Visible-light-driven Ag/Bi3O4Cl nanocomposite photocatalyst with enhanced photocatalytic activity for degradation of tetracycline

被引:71
作者
Jiang, Enhui [1 ]
Liu, Xiaoteng [2 ]
Che, Huinan [1 ]
Liu, Chunbo [2 ]
Dong, Hongjun [2 ]
Che, Guangbo [3 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Univ, Sch Chem & Chem Engn, Inst Green Chem & Chem Technol, Zhenjiang 212013, Peoples R China
[3] Jilin Normal Univ, Minist Educ, Key Lab Preparat & Applicat Environm Friendly Mat, Changchun 130103, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
MINERALIZATION EFFICIENCY; ELECTROCHEMICAL-BEHAVIOR; PLASMONIC PHOTOCATALYST; HETEROJUNCTION; PERFORMANCE; FABRICATION; G-C3N4; TIO2; HETEROSTRUCTURE; OXYTETRACYCLINE;
D O I
10.1039/c8ra07482h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, a novel Ag/Bi3O4Cl photocatalyst has been synthesized by a facile photodeposition process. Its photocatalytic performance was evaluated from the degradation of tetracycline (TC) under visible light irradiation (lambda > 420 nm). The 1.0 wt% Ag/Bi3O4Cl photocatalyst could significantly enhance the degradation of TC compared with pure Bi3O4Cl, with the degradation level reaching 94.2% in 120 minutes. The enhancement of photocatalytic activity could be attributed to the synergetic effect of the photogenerated electrons (e(-)) of Bi3O4Cl and the surface plasmon resonance (SPR) caused by Ag nanoparticles, which could improve the absorption capacity of visible light and facilitate the separation of photogenerated electron-hole pairs. In addition, electron spin resonance (ESR) analysis and trapping experiments demonstrated that the superoxide radicals (center dot O2-), hydroxyl radicals (center dot OH) and holes (h(+)) played crucial roles in the photocatalytic process of TC degradation. The present work provides a promising approach for the development of highly efficient photocatalysts to address current environmental pollution, energy issues and other related areas.
引用
收藏
页码:37200 / 37207
页数:8
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