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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/394
DC FieldValueLanguage
dc.contributor.authorŠljukić Paunković, Biljanaen_US
dc.contributor.authorSantos, D. M.F.en_US
dc.contributor.authorSequeira, C. A.C.en_US
dc.date.accessioned2022-12-13T18:50:33Z-
dc.date.available2022-12-13T18:50:33Z-
dc.date.issued2013-01-01-
dc.identifier.issn1572-6657en
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/394-
dc.description.abstractElectrocatalysts of manganese dioxide (MnO2) supported on activated carbon (AC) were prepared by low-temperature (ltMnO2/AC) and high-temperature (htMnO2/AC) procedures. Structure, morphology and composition of the synthesised materials were investigated by X-ray diffraction analysis, transmission electron microscopy and thermogravimetric analysis. Activity of the two prepared electrocatalysts for the oxygen reduction reaction (ORR) was investigated in alkaline media and ORR kinetic parameters evaluated from rotating disc electrode measurements. It was found that the ORR proceeds as two-electron process at ltMnO2/AC-based electrode, while it proceeds as four-electron process at htMnO2/AC-based electrode. The two electrocatalysts were further investigated for application as cathode materials in direct borohydride fuel cells. For that purposes the ORR at MnO2/AC was investigated in the presence of borohydride in alkaline solution and in the temperature range from 25 to 65 °C. It could be observed that the activity of ltMnO2/AC for the ORR is significantly suppressed in the borohydride-containing solution whereas htMnO2/AC still showed high activity for the ORR. © 2013 Elsevier B.V. All rights reserved.en
dc.relation.ispartofJournal of Electroanalytical Chemistryen
dc.subjectCarbon-supported electrocatalysten
dc.subjectDirect borohydride fuel cellen
dc.subjectManganese dioxide-based cathodeen
dc.subjectOxygen reduction reactionen
dc.titleManganese dioxide electrocatalysts for borohydride fuel cell cathodes?en_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.jelechem.2013.01.044-
dc.identifier.scopus2-s2.0-84875193015-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84875193015-
dc.relation.firstpage77en
dc.relation.lastpage83en
dc.relation.volume694en
item.grantfulltextnone-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
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