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dc.creatorOmymen, Waleed M.
dc.creatorEbshish, Ali S.
dc.creatorJugović, Branimir
dc.creatorTrišović, Tomislav
dc.creatorGvozdenović, Milica M.
dc.creatorGrgur, Branimir
dc.date.accessioned2018-01-30T10:09:11Z
dc.date.available2018-01-30T10:09:11Z
dc.date.issued2016
dc.identifier.issn0013-4686
dc.identifier.urihttp://dais.sanu.ac.rs/123456789/15997
dc.description.abstractThe fast reaction of forced hydrolysis of iron(III) nitrate in hypochlorite solution at room temperature, leads to the formation of mainly hematite, α-Fe2O3. Successive ion adsorption and reaction (SILAR) is applied to decorate an electrochemically formed TiO2 nanotube electrode. The anodic photoelectrochemical 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.eng
dc.format203 (2016) 136-143
dc.languageen
dc.publisherElsevier
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172046/RS//
dc.rightsrestrictedAccess
dc.sourceElectrochimica Actaeng
dc.subjectHematite
dc.subjectForced hydrolysis
dc.subjectPhotoelectrochemical cell
dc.subjectBand gap
dc.subjectFlat band potential
dc.titlePhotoelectochemical behavior of TiO2-NT’s modified with SILAR deposited iron oxideeng
dc.typearticle
dc.rights.licenseARR
dcterms.abstractОмyмен, Wалеед М.; Ебсхисх, Aли С.; Гргур, Бранимир Н.; Тришовић, Томислав Љ.; Гвозденовић, Милица М.; Југовић, Бранимир З.;
dc.citation.spage136
dc.citation.epage143
dc.citation.volume203
dc.identifier.wos000376133200016
dc.identifier.doi10.1016/j.electacta.2016.04.038
dc.identifier.scopus2-s2.0-84963606979
dc.type.versionpublishedVersion


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