材料科学
催化作用
电解质
粒径
降级(电信)
粒子(生态学)
化学工程
电极
复合材料
纳米技术
电气工程
化学
工程类
物理化学
地质学
海洋学
生物化学
作者
Lei Cheng,Kaustubh Khedekar,Morteza Rezaei Talarposhti,A. Perego,Michael Metzger,Saravanan Kuppan,S. Michael Stewart,Plamen Atanassov,Nobumichi Tamura,Nathan Craig,Iryna V. Zenyuk,Christina Johnston
标识
DOI:10.1002/aenm.202000623
摘要
Abstract Pt catalysts in polymer electrolyte fuel cells degrade heterogeneously as the catalyst particles are exposed to local variations throughout the catalyst layer during operation. State‐of‐the‐art analytical techniques for studying degradation of Pt catalysts do not possess fine spatial resolution to elucidate such non‐uniform degradation behavior at a large electrode level. A new methodology is developed to spatially resolve and quantify the heterogeneous Pt catalyst degradation over a large area (several cm 2 ) of aged MEAs based on synchrotron X‐ray microdiffraction. PEFC single cells are aged using voltage cycling as an accelerated stress test and the degradation heterogeneity at a micrometer length scale is visualized by mapping Pt catalyst particle size after voltage cycling. It is demonstrated in detail that the Pt catalyst particle size growth is non‐uniform and follows the flow field geometry. The Pt particle size growth is greater in the area under the flow field land, while it is minimal in the area under the flow field channel. Additional non‐uniformity is observed with the Pt particle size increasing more rapidly at the air outlet area than the Pt particle size at the inlet area.
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