Characterization and photocatalytic properties of N-doped BiVO4 synthesized via a sol-gel method

被引:144
作者
Wang, Min [1 ]
Liu, Qiong [1 ]
Che, Yinsheng [1 ]
Zhang, Lifang [1 ]
Zhang, Dong [1 ]
机构
[1] Shenyang Ligong Univ, Coll Environm & Chem Engn, Shenyang 110165, Peoples R China
基金
中国国家自然科学基金;
关键词
BiVO4; Photocatalytic activity; N-doped; Methyl orange solution; MONOCLINIC BIVO4; LOW-TEMPERATURE; METHYLENE-BLUE; DEGRADATION; COMPOSITE; DYE; WATER; PERFORMANCE; SURFACTANT; MORPHOLOGY;
D O I
10.1016/j.jallcom.2012.08.140
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
A N-doped BiVO4 photocatalyst with high visible light activity was synthesized by the complexing sol-gel method using citric acid as a chelate and hexamethylene tetramine (C6H12N4) as a nitrogen source. The as-prepared N-doped BiVO4 samples were characterized by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), scanning electron microscopy (SEM), specific surface area (BET) and UV-Vis diffuse reflectance spectroscopy (DRS). The photocatalytic activity was evaluated by photocatalytic degradation of methyl orange (MO) solution under visible light. This technique revealed that pure BiVO4 and all the N-doped samples were in a monoclinic phase; no peaks of any other phases or impurities were detected. Nitrogen atoms were doped into the BiVO4 lattice and filled the atomic sites of oxygen to form O-Bi-N-V-O bonds, which contributed to the appearance of the more active species V4+ and oxygen vacancies. The doped nitrogen resulted in a red shift in the absorption edge. However, the N-doping only slightly changed the morphologies and BET special surface areas of the samples. The photocatalytic activity of BiVO4 significantly depended on the N-doping content and the calcination temperature. The maximum activity was observed for the catalyst obtained via calcination at 500 degrees C, for which the molar ratio of N to Bi was 0.20. Excess N-doping decreased the light absorption. (c) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:70 / 76
页数:7
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