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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/367
DC FieldValueLanguage
dc.contributor.authorMilikić, Jadrankaen_US
dc.contributor.authorFuentes, Rodolfo O.en_US
dc.contributor.authorTasca, Julia E.en_US
dc.contributor.authorSantos, Diogo M.F.en_US
dc.contributor.authorŠljukić Paunković, Biljanaen_US
dc.contributor.authorFigueiredo, Filipe M.L.en_US
dc.date.accessioned2022-12-13T18:50:29Z-
dc.date.available2022-12-13T18:50:29Z-
dc.date.issued2022-08-01-
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/367-
dc.description.abstractNickel-doped ceria (Ce1−xNixO2−δ) nanopowders (7 to 5 nm in size) synthesized by the cation complexation method with 5, 10, 15, and 20 Ni at.% are studied with respect to their electrochemical activity for the oxygen reduction (ORR) and oxygen evolution (OER) reactions in alkaline medium. One finds good bifunctional electrocatalytic activity of the four Ce1−xNixO2−δ electrocatalysts. The Tafel analysis of the ORR in the 0.57–0.78 V vs. RHE potential window leads to slopes in the 70–108 mV dec−1 range. The number of electrons exchanged during ORR is between 2 and 2.7. The OER Tafel slopes are determined to be in the range 192 –281 mV dec−1. OER activation energies are found to range between 28 and 43 kJ mol−1. The specific capacitance of Ce1−xNixO2−δ electrocatalysts measured at a scan rate of 100 mV s−1 varies between 0.7 and 1.4 Fg−1. The results demonstrate that Ce1−xNixO2−δ nanopowders can act as bifunctional electrocatalysts for ORR/OER for potential application in the oxygen electrode of devices such as rechargeable metal–air batteries.en
dc.relation.ispartofBatteriesen
dc.subjectnickel-doped ceriaen
dc.subjectoxygen evolution reactionen
dc.subjectoxygen reduction reactionen
dc.subjectrechargeable metal–air batteriesen
dc.titleNickel-Doped Ceria Bifunctional Electrocatalysts for Oxygen Reduction and Evolution in Alkaline Mediaen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/batteries8080100-
dc.identifier.scopus2-s2.0-85137340400-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85137340400-
dc.relation.issue8en
dc.relation.volume8en
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