• 文献标题:   Novel 3D flowerlike BiOCl0.7Br0.3 microspheres coupled with graphene sheets with enhanced visible-light photocatalytic activity for the degradation of rhodamine B
  • 文献类型:   Article
  • 作  者:   TANG GG, DONG JZ, WU KQ, LIANG W, ZHOU DY, MA SB, TANG H, LI CS
  • 作者关键词:   composite, bismuth mixed oxyhalidesare, solid solution, graphene sheet, visiblelight photocatalysi
  • 出版物名称:   CERAMICS INTERNATIONAL
  • ISSN:   0272-8842 EI 1873-3956
  • 通讯作者地址:   Jiangsu Univ
  • 被引频次:   14
  • DOI:   10.1016/j.ceramint.2015.11.110
  • 出版年:   2016

▎ 摘  要

Highly efficient visible-light-driven 3D flowerlike BiOCl0.Br-3(0.3) microspheres coupled with graphene sheets with different graphene contents have been synthesized by a facile solvothermal process. The as-prepared samples were characterized by power X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), N-2 adsorption-desorption analysis and UV-vis diffuse reflectance spectra (DRS). Characterization results showed BiOCl0.7Br0.3 microspheres were composed of numerous nanoplates with a thickness of about 20 nm and dispersed uniformly on the surface of graphene. Moreover, the photocatalytic activities of these BiOCl0.7Br0.3/graphene composites under visible-light irradiation (lambda > 420 nm) were evaluated by the degradation of rhodamine B (RhB). The results indicate all BiOCl0.7Br0.3/graphene composites exhibited much higher photocatalytic activities than pristine BiOCl0.7Br0.3, pure BiOBr and BiOCl, and the highest activity was reached by the BiOCl0.7Br0.3/graphene composite photocatalyst with 10 wt% of graphene. The enhanced photocatalytic activity could be largely ascribed to more effective charge transportations and separations, larger BET surface areas and the increased light absorption. In addition, a possible photocatalytic mechanism of the BiOCl0.7Br0.3/graphene composites on basis of the experimental results was also proposed. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.