refrigerated centrifuge (model number 6930) manufactured by Kubota Manufacturing Co., Ltd., and the polymerization stock solution was directly centrifuged at 25° C. for 30 minutes at a centrifugal force of 20,000 G. Since the precipitated solid (cake) and the supernatant liquid (coating liquid) could be clearly separated, the supernatant liquid was collected.
  • NMP was removed by distillation under reduced pressure at 80° C. with stirring until the polymer concentration became 14% by mass, and further pressure filtration was performed using a 5 ⁇ m polyethylene filter to obtain coating liquid p2.
  • the viscosity of this coating liquid p2 was 1,000 mPa ⁇ s.
  • Coating liquid p3 Coating liquid containing polyarylene block copolymer P3 represented by the following general formula (G10) 540 mL of dried N,N-dimethylacetamide (DMAc) was mixed with 3-(2,5-dichloro 135.0 g (0.336 mol) of neopentyl benzenesulfonate and 40.7 g (5.6 mmol) of the nonionic oligomer represented by general formula (G6) synthesized in Synthesis Example 6, 2,5-dichloro -4'-(1-imidazolyl)benzophenone 6.71g (16.8mmol), bis(triphenylphosphine)nickel dichloride 6.71g (10.3mmol), triphenylphosphine 35.9g (0.137mol), iodide It was added to a mixture of 1.54 g (10.3 mmol) of sodium and 53.7 g (0.821 mol) of zinc under nitrogen.
  • G10 dried N,N-dimethylace
  • the reaction system was heated while stirring (finally heated to 79°C) and reacted for 3 hours. An increase in viscosity in the system was observed during the reaction.
  • the polymerization reaction solution was diluted with 730 mL of DMAc, stirred for 30 minutes, and filtered using Celite as a filter aid.
  • the filtrate was concentrated using an evaporator, 43.8 g (0.505 mol) of lithium bromide was added to the filtrate, and the mixture was reacted at an internal temperature of 110° C. for 7 hours under a nitrogen atmosphere. After the reaction, the mixture was cooled to room temperature, poured into 4 L of acetone, and solidified. The coagulated material was collected by filtration, air-dried, pulverized with a mixer, and washed with 1,500 mL of 1N hydrochloric acid while stirring. After filtration, the product was washed with ion-exchanged water until the pH of the washing solution was 5 or higher. Thereafter, it was dried at 80° C.
  • polyarylene block copolymer P3 The weight average molecular weight of this polyarylene block copolymer P3 was 190,000, and the ion exchange capacity (IEC) was 2.0.
  • [Coating liquid p4] Coating liquid containing polyethersulfone-based block copolymer P4 Weighed 0.23 g of the block copolymer precursor b1 obtained in Synthesis Example 7, and added 0.16 g of lithium bromide monohydrate. and NMP (8 mL), and the mixture was reacted at 120° C. for 24 hours. The reaction mixture was poured into 80 mL of 6 mol/L hydrochloric acid and stirred for 1 hour. The precipitated solid was separated by filtration. The separated solid was dried to obtain a gray-white block copolymer P4 consisting of a segment represented by the above general formula (G9) and a segment represented by the following chemical formula (G11).
  • the weight average molecular weight of the obtained polyethersulfone block copolymer P4 was 190,000, and the ion exchange capacity (IEC) was 2.0.
  • p4 was obtained.
  • the viscosity of coating liquid p4 was 1,300 mPa ⁇ s.
  • Coating liquids q1 to q10 were prepared in the following manner.
  • Coating liquids q2 to q7 were prepared in the same manner as coating liquid q1, except that the ratio of polymer to particles (P/F) was changed as shown in Table 1.
  • Coating liquid q8 was prepared in the same manner as coating liquid q1 except that particles were not used.
  • Coating liquid q9 was prepared in the same manner as coating liquid q1, except that the particles were changed from carbon black to cerium (IV) oxide manufactured by Fuji Film Wako Pure Chemical Industries, Ltd. (average particle size: 50 nm).
  • Coating liquid q10 was prepared in the same manner as coating liquid q8 except that the polymer was changed to PVDF (polyvinylidene fluoride) manufactured by Solvey.
  • the anode catalyst layer was formed by casting the following coating solution for an anode catalyst layer on a commercially available polytetrafluoroethylene film so that the amount of iridium was 1.0 mg/cm 2 and drying at 100°C for 4 hours. A transfer sheet was produced.
  • ⁇ Coating liquid for anode catalyst layer Particles (10 parts by mass of IrO 2 catalyst Elyst Ir75 0480 (Ir content 75%) manufactured by Umicore) and fluoropolymer electrolyte (“Nafion” (registered trademark) product number D2020 manufactured by Chemours Co., Ltd.) in terms of solid content. It was prepared by dispersing 1.2 parts by mass in 28.8 parts by mass of water, 30 parts by mass of 1-propanol, and 30 parts by mass of t-butanol.
  • cathode catalyst layer transfer sheet A cathode catalyst layer was formed by casting the following coating solution for cathode catalyst layer on a commercially available polytetrafluoroethylene film so that the amount of platinum was 0.3 mg/cm 2 and drying at 100°C for 4 hours. A transfer sheet was produced.
  • ⁇ Coating liquid for cathode catalyst layer 10 parts by mass of catalyst particles (Tanaka Kikinzoku Kogyo Co., Ltd. platinum catalyst-supported carbon particles TEC10E50E (platinum loading rate 50 mass%)) and a fluoropolymer electrolyte (“Nafion” (registered trademark) product number manufactured by Chemours Co., Ltd.) D2020) was dispersed in 25 parts by mass of water, 30 parts by mass of 1-propanol, and 30 parts by mass of t-butanol.
  • Coating liquid q1 was cast onto the layer (A) and dried at 100° C. for 4 hours, thereby layering the layer (B-1) (thickness: 3 ⁇ m) on the layer (A). Subsequently, coating liquid q8 was cast onto the layer (B-1) and dried at 100° C. for 4 hours, thereby laminating the layer (B-2) (thickness: 3 ⁇ m).
  • Example 2 An electrolyte membrane was produced in the same manner as in Example 1, except that the coating liquid for the (B-1) layer and the coating liquid for the (B-2) layer were changed as shown in Table 2.
  • Example 12 to 14 An electrolyte membrane was produced in the same manner as in Example 1, except that the coating liquid p1 for layer was changed as shown in Table 2.
  • the (A) layer was prepared in the same manner as in Example 1, and the coating liquid q8 was cast onto the (A) layer and dried at 100°C for 4 hours, thereby leaving only the polymer on the (A) layer.
  • An electrolyte membrane was produced by laminating a single (B) layer (film thickness: 6 ⁇ m) consisting of:
  • the (A) layer was prepared in the same manner as in Example 1, and coating liquid q7 was cast onto the (A) layer and dried at 100°C for 4 hours to form particles and particles on the (A) layer.
  • An electrolyte membrane was produced by stacking a single (B) layer (6 ⁇ m thick) containing a polymer.
  • catalyst layer/(B) layer transfer sheet Coating liquid q8 was cast onto the catalyst layer of the anode catalyst layer transfer sheet described above, and the (B-2) layer (thickness: 3 ⁇ m) was laminated by drying at 100°C for 4 hours. The coating liquid q1 was cast onto the (B-2) layer and dried at 100° C. for 4 hours to form the (B-1) layer (thickness: 3 ⁇ m).
  • This catalyst layer/(B) layer transfer sheet is a catalyst layer/(B) layer in which a catalyst layer and a (B) layer ((B-2) layer/(B-1) layer) are sequentially laminated on a transfer base material. (B-2) layer/(B-1) layer layer transfer sheet, and was used to produce CCM.
  • Coating liquid q1 was cast onto layer (A) prepared in the same manner as in Example 1, and dried at 100°C for 4 hours to form layer (B-1) (film thickness) on layer (A). A laminate in which 3 ⁇ m) was laminated was obtained.
  • catalyst layer/(B-2) layer transfer sheet Coating liquid q8 was cast onto the catalyst layer of the above-mentioned anode catalyst layer transfer sheet and dried at 100° C. for 4 hours to form a layer (B-2) (thickness: 3 ⁇ m).
  • This catalyst layer/(B-2) layer transfer sheet had a catalyst layer and a (B-2) layer sequentially laminated on a transfer substrate, and was used to produce a CCM.
  • the anode catalyst layer transfer sheet was superimposed on the (B) layer side of the electrolyte membranes prepared in Examples 1 to 14 and Comparative Examples 1 to 3 above, and heated and pressed at 150°C and 5 MPa for 3 minutes. After the temperature was lowered to 40° C. or lower, the pressure was released to obtain CCM. Regarding these CCMs and the CCMs produced in Examples 15 and 16, the bondability between the electrolyte membrane and the catalyst layer was evaluated according to "(4) Evaluation of interlayer bondability (peelability)" above. The results are shown in Table 2.
  • particles "CB” represent carbon black, and “Ce” represents cerium oxide.
  • Example 22 An electrolyte membrane was produced in the same manner as in Example 21, except that the layer coating liquid was changed to coating liquid q5.
  • the cathode catalyst layer transfer sheet was superimposed on the (B) layer side of the electrolyte membrane prepared in the above Examples and Comparative Examples, and hot pressed at 150°C and 5 MPa for 3 minutes, and the temperature was lowered to 40°C or less under pressure. After that, the pressure was released and CCM was obtained. Regarding these CCMs, the bondability between the electrolyte membrane and the catalyst layer was evaluated according to "(4) Evaluation of interlayer bondability (peelability)" above. The results are shown in Table 3.
  • Coating liquid q8 was cast onto a commercially available polytetrafluoroethylene film and dried at 100° C. for 4 hours to form a layer (B-2) (thickness: 3 ⁇ m). Furthermore, the (B-1) layer (thickness: 3 ⁇ m) was laminated by casting coating liquid q1 on the (B-2) layer and drying it at 100°C for 4 hours, thereby forming the (B) layer transfer sheet. I got D1.
  • Example 32 [(B) Production of layer transfer sheet D3] A (B) layer transfer sheet D3 was prepared in the same manner as the above (B) layer transfer sheet D1, except that the (B-1) layer coating liquid q1 was changed to a coating liquid q9.
  • Example 34 to 36 An electrolyte membrane was produced in the same manner as in Example 31, except that the layer coating liquid p1 was changed as shown in Table 4 [Comparative Example 31] (B) An electrolyte membrane was produced in the same manner as in Example 31 except that the layer was not laminated.
  • An anode catalyst layer transfer sheet was placed on the anode side (B) layer of the electrolyte membrane prepared in the above Examples and Comparative Examples, and a cathode catalyst layer transfer sheet was placed on the cathode side (B) layer of the electrolyte membrane, and heated at 150°C. Heat pressing was performed at 5 MPa for 3 minutes, and the temperature was lowered to 40° C. or less under pressure, and then the pressure was released to obtain a CCM. The durability of these CCMs was evaluated according to "(5) Evaluation of durability" above. The results are shown in Table 4.
  • Electrolyte membrane 10 (A) Layers 20, 20a, 20b (B) Layers 21, 21a, 21b (B) Layer's (A) layer side interface region 22, 22a, 22b (B) Layer's (A) Interface region on the opposite side of the layer 30, 40 Catalyst layer 50 Anode catalyst layer 60 Cathode catalyst layer 100, 200 Electrolyte membrane with catalyst layer

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JP2008512844A (ja) 2004-09-08 2008-04-24 ポリフューエル・インコーポレイテッド 接着性促進層を有する膜及び膜電極アセンブリー
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