电催化剂
催化作用
化学
电化学
溶解
纳米颗粒
动力学
分子
粒子(生态学)
扫描电化学显微镜
无机化学
光化学
化学工程
纳米技术
材料科学
电极
物理化学
有机化学
地质学
工程类
物理
海洋学
量子力学
作者
Yuwei Zhang,Tao Chen,Shaun M Alia,Bryan S. Pivovar,Weilin Xu
标识
DOI:10.1002/ange.201511071
摘要
Abstract By coupling a Pt‐catalyzed fluorogenic reaction with the Pt‐electrocatalyzed hydrogen‐oxidation reaction (HOR), we combine single‐molecule fluorescence microscopy with traditional electrochemical methods to study the real‐time deactivation kinetics of a Pt/C electrocatalyst at single‐particle level during electrocatalytic hydrogen‐oxidation reaction. The decay of the catalytic performance of Pt/C could be mainly attributed to the electrocatalysis‐induced etching or dissolution of Pt nanoparticles. Spontaneous regeneration of activity and incubation period of the Pt electrocatalyst were also observed at single‐particle level. All these new insights are practically useful for the understanding and rational design of highly efficient electrocatalysts for application in fuel cells.
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