S vacant CuIn5S8 confined in a few-layer MoSe2 with interlayer-expanded hollow heterostructures boost photocatalytic CO2 reduction

被引:48
作者
Chen, Li-Juan [1 ]
Liu, Ting-Ting [1 ]
Liu, Shu-Ming [1 ]
Cai, Sheng [1 ]
Zou, Xiao-Xiao [1 ]
Jiang, Jing-Wen [1 ]
Mei, Zhi-Yuan [1 ]
Zhao, Gen-Fu [1 ]
Yang, Xiao-Fei [2 ]
Guo, Hong [1 ]
机构
[1] Yunnan Univ, Sch Mat & Energy, Kunming 650091, Yunnan, Peoples R China
[2] Western Univ, Nanomat & Energy Lab, Dept Mech & Mat Engn, London, ON N6A 5B9, Canada
基金
中国国家自然科学基金;
关键词
Sulfur vacancy; CuIn5S8; MoSe2; heterojunction; Photocatalytic CO2 reduction; GRAPHITIC CARBON NITRIDE; HYDROGEN EVOLUTION; ZNIN2S4; MONOLAYER; DEGRADATION;
D O I
10.1007/s12598-021-01809-x
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The conversion of CO2 into CO, CH4 and other hydrocarbons through solar energy can alleviate the energy shortage problem. We design a novel photocatalyst with S defects CuIn5S8@MoSe2 hollow structure. The interlayer-expanded MoSe2 can increase the adsorption of intermediates. The unique hollow structure can improve the light utilization efficiency and the electron-holes separation. CuIn5S8 with S vacancies in bimetallic sites has high selectivity and photocatalytic reduction of CO2 activity. Therefore, S vacant CuIn5S8 confined in a few-layers MoSe2 with interlayer-expanded hollow heterostructures exhibit super performance for photocatalytic CO2 reduction. After 8-h light reaction, the outputs of CO and CH4 for the 15.3 wt% CuIn5S8@MoSe2 sample containing S vacancies (V-s) are 30.4 and 14.7 mu mol center dot g(-1), respectively. The mechanism is also investigated in detail through in situ Fourier transform infrared spectroscopy technology.
引用
收藏
页码:144 / 154
页数:11
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