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通过无机-有机杂化转变原位制备Ag修饰的多孔ZnO光催化剂用于有机污染物降解和细菌灭活。

In situ fabrication of Ag decorated porous ZnO photocatalyst via inorganic-organic hybrid transformation for degradation of organic pollutant and bacterial inactivation.

作者信息

Song Min Seok, Patil Ruturaj P, Hwang In Seon, Mahadik Mahadeo A, Jang Tae-Hu, Oh Byung Taek, Chae Weon-Sik, Choi Sun Hee, Lee Hyun Hwi, Jang Jum Suk

机构信息

Division of Biotechnology, Safety, Environment, and Life Science Institute, College of Environmental and Bioresource Sciences, Jeonbuk National University, Iksan, 54596, Republic of Korea.

Analysis Research Division, Daegu Center, Korea Basic Science Institute, Daegu, 702-701, Republic of Korea.

出版信息

Chemosphere. 2023 Nov;341:140057. doi: 10.1016/j.chemosphere.2023.140057. Epub 2023 Sep 4.

DOI:10.1016/j.chemosphere.2023.140057
PMID:37673185
Abstract

In this study, in situ silver (Ag) - porous ZnO photocatalysts were synthesized via solvothermal and post-annealing treatment. The formation of the porous ZnO structure due to the removal of organic moieties from the inorganic-organic hybrids Ag-ZnS(en) during the annealing process. The optimal Ag-ZnO photocatalyst showed excellent photocatalytic degradation activity, with 95.5% orange II dye and 97.2% bisphenol A (BPA) degradation under visible light conditions. Additionally, the photocatalytic inactivation of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) led to a 97% inactivation rate after 2 h under dark conditions. Trapping experiments suggest that the superoxide anion (O) radicals are the main active species to degrade the organic dye. The improved photocatalytic dye degradation activity and inactivation of bacteria were attributed to the synergistic effect of Ag and porous ZnO structure, increased surface area, and efficiently separated the photoexcited charge carriers. This work could provide an effective strategy for the synthesis of porous structures toward organic pollutant degradation and bacterial inactivation in wastewater.

摘要

在本研究中,通过溶剂热和退火后处理合成了原位银(Ag)-多孔氧化锌光催化剂。在退火过程中,由于无机-有机杂化物Ag-ZnS(en)中有机部分的去除,形成了多孔氧化锌结构。最佳的Ag-ZnO光催化剂表现出优异的光催化降解活性,在可见光条件下,橙色II染料的降解率为95.5%,双酚A(BPA)的降解率为97.2%。此外,在黑暗条件下2小时后,大肠杆菌(E. coli)和金黄色葡萄球菌(S. aureus)的光催化失活导致失活率达到97%。捕获实验表明,超氧阴离子(O)自由基是降解有机染料的主要活性物种。光催化染料降解活性的提高和细菌的失活归因于Ag与多孔ZnO结构的协同效应、表面积的增加以及光激发电荷载流子的有效分离。这项工作可为合成多孔结构以降解废水中的有机污染物和使细菌失活提供一种有效的策略。

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