Fabrication of rGO/CdS@2H, 1T, amorphous MoS2 heterostructure for enhanced photocatalytic and electrocatalytic activity

被引:26
作者
Zhao, Yue [1 ]
Zhang, Xiao [2 ,3 ]
Wang, Tao [1 ]
Song, Tong [1 ]
Yang, Ping [1 ]
机构
[1] Univ Jinan, Sch Mat Sci & Engn, Jinan 250022, Peoples R China
[2] Curtin Univ, Fuels & Energy Technol Inst, Perth, WA 6845, Australia
[3] Curtin Univ, Dept Chem Engn, Perth, WA 6845, Australia
基金
中国国家自然科学基金;
关键词
MoS2; CdS; Photocatalysis; Electrocatalysis; Heterojunction; ULTRATHIN NANOSHEETS; H-2; EVOLUTION; EFFICIENT; HETEROJUNCTION; NANOCOMPOSITES; SULFIDE; CUBES;
D O I
10.1016/j.ijhydene.2020.05.217
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 synthesis of high efficiency noble metal free catalysts is an important target for H-2 production by water-splitting. In this work, rGO/CdS@MoS2 heterostructure with two catalytic paths was successfully synthesized and as the first applied the heterostructure in the field of electrocatalysis. The MoS2 structure is adjusted by controlling hydrothermal process. Moreover, the effects of structure and loading amount of 2H-MoS2, 1T-MoS2 and amorphous MoS2 (A-MoS2) on catalytic performance were also studied. The catalytic activity of rGO/CdS@MoS2 heterostructure has been improved obviously. Compared with 2H-MoS2, the distortion of 1T-MoS2 and the defect of A-MoS2 make it have more unsaturated S, so rGO/CdS@1T-MoS2 and rGO/CdS@A-MoS2 have better catalytic activity. For photo- catalytic H-2 evolution, loading MoS2 and rGO on catalysts changes the energy band structure, promotes the separation of electron-holes and provides a large number of active sites. Among them, the visible light photocatalytic H-2 production rate of rGO/CdS@1T-MoS2 with 0.1 mol of 1T-MoS2 (CT0.1-C1) is 18.26 mmol/g/h. During the electrocatalytic H-2 evolution, introducing MoS2 and rGO improves electronic structure and increases active sites. rGO/CdS@1T-MoS2 with 0.5 mol of 1T-MoS2 (CT0.5-G1) shows the low overpotential (312 mV) and Tafel slopes (85 mV/dec). (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:21409 / 21421
页数:13
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