离聚物
相对湿度
化学
分析化学(期刊)
催化作用
玻璃碳
电化学
膜电极组件
剥离(纤维)
碳纤维
降级(电信)
扩散
质子交换膜燃料电池
阴极
材料科学
电极
复合材料
电解质
循环伏安法
色谱法
聚合物
有机化学
电信
物理
物理化学
复合数
计算机科学
共聚物
热力学
作者
Patrick Schneider,Anne-Christine Scherzer,Brian D. Storey,Matthias Klingele,Nada Zamel,Dietmar Gerteisen
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2023-10-01
卷期号:170 (10): 104505-104505
被引量:9
标识
DOI:10.1149/1945-7111/acff1f
摘要
The effect of ionomer to carbon (I/C) weight ratio and relative humidity (RH) on cathode catalyst degradation was investigated by comprehensive in situ characterization. Membrane electrode assemblies (MEA) with I/C ratios of 0.5, 0.8 and 1.2 were subjected to an accelerated stress test performed at 40, 70 and 100% RH. The results show an increasing loss in electrochemical active surface area (ECSA) for both higher I/C ratios and RH during voltage cycling. To differentiate between ionomer and water connected ECSA, carbon monoxide stripping measurements were performed at varying RH. Before degradation, all MEAs show comparable total ECSA values, while higher I/C ratios lead to a larger fraction of ionomer connected ECSA. After degradation, ECSA measurements of the lowest I/C ratio showed a relatively higher loss of Pt in contact with ionomer than Pt in contact with water, while an opposite trend was observed for higher I/C ratios. H 2 /N 2 impedance measurements showed drastically increasing protonic catalyst layer resistances for decreasing RH especially at low I/C ratios, which might hinder Pt 2+ ion diffusion towards the membrane, hence decreasing the ECSA loss. Limiting current measurements show increasing molecular O 2 diffusion resistances at end of test for samples with higher I/C ratios and higher ECSA loss.
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