Trace tungsten and iron-doped nickel hydroxide nanosheets for an efficient oxygen evolution reaction

被引:9
|
作者
Li, Chun [1 ]
Tian, Peng [1 ]
Pang, Hongchang [1 ]
Gong, Weitao [1 ]
Ye, Junwei [1 ]
Ning, Guiling [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
来源
SUSTAINABLE ENERGY & FUELS | 2020年 / 4卷 / 06期
关键词
CARBON CLOTH; HYDROGEN EVOLUTION; WATER OXIDATION; FE-SITES; ELECTROCATALYSTS; NI; CO; (OXY)HYDROXIDE; PERFORMANCE; ELECTRODES;
D O I
10.1039/d0se00205d
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
FexNi1-x(O)OH has been proven to be an efficient, earth-abundant and nonprecious catalyst for the oxygen evolution reaction (OER). However, the weak binding of oxygenated intermediates and the exposure of a few active sites on NiFe hydroxides considerably hinder their catalytic activity. Based on the fact that the W6+ ions possess higher valency. and similar ionic radius with respect to the Fe2+, Fe3+, and Ni2+ ions, which can modulate the (NiO6) crystal structure and enhance the interaction of block electrons, we have tried to introduce a trace amount of W6+ into FexNi1-x(O)OH. To our surprise, the target product Fe0.03W0.03-Ni LDHB exhibited the lowest overpotential of 205(+/- 3) mV at 10 mA cm(-2), Tafel slope of 60 mV dec(-1), and no obvious decrease in the electrocatalytic activity after more than 50 hour operation or 3000 cyclic voltammetry cycles. X-ray diffraction, Raman spectroscopy, UV-Vis spectroscopy, X-ray photoelectron spectroscopy and electrochemical studies revealed a synergistic interplay among tungsten, iron and nickel for producing a favorable local coordination environment and electronic structure, which enhanced the OER performance.
引用
收藏
页码:2792 / 2799
页数:8
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