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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/332
DC FieldValueLanguage
dc.contributor.authorMladenović, Dušanen_US
dc.contributor.authorSantos, Diogo M.F.en_US
dc.contributor.authorBozkurt, Gamzeen_US
dc.contributor.authorSoylu, Gulin S.P.en_US
dc.contributor.authorYurtcan, Ayşe B.en_US
dc.contributor.authorMiljanić, Šćepanen_US
dc.contributor.authorŠljukić Paunković, Biljanaen_US
dc.date.accessioned2022-12-13T18:50:21Z-
dc.date.available2022-12-13T18:50:21Z-
dc.date.issued2021-03-01-
dc.identifier.issn1388-2481en
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/332-
dc.description.abstractThree different metal oxides based on Mn2O3 with TiO2 or NiO were synthesised. Pt or PtNi nanoparticles were anchored on each support, creating a set of nine samples that were tested for the oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER). PtNi/Mn2O3-NiO showed the most promising results for ORR as evidenced by the lowest Tafel slope, the highest diffusion-limited current density and number of electrons exchanged, along with the highest stability. The best performance of PtNi/Mn2O3-NiO reflects its highest electrochemical surface area and the lowest charge-transfer resistance. Furthermore, this catalyst showed high activity for the OER as evidenced by the low Tafel slope and high current density at an overpotential of 400 mV. The present study indicated different active sites for the two reactions, i.e., PtNi NPs for the ORR and NiO for the OER.en
dc.relation.ispartofElectrochemistry Communicationsen
dc.subjectBinary metal oxidesen
dc.subjectNickelen
dc.subjectOxygen evolution reactionen
dc.subjectOxygen reduction reactionen
dc.subjectPlatinumen
dc.subjectUnitised regenerative fuel cellen
dc.titleTailoring metal-oxide-supported PtNi as bifunctional catalysts of superior activity and stability for unitised regenerative fuel cell applicationsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.elecom.2021.106963-
dc.identifier.scopus2-s2.0-85101385072-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85101385072-
dc.relation.volume124en
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.orcid0000-0003-4362-7324-
crisitem.author.orcid0000-0003-1955-1913-
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