Electrodeposition of Ni-P alloy from deep eutectic solvent and its electrocatalytic activity toward hydrogen evolution reaction

被引:8
作者
Li, Lin [1 ]
Sheng, Shizhan [1 ]
Wang, Huihua [1 ]
Qu, Tianpeng [1 ]
Hou, Dong [1 ]
Wang, Deyong [1 ]
Sheng, Minqi [1 ]
机构
[1] Soochow Univ, Sch Iron & Steel, Suzhou 215000, Peoples R China
基金
中国国家自然科学基金;
关键词
catalytic activity; choline chloride-ethylene glycol; electrodeposition; hydrogen evolution reaction; Ni-P alloys; ELECTROCHEMICAL SYNTHESIS; CATALYTIC-ACTIVITY; IONIC LIQUIDS; EFFICIENT; NICKEL; COATINGS; ALKALINE; MO; COBALT; FABRICATION;
D O I
10.1002/cjce.24337
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Ni-P alloys have been successfully electrodeposited in the choline chloride and ethylene glycol with a molar proportion of 1:2(CE) electrolyte and their activities toward hydrogen evolution reaction (HER) have been also evaluated. The electrodeposition of Ni-P alloy follows a co-deposition process, and the bulk growth of which depends on an instantaneous nucleation under diffusion control. The morphologies of Ni-P alloys are significantly influenced by the P content, and low P content can lead to a smooth surface. As expected, Ni-9.0 wt.% P alloy shows an impressive HER catalytic performance with a Tafel slope (b) of 72.9 mV dec(-1) and an overpotential of 105 mV at 50 mA, in agreement with its large ECSA (C-dl = 3.25 mF cm(-2)) and small interface charge-transfer resistance. More interestingly, Ni-9.0 wt.% P alloy exhibits a sustainable catalytic activity toward HER after 1000 cycling test with a tiny potential decline of similar to 10 mV at 100 mA cm(-2). Such a striking HER activity of Ni-9.0 wt.% P alloy can be attributed to the synergistic effect among the induced active sites from lattice contraction, negatively charged P incorporation, and a mixed nanometre crystal and amorphous structure. Thus, Ni-P alloy electrodeposited in a CE-based electrolyte can be used as a promising electrode material with high HER activity in alkaline solutions for hydrogen production.
引用
收藏
页码:3381 / 3394
页数:14
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