Efficient photocatalytic degradation of potent greenhouse gas SF6 at liquid-solid interface

Sulfur hexafluoride (SF6), widely used in industries, poses a significant threat as the strongest greenhouse gas. Current methods for degrading SF6 are hindered by high energy consumption and costs, thus there is an urgent need for a low-cost, convenient, and efficient solution. In response, we esta...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2025-04, Vol.363, p.124773, Article 124773
Hauptverfasser: Zhou, Wenhui, Zhao, Yue, Dong, Boxu, Guo, Hongran, Si, Ziqi, Ma, Fengxiang, Zhu, Shan, Zai, Jiantao, Qian, Xuefeng
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Sprache:eng
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Zusammenfassung:Sulfur hexafluoride (SF6), widely used in industries, poses a significant threat as the strongest greenhouse gas. Current methods for degrading SF6 are hindered by high energy consumption and costs, thus there is an urgent need for a low-cost, convenient, and efficient solution. In response, we established a gas-liquid-solid three-phase (GLS) system for efficient photocatalytic SF6 degradation by Bi2O2CO3, whose efficiency was approximately 20 times that of traditional gas-solid systems. Further, possible degradation mechanisms were demonstrated through the detection of material changes in three phases, respectively. Detailed studies revealed Bi2O2CO3 can in-situ form Bi2S3 heterojunction during the reaction, facilitating carrier separation. Besides, O2 can transform to ·O2− and accelerate the photodegradation process. This approach offered a novel toolbox for SF6 degradation. We predict this method will have a wider range of applications in the field of solar-powered catalytic degradation of extremely stable fluorinated pollutants at lower costs in the future. [Display omitted] •This work provides a novel photocatalyst route for SF6 degradation.•Three-phase system is designed for high-performance SF6 degradation at lower cost.•Solid-liquid interface is conducive to product transfer.•Formation of heterojunction accelerates catalytic degradation.
ISSN:0926-3373
DOI:10.1016/j.apcatb.2024.124773