Gallium- and iodine-co-doped titanium dioxide for photocatalytic degradation of 2-chlorophenol in aqueous solution: Role of gallium

被引:33
作者
Song, Shuang [1 ]
Wang, Cheng [1 ]
Hong, Fangyue [1 ]
He, Zhiqiao [1 ]
Cai, Qiaolan [1 ]
Chen, Jianmeng [1 ]
机构
[1] Zhejiang Univ Technol, Coll Biol & Environm Engn, Hangzhou 310032, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
TiO2; Iodine; Gallium; Photocatalysis; 2-Chlorophenol; Visible light; TIO2; PHOTODEGRADATION; OXIDATION; BEHAVIOR; ANATASE; ACID; GA;
D O I
10.1016/j.apsusc.2010.11.040
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Visible-light-driven TiO2-based catalysts for the degradation of pollutants have become the focus of attention. In the present work, iodine-doped titania photocatalysts (I-TiO2) were improved by doping with gallium (Ga,I-TiO2) and the resulting physicochemical properties and photocatalytic activity were investigated. The structural properties of the catalysts were determined by X-ray diffraction, UV-vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, Brunauer-Emmett-Teller analysis and transmission electron microscopy. We found that Ga probably enters the TiO2 framework for doping levels <0.5 mol%. A further increase in Ga content probably leads to dispersal of excess Ga on the TiO2 surface. The photocatalytic activity of Ga, I-TiO2 catalysts was evaluated using 2-chlorophenol (2-CP) as a model compound under visible and UV-vis light irradiation. The results indicate that 0.5 mol% Ga loading and calcination at 400 degrees C represent optimal conditions in the calcining temperature range 400-600 degrees C and with doping levels from 0.1% to 1 mol%. The effective enhancement of 2-CP degradation might be attributed to the formation of oxygen vacancies by Ga doping, which could decrease the recombination of electron-hole pairs. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:3427 / 3432
页数:6
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