Efficient photocatalytic hydrogen evolution with high-crystallinity and noble metal-free red phosphorus-CdS nanorods

被引:27
|
作者
Xu, Mengying [1 ,2 ,3 ]
Jiang, Linlin [1 ,2 ,3 ]
Wang, Junting [1 ,2 ,3 ]
Feng, Shuying [1 ,2 ,3 ]
Tremblay, Pier-Luc [1 ,2 ]
Zhang, Tian [1 ,2 ,3 ]
机构
[1] Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
[2] Wuhan Univ Technol, Sch Chem Chem Engn & Life Sci, Wuhan 430070, Peoples R China
[3] Wuhan Univ Technol, Sch Mat Sci & Engn, Wuhan 430070, Peoples R China
关键词
Photocatalytic H-2 evolution; CdS nanorods; Red phosphorus; Facile synthesis; Crystallinity; CADMIUM-SULFIDE NANORODS; ONE-POT SYNTHESIS; H-2; EVOLUTION; OPTICAL-PROPERTIES; TEMPLATED SYNTHESIS; WATER; DRIVEN; NANOSHEETS; SEMICONDUCTOR; FABRICATION;
D O I
10.1016/j.ijhydene.2020.04.200
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 photocatalytic production of H-2 by low-cost semiconductors is a promising approach to store solar energy. Photocatalysts with heterojunctions convert visible light into H-2 faster because of more efficient charge separation. The morphology, the structure, and the crystallinity are additional factors to consider when developing a photocatalyst. Here, highly-crystalline CdS nanorod (NR) were synthesized by a facile one-pot process. Under visible light, pure CdS NR produced H-2 2.1 times faster than conventional CdS nano-particles (NP). CdS NR were then combined with the semiconductor red phosphorus (RPh). A CdS NR-based heterojunction photocatalyst with RPh5% had an excellent photocatalytic H-2 evolution rate of 11.72 mmol g(-1)h(-)(1), which was 3.6 times higher than pure CdS NR. The apparent quantum efficiency of RPh5%/CdS NR was 19.57%. Furthermore, RPh5%/CdS NR exhibited a superior photogenerated charge separation efficiency and was stable with little photocorrosion compared to CdS NP showing the high potential of this heterojunction photocatalyst. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:17354 / 17366
页数:13
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