催化作用
过电位
双金属片
无机化学
碱性水电解
化学工程
材料科学
离子交换
分解水
镍
钴
氢氧化物
碱金属
双功能
化学
膜
扫描电子显微镜
X射线光电子能谱
卤化物
碱土金属
氢氧化钠
电子转移
制氢
电解质
氢
锶
氯化物
双功能催化剂
过氧化氢
电催化剂
感应耦合等离子体
电解水
氢氧化钾
法拉第效率
拉曼光谱
作者
Abin Sebastian,Y. Fujii,Rajith Illathvalappil,Hidenori Kuroki,Gopinathan M. Anilkumar,Takeo Yamaguchi
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2025-11-14
卷期号:39 (50): 23881-23890
被引量:1
标识
DOI:10.1021/acs.energyfuels.5c03164
摘要
We report the fabrication of a cobalt–molybdenum (Co–Mo) heterohierarchical thin-film catalyst electrodeposited on nickel foam (NF) via a facile one-step electrodeposition method for efficient hydrogen evolution reaction (HER) under alkaline conditions. A comprehensive study of alkali and alkaline earth metal halide coelectrolytes demonstrated that the coelectrolyte used during electrodeposition directly governs the Co–Mo catalyst morphology and the degree of Mo incorporation. Scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, and inductively coupled plasma–atomic emission spectroscopy analyses showed that using calcium chloride (CaCl2) as the coelectrolyte considerably improved uniform Mo incorporation and facilitated cobalt hydroxide deposition. The optimized Co–Mo/NF–CaCl2 catalyst showed an overpotential of 100 ± 6 mV at −10 mA/cm2, along with improved charge transfer and active site density, attributed to the better double-layer capacitance and tailored surface microstructure. This study is the first to correlate the coelectrolyte identity in electrodeposited Co–Mo catalysts with HER performance and contributes insights into the bimetallic electrodeposition technique. The high performance and alkaline compatibility of the catalyst make it a promising candidate for sustainable hydrogen generation via anion exchange membrane water electrolysis.
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