膜
阳极
电化学
阴极
电极
降级(电信)
化学工程
材料科学
扫描电子显微镜
聚合物
膜电极组件
离子
分析化学(期刊)
化学
复合材料
色谱法
有机化学
电气工程
物理化学
生物化学
工程类
作者
Ami C. Yang-Neyerlin,Samantha Medina,Kelly M. Meek,Derek Strasser,Cheng He,Daniel M. Knauss,William E. Mustain,Svitlana Pylypenko,Bryan S. Pivovar
标识
DOI:10.1149/1945-7111/abf77f
摘要
A series of spirocyclic copolymer membranes with varying ion exchange capacities (IECs) were investigated to probe the impact of polymer properties on in situ fuel cell performance and stability. In-situ electrochemical tests and post-mortem electron microscopy analysis of cross-sectioned membrane electrode assemblies (MEAs) have been combined with voltage loss breakdown analysis to evaluate the performance and degradation of different MEAs, and to probe the catalyst morphology and electrode structure at different stages of operation. Voltage loss breakdown results show that membrane degradation and kinetic losses played only a minor role in observed performance degradation and that performance losses were primarily related to increasing mass transport losses. From microscopy studies, carbon corrosion and Pt nanoparticle growth were identified at both the cathode and anode although more pronounced on the cathode resulting in significant structural changes. The membrane with the lowest IEC (1.3 mmolg −1 ) demonstrated the lowest peak power density ~ 1.16 W cm −2 , however, it showed the most stable performance (constant 0.6 A cm −2 hold) with ~ 5% degradation over 540 h. Isolation of performance losses and microscopic analysis of electrodes for anion exchange membrane fuel cells has not been reported previously, and these results help identify critical performance degradation concerns.
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