构建用于光降解四环素的 g-C3N4-x/MoO3 Z 型异质结

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL
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引用次数: 0

摘要

利用光催化技术降解废水中的抗生素是一项重要战略。本文合成了一种由富含缺陷的多孔 g-C3N4 和 MoO3 组成的 Z 型异质结,其对四环素(TC)的光催化降解效果显著。研究结果表明,与多孔 g-C3N4-x 相比,最佳异质结样品的降解效率提高了 2.47 倍。表征分析表明,这种显著提高归因于 Z 型异质结构和氮(N)缺陷的引入所产生的协同效应,它们共同提高了材料的电荷分离和光吸收能力。电子顺磁共振(EPR)光谱和自由基淬灭实验表明,降解的关键机制是 -O2- 和 -OH 对四环素的攻击。此外,LC-MS 研究还证明了 TC 可能的中间产物和降解途径。毒性模拟分析表明,异质结样品能有效减轻四环素溶液的毒性。这种催化剂在消除水生环境中的抗生素方面具有广阔的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Constructing g-C3N4-x/MoO3 Z-scheme heterojunction for photodegradation of tetracycline

Constructing g-C3N4-x/MoO3 Z-scheme heterojunction for photodegradation of tetracycline

Utilizing photocatalysis to degrade antibiotics in wastewater is a vital strategy. Here, a Z-scheme heterojunction was synthesized, consisting of defect-rich porous g-C3N4 and MoO3, which exhibits remarkable photocatalytic degradation of tetracycline (TC). The results revealed that the optimal heterojunction sample exhibited a 2.47-fold enhancement of degradation efficiency compared with porous g-C3N4-x. Characterization analysis shows that the significant enhancement is attributed to the synergistic effects arising from the Z-scheme heterostructure and the introduction of nitrogen (N) defects, which collectively enhance the charge separation and light absorption capabilities of the material. Electron paramagnetic resonance (EPR) spectroscopy and free radical quenching experiments indicate that the vital degradation mechanism is the assault of •O2 and •OH on tetracycline. Additionally, the LC-MS studies demonstrated possible intermediates and degradation pathway of TC. The toxicity simulation analysis revealed that the heterojunction sample effectively mitigated the toxicity of tetracycline solution. This catalyst exhibits promising potential for applications in the elimination of antibiotics from aquatic environments.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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