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揭示CeO/MnO p-n异质结增强氧物种活化以实现甲苯高效光热矿化的机理洞察。

Unveiling mechanistic insight into boosting oxygen species activation over CeO/MnO p-n heterojunction for efficient photothermal mineralization of toluene.

作者信息

Gan Guangmei, Shen Han, Cheng Qiang, Li Yuan, Zhang Gaoke

机构信息

Hubei Key Laboratory of Mineral Resources Processing and Environment, Key Laboratory of Green Utilization of Critical Non-metallic Mineral Resources, Ministry of Education, State Key Laboratory of Silicate Materials for Architectures, Wuhan University of Technology, 122 Luoshi Road, Wuhan 430070, People's Republic of China.

Hubei Key Laboratory of Mineral Resources Processing and Environment, Key Laboratory of Green Utilization of Critical Non-metallic Mineral Resources, Ministry of Education, State Key Laboratory of Silicate Materials for Architectures, Wuhan University of Technology, 122 Luoshi Road, Wuhan 430070, People's Republic of China; College of Urban and Environmental Sciences, Huangshi Key Laboratory of Prevention and Control of Soil Pollution, Hubei Normal University, Huangshi, Hubei 435002, People's Republic of China.

出版信息

J Hazard Mater. 2025 May 5;488:137423. doi: 10.1016/j.jhazmat.2025.137423. Epub 2025 Jan 26.

Abstract

The activation mechanism of oxygen species activation (including lattice oxygen and gaseous oxygen) in the photothermal catalytic reaction process is important for boosting the efficient removal of VOCs. Herein, we have successfully synthesized a p-n heterojunction photothermal catalyst CeO/MnO for exploring the activation of molecular oxygen and lattice oxygen in toluene catalytic reaction under full spectrum conditions. Various characterization tests and theoretical calculations showed that the formed composite has enhanced light absorption ability, oxygen species migration and transformation ability as well as nice redox cycles, which is conducive to the fast replenishment of surface lattice oxygen and continuous capture and activation of molecular oxygen. Meanwhile, the results of in-situ DRIFTS tests not only confirmed the enhanced activation process of surface lattice oxygen and molecular oxygen under the synergistic effect of light and heat, but also revealed the pathway and mechanism of photothermal catalytic toluene over CeO/MnO.

摘要

光热催化反应过程中氧物种(包括晶格氧和气态氧)的活化机制对于促进挥发性有机化合物(VOCs)的高效去除至关重要。在此,我们成功合成了一种p-n异质结光热催化剂CeO/MnO,用于探索全光谱条件下甲苯催化反应中分子氧和晶格氧的活化。各种表征测试和理论计算表明,所形成的复合材料具有增强的光吸收能力、氧物种迁移和转化能力以及良好的氧化还原循环,这有利于表面晶格氧的快速补充以及分子氧的持续捕获和活化。同时,原位漫反射红外傅里叶变换光谱(DRIFTS)测试结果不仅证实了在光和热的协同作用下表面晶格氧和分子氧的活化过程增强,还揭示了CeO/MnO光热催化甲苯的途径和机制。

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