Optimized design of BiVO4/NH2-MIL-53(Fe) heterostructure for enhanced photocatalytic degradation of methylene blue and ciprofloxacin under visible light

被引:46
作者
Wang, Dandan [1 ,2 ]
Li, Hongji [1 ,2 ]
Han, Qian [1 ,2 ]
Jiang, Wei [1 ,2 ]
Liu, Chunbo [1 ,2 ]
Che, Guangbo [1 ,2 ]
机构
[1] Jilin Normal Univ, Key Lab Preparat & Applicat Environm Friendly Mat, Minist Educ, Changchun 130103, Peoples R China
[2] Jilin Normal Univ, Coll Environm Sci & Engn, Siping 136000, Peoples R China
基金
中国国家自然科学基金;
关键词
BiVO4; NH2-MIL-53(Fe); Type II heterostructure; Visible light; Photocatalysis; HYDROGEN EVOLUTION; CHARGE SEPARATION; DRIVEN; CR(VI); CARBON; BIVO4; MIL-100(FE); REDUCTION; OXIDATION; REMOVAL;
D O I
10.1016/j.jpcs.2021.110027
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Visible-light-driven type II BiVO4/NH2-MIL-53(Fe) (BNMF) heterostructure have been synthesized by a facile stepwise hydrothermal method. Specifically, four BNMF heterostructures with different material ratios (BNMF-10, BNMF-20, BNMF-30, and BNMF-40) have been obtained by adjusting the amount of NH2-MIL-53(Fe) (10, 20, 30, or 40 mg) on the BiVO4-based photocatalyst. The BNMF-30 sample exhibited enhanced photocatalytic activity under visible light, degrading 90.2% of methylene blue in 180 min and 80.8% of ciprofloxacin in 120 min. The apparent rate constants for methylene blue and ciprofloxacin degradation over BNMF-30 were 2.8 and 1.4 times higher than those over pure BiVO4. The enhanced photocatalytic activity of BNMF-30 can be mainly ascribed to the formation of a tight joint interface between BiVO4 and NH2-MIL-53(Fe), which not only facilitates the separation of photo-induced charge carriers, but also extends the light absorption range. Meanwhile, the NH2-MIL-53(Fe) component facilitates the adsorption of pollutants, expediting the interfacial oxidation-reduction kinetics. Moreover, superior stability of the BNMF-30 photocatalyst was observed over repeated cycles. Furthermore, (OH)-O-center dot, O-center dot(2)-, and h(+) have been identified as the main active radicals through trapping experiments, providing a mechanism for the enhanced catalytic performance.
引用
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页数:12
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