Thermodecomposition synthesis of WO3/H2WO4 heterostructures with enhanced visible light photocatalytic properties

被引:254
作者
Cao, Jing [1 ]
Luo, Bangde [1 ]
Lin, Haili [1 ]
Xu, Benyan [1 ]
Chen, Shifu [1 ]
机构
[1] Huaibei Normal Univ, Coll Chem & Mat Sci, Huaibei 235000, Anhui, Peoples R China
关键词
WO3/H2WO4; Thermodecomposition; Photocatalytic activity; Mechanism; COMPOSITE PHOTOCATALYST; EFFICIENT DECOMPOSITION; TUNGSTEN TRIOXIDES; COMPLETE OXIDATION; REACTION-MECHANISM; ORGANIC-COMPOUNDS; METHYL-ORANGE; X-RAY; WO3; TIO2;
D O I
10.1016/j.apcatb.2011.10.010
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
Novel WO3/H2WO4 heterostructures with different contents of WO3 were synthesized through a simple thermodecomposition method. Thermogravimetry and differential thermal analysis (TG-DTA), X-ray powder diffraction (XRD), Fourier transform infrared spectrometry (FT-IR), UV-vis diffuse reflectance spectroscopy (DRS) and N-2 adsorption and desorption isotherms were employed to study the structures, morphologies, optical properties and specific surface area of the as-prepared samples. Degradation of rhodamine B (RhB) was carried out to evaluate the photocatalytic activity of samples under visible light irradiation (lambda > 420 nm). WO3/H2WO4 heterostructure with 51.04 wt% WO3 presented the highest photocatalytic activity with apparent k(app) of 0.0330 min(-1). The increased photocatalytic activity of WO3/H2WO4 could be attributed to the formation of the heterojunction between WO3 and H2WO4, which suppresses the recombination of photoinduced electron-hole pairs. Moreover, the tests of radical scavengers confirmed that O-center dot(2)- and h(+) were the main reactive species for the degradation of RhB. (C) 2011 Elsevier B.V. All rights reserved.
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页码:288 / 296
页数:9
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