Facile electrochemical synthesis of Ni(OH)2/MoSx catalyst on oxidized carbon fiber for efficient alkaline hydrogen evolution reaction

被引:6
作者
Deng, Yilin [1 ]
Lai, Wei [1 ]
He, Xiaoyang [1 ]
Xu, Li [1 ]
Xu, Bin [2 ]
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
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Electrocatalysis; Alkaline hydrogen evolution reaction; Ni(OH)(2)/MoSx; Oxidized carbon fiber; Synergistic effect; AMORPHOUS MOLYBDENUM SULFIDE; SULFUR-ATOMS; NICKEL FOAM; ELECTROCATALYSTS; NANOSHEETS; CLOTH; RAMAN; MOS2; SPECTROSCOPY; SITES;
D O I
10.1016/j.cep.2020.108090
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The efficient electrochemical hydrogen evolution reaction in alkaline media through the use of earth-abundant catalysts has received significant attention, as it is a crucial means for sustainable H-2 production. Here, we present a facile synthesis approach for Ni(OH)(2)/MoSx (MoSx: amorphous molybdenum sulfide) catalyst on oxidized carbon fiber support. Carbon fibers are first oxidized by a hydrothermal treatment in a concentrated HNO3 solution, while Ni(OH)(2) and MoSx films are consecutively deposited onto the substrate through simple electro-deposition methods from their plating solutions. Benefiting from the hydrophilicity of the oxidized carbon fiber, the abundant electrochemically reactive sites and the synergistic effect between Ni(OH)(2) and MoSx, this hybrid catalyst shows a low HER onset potential of 80 mV at 1 mA/cm(2), an overpotential of 180 mV at 10 mA/cm(2) and a remarkable stability of at least 35 working hours at a H-2-evolving current density of 10 mA/cm(2) without any obvious overpotential changes.
引用
收藏
页数:6
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