Boosting photocatalytic performances of lamellar BiVO4 by constructing S-scheme heterojunctions with AgBr for efficient charge transfer

被引:5
|
作者
Wang, Haoran [1 ,2 ]
Hailili, Reshalaiti [2 ,3 ]
Jiang, Xiaoyu [1 ]
Yuan, Guoliang [1 ]
Bahnemann, Detlef W. [2 ]
Wang, Xiong [1 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Mat Sci & Engn, Nanjing 210094, Peoples R China
[2] Leibniz Univ Hannover, Inst Tech Chem, D-30167 Hannover, Germany
[3] Beijing Univ Technol, MOE Key Lab Enhanced Heat Transfer & Energy Conser, Beijing Key Lab ofHeat Transfer & Energy Convers, Beijing 100124, Peoples R China
基金
中国国家自然科学基金;
关键词
photocatalytic activity; AgBr; BiVO4; heterojunction; hydrothermal; VISIBLE-LIGHT; ESCHERICHIA-COLI; HIGHLY EFFICIENT; DEGRADATION; COMPOSITE; MORPHOLOGY; PHOTODEGRADATION; HETEROSTRUCTURE; NANOPARTICLES; TETRACYCLINE;
D O I
10.1088/1361-6528/acbb7c
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Successful construction of heterojunction can improve the utilization efficiency of solar light by broadening the absorption range, facilitating charge-carrier separation, promoting carrier transportation and influencing surface-interface reaction. Herein, visible-light-driven AgBr was deposited on the surface of lamellar BiVO4 which was prepared by a facile hydrothermal process to improve charge carrier separation, and subsequent photocatalytic effectiveness. The catalyst with an optimal AgBr/BiVO4 ratio exhibited a superbly enhanced photocatalytic decolorization ability (about 6.85 times higher than that of pure BiVO4) and high stability after four cycles. The unique photocatalytic mechanism of S-scheme carrier migration was investigated on the bases of radical trapping tests and photo/electrochemical characterizations. Results showed that the enhanced migration strategy and intimately interfacial collaboration guaranteed the effective charge carriers separation/transfer, leading to magnificent photocatalytic performance as well as excellent stability.
引用
收藏
页数:9
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