发明公开
EP3035424A1 PRODUCTION METHOD FOR ELECTRODE CATALYST, ELECTRODE CATALYST, COMPOSITION FOR FORMING GAS DIFFUSION ELECTRODE, GAS DIFFUSION ELECTRODE, MEMBRANE-ELECTRODE ASSEMBLY (MEA), AND FUEL CELL STACK
有权
电极催化剂的生产方法,电极催化剂,形成气体扩散电极的组合物,气体扩散电极,膜电极组件(MEA)和燃料电池堆
- 专利标题: PRODUCTION METHOD FOR ELECTRODE CATALYST, ELECTRODE CATALYST, COMPOSITION FOR FORMING GAS DIFFUSION ELECTRODE, GAS DIFFUSION ELECTRODE, MEMBRANE-ELECTRODE ASSEMBLY (MEA), AND FUEL CELL STACK
- 专利标题(中): 电极催化剂的生产方法,电极催化剂,形成气体扩散电极的组合物,气体扩散电极,膜电极组件(MEA)和燃料电池堆
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申请号: EP15769321.9申请日: 2015-03-27
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公开(公告)号: EP3035424A1公开(公告)日: 2016-06-22
- 发明人: NAKAMURA, Yoko , NAGAMORI, Kiyotaka , MIZUSAKI, Tomoteru , TSUBAKI, Takuya
- 申请人: N.E. Chemcat Corporation
- 申请人地址: 4-1, Hamamatsu-cho 2-chome Minato-ku Tokyo 105-6124 JP
- 专利权人: N.E. Chemcat Corporation
- 当前专利权人: N.E. Chemcat Corporation
- 当前专利权人地址: 4-1, Hamamatsu-cho 2-chome Minato-ku Tokyo 105-6124 JP
- 代理机构: von Füner, Nicolai
- 优先权: JP2014070627 20140328
- 国际公布: WO2015147309 20151001
- 主分类号: H01M4/88
- IPC分类号: H01M4/88 ; H01M4/86 ; H01M4/90 ; H01M4/92 ; H01M8/02 ; H01M8/10
摘要:
Provided is a production method of an electrode catalyst that can reduce the content of chlorine species reliably and sufficiently through a simple operation, even when using an electrode catalyst precursor containing a high concentration of chlorine (Cl) species as a raw material of the electrode catalyst. The production method of the electrode catalyst has a core-shell structure including a core part formed on a support and a shell part formed to cover at least a part of a surface of the core part. The production method includes a first step (1) of preparing a first liquid with an electrode catalyst precursor (I) being dispersed in ultrapure water by adding the electrode catalyst precursor (I) to the ultrapure water, the electrode catalyst precursor (I) being produced using a material containing chlorine (Cl) species, and exhibiting a chlorine (Cl) species concentration not lower than a first chlorine (Cl) species concentration when measured by X-ray fluorescence (XRF) spectroscopy; and a second step (2) of preparing a second liquid by dispersing an electrode catalyst precursor (II), the electrode catalyst precursor (II) being obtained by filtrating and washing the electrode catalyst precursor (I) contained in the first liquid with ultrapure water , and then performing washing until an electric conductivity p of a filtrate has become a first value or lower.
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