物理化学学报 >> 2026, Vol. 42 >> Issue (5): 100187.doi: 10.1016/j.actphy.2025.100187

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无机/有机S型异质结构建及高级氧化技术协同光热降解抗生素研究

程强1, 李静萍1, 柯振东2,*(), 李嘉明1, 王楷1,*()   

  1. 1 湖北师范大学城市与环境学院, 黄石市土壤污染防治重点实验室, 湖北 黄石 435002
    2 湖北省生态环境厅黄石生态环境监测中心, 湖北 黄石 435000
  • 收稿日期:2025-08-21 修回日期:2025-09-14 录用日期:2025-09-14 发布日期:2026-01-23
  • 通讯作者: Email: 13807231662@163.com (柯振东)wangkai@hbnu.edu.cn (王楷)

Advanced oxidation technology synergistic photothermal degradation of antibiotics over inorganic/organic S-scheme heterojunction

Qiang Cheng1, Jingping Li1, Zhendong Ke2,*(), Jiaming Li1, Kai Wang1,*()   

  1. 1 College of Urban and Environmental Sciences, Huangshi Key Laboratory of Prevention and Control of Soil Pollution, Hubei Normal University, Huangshi 435002, Hubei Province, China
    2 Huangshi Ecological Environment Monitoring Center, Department of Ecology and Environment of Hubei Province, Huangshi 435000, Hubei Province, China
  • Received:2025-08-21 Revised:2025-09-14 Accepted:2025-09-14 Published:2026-01-23
  • Contact: Email: 13807231662@163.com (Zhendong Ke)wangkai@hbnu.edu.cn (Kai Wang)

摘要:

通过合理设计能够同时利用太阳能和高级氧化工艺(AOPs)的无机/有机催化剂,对抗生素污染物的降解具有重要前景。本研究采用超声辅助技术开发了具有氧空位的MoO2-x/g-C3N4 (MOCN) S型异质结,并将其作为太阳能驱动的过一硫酸盐(PMS)催化剂用于抗生素降解。利用密度泛函理论、飞秒瞬态吸收光谱和原位XPS分析,证实了MoO2-x与g-C3N4之间内建电场的形成以及S型异质结中的电荷转移路径。同时,MOCN异质结的氧空位和光热效应进一步加速了电子迁移速率。与原始MoO2-x和g-C3N4相比,优化后的MOCN-2催化剂在20 min内对四环素(TC)去除率达到了90.9%。连续流实验和抗菌活性实验共同验证了该催化剂在水处理应用中的实际可行性。基于上述分析,提出了TC降解的可能机制。本研究为合成S型异质结以改善废水处理提供了新策略。

关键词: 高级氧化技术, 无机/有机异质结, S型机制, 抗生素降解, 光热效应

Abstract:

The rational engineering of inorganic/organic catalysts capable of concomitant utilization of solar energy and advanced oxidation processes (AOPs) holds significant promise for the degradation of antibiotic contaminants. The study developed MoO2-x/g-C3N4 (MOCN) S-scheme heterojunctions with oxygen vacancies using an ultrasonic-assisted integration technique, employing them as solar-driven peroxymonosulfate (PMS) catalysts for the degradation of antibiotics. The formation of an internal electric field between MoO2-x and g-C3N4, along with the charge transfer pathway in the S-scheme heterojunction, was confirmed using density functional theory, femtosecond transient absorption spectroscopy, and in-situ XPS analysis. Meanwhile, the oxygen vacancy and photothermal effect of the MOCN heterojunction further accelerate the electron migration rate. The optimized MOCN-2 catalyst achieved 90.9 % tetracycline (TC) removal within 20 min compared to pristine MoO2-x and g-C3N4. Continuous flow experiments and bactericidal activity experiments together validated the practical feasibility of this catalyst for water treatment applications. The analysis above led to the proposal of a possible mechanism for TC degradation. This research brings forward new strategies for the synthesis of S-scheme heterojunctions to improve wastewater treatment.

Key words: Advanced oxidation technology, Inorganic/organic heterojunction, S-scheme mechanism, Antibiotics degradation, Photothermal effect