Solar-matched S-scheme ZnO/g-C3N4 for visible light-driven paracetamol degradation

dc.contributorAalto-yliopistofi
dc.contributorAalto Universityen
dc.contributor.authorHassan, Fahaden_US
dc.contributor.authorBacker, Sumina Namboorimadathilen_US
dc.contributor.authorAlmanassra, Ismail W.en_US
dc.contributor.authorAli Atieh, Muatazen_US
dc.contributor.authorElbahri, Madyen_US
dc.contributor.authorShanableh, Abdallahen_US
dc.contributor.departmentDepartment of Chemistry and Materials Scienceen
dc.contributor.groupauthorNanochemistry and Nanoengineeringen
dc.contributor.organizationUniversity of Sharjahen_US
dc.date.accessioned2024-08-06T07:34:21Z
dc.date.available2024-08-06T07:34:21Z
dc.date.issued2024-05-28en_US
dc.descriptionPublisher Copyright: © The Author(s) 2024.
dc.description.abstractIn pursuit of an efficient visible light driven photocatalyst for paracetamol degradation in wastewater, we have fabricated the ZnO/g-C3N4 S-Scheme photocatalysts and explored the optimal percentage to form a composite of graphitic carbon nitride (g-C3N4) with zinc oxide (ZnO) for enhanced performance. Our study aimed to address the urgent need for a catalyst capable of environmentally friendly degradation of paracetamol, a common pharmaceutical pollutant, using visible light conditions. Here, we tailored the band gap of a photocatalyst to match solar radiation as a transformative advancement in environmental catalysis. Notably, the optimized composite, containing 10 wt.% g-C3N4 with ZnO, demonstrated outstanding paracetamol degradation efficiency of 95% within a mere 60-min exposure to visible light. This marked enhancement represented a 2.24-fold increase in the reaction rate compared to lower wt. percentage composites (3 wt.% g-C3N4) and pristine g-C3N4. The exceptional photocatalytic activity of the optimized composite can be attributed to the band gap narrowing that closely matched the maximum solar radiation spectrum. This, coupled with efficient charge transfer mechanisms through S-scheme heterojunction formation and an abundance of active sites due to increased surface area and reduced particle size, contributed to the remarkable performance. Trapping experiments identified hydroxyl radicals as the primary reactive species responsible for paracetamol photoreduction. Furthermore, the synthesized ZnO/g-C3N4 composite exhibited exceptional photostability and reusability, underscoring its practical applicability. Thus, this research marks a significant stride towards the development of an effective and sustainable visible light photocatalyst for the removal of pharmaceutical contaminants from aquatic environments.en
dc.description.versionPeer revieweden
dc.format.extent16
dc.format.mimetypeapplication/pdfen_US
dc.identifier.citationHassan, F, Backer, S N, Almanassra, I W, Ali Atieh, M, Elbahri, M & Shanableh, A 2024, 'Solar-matched S-scheme ZnO/g-C 3 N 4 for visible light-driven paracetamol degradation', Scientific Reports, vol. 14, no. 1, 12220. https://doi.org/10.1038/s41598-024-60306-0en
dc.identifier.doi10.1038/s41598-024-60306-0en_US
dc.identifier.issn2045-2322
dc.identifier.otherPURE UUID: 306570ec-1fc9-45db-9ff3-25b4f3f88220en_US
dc.identifier.otherPURE ITEMURL: https://research.aalto.fi/en/publications/306570ec-1fc9-45db-9ff3-25b4f3f88220en_US
dc.identifier.otherPURE FILEURL: https://research.aalto.fi/files/150888297/CHEM_Hassan_et_al_Solar-matched_S-scheme_2024_Scientific_Reports.pdf
dc.identifier.urihttps://aaltodoc.aalto.fi/handle/123456789/129628
dc.identifier.urnURN:NBN:fi:aalto-202408065201
dc.language.isoenen
dc.publisherNature Publishing Group
dc.relation.ispartofseriesScientific Reportsen
dc.relation.ispartofseriesVolume 14, issue 1en
dc.rightsopenAccessen
dc.subject.keywordBand alignmenten_US
dc.subject.keywordDegradation pathwayen_US
dc.subject.keywordGraphitic carbon nitrideen_US
dc.subject.keywordPhotodegradationen_US
dc.subject.keywordZinc oxideen_US
dc.titleSolar-matched S-scheme ZnO/g-C3N4 for visible light-driven paracetamol degradationen
dc.typeA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessäfi
dc.type.versionpublishedVersion

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