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Visible-light-driven photocatalytic activity of WO3/ZIF-67 S-scheme heterojunction for upgrading degradation of oxytetracycline

异质结 光催化 纳米复合材料 材料科学 降级(电信) 纳米结构 化学工程 可见光谱 热液循环 纳米技术 光电子学 催化作用 化学 计算机科学 有机化学 工程类 电信
作者
Shahram Nazari,Esrafil Asgari,Amir Sheikhmohammadi,S. Ahmad Mokhtari,Hassan Alamgholiloo
出处
期刊:Journal of environmental chemical engineering [Elsevier]
卷期号:11 (5): 110393-110393 被引量:62
标识
DOI:10.1016/j.jece.2023.110393
摘要

The S-scheme heterojunction engineering has been regarded as a promising strategy for sufficiently using photogenerated charge carriers. Therefore, how to design a suitable nanostructure for efficient photogenerated carrier transfer/separation can be the key to upgrading the photocatalytic activity. The present study was planned for the design and fabrication new type of S-scheme WO3/ZIF-67 heterojunction for the degradation of oxytetracycline (OTC) under visible light irradiation. First, the WO3 nanostructure was fabricated with the hydrothermal method. Subsequently, microcrystals ZIF-67 were grown onto WO3 nanoplate with the sol-gel method for designing a new type of WO3/ZIF-67 nanocomposite. HA–XRD pattern revealed epitaxial growth of ZIF-67 on the monoclinic α-WO3 surface. According to FESEM and TEM images, WO3 had a plate-like nanostructure with a thickness of about 90 nm that was spread heterogeneously on the surface and core of ZIF-67. The results revealed that 91.5% of OTC is degraded in 60 min of 20 W LED light following pseudo-first-order kinetics. Investigating the reaction mechanism and quenching tests indicated hydroxyl and superoxide anion radicals play a vital role in OTC degradation. The reusable ability of the prepared WO3/ZIF-67 nanocomposite was tested up to six runs with 82% removal efficiency, confirming the suitable recyclability and stability of the proposed photocatalyst. The smart strategy of designing metal organic framework-based photocatalysts provides an innovative perspective for the development of S-scheme heterojunctions for organic contamination degradation.
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