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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/2520
DC FieldValueLanguage
dc.contributor.authorGočanin, Kristinaen_US
dc.contributor.authorAykut, Yaseminen_US
dc.contributor.authorMladenović, Dušanen_US
dc.contributor.authorSantos, Diogo M Fen_US
dc.contributor.authorBayrakçeken, Ayşeen_US
dc.contributor.authorSoylu, Gulin S Pen_US
dc.contributor.authorŠljukić Paunković, Biljanaen_US
dc.date.accessioned2025-11-05T13:20:19Z-
dc.date.available2025-11-05T13:20:19Z-
dc.date.issued2025-09-23-
dc.identifier.issn14779226-
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/2520-
dc.description.abstractDeveloping efficient, low-cost catalysts for oxygen reduction and evolution reactions (ORR and OER) is key to advancing metal-air batteries and regenerative fuel cells. In this study, nitrogen-doped binary metal (Mn and Ni) oxides (N-BMOs) and Pt-decorated N-BMOs were synthesised using three methods and tested as ORR and OER catalysts in alkaline media. Their physicochemical properties were characterised by XRD, N2-sorption, TEM, and XPS, while their electrochemical performance was evaluated using voltammetry and impedance spectroscopy. Among all tested materials, the best bifunctional catalyst proved to be Pt/N-Mn2O3-NiO (1 : 1) (S3) with the highest achieved diffusion limited current density (-4.98 mA cm-2 at 1800 rpm), the highest kinetic current density (-15.3 mA cm-2), low Tafel slope (75 mV dec-1) in ORR potential region, and overpotential of 0.56 V to reach benchmark current value of 10 mA cm-2 during OER. The ΔE was calculated to be 0.95 V, comparable to or even better than that of similar materials reported in the literature. Pt/N-Mn2O3-NiO (1 : 1) (S3) demonstrated striking stability during long-term operation with preserved morphology and catalytic activity.en_US
dc.language.isoenen_US
dc.relation.ispartofDalton transactions (Cambridge, England : 2003)en_US
dc.titleAdvanced nitrogen-doped transition metal oxides decorated with Pt: synthesis and composition strategies for maximised electrochemical performanceen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1039/d5dt01211b-
dc.identifier.pmid40916773-
dc.identifier.scopus2-s2.0-105016797785-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/105016797785-
dc.relation.firstpage13934en_US
dc.relation.lastpage13949en_US
dc.relation.issue37en_US
dc.relation.volume54en_US
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeJournal Article-
crisitem.author.orcid0000-0003-4362-7324-
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