Effect of tantalum addition on anatase phase stability and photoactivity of aqueous sol-gel derived mesoporous titania

被引:52
作者
Baiju, K. V.
Shajesh, P.
Wunderlich, W.
Mukundan, P.
Kumar, S. Rajesh
Warrier, K. G. K. [1 ]
机构
[1] Natl Inst Interdisciplinary Sci & Technol, Reg Res Lab, CSIR, Mat & Mineral Div, Thiruvananthapuram 695019, Kerala, India
[2] Tokai Univ, Fac Engn, Dept Mat Sci, Kanagawa 2591292, Japan
[3] Ctr Mat Elect Technol, Hyderabad 500051, Andhra Pradesh, India
关键词
sol-gel; titanyl oxysulphate; photocatalyst; anatase; rutile;
D O I
10.1016/j.molcata.2007.06.017
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
The effect of the addition of tantalum to nanocrystalline titania matrix on the photocatalytic activity is presented. The tantalum addition increases the anatase phase stability to above 1000 degrees C by inhibiting the increase in crystallite size of titania. All the tantalum added titania compositions have higher surface area than pure titania. Transmission electron micrograph images support the reduction in crystallite size of titanium oxide in presence of tantalum. Addition of tantalum above I mole percentage increases photocatalytic activity considerably and the activity is much higher than that of commercially available Hombikat UV 100 titania. All the compositions containing tantalum have higher photoactivity than pure titania. The synergistic effect of high surface area and small crystallite size is found to be responsible for the observed photocatalytic activity rates. The aqueous sol-gel method adopted for the preparation of tantalum added titania from cheaper salt precursors and the resultant highly photoactive titania make this investigation promising for various technological applications. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:41 / 46
页数:6
相关论文
共 30 条
[1]   The design and development of highly reactive titanium oxide photocatalysts operating under visible light irradiation [J].
Anpo, M ;
Takeuchi, M .
JOURNAL OF CATALYSIS, 2003, 216 (1-2) :505-516
[2]   PHOTOCATALYTIC HYDROGENATION OF CH3CCH WITH H2O ON SMALL-PARTICLE TIO2 - SIZE QUANTIZATION EFFECTS AND REACTION INTERMEDIATES [J].
ANPO, M ;
SHIMA, T ;
KODAMA, S ;
KUBOKAWA, Y .
JOURNAL OF PHYSICAL CHEMISTRY, 1987, 91 (16) :4305-4310
[3]   Thermophoresis-assisted vapour phase synthesis of CeO2 and CexY1-xO2-δ nanoparticles [J].
Bai, W ;
Choy, KL ;
Stelzer, NHJ ;
Schoonman, J .
SOLID STATE IONICS, 1999, 116 (3-4) :225-228
[4]   HETEROGENEOUS PHOTOCATALYSIS [J].
FOX, MA ;
DULAY, MT .
CHEMICAL REVIEWS, 1993, 93 (01) :341-357
[5]   HETEROGENEOUS PHOTOCATALYTIC OXIDATION OF AROMATIC-COMPOUNDS ON TIO2 [J].
FUJIHIRA, M ;
SATOH, Y ;
OSA, T .
NATURE, 1981, 293 (5829) :206-208
[6]  
Fujishima A., 1999, TIO2 PHOTOCATALYSIS
[7]   Photoelectrochemical cells [J].
Grätzel, M .
NATURE, 2001, 414 (6861) :338-344
[8]  
Gregg S. J., 1982, ADSORPTION SURFACE A, P287
[9]   Evidence for bicarbonate formation on vacuum annealed TiO2(110) resulting from a precursor-mediated interaction between CO2 and H2O [J].
Henderson, MA .
SURFACE SCIENCE, 1998, 400 (1-3) :203-219
[10]   Photocatalytic degradation pathway of methylene blue in water [J].
Houas, A ;
Lachheb, H ;
Ksibi, M ;
Elaloui, E ;
Guillard, C ;
Herrmann, JM .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2001, 31 (02) :145-157