Direct Z-scheme Bi2O2CO3/porous g-C3N4 heterojunction for improved photocatalytic degradation performance

被引:23
作者
Duan, Yongzheng [1 ,2 ]
Li, Jing [1 ,2 ]
Li, Yuejin [1 ,2 ]
Shang, Xili [1 ,2 ]
Jia, Dongmei [1 ,2 ]
Li, Changhai [1 ,2 ]
机构
[1] Binzhou Univ, Dept Chem Engn & Safety, Binzhou 256603, Peoples R China
[2] Engn Res Ctr Wastewater Resource Shandong Prov, Binzhou 256603, Peoples R China
关键词
Bi2O2CO3; Porous g-C3N4 nanosheets; Photocatalytic; Simulated solar light illumination; IN-SITU FABRICATION; MOLECULAR-OXYGEN ACTIVATION; GRAPHITIC CARBON NITRIDE; RHODAMINE-B; COMPOSITE PHOTOCATALYSTS; HYDROTHERMAL SYNTHESIS; POLLUTANT DEGRADATION; HYDROGEN EVOLUTION; DOPED G-C3N4; LIGHT;
D O I
10.1016/j.jtice.2019.08.013
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this study, a series of direct Z-scheme bismuth subcarbonate (Bi2O2CO3)/porous graphitic carbon nitride (g-C3N4) composites was prepared by using a simple two-stage template free process. The structure, morphology, textural and optical properties were characterized by X-ray diffraction, N-2-physisorption, transmission electron microscopy, Fourier transform infrared spectra, X-ray photoelectron spectroscopy, UV-vis analysis and photoluminescence spectroscopy. The catalytic properties of Bi2O2CO3/porous g-C3N4 composites were assessed using tetracycline hydrochloride under simulated solar light illumination. When the loading amount of Bi2O2CO3 was 2 wt%, the composite showed the highest catalytic activity, which was 5.1 times that of porous g-C3N4 nanosheets (PCNS). The enhanced photocatalytic properties of Bi2O2CO3/porous g-C3N4 may be attributed to the formation of heterojunction between Bi2O2CO3 and PCNS, resulting in the effective separation of photogenerated carriers and enhanced absorption of visible light. Furthermore, the novel photocatalyst had an excellent catalytic stability and could be recycled for five times without distinct loss of catalytic activity. (C) 2019 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:74 / 85
页数:12
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