A dual-cathode photoelectrocatalysis-electroenzymatic catalysis system by coupling BiVO4 photoanode with hemin/Cu and carbon cloth cathodes for degradation of tetracycline

被引:34
作者
Cheng, Ling [1 ]
Jiang, Tao [1 ]
Yan, Kai [1 ]
Gong, Jianyu [2 ]
Zhang, Jingdong [1 ]
机构
[1] Huazhong Univ Sci & Technol, Key Lab Mat Chem Energy Convers & Storage, Minist Educ, Sch Chem & Chem Engn, Luoyu Rd 1037, Wuhan 430074, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Environm Sci & Engn, Luoyu Rd 1037, Wuhan 430074, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Photoelectrocatalysis; Electroenzymatic catalysis; Dual cathodes; Tetracycline; BiVO4; TIO2; NANOPARTICLES; OXIDATION; WATER; PERFORMANCE; ENZYME; FILM; H2O2; GENERATION; BIOSENSOR; SURFACE;
D O I
10.1016/j.electacta.2018.12.086
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
When photoelectrocatalysis (PEC) couples with electroenzymatic catalysis (EEC), effective utilization of electrons from PEC process for yield of H2O2 plays an important role in the enzymatic catalysis. In the present work, we designed a novel dual-cathode PEC-EEC system for pollutant removal. In this system, BiVO4 photoanode was prepared by electrodeposition for visible light-driven PEC process while carbon cloth was used as the first cathode for electrogeneration of H2O2 and hemin/Cu prepared by electrophoretic deposition acted as the second cathode for enzymatic catalysis. The performances of the constructed dual-cathode PEC-EEC system were evaluated by decoloring Rhodamine B (RhB), which showed high decoloration percentage with acceptable stability and reusability. Further, the system was applied to degradation of tetracycline (TC), indicating that about 93.6% of TC was removed after 2-h treatment. A pathway for TC degradation in such a dual-cathode PEC-EEC system was proposed based on the intermediates determined by liquid chromatography coupled to mass spectrometry in tandem (LC-ESI-MS/MS). (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:561 / 569
页数:9
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