Preparation of g-C3N4(Ag)/Gr/TiO2 Z-scheme photocatalyst with enhanced reduction property and the efficient degradation of rhodamine B

被引:13
|
作者
Xue, Shuai [1 ]
Li, Houfen [1 ]
Cao, Fang [1 ]
Cao, Yajie [1 ]
Yue, Xiuping [1 ]
机构
[1] Taiyuan Univ Technol, Coll Environm Sci & Engn, Taiyuan 030024, Peoples R China
基金
中国国家自然科学基金; 山西省青年科学基金; 中国博士后科学基金;
关键词
g-C3N4; TiO2; Z-scheme system; Photodegradation; Mineralization; HIGHLY EFFICIENT; WASTE-WATER; GRAPHENE OXIDE; FABRICATION; HETEROJUNCTION; PERFORMANCE; DYES; AG; DECOLORIZATION; NANOCOMPOSITES;
D O I
10.1016/j.jallcom.2021.162759
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, to enhance the mineralization of the organic dyes, the g-C3N4(Ag)/Gr/TiO2 Z-scheme photo catalyst was successfully prepared by hydrothermal method. The XRD and XPS results showed that the nanocomposite was constructed. The SEM and EDS results showed that the morphology of g-C3N4(Ag)/Gr/ TiO2 was that TiO2 nanoparticles distributed on the surface of the Gr/g-C3N4 layers. The photocatalytic performance of the prepared samples was evaluated by the photocatalytic degradation and mineralization of RhB under visible light irradiation. The degradation efficiency of RhB on g-C3N4(Ag)/Gr/TiO2 reached 99.7% within 2 h, and the kinetic rate (0.0431 min-1) was 7.1, 7.1, 2.2, 2.0 and 1.3 times higher than those of g-C3N4, TiO2, g-C3N4(Ag)/Gr, g-C3N4/TiO2, and g-C3N4/Gr/TiO2, respectively. The total organic carbon (TOC) removal results showed that the mineralization efficiency of RhB on this composite was as high as 74.5% after 2 h of reaction time. During the photocatalytic process, it was speculated that Gr acted as the electron transporter between TiO2 and g-C3N4, which reduced the recombination efficiency of photo-generated charge carriers, and silver clusters acted as an electron reservoir to accelerate the reduction reaction of photo-generated electrons on the g-C3N4 conduction band, and further improved the photocatalytic performance. (C) 2021 Elsevier B.V. All rights reserved.
引用
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页数:11
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