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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/2349
DC FieldValueLanguage
dc.contributor.authorPerović, Ivanaen_US
dc.contributor.authorMitrović, Stefanen_US
dc.contributor.authorBrković, Snežanaen_US
dc.contributor.authorZdolšek, Nikolaen_US
dc.contributor.authorSeović, Minaen_US
dc.contributor.authorTasić, Gvozdenen_US
dc.contributor.authorPašti, Igoren_US
dc.date.accessioned2024-11-05T15:26:18Z-
dc.date.available2024-11-05T15:26:18Z-
dc.date.issued2024-04-25-
dc.identifier.issn03603199-
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/2349-
dc.description.abstractThis study investigates the impact of Co–Mo–W ionic activators on the hydrogen evolution reaction (HER) in alkaline electrolysis, comparing their performance to Co–Mo and Co–W systems. The research focuses on analyzing the catalytic efficiency of these activators under varying conditions, including temperature and current density variations. Key findings reveal that the Co–Mo–W activator enhances HER performance, with a significant 17% reduction in energy consumption compared to plain electrolyte, mirroring the efficiency of Co–Mo. Tafel analysis gave the insight of the reaction mechanism for HER for all activators, with Co–Mo–W exhibiting a lower Tafel slope, suggesting improved catalytic activity. Structural and morphological analysis of electrode coatings shows a highly developed surface for Co–Mo–W, with a roughness factor similar to or slightly lower than the most developed Co–Mo coating. The study concludes that the synergistic combination of Co, Mo, and W in a tri-component ionic activator offers a promising catalytic activity for HER, outperforming bi-component systems and presenting significant potential for industrial-scale alkaline water electrolysis applications.en_US
dc.relation.ispartofInternational Journal of Hydrogen Energyen_US
dc.titleOn the use of WO<inf>4</inf><sup>2−</sup> as a third component to Co–Mo ionic activator for HER in alkaline water electrolysisen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.ijhydene.2024.03.267-
dc.identifier.scopus2-s2.0-85188961729-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85188961729-
dc.relation.firstpage196en_US
dc.relation.lastpage204en_US
dc.relation.volume64en_US
item.openairetypeArticle-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
crisitem.author.orcid0000-0002-1000-9784-
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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