丝绒球状S-Scheme FeOOH/ZnMn2O4异质结在可见光下降解四环素的研究

IF 2.3 4区 化学 Q3 CHEMISTRY, PHYSICAL
Guangling Zuo, Hongyong Ye, Luyao Zhao, Jinping Lai, Jia Du, Xin Ding
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引用次数: 0

摘要

为解决ZnMn2O4 (ZMO)光催化剂中电子-空穴对复合率高、量子效率低的问题,采用浸染法将FeOOH (FOH)负载在ZMO上,构建了S-scheme FeOOH/ZnMn2O4 (FOH/ZMO)异质结复合材料。采用各种表征方法对FOH/ZMO的微观结构、光电性能和晶体结构进行了系统表征。通过对模拟废水中盐酸四环素(TC)的降解,研究了FOH/ZMO的光催化活性。表征结果表明,FOH/ZMO复合材料保留了ZMO的四方尖晶石结构,形成了独特的“丝绒球状”形貌。此外,FOH被均匀而紧密地加载在ZMO表面,并在两种材料的界面处成功构建了s型异质结结构。该异质结通过优化界面电荷转移路径、保留高活性氧化还原位点、促进载流子定向分离等协同作用,显著增强了FOH/ZMO的光催化活性。猝灭实验进一步证实了超氧自由基(·O2−)和羟基自由基(·OH)是降解过程中的主要活性物质。在降解性能测试中,FOH/ZMO表现出优异的可见光催化活性。在催化剂投加量为0.6 g/L、TC初始浓度为20 mg/L、pH为7的条件下,FOH/ZMO中FOH投加量为6 wt%时,降解效果最佳,可见光照射100 min后降解效率为98.29%。值得注意的是,该催化剂表现出优异的磁可分离性。经过4次循环使用,该催化剂仍能保持93.79%的降解效率,具有良好的稳定性。该研究不仅为zmo基光催化剂的设计提供了一种新的策略,而且为s型异质结材料的开发和实际应用提供了有价值的见解。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Velvet-Ball-Like S-Scheme FeOOH/ZnMn2O4 Heterojunction for Degradation of Tetracycline Under Visible-Light Irradiation

Velvet-Ball-Like S-Scheme FeOOH/ZnMn2O4 Heterojunction for Degradation of Tetracycline Under Visible-Light Irradiation

To address the issues of high electron-hole pair recombination rate and low quantum efficiency in the ZnMn2O4 (ZMO) photocatalyst, an S-scheme FeOOH/ZnMn2O4 (FOH/ZMO) heterojunction composite was constructed by loading FeOOH (FOH) onto ZMO using an impregnation method. The microstructure, optoelectronic properties, and crystal structure of FOH/ZMO were systematically characterized using various characterization methods. The photocatalytic activity of FOH/ZMO was investigated by degrading tetracycline hydrochloride (TC) in simulated wastewater. Characterization results revealed that the FOH/ZMO composite material retained the tetragonal spinel structure of ZMO and formed a unique “velvet-ball-like” morphology. Moreover, FOH was uniformly and closely loaded on the surface of ZMO, and an S-scheme heterojunction structure was successfully constructed at the interface between the two materials. Through the synergistic effects of optimizing the interfacial charge transfer path, retaining highly active redox sites, and promoting the directional separation of carriers, this heterojunction significantly enhanced the photocatalytic activity of FOH/ZMO. Quenching experiments further confirmed that superoxide radicals (·O2) and hydroxyl radicals (·OH) were the primary reactive species in the degradation process. During the degradation performance tests, FOH/ZMO demonstrated outstanding visible-light catalytic activity. The optimal performance was achieved with 6 wt% FOH loading in FOH/ZMO under conditions of 0.6 g/L catalyst dosage, 20 mg/L initial TC concentration, and pH 7, reaching a degradation efficiency of 98.29% after 100 min of visible-light irradiation. Notably, the catalyst demonstrated excellent magnetic separability. After 4 cycles of use, the catalyst could still maintain a degradation efficiency of 93.79%, demonstrating sound stability. This study not only proposes a novel strategy for designing ZMO-based photocatalysts but also provides valuable insights into the development and practical applications of S-scheme heterojunction materials.

Graphical Abstract

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来源期刊
Catalysis Letters
Catalysis Letters 化学-物理化学
CiteScore
5.70
自引率
3.60%
发文量
327
审稿时长
1 months
期刊介绍: Catalysis Letters aim is the rapid publication of outstanding and high-impact original research articles in catalysis. The scope of the journal covers a broad range of topics in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis. The high-quality original research articles published in Catalysis Letters are subject to rigorous peer review. Accepted papers are published online first and subsequently in print issues. All contributions must include a graphical abstract. Manuscripts should be written in English and the responsibility lies with the authors to ensure that they are grammatically and linguistically correct. Authors for whom English is not the working language are encouraged to consider using a professional language-editing service before submitting their manuscripts.
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