Fabrication of CdS@1T-MoS2 core-shell nanostructure for enhanced visible-light-driven photocatalytic H2 evolution from water splitting

被引:11
作者
Lian, Zhongqin [1 ]
Liu, Yichen [1 ]
Liu, Hong [1 ]
Zhou, Hualei [1 ]
Chang, Zhidong [1 ]
Li, Wenjun [1 ]
机构
[1] Univ Sci & Technol Beijing, Dept Chem & Chem Engn, Beijing Key Lab Sci & Applicat Funct Mol & Crysta, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; Hydrogen evolution; 1T-MoS2; Core-shell structure; Water splitting; HYDROGEN EVOLUTION; MOS2; NANOSHEETS; MODIFIED G-C3N4; EFFICIENT; CDS; PERFORMANCE; COCATALYST; HETEROSTRUCTURE; CATALYSTS; 1T-MOS2;
D O I
10.1016/j.jtice.2019.10.002
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
CdS@1T-MoS2 composites with core-shell structure were synthesized through a hydrothermal treatment followed by a solvothermal treatment. Nanosized CdS particles were coated by a thin 1T-MoS2 shell to form efficient heterojunction, as demonstrated by transmission electron microscopy images and X-ray photoelectron spectroscopy. Under visible-light irradiation, CdS@1T-MoS2 composites with the MoS2/CdS weight ratio of 0.5 exhibit the highest photocatalytic performance and the H-2 evolution rate reached 2.67 mmol h(-1) g(-1), which is 50 times that of single 1T-MoS2 and 10 times that of single CdS. 1T-MoS2, as a cocatalyst, donates the composites fast charge transfer ability and the high H-2 evolution activity, while the intimate heterojunction between CdS core and 1T-MoS2 shell greatly increase the separation efficiency of photo-induced electron-hole pairs, as demonstrated by the electrochemical and PL results, resulting in the remarkable photocatalytic performance of the composites. This study supplies a facile and efficient strategy to develop the photocatalysts with boosted performance for hydrogen energy application. (C) 2019 Published by Elsevier B.V. on behalf of Taiwan Institute of Chemical Engineers.
引用
收藏
页码:57 / 64
页数:8
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