Constructing reconstruction-inhibited nickel selenide electrocatalysts via incorporating Ag single atom for durable and efficient water oxidation

被引:14
|
作者
Wang, Fangqing [1 ,2 ]
Zhao, Xueru [3 ]
Li, Ying [1 ,2 ]
Liang, Limin [1 ,2 ]
Sasaki, Kotaro [3 ]
Hao, Qiuyan [1 ,2 ]
Yuan, Wenhao [4 ]
Li, Sijia [1 ,2 ]
Liu, Hui [1 ,2 ]
机构
[1] Hebei Univ Technol, Key Lab Special Funct Mat Ecol Environm & Informat, Minist Educ, Tianjin 300130, Peoples R China
[2] Hebei Univ Technol, Sch Mat Sci & Engn, Tianjin 300130, Peoples R China
[3] Brookhaven Natl Lab, Chem Dept, Upton, NY 11973 USA
[4] Natl Univ Singapore, Coll Design & Engn, Dept Mat Sci & Engn, Singapore 117575, Singapore
关键词
Ag single atom; Se vacancies; Oxygen evolution; Density functional theory; OXYGEN EVOLUTION; NANOSHEETS; HYDROGEN; CATALYSTS; DESIGN;
D O I
10.1016/j.apcatb.2024.123830
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
Transition-metal selenides exhibit excellent catalytic activity towards oxygen evolution reaction (OER), but suffering from serious performance degradation due to the surface reconstruction during OER. Herein, we found that the incorporation of Ag single atoms in NiSe2 electrocatalyst (Ag-SA-NiSe2) could suppress the surface reconstruction, improving both catalytic activity (179 mV@10 mA cm(-2)) and stability (500 h @ similar to 100 mA cm(-2)) for OER in 1.0 M KOH. The aberration corrected transmission electron microscope and X-ray absorption structure analysis reveal the co-existence of the Ag single atoms and Se vacancies in NiSe2 matrix. In-situ Raman spectroscopy demonstrates that the introduction of single-atom Ag and Se vacancies in NiSe2 successfully inhibits the formation of NiOOH species on the surface during OER, accounting for the excellent stability. The theoretical calculation result indicates that the Ag single atom and Se vacancies in NiSe2 synergistically optimizes the adsorption/desorption of OER intermediates, boosting the intrinsic activity.
引用
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页数:9
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