催化作用
铂金
质子交换膜燃料电池
材料科学
氧还原反应
化学工程
旋转圆盘电极
电极
纳米技术
化学
电化学
物理化学
有机化学
循环伏安法
工程类
作者
Jiantao Fan,Ming Chen,Zhiliang Zhao,Zhen Zhang,Siyu Ye,Shaoyi Xu,Haijiang Wang,Hui Li
出处
期刊:Nature Energy
[Springer Nature]
日期:2021-05-21
卷期号:6 (5): 475-486
被引量:357
标识
DOI:10.1038/s41560-021-00824-7
摘要
Ultralow platinum loading and high catalytic performance at the membrane electrode assembly (MEA) level are essential for reducing the cost of proton exchange membrane fuel cells. The past decade has seen substantial progress in developing a variety of highly active platinum-based catalysts for the oxygen reduction reaction. However, these high activities are almost exclusively obtained from rotating disk electrode (RDE) measurements and have rarely translated into MEA performance. In this Review, we elucidate the intrinsic limitations that lead to a persistent failure to transfer catalysts’ high RDE activities into maximized MEA performance. We discuss catalyst-layer engineering strategies for controlling mass transport resistances at local catalyst sites, in the bulk of the catalyst layer and at the interfaces of the MEA to achieve high performance with ultralow platinum loading. We also examine promising intermediate testing methods for closing the gap between RDE and MEA experiments.
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