Hydrothermal synthesis of InVO4/Graphitic carbon nitride heterojunctions and excellent visible-light-driven photocatalytic performance for rhodamine B

被引:112
作者
Shi, Weilong [1 ]
Guo, Feng [1 ]
Chen, Jibin [2 ]
Che, Guangbo [1 ]
Lin, Xue [1 ]
机构
[1] Jilin Normal Univ, Key Lab Preparat & Applicat Environm Friendly Mat, Minist Educ, Siping 136000, Jilin Province, Peoples R China
[2] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Jiangsu, Peoples R China
关键词
C3N4; InVO4; Heterojunction; Hydrothermal method; Photocatalysis; GRAPHITE-LIKE C3N4; HYDROGEN EVOLUTION; TITANIUM-DIOXIDE; COMPOSITE PHOTOCATALYSTS; METHYL-ORANGE; TIO2; IRRADIATION; OXIDATION; WATER; CATALYSTS;
D O I
10.1016/j.jallcom.2014.05.207
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
In this work, n-type graphite-like C3N4 (denoted as g-C3N4) was fabricated and modified with p-type Indium vanadate (InVO4) to form a novel InVO4/g-C3N4 p-n heterojunction photocatalyst for the efficient photocatalytic degradation of rhodamine B (Rh B). The photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-vis diffuse reflectance spectroscopy (DRS), photoluminescence (PL) and Fourier transform infrared spectroscopy (FT-IR). The photocatalytic activities were evaluated in the degradation of Rh B aqueous solution. The results showed that the as-prepared InVO4/g-C3N4 hybrid materials displayed much higher photocatalytic activity than the pure g-C3N4 and InVO4 particles. Among them, the 30 wt% InVO4/g-C3N4 sample exhibited the highest photocatalytic activity. The visible-light photocatalytic activity enhancement of InVO4/g-C3N4 heterojunction photocatalyst could be attributed to its strong absorption in the visible region and low recombination rate of the electron-hole pairs. It was further found that the photodegradation of Rh B molecules is mainly attributed to the oxidation action of the generated O-2(is approximately equal to) radicals and partly to the oxidation process of (OH)-O-center dot radicals. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 148
页数:6
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