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Inert Copper Incorporation Enables the High Activity and Durability of NiW Electrocatalyst for Alkaline Hydrogen Oxidation Reaction
Author(s) -
Liu Guimei,
Liu Yushen,
Qiu Xiaoyi,
Zhang Bingxing,
Jang Juhee,
Cui Yingdan,
Xiao Fei,
Zhao Qinglan,
Wang Wenjun,
KIM Yoonseob,
Xing Wei,
Shao Minhua
Publication year - 2025
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.202405127
Subject(s) - materials science , electrocatalyst , durability , copper , inert , hydrogen , inert gas , inorganic chemistry , chemical engineering , metallurgy , electrochemistry , composite material , chemistry , organic chemistry , electrode , engineering
Abstract The slow reaction kinetics of hydrogen oxidation reaction (HOR) on existing catalysts in alkaline hinders the commercialization of anion exchange membrane fuel cells (AEMFCs). In this work, a Cu‐incorporated NiW alloy (Cu i ‐NiW) without any platinum group metal (PGM) is designed and evaluated in both liquid cells and AEMFCs. This catalyst enabled the achievement of an electrochemical surface area‐normalized exchange current density of 70 µA cm −2 and robust stability, outperforming most PGM‐free catalysts. Furthermore, the incorporation of Cu into other systems such as NiMo and NiV using the same method also showcased excellent HOR activity and durability. The fuel cells assembled with Cu i ‐NiW as the anode and Pt/C or Fe‐N‐C as the cathode delivered peak power densities of 480 and 340 mW cm −2 , respectively. Experimental and theoretical studies reveal that the incorporated Cu is chemically inert but enhances the overall oxidation resistance of the catalysts. Moreover, it weakens hydrogen adsorption and promotes the adsorption of hydroxide ions, thereby enhancing the HOR activity significantly. These results may open a door for rational design of high‐performance and durable PGM‐free HOR catalysts.

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