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Platinum/nitrogen-co-doped TiO2 as photocatalyst and light-free catalytic adsorbent for gaseous formaldehyde

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dc.contributor.authorLim, Daehwan-
dc.contributor.authorMaitlo, Hubdar Ali-
dc.contributor.authorYounis, Sherif A.-
dc.contributor.authorBoukhvalov, Danil W.-
dc.contributor.authorKim, Ki Hyun-
dc.contributor.authorLee, Jechan-
dc.date.accessioned2025-09-22T07:00:08Z-
dc.date.available2025-09-22T07:00:08Z-
dc.date.issued2026-01-
dc.identifier.issn0021-9797-
dc.identifier.issn1095-7103-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/208785-
dc.description.abstractPlatinum and nitrogen co-doped titanium dioxide (Pt/N-TiO<inf>2</inf>, with 1 wt% Pt and an N/Ti molar ratio of 1) has been synthesized. This Pt/N co-doping strategy creates Schottky junctions, reduces the bandgap energy (3.25 to 2.12 eV), and introduces a new energy level (N 2p). The modified catalyst exhibits dual functionality, serving as both a photocatalyst under light irradiation (λ = 365 nm, 32 W) and a light-free catalytic adsorbent against gaseous formaldehyde (FA). The Pt/N-TiO<inf>2</inf> catalysts are immobilized on ceramic bead supports, placed in a tubular reactor system, and tested under controlled operating conditions, including FA concentrations (100–500 ppm), oxygen levels (0–21%), relative humidity (RH; 0–100%), and gas flow rates (100–500 mL min−1). The Pt/N-TiO<inf>2</inf> achieves a photocatalytic oxidation efficiency of 94.2% (reaction rate of 9.24 μmol mg−1 h−1 and apparent quantum yield of 5.58%) against 200 ppm FA (100% RH). The catalyst's efficiency stems from a synergistic dual mechanism, as evidenced by molecular simulation using density functional theory. First, N doping enhances light absorption and extends the charge carrier lifetime, while the Pt as a co-catalyst promotes charge separation by acting as an electron sink. Second, the catalyst's ability to efficiently trap H<inf>2</inf>O and O<inf>2</inf> molecules also contributes to the efficient mineralization of FA through the facile generation of reactive oxygen species. This dual functionality extends to dark conditions as a catalytic adsorbent, achieving a FA removal efficiency of 78.9% with a CO<inf>2</inf> yield of 57%. In-situ diffuse reflectance infrared Fourier transform spectroscopy analysis confirms this mechanism by identifying the generation of Pt-OH hydroxylation and •O<inf>2</inf>− radicals from H<inf>2</inf>O vapor and O<inf>2</inf>, respectively. Overall, this research provides a practical guideline for constructing an advanced VOC abatement platform.-
dc.format.extent21-
dc.language영어-
dc.language.isoENG-
dc.publisherAcademic Press-
dc.titlePlatinum/nitrogen-co-doped TiO2 as photocatalyst and light-free catalytic adsorbent for gaseous formaldehyde-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.jcis.2025.138895-
dc.identifier.scopusid2-s2.0-105014800668-
dc.identifier.wosid001566736300007-
dc.identifier.bibliographicCitationJournal of Colloid and Interface Science, v.702, pp 1 - 21-
dc.citation.titleJournal of Colloid and Interface Science-
dc.citation.volume702-
dc.citation.startPage1-
dc.citation.endPage21-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.subject.keywordPlusGAS-PHASE-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusNANOCOMPOSITES-
dc.subject.keywordAuthorPt/N-TiO2 catalyst-
dc.subject.keywordAuthorVolatile organic compounds (VOCs)-
dc.subject.keywordAuthorFormaldehyde-
dc.subject.keywordAuthorCatalytic adsorption-
dc.subject.keywordAuthorPhotocatalytic degradation-
dc.subject.keywordAuthorIndoor air pollution control-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0021979725022878?via%3Dihub-
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