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Photogeneration of singlet oxygen catalyzed by hexafluoroisopropanol for selective degradation of dyes

Singlet oxygen ((1)O(2)) shows great potential for selective degradation of dyes in environmental remediation of wastewater. In this study, we showcased that (1)O(2) can be effectively generated from an anion complex composed of deprotonated hexafluoroisopropanol anion ([HFIP(-H)](‒)) with hydropero...

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Detalles Bibliográficos
Autores principales: Han, Jia, Wang, Lei, Cao, Wenjin, Yuan, Qinqin, Zhou, Xiaoguo, Liu, Shilin, Wang, Xue-Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374460/
https://www.ncbi.nlm.nih.gov/pubmed/37520730
http://dx.doi.org/10.1016/j.isci.2023.107306
Descripción
Sumario:Singlet oxygen ((1)O(2)) shows great potential for selective degradation of dyes in environmental remediation of wastewater. In this study, we showcased that (1)O(2) can be effectively generated from an anion complex composed of deprotonated hexafluoroisopropanol anion ([HFIP(-H)](‒)) with hydroperoxyl radical (⋅HO(2)) via ultraviolet (UV) photodetachment. Electronic structure calculations and cryogenic negative ion photoelectron spectroscopy unveil critical proton transfer upon complex formation and electron ejection, effectively photoconverting prevalent triplet ground state (3)O(2) to long-lived excited (1)O(2), stabilized by nearby HFIP. Inspired by this spectroscopic study, a novel “photogeneration” strategy is proposed to produce (1)O(2) with the incorporation of atmospheric O(2) and HFIP, acting as a catalyst. Conceptually, the designed catalytic cycle upon UV irradiation and electron injection is able to achieve different degradations of dye molecules in a controllable fashion from decolorization to complete mineralization, shedding new light on potential water purification.