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Schottky junction–engineered titanium dioxide/microporous carbon composites for visible light–driven mineralization of formaldehyde under mild conditions

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dc.contributor.authorKim, Won-Ki-
dc.contributor.authorAhmadi, Younes-
dc.contributor.authorMaitlo, Hubdar Ali-
dc.contributor.authorKim, Ki-Hyun-
dc.date.accessioned2026-03-30T01:00:30Z-
dc.date.available2026-03-30T01:00:30Z-
dc.date.issued2026-01-
dc.identifier.issn0301-4797-
dc.identifier.issn1095-8630-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/211715-
dc.description.abstractA series of multifunctional composite catalysts, ATx-K, are synthesized by combining activated carbon (AC: A) and titanium dioxide (TiO2: T), followed by a potassium hydroxide (KOH: K) treatment, where the subscript x denotes the T/A mass ratio. These catalysts are then used for the photocatalytic oxidation (PCO) of formaldehyde (FA) in air. The best performing catalyst, AT9-K, achieves complete mineralization of FA into carbon dioxide with a maximum reaction rate (rmax) of 3272 μmol g−1 h−1 and an apparent quantum yield (AQY) of 6.14 % at a gas hourly space velocity (GHSV) of 400 L g−1 h−1. This enhanced activity is attributed to a dual mechanism. Firstly, the KOH treatment creates abundant surface hydroxyl (–OH) groups on AC and reduces the TiO2 bandgap from 3.21 to 2.96 eV, promoting visible-light absorption. Secondly, the formation of a Schottky junction between AC and TiO2 facilitates the separation and transfer of photogenerated electron–hole pairs. In-situ diffuse reflectance infrared Fourier transform spectroscopy confirms that the PCO of FA proceeds through dioxymethylene and formate intermediates. These findings collectively demonstrate that AT9-K is a promising and scalable photocatalyst for indoor air purification applications.-
dc.format.extent20-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD-
dc.titleSchottky junction–engineered titanium dioxide/microporous carbon composites for visible light–driven mineralization of formaldehyde under mild conditions-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.jenvman.2025.128172-
dc.identifier.scopusid2-s2.0-105023837245-
dc.identifier.wosid001636975600001-
dc.identifier.bibliographicCitationJOURNAL OF ENVIRONMENTAL MANAGEMENT, v.397, pp 1 - 20-
dc.citation.titleJOURNAL OF ENVIRONMENTAL MANAGEMENT-
dc.citation.volume397-
dc.citation.startPage1-
dc.citation.endPage20-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEnvironmental Sciences & Ecology-
dc.relation.journalWebOfScienceCategoryEnvironmental Sciences-
dc.subject.keywordPlusPHOTOCATALYTIC ACTIVITY-
dc.subject.keywordPlusCHARGE SEPARATION-
dc.subject.keywordPlusACTIVATED CARBON-
dc.subject.keywordPlusSOL-GEL-
dc.subject.keywordPlusTIO2-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusREMOVAL-
dc.subject.keywordPlusPHOTODEGRADATION-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordAuthorActivated carbon-
dc.subject.keywordAuthorTiO2-
dc.subject.keywordAuthorFormaldehyde-
dc.subject.keywordAuthorBase treatment-
dc.subject.keywordAuthorPhotocatalysis-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0301479725041489?via%3Dihub-
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