塔菲尔方程
过电位
拉曼光谱
循环伏安法
材料科学
电化学
催化作用
电解质
异质结
电极
化学工程
极化(电化学)
可逆氢电极
无机化学
分析化学(期刊)
化学
物理化学
工作电极
光电子学
光学
物理
工程类
色谱法
生物化学
作者
Wei Lai,Lihong Ge,Huaming Li,Yilin Deng,Bin Xu,Bo Ouyang,Erjun Kan
标识
DOI:10.1016/j.ijhydene.2021.05.158
摘要
The electrochemical water splitting to produce H2 in high efficiency with earth-abundant-metal catalysts remains a challenge. Here, we describe a simple “cyclic voltammetry + ageing” protocol at room temperature to activate Ni electrode (AC-Ni/NF) for hydrogen evolution reaction (HER), by which Ni/Ni(OH)2 heterostructure is formed at the surface. In situ Raman spectroscopy reveals the gradual growth of Ni/Ni(OH)2 heterostructure during the first 30 min of the aging treatment and combined with polarization measurements, it suggests a positive relation between the Ni/Ni(OH)2 amount and HER performance of the electrode. The obtained AC-Ni/NF catalyst, with plentiful Ni–Ni(OH)2 interfaces, exhibits remarkable performance towards HER, with the low overpotential of only 30 mV at a H2-evolving current density of 10 mA/cm2 and 153 mV at 100 mA/cm2, as well as a small Tafel slope of 46.8 mV/dec in 1 M KOH electrolyte at ambient temperature. The excellent HER performance of the AC-Ni/NF could be maintained for at least 24 h without obvious decay. Ex situ experiments and in situ electrochemical-Raman spectroscopy along with density functional theory (DFT) calculations reveal that Ni/Ni(OH)2 heterostructure, although partially reduced, can still persist during HER catalysis and it is the Ni–Ni(OH)2 interface reducing the energy barrier of H∗ adsorption thus promoting the HER performance.
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