rGO/Bi2WO6 composite as a highly efficient and stable visible-light photocatalyst for norfloxacin degradation in aqueous environment

被引:58
|
作者
Zhao, Yanyan [1 ,2 ]
Liang, Xuhua [1 ,2 ]
Hu, Xiaoyun [4 ]
Fan, Jun [3 ]
机构
[1] Shangluo Univ, Coll Biol Pharm & Food Engn, Shangluo 726000, Peoples R China
[2] Shaanxi Qinling Ind Technol Res Inst Special Biol, Shangluo 726000, Peoples R China
[3] Northwest Univ, Coll Food Sci & Technol, Xian 710069, Peoples R China
[4] Northwest Univ, Sch Phys, Xian 710069, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; rGO/Bi2WO6; composite; Visible light; Norfloxacin; Degradation;
D O I
10.1016/j.jcis.2021.01.016
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Fabrication of binary composite has proved to be an efficient approach to improve the photocatalytic activity of monomer photocatalyst. In this contribution, an effective Reduced Graphene Oxide/Bismuth Tungsten Oxide (rGO/Bi2WO6) composite with outstanding photocatalytic activity was designed by employing Bi(2)WO(6 )as a primary photocatalyst and rGO as an electron acceptor and transporter for norfloxacin degradation in aquatic environment. The rGO/Bi2WO6 composite displayed higher photocatalytic activity compare with pure Bi2WO6, which could degrade about 87.49% of norfloxacin with 180 min under visible light irradiation. The results of the UV-vis diffuse reflection spectrum, photoluminescence spectra and transient photocurrent response implied that the enhanced photocatalytic activity of the rGO/Bi2WO6 composite could be attributed to the improved visible light-harvesting ability and the efficient charge separation ability. Additionally, the reactive-species-trapping experiments indicated that center dot OH and e played dominant roles during the photocatalytic degradation process. Four possible intermediates and two possible transformation pathways of norfloxacin degradation were detected by LC-MS. This present work provided a low-cost and facile green method to design of Bi-based composite. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:336 / 346
页数:11
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