催化作用
合金
化学
吸附
电催化剂
解吸
氢
高熵合金
化学工程
材料科学
无机化学
物理化学
冶金
电化学
有机化学
工程类
生物化学
电极
作者
Yana Men,Dean Wu,Youcheng Hu,Lei Li,Peng Li,Shuangfeng Jia,Jianbo Wang,Gongzhen Cheng,Shengli Chen,Wei Luo
标识
DOI:10.1002/anie.202217976
摘要
Abstract High‐entropy alloy (HEA) catalysts have been widely studied in electrocatalysis. However, identifying atomic structure of HEA with complex atomic arrangement is challenging, which seriously hinders the fundamental understanding of catalytic mechanism. Here, we report a HEA‐PdNiRuIrRh catalyst with remarkable mass activity of 3.25 mA μg −1 for alkaline hydrogen oxidation reaction (HOR), which is 8‐fold enhancement compared to that of commercial Pt/C. Through machine learning potential‐based Monte Carlo simulation, we reveal that the dominant Pd−Pd−Ni/Pd−Pd−Pd bonding environments and Ni/Ru oxophilic sites on HEA surface are beneficial to the optimized adsorption/desorption of *H and enhanced *OH adsorption, contributing to the excellent HOR activity and stability. This work provides significant insights into atomic structure and catalytic mechanism for HEA and offers novel prospects for developing advanced HOR electrocatalysts.
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