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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/340
DC FieldValueLanguage
dc.contributor.authorMladenović, Dušanen_US
dc.contributor.authorVujković, Milicaen_US
dc.contributor.authorMentus, Slavkoen_US
dc.contributor.authorSantos, Diogo M Fen_US
dc.contributor.authorRocha, Raquel Pen_US
dc.contributor.authorC Sequeira, Cesar Aen_US
dc.contributor.authorFigueiredo, Jose Luisen_US
dc.contributor.authorŠljukić Paunković, Biljanaen_US
dc.date.accessioned2022-12-13T18:50:24Z-
dc.date.available2022-12-13T18:50:24Z-
dc.date.issued2020-09-10-
dc.identifier.issn2079-4991en
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/340-
dc.description.abstractMolybdenum carbide (Mo2C)-based electrocatalysts were prepared using two different carbon supports, commercial carbon nanotubes (CNTs) and synthesised carbon xerogel (CXG), to be studied from the point of view of both capacitive and electrocatalytic properties. Cation type (K+ or Na+) in the alkaline electrolyte solution did not affect the rate of formation of the electrical double layer at a low scan rate of 10 mV s-1. Conversely, the different mobility of these cations through the electrolyte was found to be crucial for the rate of double-layer formation at higher scan rates. Molybdenum carbide supported on carbon xerogel (Mo2C/CXG) showed ca. 3 times higher double-layer capacity amounting to 75 mF cm-2 compared to molybdenum carbide supported on carbon nanotubes (Mo2C/CNT) with a value of 23 mF cm-2 due to having more than double the surface area size. The electrocatalytic properties of carbon-supported molybdenum carbides for the oxygen reduction reaction in alkaline media were evaluated using linear scan voltammetry with a rotating disk electrode. The studied materials demonstrated good electrocatalytic performance with Mo2C/CXG delivering higher current densities at more positive onset and half-wave potential. The number of electrons exchanged during oxygen reduction reaction (ORR) was calculated to be 3, suggesting a combination of four- and two-electron mechanism.en
dc.language.isoenen
dc.relation.ispartofNanomaterials (Basel, Switzerland)en
dc.subjectalkaline fuel cellen
dc.subjectcarbon nanotubesen
dc.subjectcarbon xerogelen
dc.subjectmolybdenum carbideen
dc.subjectoxygen reduction reactionen
dc.titleCarbon-Supported Mo2C for Oxygen Reduction Reaction Electrocatalysisen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.3390/nano10091805-
dc.identifier.pmid32927755-
dc.identifier.scopus2-s2.0-85090765590-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85090765590-
dc.relation.firstpage1en
dc.relation.lastpage12en
dc.relation.issue9en
dc.relation.volume10en
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.orcid0000-0003-4362-7324-
crisitem.author.orcid0000-0002-0518-8837-
crisitem.author.orcid0000-0001-8155-8003-
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