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dc.creatorŠalipur, Hristina
dc.creatorLončarević, Davor
dc.creatorDostanić, Jasmina
dc.creatorLikozar, Blaž
dc.creatorPrašnikar, Anže
dc.creatorManojlović, Dragan D.
dc.date.accessioned2022-06-01T09:41:27Z
dc.date.available2022-06-01T09:41:27Z
dc.date.issued2022
dc.identifier.issn0360-3199
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0360319922006036
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/5207
dc.description.abstractIn this work hydrogen production activity of a series of the nickel-loaded, nitrogen-doped titanate-based photocatalysts was tested by water splitting reaction in isopropanol-water mixture. The utilization of ammonium ions during catalyst synthesis and subsequent calcination led to successful formation of nitrogen-doped nanotubular titanates with lower sodium content, favored titanate-to-anatase transformation and enhanced textural, morphological and interface properties. The photocatalytic tests revealed that hydrogen production activity of nitrogen-doped titanates is ten times higher compared to nitrogen-free titanates. The presence of highly photoactive anatase phase, improved anatase crystallinity and lower amount of sodium ions are found to be decisive factors for increased hydrogen production activity. The optimal nickel loading was determined and the variation in photocatalytic activity with reduction temperature was explained. Stability tests gave quantitative analysis of the effects of reaction products accumulation and photocorrosion on the catalyst deactivation.
dc.languageen
dc.publisherElsevier
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200026/RS//
dc.relationCOST Action [Grant number: 18234]
dc.rightsrestrictedAccess
dc.sourceInternational Journal of Hydrogen Energy
dc.subjectDye
dc.subjectHydrogen
dc.subjectNickel
dc.subjectPhotocatalysis
dc.subjectTiO
dc.subjectWater
dc.titleNickel-loaded nitrogen-doped titanate nanostructured catalysts for solar-light driven hydrogen evolution and environmental remediation
dc.typearticleen
dc.rights.licenseARR
dc.citation.volume47
dc.citation.issue26
dc.citation.spage12937
dc.citation.epage12952
dc.identifier.wos00078346700001
dc.identifier.doi10.1016/j.ijhydene.2022.02.054
dc.citation.rankM21~
dc.type.versionpublishedVersion
dc.identifier.scopus2-s2.0-85125470996


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