近中性条件下协同去除氟喹诺酮类抗生素的光热效应和芬顿类氧化作用

IF 3 4区 化学 Q3 CHEMISTRY, PHYSICAL ChemPhotoChem Pub Date : 2024-07-01 DOI:10.1002/cptc.202400103
Lanya Jiao, Dr. Jiao Meng, Shujun Wang, Prof. Xuan Sun
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引用次数: 0

摘要

研究人员构建了富含缺陷的介孔氧化铜纳米片(NSs),以研究光-芬顿催化和光热-芬顿催化在降解氟喹诺酮类抗生素(FQ)中的协同作用。氧空位提供了丰富的活性位点,可结合底物并抑制电荷重组,从而提高芬顿催化活性。在 CuO NS 上实现了光激发和光热转换两种不同的光谱选择功能,从而协同促进了 Fenton 活性。可见光诱导光激发以促进 Cu+ 和 -OH 的生成,而近红外光则转化为热量以促进电荷分离和加速介质传输。最终,作为一个单元催化剂系统,CuO NS 集成了路易斯酸催化、类芬顿催化和光热催化,可在近中性条件下快速、持续地降解抗生素。
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Photothermal Effect and Fenton-Like Oxidation for Synergistic Removal of Fluoroquinolones Antibiotics under Near-Neutral Conditions

Defect-enriched mesoporous CuO nanosheets (NSs) were constructed to investigate the cooperative photo-Fenton and photothermal-Fenton catalysis on degradation of fluoroquinolones (FQ) antibiotics. The oxygen vacancies provide abundant active sites to bind the substrates and inhibit charge recombination, by all means to enhance Fenton-like activity. Two disparate spectral selective functions of photoexcitation and photothermal conversion were achieved on CuO NS, which to promote the Fenton activity synergistically. Visible light induced photoexcitation to facilitate the generation of Cu+ and ⋅OH, while near-infrared light converted into heat to promote charge separation and accelerate medium transport. Ultimately, as a unitary catalyst system, the CuO NS integrated the Lewis acid catalysis, Fenton-like catalysis and photothermal catalysis that rapidly and sustainably degraded antibiotics under near-neutral conditions.

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来源期刊
ChemPhotoChem
ChemPhotoChem Chemistry-Physical and Theoretical Chemistry
CiteScore
5.80
自引率
5.40%
发文量
165
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