Double-catalytic-site engineering of nickel-based electrocatalysts by group VB metals doping coupling with in-situ cathodic activation for hydrogen evolution

被引:39
|
作者
Shang, Xiao [1 ]
Zhang, Xin-Yu [1 ]
Xie, Jing-Yi [1 ,2 ]
Dong, Bin [1 ,2 ]
Chi, Jing-Qi [1 ]
Guo, Bao-Yu [1 ,2 ]
Yang, Min [1 ]
Chai, Yong-Ming [1 ]
Liu, Chen-Guang [1 ]
机构
[1] China Univ Petr East China, Inst New Energy, State Key Lab Heavy Oil Proc, Qingdao 266580, Shandong, Peoples R China
[2] China Univ Petr East China, Coll Sci, Qingdao 266580, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Double-site catalysis; Group VB transition metal; In-situ cathodic activation; Coupling strategy; Alkaline hydrogen evolution; ELECTROCHEMICAL PRODUCTION; DOUBLE HYDROXIDE; EFFICIENT; GENERATION; NANOSHEETS; SULFIDE; FILMS; NANOPARTICLES; PHOSPHORUS; OXIDATION;
D O I
10.1016/j.apcatb.2019.117984
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 hydrogen evolution reaction (HER) in alkaline media is limited by poor-proton environment with the water dissociation step. Herein, we report a double-catalytic-site construction strategy for nickel-based materials (e.g., sulfides, selenides, phosphides and oxides) for HER, utilizing group VB metals (V, Nb or Ta) doping coupled with the subsequent in-situ cathodic activation (ICA). For V-doped nickel sulfide, ICA creates Ni-V oxides species as new active sites for water dissociation. Moreover, V dopants enhance the intrinsic activity of nickel sulfide by the electronic interaction between Ni and V during the ICA process. As a result, the double-catalytic-site system composed of Ni V sulfides-oxides hybrid achieves 4-fold higher intrinsic activity and 15-fold larger current density at the overpotential of 300 mV than those of pristine nickel sulfide. Our work may open up a new avenue for designing multi-site systems, which may be promisingly applied for other transition metal materials in the electrolysis field.
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页数:8
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