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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/1060
DC FieldValueLanguage
dc.contributor.authorJašin, Danijelaen_US
dc.contributor.authorAbu-Rabi, Andjelaen_US
dc.contributor.authorMentus, Slavkoen_US
dc.contributor.authorJovanović, Dušanen_US
dc.date.accessioned2022-12-16T17:30:02Z-
dc.date.available2022-12-16T17:30:02Z-
dc.date.issued2007-03-20-
dc.identifier.issn0013-4686en
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/1060-
dc.description.abstractFrom aqueous solutions, gold was deposited on freshly polished titanium surface either by displacement reaction or by potentiodynamic polarization. Both of these procedures resulted in the formation of Au/TiO2 composite layer over the titanium surface, although with quite different Au content. The electrochemical behaviour of these composite layers was examined in 0.1 M NaOH solution, both oxygen free and oxygen saturated, using rotating disc technique. In the potential region of oxygen reduction reaction, the Au/TiO2 layer obtained by potentiodynamic polarization, displayed the voltammetric curve similar to that observed on (1 0 0) plane of Au monocrystal. The Koutecky-Levich analysis evidenced that 4e- route of oxygen reduction dominates on both type of composite layers. © 2007 Elsevier Ltd. All rights reserved.en
dc.relation.ispartofElectrochimica Actaen
dc.subjectElectrocatalysisen
dc.subjectGolden
dc.subjectOxygen reduction reactionen
dc.subjectRotating disk electrodeen
dc.subjectTitanium dioxideen
dc.titleOxygen reduction reaction on spontaneously and potentiodynamically formed Au/TiO<inf>2</inf> composite surfacesen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.electacta.2006.12.071-
dc.identifier.scopus2-s2.0-33847608280-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/33847608280-
dc.relation.firstpage4581en
dc.relation.lastpage4588en
dc.relation.issue13en
dc.relation.volume52en
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.orcid0000-0001-8155-8003-
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University of Belgrade
Faculty of Physical Chemistry
Studentski trg 12-16
11158 Belgrade 118
PAC 105305
SERBIA
University of Belgrade Faculty of Physical Chemistry