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
Quantum-sized BiVO4 modified TiO2 microflower composite heterostructures: efficient production of hydroxyl radicals towards visible light-driven degradation of gaseous toluene
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论文类型:期刊论文
发表时间:2015-01-01
发表刊物:JOURNAL OF MATERIALS CHEMISTRY A
收录刊物:SCIE、EI、Scopus
卷号:3
期号:43
页面范围:21655-21663
ISSN号:2050-7488
摘要:In an effort to develop visible-light-driven heterostructured photocatalysts with high activity, a novel quantum-sized tubelike BiVO4 sensitized TiO2 microflower catalytic system was successfully fabricated by using a facile hydrothermal and ultrasonic adhering approach. The structural and optical properties of the as-prepared samples were comparatively characterized. The staggered band structure of quantumsized BiVO4 decorated TiO2 not only extended the photo-response range but also promoted photoexcited charges transfer and separation. Photocatalytic activities of the as-prepared samples were examined by the degradation of toluene under visible light irradiation (A > 400 nm). Compared to the individual TiO2 microflower, BiVO4 quantum tube, BiVO4 nanoparticle and nano-BiVO4/TiO2, the quantum-BiVO4/Ti02 (Q-BiVO4/TiO2) composite exhibited higher photo activities. Electron spin resonance (ESR) examinations confirmed the generation of the photo-induced reactive oxygen species (*OH and *02) which were involved in the photocatalytic process of Q-BiVO4/TiO2 composites. Furthermore, the enhanced photocatalytic activity of the Q-BiVO4/TiO2 composite mainly originated from the high separation efficiency of photo-induced electron-hole pairs and the efficient production of hydroxyl radicals. A detailed mechanism accounting for the superior photocatalytic activity was proposed in terms of the energy band structures of the components.