Construction of Ni2P/WS2/CoWO4@C multi-heterojunction electrocatalysis derived from heterometallic clusters for superior overall water splitting

被引:0
|
作者
Yang, Yu-Ying [1 ]
Pan, Fu-Chun [1 ]
Li, Jia-Ling [1 ]
Gong, Feng [1 ]
Hu, Jisong [2 ]
Zheng, Qiaoji [1 ]
Lin, Dunmin [1 ]
Huo, Yu [1 ]
机构
[1] Sichuan Normal Univ, Coll Chem & Mat Sci, Chengdu 610066, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Opt & Elect Informat, Wuhan 430074, Peoples R China
关键词
Overall water splitting; Bifunctional electrocatalyst; Multiple heterointerfaces; Heterometallic clusters; EFFICIENT; ARRAY;
D O I
10.1016/j.jcis.2025.01.075
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 reasonable design of an economical and robust bifunctional electrocatalyst for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is both essential but challenging. Herein, we synthesized a multiinterfacial Ni2P/WS2/CoWO4@C hybrid electrocatalyst devived from the heterometallic clusters [Co-24(TC(4)A)(6)(WO4)(8)Cl-6][HPW12O40], in which Ni2P was incorporated into WS2/CoWO4@C nanosheets via interfacial interactions by in situ phosphorization processes. Theoretical calculations revealed that moderate electron transfer from CoWO4 and Ni2P to WS2 induced by the multi-heterojunction significantly regulate the binding energies of the reactive intermediates, thus enhacing its intrinsic activity. Under alkaline medium, the overpotential of the optimized Ni2P/WS2/CoWO4@C electrocatalyst for OER and HER is only 206 mV and 90 mV at 10 mA cm(-2), respectively, with extraordinary stability more than 100 h, and the potential of overall water splitting is only 1.46 V. This work motivates further research and presents a reliable design route for other heterojunction engineered cost-effective bifuctional electrocatalysts.
引用
收藏
页码:196 / 204
页数:9
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