降级(电信)
光催化
异质结
化学
化学工程
环境化学
材料科学
计算机科学
光电子学
工程类
电信
有机化学
催化作用
作者
Qilai Chen,Ling Hu,Yingzhang Shi,Cheng Liu,Yidong Hou,Jinhong Bi,Jimmy C. Yu,Ling Wu
出处
期刊:Chemosphere
[Elsevier BV]
日期:2024-02-12
卷期号:352: 141446-141446
被引量:12
标识
DOI:10.1016/j.chemosphere.2024.141446
摘要
Heterogeneous photocatalytic degradation of antibiotic involves the activation of antibiotic molecules and the photocatalytic oxidation process. However, the simultaneous improvement of these processes is still a challenge. Herein, S-scheme heterojunctions consisted of Cu2O nanocluster with defective WO3 nanosheets were constructed for efficient photocatalytic degradation of levofloxacin (LVX). The typical CNS-5 composite (5 wt% Cu2O/WO3) achieves an optimal LVX degradation efficiency of 97.9% within 80 min. The spatial charge separation and enhancement of redox capacity were realized by the formation of S-scheme heterojunction between Cu2O and WO3. Moreover, their interfacial interaction would lead to the loss of lattice oxygen and the generation of W5+ sites. It is witnessed that the C–N of piperazine ring and CO of carboxylic acid in LVX are coordinated with W5+ sites to build the electronic bridge to activate LVX, greatly promoting the further degradation. This work highlights the important role of selective coordination activation cooperated with S-type heterojunctions for the photocatalytic degradation and offers a new view to understand the degradation of antibiotics at molecular level.
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