Precisely tailoring the d-band center of nickel sulfide for boosting overall water splitting

被引:8
|
作者
Zhou, Jianqing [1 ]
Li, Pengfei [1 ]
Xia, Xinyi [1 ]
Zhao, Yi [1 ]
Hu, Zhihao [1 ]
Xie, Yunlong [1 ]
Yang, Lun [1 ]
Liu, Yisi [1 ]
Du, Yue [1 ]
Zhou, Qiancheng [2 ]
Yu, Luo [3 ,4 ,5 ]
Yu, Ying [2 ]
机构
[1] Hubei Normal Univ, Sch Mat Sci & Engn, Hubei Key Lab Photoelect Mat & Devices, Huangshi 435002, Hubei, Peoples R China
[2] Cent China Normal Univ, Coll Phys Sci & Technol, Wuhan 430079, Peoples R China
[3] Univ Houston, Univ Houston TcSUH, Dept Phys, Houston, TX 77204 USA
[4] Univ Houston, Univ Houston TcSUH, Texas Ctr Superconduct, Houston, TX 77204 USA
[5] China Univ Geosci, Fac Mat Sci & Chem, Lab Solar Fuel, Wuhan 430078, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTRONIC-STRUCTURE; ELECTROCATALYST; PERFORMANCE; EFFICIENT; PLATINUM; SURFACE; ARRAYS;
D O I
10.1016/j.apcatb.2024.124461
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
d-band center engineering is an effective approach to manipulate the electronic structure of an electrocatalyst for boosting water splitting performance. However, it is still challenging to precisely tailor the electronic structure with an optimized d-band center for efficient hydrogen and oxygen evolution reactions (HER and OER) on one single catalyst simultaneously. Focusing on nickel sulfide (Ni3S2), herein we applied dual-atom modification to precisely regulate the d-band center of Ni3S2, which dramatically enhances its bifunctional activity with outstanding HER and OER performance. Specifically, the V and Fe co-modified N(i)3S(2) achieves ultra-low overpotentials of 68 and 190 mV to output 10 mA cm(-2) in 1 M KOH for HER and OER, respectively. Theoretical calculations reveal that the strong electronic interactions between Ni 3d and V 3d/Fe 3d orbitals effectively tailor the d-band center of Ni3S2, resulting in optimized HER and OER intermediate adsorption, thus boosting the HER and OER simultaneously.
引用
收藏
页数:9
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