Mo doping and Se vacancy engineering for boosting electrocatalytic water oxidation by regulating the electronic structure of self-supported Co9Se8@NiSe

被引:50
作者
Tian, Lin [1 ,2 ,3 ]
Chen, Zhenyang [1 ]
Wang, Tingjian [1 ]
Cao, Ming [1 ]
Lu, Xinhua [1 ]
Cheng, Wenjing [2 ,3 ]
He, Changchun [1 ]
Wang, Ju [1 ]
Li, Zhao [1 ]
机构
[1] Xuzhou Univ Technol, Sch Mat & Chem Engn, Xuzhou 221018, Peoples R China
[2] Yili Normal Univ, Sch Chem & Environm Sci, University & Coll Key Lab Nat Prod Chem & Applicat, Yili 835000, Peoples R China
[3] Yili Normal Univ, Sch Chem & Environm Sci, Key Lab Pollutant Chem & Environm Treatment, Yili 835000, Peoples R China
基金
中国国家自然科学基金;
关键词
HYDROGEN EVOLUTION; ETHANOL;
D O I
10.1039/d2nr05410h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Oxygen evolution reactions (OERs) are regarded as the rate-determining step of electrocatalytic overall water splitting, which endow OER electrocatalysts with the advantages of high activity, low cost, good conductivity, and excellent stability. Herein, a facile H2O2-assisted etching method is proposed for the fabrication of Mo-doped ultrathin Co9Se8@NiSe/NF-X heterojunctions with rich Se vacancies to boost electrocatalytic water oxidation. After step-by-step electronic structure modulation by Mo doping and Se vacancy engineering, the self-standing Mo-Co9Se8@NiSe/NF-60 heterojunctions deliver a current density of 50 mA cm(-2) with an overpotential of 343 mV and a cell voltage of only 1.87 V at 50 mA cm(-2) for overall water splitting in 1.0 M KOH. Our study opens up the possibility of realizing step-by-step electronic structure modulation of nonprecious OER electrocatalysts via heteroatom doping and vacancy engineering.
引用
收藏
页码:259 / 265
页数:7
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