In-situ exsolved NiS nanoparticle-socketed CdS with strongly coupled interfaces as a superior visible-light-driven photocatalyst for hydrogen evolution

被引:42
作者
Li, Kailu [1 ]
Pan, Hui [1 ]
Wang, Fang [1 ]
Zhang, Zhengguo [1 ]
Min, Shixiong [1 ]
机构
[1] North Minzu Univ, Sch Chem & Chem Engn, Yinchuan 750021, Peoples R China
基金
中国科学院西部之光基金; 中国国家自然科学基金;
关键词
CdS particles; NiS cocatalyst; In-situ exsolution; Visible light; H2; evolution; GRAPHITIC CARBON NITRIDE; METAL-FREE COCATALYST; H-2; EVOLUTION; QUANTUM DOTS; EFFICIENT; CO; CATALYSTS; GROWTH; PHOTODEPOSITION; EXSOLUTION;
D O I
10.1016/j.apcatb.2022.122028
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
Herein, a NiS nanoparticle-socketed CdS photocatalyst (NiS/CdS-e) is developed by hydrothermal sulfurization of Ni-doped Cd(OH)2 precursor, where the Cd(OH)2 particles are converted into CdS while the doped Ni species are exsolved and socketed on the surfaces of CdS. 2% NiS/CdS-e presents a high H2 evolution rate of 18.9 mmol g-1 h-1 with an apparent quantum efficiency (AQE) of 13.9% at 420 nm, much superior to those of pristine CdS (0.5 mmol g-1 h-1) and 2% NiS/CdS-h (9.9 mmol g-1 h-1) prepared by impregnation-hydrothermal sulfurization. The enhanced activity originates from the strongly coupled interface between exsolved NiS and CdS that effi-ciently promote the charge separation, while the exsolved NiS nanoparticles serve as highly active H2 evolution sites. Moreover, the strongly coupled interfaces enable improved H2 evolution stability for 2% NiS/CdS-e over a 30-h cycling reaction. This work provides an effective strategy toward strongly coupled cocatalyst/semi-conductor photocatalysts for efficient solar energy conversion.
引用
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页数:12
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