INORGANIC MATERIALS AND CERAMIC MATRIX COMPOSITES |
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Construction of Wide-spectrum-driven Cu2(OH)2CO3/g-C3N4 Heterojunction and Its Improved Photocatalysis Towards Tetracycline Degradation: Degradation Pathways and Mechanism |
LIANG Hongyu1,*, XU Jiazhi1, LI Zheng1, LU Guang2, WANG Bin3, LI Tongyu1, LIU Yujia1
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1 School of Environmental and Safety Engineering, Liaoning Petrochemical University, Fushun 113001, Liaoning, China 2 School of Civil Engineering, Liaoning Petrochemical University, Fushun 113001, Liaoning, China 3 Lanpec Technologies Limited, Shanghai 201518, China |
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Abstract Awide-spectrum-driven Cu2(OH)2CO3/g-C3N4(Cu/g-C3N4) heterojunction catalyst was designed and the photocatalytic tetracycline degradation was investigated in the present work. The morphologies, crystal phases, optical property and so on of the as-prepared photocatalysts were characterized by means of TEM, SEM, XRD, UV-visible light spectroscopy, photoluminescence spectroscopy, etc. Experimental results indicated that the component Cu2(OH)2CO3 gave heterojunction a broad spectrum response to simulated sunlight due to its absorption of visible and near infrared light, and the consist of Z-scheme heterojunction with g-C3N4 enhanced photochemical energy conversion efficiency. Particularly, Cu/g-C3N4 (1∶4) heterojunction showed the best photocatalytic activity towards TC degradation, including an one order reaction rate constant of 0.017 6 min-1, which was 3 and 2.1 times higher than that of neat Cu2(OH)2CO3 and g-C3N4, as well as perfect photocatalytic stability. Moreover, this work hypothesized three possible photocatalytic degradation pathways of TC over Cu/g-C3N4 (1∶4) heterojunction.
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Published: 10 October 2025
Online: 2025-09-24
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