Micro-arc oxidation of TC4 substrates to fabricate TiO2/YAG:Ce3+ compound films with enhanced photocatalytic activity

被引:39
作者
Jiang, Xudong [1 ,2 ]
Wang, Yongqian [1 ,2 ,3 ]
Pan, Chunxu [1 ,2 ]
机构
[1] Wuhan Univ, Dept Phys, Minist Educ, Wuhan 430072, Hubei, Peoples R China
[2] Wuhan Univ, Key Lab Acoust & Photon Mat & Devices, Minist Educ, Wuhan 430072, Hubei, Peoples R China
[3] China Univ Geosci, Minist Educ, Engn Res Ctr Nanogeomat, Wuhan 430074, Peoples R China
关键词
TiO2 photocatalytic film; YAG:Ce3+ semiconductor; Micro-arc oxidation; Compounded film; TIO2 NANOTUBE ARRAYS; TITANIUM-DIOXIDE; ANODIZATION; GROWTH;
D O I
10.1016/j.jallcom.2010.12.131
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
This paper introduces a process for "in situ" preparing TiO2 photocatalytic film compounded with YAG:Ce3+ semiconductor upon titanium alloy by using micro-arc oxidation (MAO). The surface morphology, chemical compositions, phase structures and photocatalytic properties of the films were characterized and measured by field emission gun scanning electron microscope (FEG-SEM), energydispersive X-ray spectrometer (EDS), X-ray diffractometer (XRD), electro-chemical workstation and UV-vis spectrophotometer. The results show that the YAG:Ce3+ semiconductor particles which were added in the electrolyte had been homogenously compounded within the TiO2 film during MAO. Compared with the pure TiO2 film, the compounded film exhibited much larger specific surface area, stronger absorption in the visible light and higher photo-generated current density, which improves the photocatalytic property markedly. It is expected that MAO will provide a simple, economic and promising approach for preparing a superior photocatalytic TiO2 film. Crown Copyright (c) 2010 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:L137 / L141
页数:5
相关论文
共 20 条
[1]   How photocatalytic activity of the MAO-grown TiO2 nano/micro-porous films is influenced by growth parameters? [J].
Bayati, M. R. ;
Golestani-Fard, F. ;
Moshfegh, A. Z. .
APPLIED SURFACE SCIENCE, 2010, 256 (13) :4253-4259
[2]   Photoinduced reactivity of titanium dioxide [J].
Carp, O ;
Huisman, CL ;
Reller, A .
PROGRESS IN SOLID STATE CHEMISTRY, 2004, 32 (1-2) :33-177
[3]   Hierarchically organized nanostructured TiO2 for photocatalysis applications [J].
Di Fonzo, F. ;
Casari, C. S. ;
Russo, V. ;
Brunella, M. F. ;
Li Bassi, A. ;
Bottani, C. E. .
NANOTECHNOLOGY, 2009, 20 (01)
[4]   Visible light photocatalytic activities of TiO2 nanocrystals doped with upconversion luminescence agent [J].
Feng, Guangjian ;
Liu, Suwen ;
Xiu, Zhiliang ;
Zhang, Yin ;
Yu, Jiaoxian ;
Chen, Yonggang ;
Wang, Ping ;
Yu, Xiaojun .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (35) :13692-13699
[5]   ELECTROCHEMICAL PHOTOLYSIS OF WATER AT A SEMICONDUCTOR ELECTRODE [J].
FUJISHIMA, A ;
HONDA, K .
NATURE, 1972, 238 (5358) :37-+
[6]   An Efficient Method To Form Heterojunction CdS/TiO2 Photoelectrodes Using Highly Ordered TiO2 Nanotube Array Films [J].
Gao, Xian-Feng ;
Sun, Wen-Tao ;
Hu, Zhu-Dong ;
Ai, Guo ;
Zhang, Yi-Ling ;
Feng, Shi ;
Li, Fei ;
Peng, Lian-Mao .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (47) :20481-20485
[7]   Influence of fluorine on the structure and photocatalytic activity of TiO2 film prepared in tungstate-electrolyte via micro-arc oxidation [J].
He, J. ;
Cai, Q. Z. ;
Ji, Y. G. ;
Luo, H. H. ;
Li, D. J. ;
Yu, B. .
JOURNAL OF ALLOYS AND COMPOUNDS, 2009, 482 (1-2) :476-481
[8]   Enhanced photoactivity of silica-embedded titania particles prepared by sol-gel process for the decomposition of trichloroethylene [J].
Jung, KY ;
Park, SB .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2000, 25 (04) :249-256
[9]   Preparation and photocatalytic activity of TiO2 nanotube powders derived by a rapid anodization process [J].
Liao, Yulong ;
Que, Wenxiu .
JOURNAL OF ALLOYS AND COMPOUNDS, 2010, 505 (01) :243-248
[10]   The structure and photocatalytic studies of N-doped TiO2 films prepared by radio frequency reactive magnetron sputtering [J].
Liu, Baoshun ;
Wen, Liping ;
Zhao, Xiujian .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2008, 92 (01) :1-10