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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/2226
DC FieldValueLanguage
dc.contributor.authorMilikić, Jadrankaen_US
dc.contributor.authorKnežević, Saraen_US
dc.contributor.authorOgnjanović, Milošen_US
dc.contributor.authorStanković, Daliboren_US
dc.contributor.authorRakočević, Lazaren_US
dc.contributor.authorŠljukić Paunković, Biljanaen_US
dc.date.accessioned2024-01-15T09:13:17Z-
dc.date.available2024-01-15T09:13:17Z-
dc.date.issued2023-08-19-
dc.identifier.issn03603199-
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/2226-
dc.description.abstractPorous cobalt (III) oxide (Co3O4) and mixed cobalt (III) oxide - tin oxide (Co3O4/SnO2) were prepared by a novel template-based hydrothermal method resulting in their spherical morphology as confirmed by thorough physico-chemical characterisation. Two oxides were systematically examined as bifunctional electrocatalysts for oxygen reduction (ORR) and evolution (OER) reaction in alkaline media by voltammetry with rotating disk electrode, electrochemical impedance spectroscopy, and chronoamperometry. Low-cost Co3O4 and Co3O4/SnO2 electrocatalysts showed excellent ORR performance with low onset and half-wave potential, low Tafel slope, and the number of exchange electrons near 4, comparable to the commercial Pt/C electrocatalyst. Low OER onset potential of 1.52 and 1.57 V was observed for Co3O4 and Co3O4/SnO2, respectively, with low charge transfer resistance under anodic polarization conditions. Finally, to test bifunctional activity and durability of the two electrocatalyst, switch OER/ORR test was carried out.en_US
dc.relation.ispartofInternational Journal of Hydrogen Energyen_US
dc.subjectBifunctional electrocatalystsen_US
dc.subjectCobalt (III) oxideen_US
dc.subjectOxygen evolution reactionen_US
dc.subjectOxygen reduction reactionen_US
dc.subjectTin oxideen_US
dc.titleTemplate-based synthesis of Co3O4 and Co3O4/SnO2 bifunctional catalysts with enhanced electrocatalytic properties for reversible oxygen evolution and reduction reactionen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.ijhydene.2023.03.433-
dc.identifier.scopus2-s2.0-85152701944-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85152701944-
dc.relation.firstpage27568en_US
dc.relation.lastpage27581en_US
dc.relation.issue71en_US
dc.relation.volume48en_US
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.orcid0000-0003-2266-6738-
crisitem.author.orcid0000-0003-0203-4012-
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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