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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.
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页码:57 / 64
页数:8
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