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Synthesis of Self-Assembled Mesoporous ZnO Microspheres Designed for Microwave-Assisted Photocatalytic Degradation of Tetracycline. | LitMetric

Synthesis of Self-Assembled Mesoporous ZnO Microspheres Designed for Microwave-Assisted Photocatalytic Degradation of Tetracycline.

Inorg Chem

Engineering Research Center of Ministry of Education for Geological Carbon Storage and Low Carbon Utilization of Resources, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Material Sciences and Technology,

Published: October 2024


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Article Abstract

Microwave-assisted photocatalysis offers a novel approach for degrading antibiotics, while the mechanism of enhancement of microwave-induced photocatalysis remains poorly understood. In this study, tetracycline (TC) was degraded using the method of microwave-assisted photocatalysis with a ZnO catalyst, which was synthesized by the combination of hydrothermal and calcination methods. The self-assembled mesoporous ZnO catalyst exhibited superior catalytic activity in degrading TC. It is found that the degradation efficiency of TC by the ZnO catalysts with microwave-assisted photocatalysis is 4.27 times higher than that of photocatalysis alone. Of particular significance, we found that the optical absorption range of ZnO increased and the band gap decreased when microwave was introduced into the photocatalytic system. Semi-in situ photochemical tests demonstrated that more photogenerated electron-hole pairs were detected under microwave, thus further improving the photocatalytic activity of ZnO. The separation efficiency and charge transfer efficiency of photogenerated electron-hole pairs also improved due to the increase of oxygen vacancies in the synergistic effect. Meanwhile, h and ·OH were the main active species in the degradation system. The mechanism of microwave-induced photocatalysis is illustrated, and an efficient way for degrading antibiotic is provided in this work.

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http://dx.doi.org/10.1021/acs.inorgchem.4c03388DOI Listing

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