材料科学
粒径
质子交换膜燃料电池
相对湿度
电解质
湿度
粒子(生态学)
入口
化学工程
电极
分析化学(期刊)
催化作用
复合材料
环境工程
降级(电信)
环境科学
环境化学
化学
热力学
电气工程
地质学
物理化学
海洋学
物理
工程类
机械工程
生物化学
作者
Kaustubh Khedekar,Morteza Rezaei Talarposhti,Münir M. Besli,Saravanan Kuppan,A. Perego,Yechuan Chen,Michael Metzger,S. Michael Stewart,Plamen Atanassov,Nobumichi Tamura,Nathan Craig,Lei Cheng,Christina Johnston,Iryna V. Zenyuk
标识
DOI:10.1002/aenm.202101794
摘要
Abstract The heterogeneity of polymer electrolyte fuel cell catalyst degradation is studied under varied relative humidity and types of feed gas. Accelerated stress tests (ASTs) are performed on four membrane electrode assemblies (MEAs) under wet and dry conditions in an air or nitrogen environment for 30 000 square voltage cycles. The largest electrochemically active area loss is observed for MEA under wet conditions in a nitrogen gas environment AST due to constant upper potential limit of 0.95 V and significant water content. The mean Pt particle size is larger for the ASTs under wet conditions compared to dry conditions, and the Pt particle size under land is generally larger than under the channel. Observations from ASTs in both conditions and gas environments indicate that water content promotes Pt particle size growth. ASTs under wet conditions and an air environment show the largest difference in Pt particle size growth for inlet versus outlet and channel versus land, which can be attributed to larger water content at outlet and under land compared to inlet and under channel. From X‐ray fluorescence experiments Pt particle size increase is a local phenomenon as Pt loading remains relatively uniform across the MEA.
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