催化作用
钯
X射线光电子能谱
材料科学
阳极
化学工程
电化学
氢
基础(拓扑)
燃料电池
无机化学
化学
电极
物理化学
有机化学
数学分析
工程类
数学
作者
Haoran Yu,Elena S. Davydova,Uri Ash,Hamish A. Miller,Leonard J. Bonville,Dario R. Dekel,Radenka Marić
出处
期刊:Nano Energy
[Elsevier BV]
日期:2019-01-02
卷期号:57: 820-826
被引量:89
标识
DOI:10.1016/j.nanoen.2018.12.098
摘要
The development of Pt-free catalyst for anion exchange membrane fuel cells is limited by the sluggish hydrogen oxidation reaction (HOR) at the anode. Previously, the use of CeO2 as a catalyst promoter facilitated drastic ennoblement of Pd for the HOR kinetics in base media. However, further optimization and understanding of the Pd–CeO2 interaction, surface properties, and their influence on HOR are still needed. In this work, three types of Pd–CeO2/C catalysts are synthesized by a flame-based process, where the Pd–CeO2 interface and the HOR activity are improved as compared to catalysts prepared by wet-chemistry processes. The correlation between the Pd–CeO2 interaction and the HOR activity is established through comparisons of three types of Pd–CeO2/C synthesized catalysts using electrochemical techniques and X-ray photoelectron spectroscopy.
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