WO2010047254A1 - Method for producing electrode catalyst for fuel cell, and electrode catalyst for fuel cell - Google Patents
Method for producing electrode catalyst for fuel cell, and electrode catalyst for fuel cell Download PDFInfo
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- WO2010047254A1 WO2010047254A1 PCT/JP2009/067772 JP2009067772W WO2010047254A1 WO 2010047254 A1 WO2010047254 A1 WO 2010047254A1 JP 2009067772 W JP2009067772 W JP 2009067772W WO 2010047254 A1 WO2010047254 A1 WO 2010047254A1
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- Prior art keywords
- fuel cell
- added
- electrode catalyst
- catalyst
- functional group
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- 239000003054 catalyst Substances 0.000 title claims abstract description 60
- 239000000446 fuel Substances 0.000 title claims abstract description 24
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 150000001875 compounds Chemical class 0.000 claims abstract description 32
- 125000000524 functional group Chemical group 0.000 claims abstract description 29
- 229910052723 transition metal Inorganic materials 0.000 claims abstract description 20
- 230000002378 acidificating effect Effects 0.000 claims abstract description 14
- 229910000510 noble metal Inorganic materials 0.000 claims abstract description 13
- 150000003624 transition metals Chemical class 0.000 claims abstract description 11
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 10
- 238000000034 method Methods 0.000 claims abstract description 10
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 9
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 8
- 239000000956 alloy Substances 0.000 claims abstract description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 6
- 239000002904 solvent Substances 0.000 claims abstract description 6
- 238000006243 chemical reaction Methods 0.000 claims abstract description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 41
- 229910052799 carbon Inorganic materials 0.000 claims description 41
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 28
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- 229910052697 platinum Inorganic materials 0.000 claims description 14
- 229910017052 cobalt Inorganic materials 0.000 claims description 11
- 239000010941 cobalt Substances 0.000 claims description 11
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 11
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 9
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- 239000011651 chromium Substances 0.000 claims description 4
- 239000011572 manganese Substances 0.000 claims description 4
- 239000010955 niobium Substances 0.000 claims description 4
- 239000010948 rhodium Substances 0.000 claims description 4
- 239000010936 titanium Substances 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 229910052741 iridium Inorganic materials 0.000 claims description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052748 manganese Inorganic materials 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 239000011733 molybdenum Substances 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 229910052758 niobium Inorganic materials 0.000 claims description 2
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 2
- 229910052762 osmium Inorganic materials 0.000 claims description 2
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims description 2
- 229910052702 rhenium Inorganic materials 0.000 claims description 2
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims description 2
- 229910052703 rhodium Inorganic materials 0.000 claims description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- 229910052709 silver Inorganic materials 0.000 claims description 2
- 239000004332 silver Substances 0.000 claims description 2
- 229910052715 tantalum Inorganic materials 0.000 claims description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 239000010937 tungsten Substances 0.000 claims description 2
- 238000006722 reduction reaction Methods 0.000 abstract description 31
- 230000003197 catalytic effect Effects 0.000 abstract description 6
- 239000003960 organic solvent Substances 0.000 abstract description 3
- 150000001412 amines Chemical class 0.000 abstract description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract description 2
- 239000003146 anticoagulant agent Substances 0.000 abstract 1
- 239000002245 particle Substances 0.000 description 29
- 230000002776 aggregation Effects 0.000 description 17
- 238000004220 aggregation Methods 0.000 description 16
- 239000003112 inhibitor Substances 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 11
- 229910002837 PtCo Inorganic materials 0.000 description 10
- 239000004020 conductor Substances 0.000 description 10
- KLFRPGNCEJNEKU-FDGPNNRMSA-L (z)-4-oxopent-2-en-2-olate;platinum(2+) Chemical class [Pt+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O KLFRPGNCEJNEKU-FDGPNNRMSA-L 0.000 description 9
- NKJOXAZJBOMXID-UHFFFAOYSA-N 1,1'-Oxybisoctane Chemical compound CCCCCCCCOCCCCCCCC NKJOXAZJBOMXID-UHFFFAOYSA-N 0.000 description 9
- CLBRCZAHAHECKY-UHFFFAOYSA-N [Co].[Pt] Chemical compound [Co].[Pt] CLBRCZAHAHECKY-UHFFFAOYSA-N 0.000 description 9
- 238000013019 agitation Methods 0.000 description 9
- FJDJVBXSSLDNJB-LNTINUHCSA-N cobalt;(z)-4-hydroxypent-3-en-2-one Chemical class [Co].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O FJDJVBXSSLDNJB-LNTINUHCSA-N 0.000 description 9
- 238000001914 filtration Methods 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 239000005518 polymer electrolyte Substances 0.000 description 6
- 229910001260 Pt alloy Inorganic materials 0.000 description 5
- 238000010248 power generation Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 4
- -1 aliphatic aldehyde Chemical class 0.000 description 4
- 230000002744 anti-aggregatory effect Effects 0.000 description 4
- 239000006229 carbon black Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 239000002923 metal particle Substances 0.000 description 4
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 4
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 4
- 239000010419 fine particle Substances 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 239000005639 Lauric acid Substances 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- 229910002836 PtFe Inorganic materials 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000007731 hot pressing Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000003223 protective agent Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 229920000557 Nafion® Polymers 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- WFDIJRYMOXRFFG-UHFFFAOYSA-N acetic anhydride Substances CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 1
- VBXBSTJDBPXOAD-UHFFFAOYSA-N acetyl acetate;platinum Chemical compound [Pt].CC(=O)OC(C)=O VBXBSTJDBPXOAD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- FJDUDHYHRVPMJZ-UHFFFAOYSA-N nonan-1-amine Chemical compound CCCCCCCCCN FJDUDHYHRVPMJZ-UHFFFAOYSA-N 0.000 description 1
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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Classifications
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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
- H01M4/90—Selection of catalytic material
- H01M4/92—Metals of platinum group
- H01M4/921—Alloys or mixtures with metallic elements
-
- 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
- H01M4/90—Selection of catalytic material
- H01M4/92—Metals of platinum group
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/89—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals
- B01J23/8913—Cobalt and noble metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
- B01J35/33—Electric or magnetic properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0215—Coating
- B01J37/0219—Coating the coating containing organic compounds
-
- 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 weakly basic functional group-containing compound used as another aggregation inhibitor in the present invention is a hydrocarbon having a weakly basic functional group having 5 to 10 carbon atoms (for example, a weakly basic functional group is carbonized with an amino group).
- Hydrogen is an aliphatic hydrocarbon, alicyclic hydrocarbon, aromatic hydrocarbon), and more specifically, an aliphatic amine having 5 to 10 carbon atoms is preferably exemplified.
- the present invention is a fuel cell electrode catalyst produced by the above method.
- a weakly acidic functional group-containing compound and a weakly basic functional group-containing compound are added to the reaction system as an aggregation inhibitor, and the weakly acidic functional group-containing compound is added.
- proton conductive material polymer electrolyte
- platinum alloy catalyst particles in which the weakly acidic functional group-containing compound is supported on a carbon support Contributes to the proximity of platinum alloy catalyst particles. Thereby, the power generation performance of the fuel cell is improved.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Inert Electrodes (AREA)
- Fuel Cell (AREA)
- Catalysts (AREA)
Abstract
Provided is a method for further improvement of the catalytic activity of a noble metal-transition metal alloy catalyst synthesized by a reduction reaction in which a noble metal component and transition metal component are dissolved in a solvent, an anti-coagulation agent, such as an amine or carboxylic acid, is added to this solution, reduction occurs, and afterwards a conductive carrier and organic solvent are added. A method for producing an electrode catalyst for a fuel cell comprising a noble metal-transition metal alloy supported on a conductive carrier in which a noble metal component and transition metal component are dissolved in a solvent, reduction occurs, and then a conductive carrier is added to support the catalyst component on the conductive carrier, wherein a compound containing weakly acidic functional groups and a compound containing weakly basic functional groups are added to the reaction system, and a C5-10 partially sulfonated hydrocarbon is used as the compound containing weakly acidic functional groups.
Description
本発明は、従来の白金合金触媒の性能向上を図った燃料電池用電極触媒の製造方法、及び製造された燃料電池用電極触媒に関する。
The present invention relates to a method for producing a fuel cell electrode catalyst in which the performance of a conventional platinum alloy catalyst is improved, and a produced fuel cell electrode catalyst.
従来、高分子電解質型燃料電池の電極触媒のカソード及びアノード触媒としては、白金又は白金合金等の貴金属をカーボンブラックに担持した触媒が用いられてきた。白金担持カーボンブラックは、塩化白金酸水溶液に、亜硫酸水素ナトリウムを加えた後、過酸化水素水と反応させ、生じた白金コロイドをカーボンブラックに担持させ、洗浄後、必要に応じて熱処理することにより調製するのが一般的である。高分子電解質型燃料電池の電極は、白金担持カーボンブラックを高分子電解質溶液に分散させてインクを調製し、そのインクをカーボンペーパーなどのガス拡散基材に塗布し、乾燥することにより作製される。この2枚の電極で高分子電解質膜を挟み、ホットプレスをすることにより電解質膜-電極接合体(MEA)が組立てられる。
Conventionally, as a cathode and an anode catalyst of an electrode catalyst of a polymer electrolyte fuel cell, a catalyst in which a noble metal such as platinum or a platinum alloy is supported on carbon black has been used. Platinum-supported carbon black is obtained by adding sodium hydrogen sulfite to a chloroplatinic acid aqueous solution, reacting with hydrogen peroxide solution, supporting the resulting platinum colloid on carbon black, washing, and heat-treating as necessary. It is common to prepare. The electrode of a polymer electrolyte fuel cell is prepared by dispersing platinum-supported carbon black in a polymer electrolyte solution, preparing an ink, applying the ink to a gas diffusion substrate such as carbon paper, and drying. . An electrolyte membrane-electrode assembly (MEA) is assembled by sandwiching a polymer electrolyte membrane between these two electrodes and performing hot pressing.
白金は高価な貴金属であり、少ない担持量で十分な性能を発揮させることが望まれている。そのため、より少量で触媒活性を高める検討がなされている。電極触媒を高性能化するには、触媒粒子の凝集を防いで粒子を小粒径に保ち、比表面積を大きくする必要がある。現在、小粒径粒子の作製方法としては保護剤を用いて表面をコートし、凝集を防止する方法が一般的となっている。例えば、下記非特許文献1には、ポリオール還元法により合成した白金合金微粒子をカーボンに担持し、燃料電池用電極触媒とする論文が記述されている。
Platinum is an expensive noble metal, and it is desired to exhibit sufficient performance with a small amount of support. Therefore, studies have been made to increase the catalytic activity with a smaller amount. In order to improve the performance of the electrode catalyst, it is necessary to prevent the agglomeration of the catalyst particles, keep the particles small, and increase the specific surface area. At present, as a method for producing small-sized particles, a method is generally used in which the surface is coated with a protective agent to prevent aggregation. For example, Non-Patent Document 1 below describes a paper in which platinum alloy fine particles synthesized by a polyol reduction method are supported on carbon and used as a fuel cell electrode catalyst.
ところで、ポリオール還元法によって作製したPtFe合金微粒子溶液を用いて合金微粒子をカーボン担体に担持する際に、溶液中におけるカーボンの分散が悪いために、PtFe粒子が凝集してしまい、十分な発電効率が得られないという問題があった。これは、余剰な保護基分子が存在することによって溶液の粘性が高くなり、カーボンが分散しないためである。
By the way, when alloy fine particles are supported on a carbon support using a PtFe alloy fine particle solution prepared by a polyol reduction method, the dispersion of carbon in the solution is poor, and PtFe particles are aggregated, so that sufficient power generation efficiency is obtained. There was a problem that it could not be obtained. This is because the presence of excess protecting group molecules increases the viscosity of the solution and does not disperse carbon.
一方、下記特許文献1には、触媒粒子の凝集を防いで粒子を小粒径に保ち、比表面積を大きくする必要がある。現在、小粒径粒子の作製方法としては保護剤を用いて表面をコートし、凝集を防止する方法では、触媒反応は表面の活性サイトで進行するため、触媒金属表面を保護剤で覆い隠すと触媒活性が低下するという課題を解決するために、触媒担体の表面に、触媒金属粒子と共有結合を形成する官能基と、その官能基と共有結合する触媒金属粒子からなる触媒が開示されている。ここでは、カーボン担体上に修飾した官能基を金属粒子表面と共有結合させて金属粒子を担体表面に安定に固定することにより、活性な金属表面を最大限露出しながら、粒子同士の凝集を防止することを目的としている。
On the other hand, in Patent Document 1 below, it is necessary to prevent the catalyst particles from agglomerating to keep the particles small and to increase the specific surface area. Currently, as a method for producing small particle size, the surface is coated with a protective agent to prevent aggregation, and the catalytic reaction proceeds at the active site on the surface. In order to solve the problem that the catalytic activity is lowered, a catalyst comprising a functional group that forms a covalent bond with the catalytic metal particle on the surface of the catalyst carrier and a catalytic metal particle that is covalently bonded to the functional group is disclosed. . Here, the functional group modified on the carbon support is covalently bonded to the surface of the metal particle to stably fix the metal particle on the support surface, thereby preventing the aggregation of the particles while exposing the active metal surface to the maximum extent. The purpose is to do.
特許文献1に開示された方法では、カーボン担体自体に特定の処理を行う必要がある。
Langmuir 23(2007)6438-6445 特開2005-87989号公報
In the method disclosed in Patent Document 1, it is necessary to perform a specific treatment on the carbon support itself.
Langmuir 23 (2007) 6438-6445 JP 2005-87989 A
Langmuir 23(2007)6438-6445
Langmuir 23 (2007) 6438-6445
本発明は、貴金属成分と遷移金属成分を溶媒中に溶解し、この溶液にアミンとカルボン酸などの凝集防止剤を添加し、還元後に導電性担体と有機溶媒を加えて還元反応で合成される貴金属-遷移金属合金触媒の更なる触媒活性を向上させることを目的とする。
In the present invention, a noble metal component and a transition metal component are dissolved in a solvent, an aggregation inhibitor such as an amine and a carboxylic acid is added to the solution, a conductive carrier and an organic solvent are added after the reduction, and then synthesized by a reduction reaction. The object is to further improve the catalytic activity of the noble metal-transition metal alloy catalyst.
本発明者は、貴金属成分と遷移金属成分を溶媒中に溶解し、この溶液に凝集防止剤を添加し、還元後に導電性担体を加えて還元反応で貴金属-遷移金属合金触媒を合成する際に、該凝集防止剤にプロトン伝導性及び電子伝導性を付与するとともに、該凝集防止剤の触媒金属への配位性を考慮することで、上記課題が解決されることを見出し、本発明に到達した。
The present inventor dissolved a noble metal component and a transition metal component in a solvent, added an anti-aggregation agent to this solution, added a conductive support after reduction, and synthesized a noble metal-transition metal alloy catalyst by a reduction reaction. The present inventors have found that the above problems can be solved by imparting proton conductivity and electron conductivity to the aggregation inhibitor and considering the coordination property of the aggregation inhibitor to the catalyst metal. did.
即ち、第1に、本発明は、貴金属成分と遷移金属成分を溶媒中に溶解し、還元後に導電性担体を加えて触媒成分を導電性担体上に析出・担持させる、導電性担体上に担持された貴金属-遷移金属合金からなる燃料電池用電極触媒の製造方法の発明であり、反応系に弱酸性官能基含有化合物と弱塩基性官能基含有化合物を添加し、且つ該弱酸性官能基含有化合物として炭素数5~10の一部スルホン化された炭化水素類を用いることを特徴とする。
That is, first, in the present invention, a noble metal component and a transition metal component are dissolved in a solvent, and after reduction, a conductive support is added to deposit and support the catalyst component on the conductive support. Is a method for producing a fuel cell electrode catalyst comprising a noble metal-transition metal alloy, wherein a weakly acidic functional group-containing compound and a weakly basic functional group-containing compound are added to the reaction system, and the weakly acidic functional group-containing compound is added. As the compound, partially sulfonated hydrocarbons having 5 to 10 carbon atoms are used.
本発明では、触媒作製後は除去の対象であった、凝集防止剤を積極的に活用し、該凝集防止剤を用いて、触媒周辺でのプロトン伝導性及び電子伝導性を確保することで、燃料電池の発電性能を向上させる。
In the present invention, the anti-aggregation agent, which was the object of removal after catalyst preparation, was actively utilized, and by using the anti-aggregation agent, proton conductivity and electron conductivity around the catalyst were ensured, Improve the power generation performance of the fuel cell.
本発明において、弱酸性官能基含有化合物と弱塩基性官能基含有化合物を添加する理由は、弱酸性官能基含有化合物は遷移金属に付着しやすく、一方弱塩基性官能基含有化合物は貴金属に付着しやすいため、弱酸性官能基含有化合物と弱塩基性官能基含有化合物を組み合わせることで、触媒成分に満遍なく付着させることができ、還元・合成反応中の粒子成長を抑制することが可能となる。
In the present invention, the reason for adding the weakly acidic functional group-containing compound and the weakly basic functional group-containing compound is that the weakly acidic functional group-containing compound easily adheres to the transition metal, while the weakly basic functional group-containing compound adheres to the noble metal. Therefore, by combining the weakly acidic functional group-containing compound and the weakly basic functional group-containing compound, it is possible to evenly adhere to the catalyst component, and it is possible to suppress particle growth during the reduction / synthesis reaction.
本発明で凝集防止剤として用いる、炭素数5~10の一部スルホン化された炭化水素類としては、カルボニル基を有することを特徴とする。例えば脂肪族カルボン酸、脂肪族ケトン、脂肪族アルデヒド、脂肪族炭化水素、脂環式炭化水素、芳香族炭化水素などの炭化水素鎖の一部をスルホン化したものである。具体的には、炭素数5~10の一部スルホン化された脂肪族カルボン酸が好ましく例示される。
The partially sulfonated hydrocarbons having 5 to 10 carbon atoms used as the aggregation inhibitor in the present invention are characterized by having a carbonyl group. For example, a part of hydrocarbon chain such as aliphatic carboxylic acid, aliphatic ketone, aliphatic aldehyde, aliphatic hydrocarbon, alicyclic hydrocarbon, aromatic hydrocarbon is sulfonated. Specifically, a partially sulfonated aliphatic carboxylic acid having 5 to 10 carbon atoms is preferably exemplified.
本発明で他の凝集防止剤として用いる、前記弱塩基性官能基含有化合物として、炭素数5~10の弱塩基性官能基を有する炭化水素類(例えば、弱塩基性官能基がアミノ基で炭化水素が脂肪族炭化水素、脂環式炭化水素、芳香族炭化水素)であって、より具体的には、炭素数5~10の脂肪族アミンが好ましく例示される。
The weakly basic functional group-containing compound used as another aggregation inhibitor in the present invention is a hydrocarbon having a weakly basic functional group having 5 to 10 carbon atoms (for example, a weakly basic functional group is carbonized with an amino group). Hydrogen is an aliphatic hydrocarbon, alicyclic hydrocarbon, aromatic hydrocarbon), and more specifically, an aliphatic amine having 5 to 10 carbon atoms is preferably exemplified.
本発明のポリオール還元反応で製造される燃料電池用電極触媒は貴金属-遷移金属系触媒である。公知の貴金属-遷移金属の組合せが広く用いられる。これらの中で、貴金属が白金、パラジウム(Pd)及び銀(Ag)から選択される1種以上であり、遷移金属が、鉄(Fe)、ルテニウム(Ru)、モリブデン(Mo)、オスミウム(Os)、コバルト(Co)、ロジウム(Rh)、イリジウム(Ir)、ニッケル(Ni)、チタン(Ti)、タングステン(W)、レニウム(Re)、クロム(Cr)、マンガン(Mn)、ニオブ(Nb)、及びタンタル(Ta)から選択される1種以上である組合せが好ましく例示される。
The fuel cell electrode catalyst produced by the polyol reduction reaction of the present invention is a noble metal-transition metal catalyst. Known noble metal-transition metal combinations are widely used. Among these, the noble metal is at least one selected from platinum, palladium (Pd), and silver (Ag), and the transition metal is iron (Fe), ruthenium (Ru), molybdenum (Mo), osmium (Os) ), Cobalt (Co), rhodium (Rh), iridium (Ir), nickel (Ni), titanium (Ti), tungsten (W), rhenium (Re), chromium (Cr), manganese (Mn), niobium (Nb) And a combination of at least one selected from tantalum (Ta) is preferable.
本発明の燃料電池用電極触媒の製造方法において出発物質となる貴金属成分として白金アセチルアセテートが、遷移金属成分として遷移金属アセチルアセテートが好ましく例示され、導電性担体としてカーボン担体が好ましく例示される。
In the method for producing an electrode catalyst for a fuel cell of the present invention, platinum acetyl acetate is preferably exemplified as a noble metal component which is a starting material, transition metal acetyl acetate is preferably exemplified as a transition metal component, and a carbon carrier is preferably exemplified as a conductive carrier.
本発明において、弱酸性官能基含有化合物の添加は、貴金属成分と遷移金属成分との還元反応前又は還元反応中に添加する。
In the present invention, the weakly acidic functional group-containing compound is added before or during the reduction reaction between the noble metal component and the transition metal component.
第2に、本発明は、上記の方法によって製造された燃料電池用電極触媒である。
Second, the present invention is a fuel cell electrode catalyst produced by the above method.
本明細書は本願の優先権の基礎である日本国特許出願2008-273943号の明細書および/または図面に記載される内容を包含する。
This specification includes the contents described in the specification and / or drawings of Japanese Patent Application No. 2008-273943 which is the basis of the priority of the present application.
本発明の方法によって製造された燃料電池用電極触媒では、反応系に凝集防止剤として、弱酸性官能基含有化合物と弱塩基性官能基含有化合物を添加し、且つ該弱酸性官能基含有化合物として炭素数5~10の一部スルホン化された炭化水素類を用いることにより、該弱酸性官能基含有化合物がカーボン担体上に担持された白金合金触媒粒子の周辺のプロトン伝導物質(高分子電解質)と白金合金触媒粒子との近接化に寄与する。これにより、燃料電池の発電性能向上をもたらす。
In the fuel cell electrode catalyst produced by the method of the present invention, a weakly acidic functional group-containing compound and a weakly basic functional group-containing compound are added to the reaction system as an aggregation inhibitor, and the weakly acidic functional group-containing compound is added. By using partially sulfonated hydrocarbons having 5 to 10 carbon atoms, proton conductive material (polymer electrolyte) around platinum alloy catalyst particles in which the weakly acidic functional group-containing compound is supported on a carbon support Contributes to the proximity of platinum alloy catalyst particles. Thereby, the power generation performance of the fuel cell is improved.
以下、実施例および比較例によって本発明をさらに詳細に説明する。
Hereinafter, the present invention will be described in more detail with reference to examples and comparative examples.
[実施例1]
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、ペンタン酸の側鎖の一部をスルホン化させた化合物1.5mmolを、ペンタニルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、ペンタン酸の炭素数は5である。 [Example 1]
A compound in which a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt are added, and a part of the side chain of pentanoic acid is sulfonated. To 1.5 mmol, 1.5 mmol of pentanylamine was added and stirred well. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Note that pentanoic acid has 5 carbon atoms.
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、ペンタン酸の側鎖の一部をスルホン化させた化合物1.5mmolを、ペンタニルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、ペンタン酸の炭素数は5である。 [Example 1]
A compound in which a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt are added, and a part of the side chain of pentanoic acid is sulfonated. To 1.5 mmol, 1.5 mmol of pentanylamine was added and stirred well. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Note that pentanoic acid has 5 carbon atoms.
[実施例2]
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、へキサン酸の側鎖の一部をスルホン化させた化合物1.5mmolを、ヘキシルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、へキサン酸の炭素数は6である。 [Example 2]
A platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt were added, and a part of the side chain of hexanoic acid was sulfonated. To 1.5 mmol of the compound, 1.5 mmol of hexylamine was added and sufficiently stirred. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Hexanoic acid has 6 carbon atoms.
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、へキサン酸の側鎖の一部をスルホン化させた化合物1.5mmolを、ヘキシルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、へキサン酸の炭素数は6である。 [Example 2]
A platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt were added, and a part of the side chain of hexanoic acid was sulfonated. To 1.5 mmol of the compound, 1.5 mmol of hexylamine was added and sufficiently stirred. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Hexanoic acid has 6 carbon atoms.
[実施例3]
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、ノナン酸の側鎖の一部をスルホン化させた化合物1.5mmol、ノニルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、ノナン酸の炭素数は9である。 [Example 3]
A compound in which a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt are added, and a part of the side chain of nonanoic acid is sulfonated. 1.5 mmol and 1.5 mmol of nonylamine were added and stirred sufficiently. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Nonanoic acid has 9 carbon atoms.
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、ノナン酸の側鎖の一部をスルホン化させた化合物1.5mmol、ノニルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、ノナン酸の炭素数は9である。 [Example 3]
A compound in which a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt are added, and a part of the side chain of nonanoic acid is sulfonated. 1.5 mmol and 1.5 mmol of nonylamine were added and stirred sufficiently. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Nonanoic acid has 9 carbon atoms.
[実施例4]
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、デカン酸の側鎖の一部をスルホン化させた化合物1.5mmol、デカニルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、デカン酸の炭素数は10である。 [Example 4]
A compound in which a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt are added, and a part of the side chain of decanoic acid is sulfonated. 1.5 mmol and decanylamine 1.5 mmol were added and stirred sufficiently. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. The decanoic acid has 10 carbon atoms.
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、デカン酸の側鎖の一部をスルホン化させた化合物1.5mmol、デカニルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、デカン酸の炭素数は10である。 [Example 4]
A compound in which a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt are added, and a part of the side chain of decanoic acid is sulfonated. 1.5 mmol and decanylamine 1.5 mmol were added and stirred sufficiently. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. The decanoic acid has 10 carbon atoms.
[比較例1(参考例)]
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元終了後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。 [Comparative Example 1 (Reference Example)]
A platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt were added and sufficiently stirred. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, the mixture was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out.
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元終了後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。 [Comparative Example 1 (Reference Example)]
A platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt were added and sufficiently stirred. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, the mixture was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out.
[比較例2]
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、酪酸の側鎖の一部をスルホン化させた化合物1.5mmol、ブチルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、酪酸の炭素数は4である。 [Comparative Example 2]
Compound 1 in which a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt are added, and a part of the side chain of butyric acid is sulfonated. .5 mmol and butylamine 1.5 mmol were added and stirred sufficiently. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Butyric acid has 4 carbon atoms.
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、酪酸の側鎖の一部をスルホン化させた化合物1.5mmol、ブチルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、酪酸の炭素数は4である。 [Comparative Example 2]
Compound 1 in which a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt are added, and a part of the side chain of butyric acid is sulfonated. .5 mmol and butylamine 1.5 mmol were added and stirred sufficiently. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Butyric acid has 4 carbon atoms.
[比較例3]
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、ラウリン酸の側鎖の一部をスルホン化させた化合物1.5mmol、ラウリルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、ラウリン酸の炭素数は12である。 [Comparative Example 3]
A compound in which a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt are added, and a part of the side chain of lauric acid is sulfonated. 1.5 mmol and 1.5 mmol of laurylamine were added and sufficiently stirred. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Note that lauric acid has 12 carbon atoms.
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、ラウリン酸の側鎖の一部をスルホン化させた化合物1.5mmol、ラウリルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、ラウリン酸の炭素数は12である。 [Comparative Example 3]
A compound in which a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt are added, and a part of the side chain of lauric acid is sulfonated. 1.5 mmol and 1.5 mmol of laurylamine were added and sufficiently stirred. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Note that lauric acid has 12 carbon atoms.
[比較例4]
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、パルミチン酸の側鎖の一部をスルホン化させた化合物1.5mmol、パルミチルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、パルミチン酸の炭素数は16である。 [Comparative Example 4]
A compound obtained by adding a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt to which a part of the side chain of palmitic acid is sulfonated. 1.5 mmol and 1.5 mmol of palmitylamine were added and stirred sufficiently. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Palmitic acid has 16 carbon atoms.
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、パルミチン酸の側鎖の一部をスルホン化させた化合物1.5mmol、パルミチルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、パルミチン酸の炭素数は16である。 [Comparative Example 4]
A compound obtained by adding a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt to which a part of the side chain of palmitic acid is sulfonated. 1.5 mmol and 1.5 mmol of palmitylamine were added and stirred sufficiently. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Palmitic acid has 16 carbon atoms.
[比較例5]
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、ステアリン酸の側鎖の一部をスルホン化させた化合物1.5mmol、ステアリルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、ステアリン酸の炭素数は17である。 [Comparative Example 5]
A compound obtained by adding a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt to which a part of the side chain of stearic acid is sulfonated. 1.5 mmol and stearylamine 1.5 mmol were added and stirred sufficiently. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Note that stearic acid has 17 carbon atoms.
ジオクチルエーテル100ml中に白金0.5gを含む白金アセチルアセトナート塩と、コバルト0.5gを含むコバルトアセチルアセトナート塩を添加し、これに、ステアリン酸の側鎖の一部をスルホン化させた化合物1.5mmol、ステアリルアミン1.5mmolを加え、十分に攪拌した。230℃で還元し、白金コバルト粒子を析出させた。還元後、冷却し、カーボン1gを添加した。十分に攪拌し、粒子をカーボン上に担持させた。液体と固形物を濾別し、PtCo粒子担持カーボン触媒を取り出した。なお、ステアリン酸の炭素数は17である。 [Comparative Example 5]
A compound obtained by adding a platinum acetylacetonate salt containing 0.5 g of platinum in 100 ml of dioctyl ether and a cobalt acetylacetonate salt containing 0.5 g of cobalt to which a part of the side chain of stearic acid is sulfonated. 1.5 mmol and stearylamine 1.5 mmol were added and stirred sufficiently. Reduction at 230 ° C. precipitated platinum cobalt particles. After the reduction, it was cooled and 1 g of carbon was added. The agitation was sufficiently performed so that the particles were supported on carbon. The liquid and the solid were separated by filtration, and the PtCo particle-supported carbon catalyst was taken out. Note that stearic acid has 17 carbon atoms.
[単セルの作成]
触媒粉末を有機溶媒に分散させ、この分散液をテフロンシートへ塗布して、触媒層を形成した。電極面積1cm2当たりのPtCo触媒の量は0.4mgとした。これらの触媒粉末から形成した電極をそれぞれナフィオンなどの高分子電解質膜を介してホットプレスにより貼り合わせ、その両側に拡散層を設置して単セル電極を形成した。 [Create single cell]
The catalyst powder was dispersed in an organic solvent, and this dispersion was applied to a Teflon sheet to form a catalyst layer. The amount of PtCo catalyst per 1 cm 2 of electrode area was 0.4 mg. Electrodes formed from these catalyst powders were bonded together by hot pressing through a polymer electrolyte membrane such as Nafion, and diffusion layers were installed on both sides to form single cell electrodes.
触媒粉末を有機溶媒に分散させ、この分散液をテフロンシートへ塗布して、触媒層を形成した。電極面積1cm2当たりのPtCo触媒の量は0.4mgとした。これらの触媒粉末から形成した電極をそれぞれナフィオンなどの高分子電解質膜を介してホットプレスにより貼り合わせ、その両側に拡散層を設置して単セル電極を形成した。 [Create single cell]
The catalyst powder was dispersed in an organic solvent, and this dispersion was applied to a Teflon sheet to form a catalyst layer. The amount of PtCo catalyst per 1 cm 2 of electrode area was 0.4 mg. Electrodes formed from these catalyst powders were bonded together by hot pressing through a polymer electrolyte membrane such as Nafion, and diffusion layers were installed on both sides to form single cell electrodes.
[性能評価]
性能評価は、単セルのセル温度を80℃に設定し、カソード側の電極に加温バブラを通過させた加湿空気をRH40%、ストイキ比7.5、アノード側の電極に加温バブラを通過させた加湿水素をRH40%、ストイキ比7.5で供給し、電子負荷を用いて電流電圧特性を測定した。出力点性能として高電流密度(1.0A/cm2)の電圧を測定した。 [Performance evaluation]
For performance evaluation, the cell temperature of the single cell is set to 80 ° C., the humidified air that has passed the heating bubbler to the cathode side electrode is RH 40%, the stoichiometric ratio is 7.5, and the heating side bubbler is passed to the anode side electrode. The humidified hydrogen was supplied at an RH of 40% and a stoichiometric ratio of 7.5, and current-voltage characteristics were measured using an electronic load. As the output point performance, a voltage having a high current density (1.0 A / cm 2 ) was measured.
性能評価は、単セルのセル温度を80℃に設定し、カソード側の電極に加温バブラを通過させた加湿空気をRH40%、ストイキ比7.5、アノード側の電極に加温バブラを通過させた加湿水素をRH40%、ストイキ比7.5で供給し、電子負荷を用いて電流電圧特性を測定した。出力点性能として高電流密度(1.0A/cm2)の電圧を測定した。 [Performance evaluation]
For performance evaluation, the cell temperature of the single cell is set to 80 ° C., the humidified air that has passed the heating bubbler to the cathode side electrode is RH 40%, the stoichiometric ratio is 7.5, and the heating side bubbler is passed to the anode side electrode. The humidified hydrogen was supplied at an RH of 40% and a stoichiometric ratio of 7.5, and current-voltage characteristics were measured using an electronic load. As the output point performance, a voltage having a high current density (1.0 A / cm 2 ) was measured.
又、非発電時のプロトン抵抗を測定するため、周波数応答解析機(FRA)を用いてインピーダンスを測定し、膜抵抗、触媒層抵抗に相当する抵抗を解析した。
Also, in order to measure proton resistance during non-power generation, impedance was measured using a frequency response analyzer (FRA), and resistance corresponding to membrane resistance and catalyst layer resistance was analyzed.
下記表1に、凝集防止剤(第2プロトン導電性物質)のカーボン数と、プロトン導電性と、出力点性能を一覧で示す。又、図1に、凝集防止剤(第2プロトン導電性物質)のカーボン数と出力点性能の関係を示す。更に、図2に、凝集防止剤(第2プロトン導電性物質)のカーボン数とプロトン導電性の関係を示す。
Table 1 below shows a list of the carbon number, proton conductivity, and output point performance of the aggregation inhibitor (second proton conductive material). FIG. 1 shows the relationship between the carbon number of the aggregation inhibitor (second proton conductive substance) and the output point performance. Furthermore, FIG. 2 shows the relationship between the carbon number of the aggregation inhibitor (second proton conductive substance) and proton conductivity.
表1、図1及び図2より、本発明の如く、炭素数5~10の一部スルホン化された炭化水素類を用いる場合に優れた発電性能を示すことが分かる。
From Table 1, FIG. 1 and FIG. 2, it can be seen that excellent power generation performance is exhibited when partially sulfonated hydrocarbons having 5 to 10 carbon atoms are used as in the present invention.
図3~図5に、本発明の実施例と比較例のイメージを示す。図3は、実施例1~4のイメージであり、プロトン導電物質と触媒をつなぐための第2のプロトン導電物質(凝集防止剤)を触媒近傍に付与することによりプロトン導電性が向上する。図4は、比較例1、2のイメージであり、プロトン導電物質と触媒をつなぐための物質がないか、第2プロトン導電物質(凝集防止剤)が微量であるためプロトン抵抗が大きく活性が低下する。図5は、比較例3~5のイメージであり、プロトン導電物質と触媒をつなぐために第2のプロトン導電物質(凝集防止剤)を触媒近接に付与したが、分子サイズが大きく、かえってプロトン抵抗が大きくなり活性が低下する。
3 to 5 show images of examples of the present invention and comparative examples. FIG. 3 is an image of Examples 1 to 4. Proton conductivity is improved by applying a second proton conductive material (aggregation inhibitor) for connecting the proton conductive material and the catalyst in the vicinity of the catalyst. FIG. 4 is an image of Comparative Examples 1 and 2, and there is no substance to connect the proton conductive material and the catalyst, or the second proton conductive material (aggregation inhibitor) is very small, so the proton resistance is large and the activity is reduced. To do. FIG. 5 is an image of Comparative Examples 3 to 5. In order to connect the proton conductive material and the catalyst, a second proton conductive material (anti-aggregation agent) was provided in the vicinity of the catalyst, but the molecular size was large and the proton resistance instead. Increases and activity decreases.
本発明の燃料電池用電極触媒は高活性であり、燃料電池の普及に貢献する。
The fuel cell electrode catalyst of the present invention is highly active and contributes to the spread of fuel cells.
本明細書で引用した全ての刊行物、特許および特許出願をそのまま参考として本明細書にとり入れるものとする。
All publications, patents and patent applications cited in this specification shall be incorporated into the present specification as they are.
Claims (6)
- 貴金属成分と遷移金属成分を溶媒中に溶解し、還元後に導電性担体を加えて触媒成分を導電性担体上に担持させる、導電性担体上に担持された貴金属-遷移金属合金からなる燃料電池用電極触媒の製造方法において、反応系に弱酸性官能基含有化合物と弱塩基性官能基含有化合物を添加し、且つ該弱酸性官能基含有化合物として炭素数5~10の一部スルホン化された炭化水素類を用いることを特徴とする燃料電池用電極触媒の製造方法。 For a fuel cell comprising a noble metal-transition metal alloy supported on a conductive support, in which a noble metal component and a transition metal component are dissolved in a solvent, and after reduction, a conductive support is added to support the catalyst component on the conductive support. In the method for producing an electrode catalyst, a weakly acidic functional group-containing compound and a weakly basic functional group-containing compound are added to a reaction system, and the partially sulfonated carbonized carbon having 5 to 10 carbon atoms is added as the weakly acidic functional group-containing compound. A method for producing an electrode catalyst for a fuel cell, comprising using hydrogen.
- 前記炭素数5~10の一部スルホン化された炭化水素類が、カルボニル基を有することを特徴とする請求項1に記載の燃料電池用電極触媒の製造方法。 2. The method for producing an electrode catalyst for a fuel cell according to claim 1, wherein the partially sulfonated hydrocarbon having 5 to 10 carbon atoms has a carbonyl group.
- 前記弱塩基性官能基含有化合物が炭素数5~10のアミノ基を有する炭化水素類であることを特徴とする請求項1又は2に記載の燃料電池用電極触媒の製造方法。 The method for producing an electrode catalyst for a fuel cell according to claim 1 or 2, wherein the weakly basic functional group-containing compound is a hydrocarbon having an amino group having 5 to 10 carbon atoms.
- 前記弱酸性官能基含有化合物と前記弱塩基性官能基含有化合物の添加が、還元前又は還元後であることを特徴とする請求項1乃至3のいずれかに記載の燃料電池用電極触媒の製造方法。 The production of the fuel cell electrode catalyst according to any one of claims 1 to 3, wherein the weakly acidic functional group-containing compound and the weakly basic functional group-containing compound are added before or after the reduction. Method.
- 前記貴金属が、白金、パラジウム(Pd)及び銀(Ag)から選択される1種以上であり、前記遷移金属が、鉄(Fe)、ルテニウム(Ru)、モリブデン(Mo)、オスミウム(Os)、コバルト(Co)、ロジウム(Rh)、イリジウム(Ir)、ニッケル(Ni)、チタン(Ti)、タングステン(W)、パラジウム(Pd)、レニウム(Re)、クロム(Cr)、マンガン(Mn)、ニオブ(Nb)、及びタンタル(Ta)から選択される1種以上であることを特徴とする請求項1乃至4のいずれかに記載の燃料電池用電極触媒の製造方法。 The noble metal is at least one selected from platinum, palladium (Pd) and silver (Ag), and the transition metal is iron (Fe), ruthenium (Ru), molybdenum (Mo), osmium (Os), Cobalt (Co), rhodium (Rh), iridium (Ir), nickel (Ni), titanium (Ti), tungsten (W), palladium (Pd), rhenium (Re), chromium (Cr), manganese (Mn), The method for producing an electrode catalyst for a fuel cell according to any one of claims 1 to 4, wherein the method is one or more selected from niobium (Nb) and tantalum (Ta).
- 請求項1乃至5のいずれかに記載の方法によって製造された燃料電池用電極触媒。 A fuel cell electrode catalyst produced by the method according to any one of claims 1 to 5.
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KR102096130B1 (en) | 2016-05-02 | 2020-04-01 | 주식회사 엘지화학 | Carrier-nano particles complex, catalyst comprising the same and method for fabricating the same |
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JP2008234900A (en) * | 2007-03-19 | 2008-10-02 | Toppan Printing Co Ltd | Manufacturing method of catalyst electrode |
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JPH0582136A (en) * | 1991-09-19 | 1993-04-02 | Nissan Motor Co Ltd | Manufacture of fuel cell electrode |
JP2001093531A (en) * | 1999-09-28 | 2001-04-06 | Asahi Glass Co Ltd | Solid polymer fuel cell and method for manufacturing electrode catalyst |
JP2006172996A (en) * | 2004-12-17 | 2006-06-29 | Fujitsu Ltd | Catalyst for fuel cell, fuel cell, and method for manufacturing them |
WO2007081538A2 (en) * | 2005-12-21 | 2007-07-19 | E. I. Du Pont De Nemours And Company | Membrane electrode assembly for organic/air fuel cells |
JP2008234900A (en) * | 2007-03-19 | 2008-10-02 | Toppan Printing Co Ltd | Manufacturing method of catalyst electrode |
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CN116133746A (en) * | 2020-07-17 | 2023-05-16 | 松下知识产权经营株式会社 | Electrode catalyst for water electrolysis cell, water electrolysis cell and water electrolysis device |
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