个人信息Personal Information
教授
博士生导师
硕士生导师
性别:男
毕业院校:中国科学院兰州化学物理研究所
学位:博士
所在单位:环境学院
办公地点:环境楼 B415
联系方式:Tel: 0411-84706658
电子邮箱:xyli@dlut.edu.cn
Construction of p-n heterojunction beta-Bi2O3/BiVO4 nanocomposite with improved photoinduced charge transfer property and enhanced activity in degradation of ortho-dichlorobenzene
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论文类型:期刊论文
发表时间:2017-12-15
发表刊物:APPLIED CATALYSIS B-ENVIRONMENTAL
收录刊物:EI、SCIE
卷号:219
页面范围:259-268
ISSN号:0926-3373
关键字:Nanostructured photocatalysts; Photo-induced charge carriers; p-n Heterojunction; In situ FTIR; ortho-Dichlorobenzene
摘要:To achieve efficient conversion of solar to chemical energy in photocatalysis, development of visible light-induced catalysts with high charge carrier mobility and superior activity is essential. In this work, a novel beta-Bi2O3/BiVO4 nanocomposite with p-n heterojuction structure, which is assembled by interconnected quantum dots, has been successfully constructed through a facile approach. The structural and optical properties of the as-prepared materials were comparatively characterized. Steady-state and transient-state photoluminescence spectra demonstrate that the photo-induced charge carriers in beta-Bi2O3/BiVO4 nanocomposite display higher separation and much longer lifetime than those in individual BiVO4 samples, which is attributed to the formation of efficient interfacial electric field between beta-Bi2O3 and BiVO4. The photocatalytic performance of the samples was explored by the degradation of ortho-dichlorobenzene (o-DCB). Electron spin resonance examinations confirmed that much more superoxide radicals were generated in the system of beta-Bi2O3/BiVO4 nanocomposite, which could be mainly responsible for the outstanding activity. In addition, the adsorption and oxidation of o-DCB over the as-prepared materials were studied by in situ FTIR spectroscopy to investigate the nature of surface intermediates formed on the catalysts. To clarify charge migration route, a detailed photocatalytic mechanism in terms of the energy band structures is proposed. (C) 2017 Elsevier B.V. All rights reserved.