Carbon-doped anatase TiO2 nanotube array/glass and its enhanced photocatalytic activity under solar light

被引:40
|
作者
Zhao, Yun [1 ]
Li, Yan [1 ]
Wang, Cheng-Wei [1 ,2 ]
Wang, Jian [1 ]
Wang, Xiang-Qian [1 ]
Pan, Zi-Wei [1 ]
Dong, Chen [1 ]
Zhou, Feng [2 ]
机构
[1] NW Normal Univ, Coll Phys & Elect Engn, Key Lab Atom & Mol Phys & Funct Mat Gansu Prov, Lanzhou 730070, Gansu, Peoples R China
[2] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Solid Lubricat, Lanzhou 730000, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
Anatase TiO2 nanotube arrays; Carbon-doped; Photocatalytic activity; Simulated solar light; VISIBLE-LIGHT; PHOTOLUMINESCENCE; POLLUTANTS; POWDERS; ARRAYS; FILMS;
D O I
10.1016/j.solidstatesciences.2012.08.008
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
To enhance the photocatalytic activity under solar light, highly ordered TiO2 nanotube arrays (TNAs) film with anatase phase was fabricated on glass and successfully doped with carbon at various temperatures of 450-550 degrees C. The characterization results indicate that, after carbon doping, the TNAs still remained nanotubular structure with anatase phase. But their optical response shifted from UV to the visible light region and the recombination of photogenerated carriers was suppressed effectively. It is more important that the carbon-doped TNAs/glass (C-TNAs) samples exhibited high solar light photocatalytic activity, and 68%, 61% and 56% MO was photodegraded in 150 min by the C-TNAs calcined at 550, 500 and 450 degrees C, respectively. Especially, the apparent reaction rate constant of C-TNAs calcined at 550 (k, 0.065 min(-1)) with the highest activity is 3.6 times that of pristine anatase TNAs (k, 0.018 min(-1)). It is clear that carbon doping enhanced the photocatalytic activity under sunlight at optimized annealing temperature. The efficient activity could be attributed to the synergetic effects of strong visible light absorption, good crystallization, large surface, and enhanced separation of photoinduced carriers. (C) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:53 / 59
页数:7
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