A novel Bi-based oxybromide SrBiO2Br: Synthesis, optical property and photocatalytic activity

被引:19
作者
He, Ying [1 ]
Huang, Hongwei [1 ]
Zhang, Yihe [1 ]
Li, Xiaowei [1 ]
Tian, Na [1 ]
Guo, Yuxi [1 ]
Luo, Yi [1 ]
机构
[1] China Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Beijing 100083, Peoples R China
关键词
Oxides; Optical properties; Catalytic properties; VISIBLE-LIGHT IRRADIATION; CRYSTAL-STRUCTURE; NANOPARTICLES; WATER; OXIDATION; CATALYSTS; GRAPHENE; BI2WO6; FILMS;
D O I
10.1016/j.materresbull.2015.01.011
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A novel Bi-based photocatalyst SrBiO2Br with layered structure was successfully synthesized via a solid state reaction method. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and UV-vis diffuse reflectance spectra (DRS). SrBiO2Br has an indirect-transition optical band-gap of 2.58 eV. Density functional calculations revealed that conduction band (CB) were composed of the Bi 6p and Br 4s orbitals, and valence band (VB) were occupied by Br 4p and O 2p. The photodecomposition of rhodamine-B (RhB) experiments demonstrated SrBiO2Br can be used as photocatalysts under ultraviolet (UV) light and visible light irradiation (lambda > 400 nm). The results revealed that SrBiO2Br calcinated at 700 degrees C exhibited the highest photocatalytic activity among the obtained SrBiO2Br samples. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:405 / 409
页数:5
相关论文
共 31 条
  • [1] Visible-light photocatalysis in nitrogen-doped titanium oxides
    Asahi, R
    Morikawa, T
    Ohwaki, T
    Aoki, K
    Taga, Y
    [J]. SCIENCE, 2001, 293 (5528) : 269 - 271
  • [2] Spontaneous Organization of Inorganic Nanoparticles into Nanovesicles Triggered by UV Light
    Bian, Tong
    Shang, Lu
    Yu, Huijun
    Perez, Maria Teresa
    Wu, Li-Zhu
    Tung, Chen-Ho
    Nie, Zhihong
    Tang, Zhiyong
    Zhang, Tierui
    [J]. ADVANCED MATERIALS, 2014, 26 (32) : 5613 - +
  • [3] A reinvestigation of quaternary layered bismuth oxyhalides of the Sillen X1 type
    Charkin, DO
    Berdonosov, PS
    Dolgikh, VA
    Lightfoot, P
    [J]. JOURNAL OF SOLID STATE CHEMISTRY, 2003, 175 (02) : 316 - 321
  • [4] ELECTROCHEMICAL PHOTOLYSIS OF WATER AT A SEMICONDUCTOR ELECTRODE
    FUJISHIMA, A
    HONDA, K
    [J]. NATURE, 1972, 238 (5358) : 37 - +
  • [5] Direct hydrolysis preparation for novel bi-based oxysalts photocatalyst Bi6O5(OH)3(NO3)5•3H2O with high photocatalytic activity
    He, Ying
    Zhang, Yihe
    Huang, Hongwei
    Tian, Na
    Luo, Yi
    [J]. INORGANIC CHEMISTRY COMMUNICATIONS, 2014, 40 : 55 - 58
  • [6] A novel Bi-based oxychloride CdBiO2Cl: Crystal structure, electronic structure and photocatalytic activity
    Huang, Fuqiang
    Wu, Jianjun
    Lin, Xinping
    Zhou, Zhen
    [J]. JOURNAL OF ALLOYS AND COMPOUNDS, 2011, 509 (03) : 764 - 768
  • [7] Ce and F Comodification on the Crystal Structure and Enhanced Photocatalytic Activity of Bi2WO6 Photocatalyst under Visible Light Irradiation
    Huang, Hongwei
    Liu, Kun
    Chen, Kai
    Zhang, Yinglei
    Zhang, Yihe
    Wang, Shichao
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2014, 118 (26) : 14379 - 14387
  • [8] Novel Bi-based iodate photocatalysts with high photocatalytic activity
    Huang, Hongwei
    He, Ying
    He, Ran
    Jiang, Xingxing
    Lin, Zheshuai
    Zhang, Yihe
    Wang, Shichao
    [J]. INORGANIC CHEMISTRY COMMUNICATIONS, 2014, 40 : 215 - 219
  • [9] Deep-Ultraviolet Nonlinear Optical Materials: Na2Be4B4O11 and LiNa5Be12B12O33
    Huang, Hongwei
    Liu, Lijuan
    Jin, Shifeng
    Yao, Wenjiao
    Zhang, Yihe
    Chen, Chuangtian
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (49) : 18319 - 18322
  • [10] Two Novel Bi-Based Borate Photocatalysts: Crystal Structure, Electronic Structure, Photoelectrochemical Properties, and Photocatalytic Activity under Simulated Solar Light Irradiation
    Huang, Hongwei
    He, Ying
    Lin, Zheshuai
    Kang, Lei
    Zhang, Yihe
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2013, 117 (44) : 22986 - 22994