In situ Raman spectroscopic study towards the growth and excellent HER catalysis of Ni/Ni(OH)2 heterostructure

被引:120
作者
Lai, Wei [1 ]
Ge, Lihong [1 ]
Li, Huaming [1 ]
Deng, Yilin [1 ,2 ]
Xu, Bin [2 ]
Ouyang, Bo [3 ,4 ]
Kan, Erjun [3 ,4 ]
机构
[1] Jiangsu Univ, Inst Energy Res, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Jiangsu Univ, Res Ctr Fluid Machinery Engn & Technol, Zhenjiang 212013, Jiangsu, Peoples R China
[3] Nanjing Univ Sci & Technol, Dept Appl Phys, Nanjing 210094, Peoples R China
[4] Nanjing Univ Sci & Technol, Inst Energy & Microstruct, Nanjing 210094, Peoples R China
基金
中国博士后科学基金;
关键词
Ni/Ni(OH)(2) heterostructure; In situ Raman spectroscopy; Hydrogen evolution reaction; Electrochemistry; Density functional theory calculations; HYDROGEN EVOLUTION REACTION; AMORPHOUS MOLYBDENUM SULFIDE; OXYGEN REDUCTION; HIGHLY EFFICIENT; ELECTROCATALYTIC HYDROGEN; SULFUR-ATOMS; NICKEL; NI; OXIDE; NANOPARTICLES;
D O I
10.1016/j.ijhydene.2021.05.158
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The electrochemical water splitting to produce H-2 in high efficiency with earth-abundant metal catalysts remains a challenge. Here, we describe a simple "cyclic voltammetry thorn 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 H-2-evolving current density of 10 mA/cm(2) and 153 mV at 100 mA/cm(2), 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. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:26861 / 26872
页数:12
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