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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/406
DC FieldValueLanguage
dc.contributor.authorMartins, M.en_US
dc.contributor.authorŠljukić Paunković, Biljanaen_US
dc.contributor.authorSequeira, C. A.C.en_US
dc.contributor.authorSoylu, G. S.P.en_US
dc.contributor.authorYurtcan, A. B.en_US
dc.contributor.authorBozkurt, G.en_US
dc.contributor.authorSener, T.en_US
dc.contributor.authorSantos, Diogo M.F.en_US
dc.date.accessioned2022-12-13T18:50:35Z-
dc.date.available2022-12-13T18:50:35Z-
dc.date.issued2018-01-15-
dc.identifier.issn0169-4332en
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/406-
dc.description.abstractPtNi nanoparticles (NPs) were synthesised by microwave irradiation technique and supported onto Mn 2 O 3 and two binary metal oxides, Mn 2 O 3 -TiO 2 and Mn 2 O 3 -NiO, prepared by solid-state dispersion method. TEM analysis revealed formation of PtNi NPs of 2–3 nm diameter on the metal oxides. Their activity for oxygen reduction reaction (ORR) and borohydride oxidation reaction (BOR) in alkaline media was studied using voltammetric, amperometric and electrochemical impedance spectroscopy techniques. The effect of electrolyte composition and operation temperature on the catalysts performance was also examined. ORR and BOR kinetic parameters, namely Tafel slope, kinetic current density, order of reaction and activation energy were evaluated, enabling direct comparison of the three electrocatalysts performance. The results show that PtNi NPs anchored on binary metal oxide supports possess superior activity for BOR in alkaline media, suggesting their potential application as anodes in low-temperature fuel cells.en
dc.relation.ispartofApplied Surface Scienceen
dc.subjectBinary metal oxidesen
dc.subjectBorohydride oxidation reactionen
dc.subjectLow-temperature fuel cellsen
dc.subjectOxygen reduction reactionen
dc.subjectPtNi nanoparticlesen
dc.titlePtNi supported on binary metal oxides: Potential bifunctional electrocatalysts for low-temperature fuel cells?en_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.apsusc.2017.09.132-
dc.identifier.scopus2-s2.0-85029799219-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85029799219-
dc.relation.firstpage31en
dc.relation.lastpage40en
dc.relation.volume428en
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.grantfulltextnone-
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