Mixed-calcination synthesis of CdWO4/g-C3N4 heterojunction with enhanced visible-light-driven photocatalytic activity

被引:69
|
作者
Tian, Na [1 ]
Huang, Hongwei [1 ]
Zhang, Yihe [1 ]
机构
[1] China Univ Geosci, Natl Lab Mineral Mat, Sch Mat Sci & Technol, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Beijing 100083, Peoples R China
关键词
g-C3N4; CdWO4; Visible-light irradiation; Heterostructures; Photocatalytic activity; GRAPHITIC CARBON NITRIDE; HYDROGEN EVOLUTION; COMPOSITE PHOTOCATALYSTS; CRYSTAL-STRUCTURE; DOPED G-C3N4; PERFORMANCE; EFFICIENT; PHOTODEGRADATION; DEGRADATION; TIO2;
D O I
10.1016/j.apsusc.2015.07.154
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
CdWO4/g-C3N4 composite photocatalysts have been successfully synthesized by a simple mixed-calcination method for the first time. X-ray diffraction (XRD), Fourier transforms infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM) and diffuse reflection spectroscopy (DRS) were carried out to analyze the crystal structure, morphology and optical property of the as-prepared samples. The photocatalytic experiments on rhodamine B (RhB) degradation showed that the 1:10 CdWO4/g-C3N4 photocatalyst exhibited the highest efficiency for degradation of RhB under visible light (lambda > 420 nm), which was almost 1.6 and 54.6 times as high as those of the pure g-C3N4 and CdWO4, respectively. This enhancement in visible-light photocatalytic activity of CdWO4/g-C3N4 composite should be attributed to the matchable band structures and interfacial interaction between CdWO4 and g-C3N4, resulting in the efficient separation and transfer of photogenerated charge carriers. It was corroborated by the photoluminescence spectroscopy (PL) and active species trapping experiments. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:343 / 349
页数:7
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