溶解
铱
质子交换膜燃料电池
阴极
电解
降级(电信)
材料科学
阳极
化学工程
催化作用
铂金
电化学
膜
电解水
沉积(地质)
膜电极组件
电极
化学
电解质
工程类
物理化学
古生物学
生物
电信
生物化学
计算机科学
沉积物
作者
Haoran Yu,Leonard J. Bonville,Jasna Janković,Radenka Marić
标识
DOI:10.1016/j.apcatb.2019.118194
摘要
The present work aims for a comprehensive understanding of the degradation of proton exchange membrane water electrolyzer (PEMWE) with a low catalyst loading of 0.3 mg cm−2 Pt and 0.08 mg cm−2 Ir after a long-term test of 4500 h at 1.8 A cm−2. For the first time, the mechanism of cathode degradation is proposed using established physical models from two aspects: (1) Pt dissolution from nanoparticles and (2) Pt dissolution due to rapid Pt oxide reduction at the start of operation. As Ir dissolves and migrates through the membrane, Pt-Ir precipitates are formed in the membrane. Furthermore, iridium dissolution and subsequent re-deposition on the cathode constitute a major portion (42%) of the anode catalyst loss. The overall picture of degradation mechanisms and the distribution of platinum and iridium across the membrane electrode assembly (MEA) are provided.
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