Issue 32, 2021

Construction of a novel Cu2(OH)3F/g-C3N4 heterojunction as a high-activity Fenton-like catalyst driven by visible light

Abstract

Inhibiting the competitive effect of O2 in copper-based Fenton reagents and improving the photogenerated electron–hole pair separation of g-C3N4 are the focus of current research. In this article, Cu2(OH)3F was successfully synthesized by the hydrothermal method and combined with g-C3N4via a simple mix-load method. The composite catalyst (CFO/CN) exhibits an excellent catalytic effect for degradation of dyes in wastewater in a photo-assisted Fenton-like system. Among the samples, CFO-40 shows the best catalytic effect, and the reaction rate is 4.67 times and 17.5 times as high as that of pure g-C3N4 and Cu2(OH)3F under the same conditions, respectively. The enhancement of the photocatalytic activity is mainly due to the formation of a photo-assisted Fenton-like effect between Cu2(OH)3F and g-C3N4, which not only accelerates the separation and transfer of photogenerated carriers, but also promotes the conversion and circulation of Cu(II) and Cu(I). In addition, it has been proved that the material has a wide pH range. The continuous degradation experiment shows that the material has superior stability and recyclability. Additionally, it is confirmed that ˙OH, O2˙, and h+ all contribute to the reaction, among which ˙OH plays a major role. This research introduces a new member to the family of photo-assisted Fenton-like technologies.

Graphical abstract: Construction of a novel Cu2(OH)3F/g-C3N4 heterojunction as a high-activity Fenton-like catalyst driven by visible light

Supplementary files

Article information

Article type
Paper
Submitted
29 Apr 2021
Accepted
06 Jul 2021
First published
27 Jul 2021

New J. Chem., 2021,45, 14458-14468

Construction of a novel Cu2(OH)3F/g-C3N4 heterojunction as a high-activity Fenton-like catalyst driven by visible light

L. Wang, Y. Lin, W. Guo, Y. Yang, R. Zhang, Y. Zhai and Y. Liu, New J. Chem., 2021, 45, 14458 DOI: 10.1039/D1NJ02091A

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