铱
质子交换膜燃料电池
阳极
电解水
电解
过电位
析氧
催化作用
材料科学
Nafion公司
化学工程
膜电极组件
聚合物电解质膜电解
分解水
电极
铂金
极化(电化学)
化学
电化学
电解质
光催化
生物化学
物理化学
工程类
作者
Maximilian Möckl,Matthias Felix Ernst,Matthias Kornherr,Frank Allebrod,Maximilian Bernt,Jan Byrknes,Christian Eickes,Christian Gebauer,Antonina Moskovtseva,Hubert A. Gasteiger
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2022-05-05
卷期号:169 (6): 064505-064505
被引量:65
标识
DOI:10.1149/1945-7111/ac6d14
摘要
Lowering the iridium loading at the anode of proton exchange membrane (PEM) water electrolyzers is crucial for the envisaged GW-scale deployment of PEM water electrolysis. Here, the durability of a novel iridium catalyst with a low iridium packing density, allowing for low iridium loadings without decreasing the electrode thickness, is being investigated in a 10-cell PEM water electrolyzer short stack. The anodes of the membrane electrode assemblies (MEAs) of the first five cells utilize a conventional iridium catalyst, at loadings that serve as benchmark for today's industry standard (2 mg Ir cm −2 ). The last five cells utilize the novel catalyst at 8-fold lower loadings (0.25 mg Ir cm −2 ). The MEAs are based on Nafion ® 117 and are tested for 3700 h by load cycling between 0.2 and 2.0 A cm −2 , with weekly polarization curves and impedance diagnostics. For both catalysts, the performance degradation at low current densities is dominated by an increase of the overpotential for the oxygen evolution reaction (OER), whereby the OER mass activity of the novel catalyst remains ≈4-fold higher after 3700 h. The temporal evolution of the OER mass activities of the two catalysts will be analyzed in order to assess the suitability of the novel catalyst for industrial application.
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