Investigation on the Different Photocatalytic Properties of Bismuths Oxychlorides: Bi12O15Cl6 versus Bi3O4Cl versus BiOCl

被引:24
作者
Gu, Wenhao [1 ]
Xu, Juan [1 ]
Teng, Fei [1 ]
Ul Abideen, Zain [1 ]
机构
[1] Nanjing Univ Informat Sci & Technol, Jiangsu Engn & Technol Res Ctr Environm Cleaning, Jiangsu Collaborat Innovat Ctr Atmospher Environm, Jiangsu Key Lab Atmospher Environm Monitoring & P, 219 Ningliu Rd, Nanjing 210044, Jiangsu, Peoples R China
基金
美国国家科学基金会;
关键词
Bi12O15Cl6; band gap; charge separation; crystal structure; surface area; PLASMONIC ABSORPTION; DOPED TIO2; DEGRADATION; PHOTOLUMINESCENCE; PERFORMANCE; ARRAYS; BANDS; BR;
D O I
10.1002/slct.201801318
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It is found that under UV light (lambda <= 420 nm) irradiation, the photo activity of Bi12O15Cl6 is 1 times higher than that of BiOCl for the degradation of methyl orange (MO), which is mainly attributed to the wider light absorption range and higher charge separation efficiency, but rather than BET area (4.5m(2)g(-1)vs. 15.9m(2)g(-1)). Under visible light (lambda>420nm) irradiation, the photo activity of Bi12O15Cl6 is 3.3 times higher than that of Bi3O4Cl for the degradation of MO, which is mainly attributed to the higher charge separation efficiency and higher BET area (0.4m(2)g(-1)), rather than light absorption range (2.86 vs. 2.63eV). Under UV light irradiation (lambda <= 420nm), the photo activity of BiOCl is 1 times higher than that of Bi3O4Cl for the degradation of MO, which is mainly ascribed to the higher BET area (15.9 vs. 0.4m(2)g(-1)) and the higher charge separation efficiency, rather than light absorption (3.4 vs. 2.63eV). This work suggests that various affecting factors should be fully investigated to correctly understand the photochemical properties of a photocatalyst.
引用
收藏
页码:10721 / 10726
页数:6
相关论文
共 35 条
[1]  
Dolgikh V. A., 1992, RUSS J INORG CHEM, V37, P488
[2]   Synthesis and structure of CaBiO2Cl and SrBiO2Cl: New distorted variants of the Sillen X1 structure [J].
Fray, SM ;
Milne, CJ ;
Lightfoot, P .
JOURNAL OF SOLID STATE CHEMISTRY, 1997, 128 (01) :115-120
[3]  
He A., 2006, SCRIPTA MATER, V54, P1221
[4]   PHOTOCHEMISTRY OF COLLOIDAL METAL SULFIDES .5. FLUORESCENCE AND CHEMICAL-REACTIONS OF ZNS AND ZNS/CDS CO-COLLOIDS [J].
HENGLEIN, A ;
GUTIERREZ, M .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1983, 87 (10) :852-858
[5]   Two Novel Bi-Based Borate Photocatalysts: Crystal Structure, Electronic Structure, Photoelectrochemical Properties, and Photocatalytic Activity under Simulated Solar Light Irradiation [J].
Huang, Hongwei ;
He, Ying ;
Lin, Zheshuai ;
Kang, Lei ;
Zhang, Yihe .
JOURNAL OF PHYSICAL CHEMISTRY C, 2013, 117 (44) :22986-22994
[6]   Dual Cocatalysts Loaded Type I CdS/ZnS Core/Shell Nanocrystals as Effective and Stable Photocatalysts for H2 Evolution [J].
Huang, Lei ;
Wang, Xiuli ;
Yang, Jinhui ;
Liu, Gang ;
Han, Jingfeng ;
Li, Can .
JOURNAL OF PHYSICAL CHEMISTRY C, 2013, 117 (22) :11584-11591
[7]   Efficient visible light-sensitive photocatalysts:: Grafting Cu(II) ions onto TiO2 and WO3 photocatalysts [J].
Irie, Hiroshi ;
Miura, Shuhei ;
Kamiya, Kazuhide ;
Hashimoto, Kazuhito .
CHEMICAL PHYSICS LETTERS, 2008, 457 (1-3) :202-205
[8]   Review of photoluminescence performance of nano-sized semiconductor materials and its relationships with photocatalytic activity [J].
Jing Liqiang ;
Qu Yichun ;
Wang Baiqi ;
Li Shudan ;
Jiang Baojiang ;
Yang Libin ;
Fu Wei ;
Fu Honggang ;
Sun Jiazhong .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2006, 90 (12) :1773-1787
[9]   Relationships of surface oxygen vacancies with photoluminescence and photocatalytic performance of ZnO nanoparticles [J].
Jing, LQ ;
Yuan, FL ;
Hou, HG ;
Xin, BF ;
Cai, WM ;
Fu, HG .
SCIENCE IN CHINA SERIES B-CHEMISTRY, 2005, 48 (01) :25-30
[10]   In situ formation of an oxygen-evolving catalyst in neutral water containing phosphate and Co2+ [J].
Kanan, Matthew W. ;
Nocera, Daniel G. .
SCIENCE, 2008, 321 (5892) :1072-1075