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dc.creatorStojadinović, Stevan
dc.creatorRadić, Nenad
dc.creatorVasilić, Rastko
dc.creatorTadić, Nenad
dc.creatorTsanev, Aleksander
dc.date.accessioned2023-01-19T23:57:15Z
dc.date.available2023-01-19T23:57:15Z
dc.date.issued2022
dc.identifier.issn1293-2558
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/5584
dc.description.abstractThe effect of selected transition metals (Mn, Ni, Co) modified TiO2 coatings formed by plasma electrolytic oxidation of titanium on their surface morphology, phase and chemical composition, optical absorption, and photocatalytic degradation of methyl orange (MO) was investigated. Coatings were formed in an alkaline electrolyte with varying concentrations of MnO, NiO, or Co3O4 powders. The morphology, thickness and phase structure of all formed coatings are nearly identical and independent of the content of transition metal ions embedded in TiO2. The X-ray diffraction and X-ray photoelectron spectroscopy results indicated that anatase TiO2 coatings were loaded with MnO, NiO, or Co3O4 from electrolytes. When up to 2.0 g/L of MnO, NiO, or Co3O4 is added to the electrolyte, the photocatalytic activity (PA) of the forming coatings is higher than for pure TiO2. The coatings formed in electrolyte with the addition of 0.75 g/L MnO, 1.5 g/L NiO, or 2.0 g/L Co3O4 had the highest PA. Increased PA is associated with a decrease in photogenerated electron/hole recombination rate, according to UV–Vis diffuse reflectance spectroscopy and photoluminescence measurements.
dc.publisherElsevier BVen
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200162/RS//en
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200026/RS//en
dc.rightsrestrictedAccess
dc.sourceSolid State Sciencesen
dc.subjectPhotocatalysis
dc.subjectTiO2
dc.subjectTransition metals
dc.subjectPlasma electrolytic oxidation
dc.subjectCoatings
dc.titlePhotocatalytic degradation of methyl orange in the presence of transition metals (Mn, Ni, Co) modified TiO2 coatings formed by plasma electrolytic oxidationen
dc.typearticleen
dc.rights.licenseARRen
dc.citation.volume129
dc.citation.spage106896
dc.citation.rankM21~
dc.identifier.doi10.1016/j.solidstatesciences.2022.106896
dc.identifier.scopus2-s2.0-85129060356
dc.identifier.wos00080038690000
dc.type.versionpublishedVersion


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