Investigation of photocatalytic performance of CuS/Bi2WO6 and degradation pathway of RhB in water

罗丹明B 光催化 材料科学 光致发光 扫描电子显微镜 光电流 纳米棒 降级(电信) 光化学 异质结 化学工程 纳米技术 化学 催化作用 光电子学 有机化学 复合材料 工程类 电信 计算机科学
作者
Houren Zhou,Jiaxiu Guo,Ningjie Fang,Juan Liang,Ting Shen,Shandong Yuan
出处
期刊:Aqua [UWA Publishing]
卷期号:69 (2): 145-159 被引量:18
标识
DOI:10.2166/aqua.2020.121
摘要

Abstract A series of CuS/Bi2WO6 composites were synthesized by solvothermal synthesis, which showed enhanced photocatalytic activity. The as-prepared samples were characterized by X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, photoluminescence ultraviolet–visible absorption spectroscopy, transient photocurrent and EIS. The results showed that as-prepared CuS/Bi2WO6 has flower-like nano microspheres self-assembled by nanoplates and CuS nanorods are uniformly dispersed on its surface. The CuS/Bi2WO6 forms heterojunctions between CuS and Bi2WO6 and shows a wide light response range and a strong light response intensity. The CuS/Bi2WO6 exhibits a better Rhodamine B (RhB) degradation effect than pure Bi2WO6 and CuS, and it can degrade 90% RhB in 50 min and achieve complete degradation in 70 min under Xe lamp irradiation. The CuS/Bi2WO6 has photocatalytic activity in a low pH environment and good stability. The formation of a heterojunction between CuS and Bi2WO6 can effectively separate photo-generated electrons and holes, greatly improving the photocatalytic activity. In the CuS/Bi2WO6-RhB reaction system, O2− is the main active species, and it can rapidly remove the ethyl group from the amino group linked to benzene rings to achieve the N-de-ethylation reaction in the process of RhB degradation. The N-de-ethylated products are simultaneously degraded to small organic molecules and even mineralized into CO2 and H2O.
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