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dc.creatorOmymen, Waleed M.
dc.creatorEbshish, Ali S.
dc.creatorJugović, Branimir
dc.creatorTrišović, Tomislav
dc.creatorGvozdenović, Milica
dc.creatorGrgur, Branimir
dc.date.accessioned2021-03-10T13:02:22Z
dc.date.available2021-03-10T13:02:22Z
dc.date.issued2016
dc.identifier.issn0013-4686
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/3257
dc.description.abstractThe fast reaction of forced hydrolysis of iron(111) nitrate in hypochlorite solution at room temperature, leads to the formation of mainly hematite, alpha-Fe203. Successive ion adsorption and reaction (SILAR) is applied to decorate an electrochemically formed TiO2 nanotube electrode. The anodic photo electrochemical behavior of pure TiO2-NT's and modified electrodes are investigated in a sulfate containing solution at pH =9.2. It is shown that such a modification leads to an increase of anodic photoactivity, as well as that at the same current density, the photoelectrochemical cell with a modified electrode operates at a voltage lower by 0.7 V. The band gap and flat band potentials are estimated, and the structure of the band gap and possible charge transfer reactions and mechanism are discussed.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172046/RS//
dc.rightsrestrictedAccess
dc.sourceElectrochimica Acta
dc.subjectHematiteen
dc.subjectForced hydrolysisen
dc.subjectPhotoelectrochemical cellen
dc.subjectBand gapen
dc.subjectFlat band potentialen
dc.titlePhotoelectochemical behavior of TiO2-NT's modified with SILAR deposited iron oxideen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage143
dc.citation.other203: 136-143
dc.citation.rankM21
dc.citation.spage136
dc.citation.volume203
dc.identifier.doi10.1016/j.electacta.2016.04.038
dc.identifier.rcubconv_5005
dc.identifier.scopus2-s2.0-84963606979
dc.identifier.wos000376133200016
dc.type.versionpublishedVersion


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