期刊
CERAMICS INTERNATIONAL
卷 40, 期 3, 页码 4631-4638出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.ceramint.2013.09.002
关键词
Semiconductors; BiVO4; Hydrothermal synthesis; X-ray diffraction; Photocatalysis
资金
- CONACYT [178895, 167018]
- SEP-PROMEP [UANL-PTC-590]
- PAICYT [IT715-11]
- Spanish Ministerio de Ciencia e Innovacion [CTQ 2008-00178]
BiVO4 photocatalyst was successfully synthesized by the hydrothermal method using Pluronic F-127 as morphology-directing agent. BiVO4 powders with a pure monoclinic phase were obtained at 80 degrees C. For optimizing the conditions of synthesis and investigate the product formation mechanism, the temperature of synthesis was systematically investigated. The structural and morphological properties of the as-synthesized BiVO4 photocatalysts were characterized by X-ray powder diffraction (XRD), and scanning electron microscopy (SEM). Nitrogen adsorption measurements (BET) were employed to analyze the specific surface area of the samples. The band gap of the as-prepared BiVO4 samples was determined from the onset of the absorption band of UV-vis diffuse reflectance spectra. The quasi-Fermi potential of electrons of the synthesized samples was determined through pH dependent photovoltage measurements. The photocatalytic activities of the as-synthesized catalysts were evaluated in the photodegradation reaction of an aqueous solution of rhodamine B under visible-light irradiation. The mechanism of formation of the as-prepared BiVO4 samples has also been proposed. (C) 2013 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据