Electron-enriched supramolecular PDI-SiO2 promoting PDS activation for enhanced photocatalytic advanced oxidation

The efficient activation of peroxydisulfate (PDS) for wastewater treatment remains a great challenge. Photocatalysis, which generates highly-reactive electrons and holes, shows great potential in activating PDS for effective degradation and deep mineralization. Herein, an electron-enriched PDI-SiO2...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2024-01, Vol.340, p.123262, Article 123262
Hauptverfasser: Li, Wenting, Zhang, Hanjie, Huang, Sijie, Xu, Jingyi, Liu, Liping, Li, Junshan, Jing, Jianfang, Zhu, Yongfa
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Sprache:eng
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Zusammenfassung:The efficient activation of peroxydisulfate (PDS) for wastewater treatment remains a great challenge. Photocatalysis, which generates highly-reactive electrons and holes, shows great potential in activating PDS for effective degradation and deep mineralization. Herein, an electron-enriched PDI-SiO2 photocatalyst was synthesized by covalently linking 3,4,9,10-perylene tetracarboxylic dianhydride (PTCDA) onto silicon dioxide (SiO2) to form π-π stacked supramolecular PDI layers for efficient PDS activation. The highly dispersed PDI generates electron-enriched PDI·- under visible light, promoting the rapid activation of PDS for bisphenol A (BPA) degradation. The PDI-SiO2 activated PDS system realized a high BPA degradation rate of 0.100 min−1 and a remarkable mineralization rate of 81%. Moreover, the charge separation efficiency is significantly improved since the electrons of PDI·- are captured by PDS, boosting oxidative degradation and improving the mineralization efficiency. This work developed a novel PDS activation strategy by constructing electron-enriched photocatalyst, and revealed the mechanism of photocatalytic activation and deep mineralization. [Display omitted] •A novel electron-enriched supramolecular PDI-SiO2 photocatalyst was prepared.•In visible light, the production of PDI·- greatly promotes the activation of PDS.•PDS activation promotes the separation of h+, enhancing the mineralization rate.•Multiple reactive species (h+, SO4·-,·OH,·O2-) accelerate the pollutants degradation.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2023.123262