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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/2180
DC FieldValueLanguage
dc.contributor.authorRmuš Mravik, Jelenaen_US
dc.contributor.authorMilanović, Igoren_US
dc.contributor.authorMilošević Govedarović, Sanjaen_US
dc.contributor.authorMraković, Anaen_US
dc.contributor.authorKorneeva, Ekaterinaen_US
dc.contributor.authorStojković Simatović, Ivanaen_US
dc.contributor.authorKurko, Sandraen_US
dc.date.accessioned2024-01-13T11:52:43Z-
dc.date.available2024-01-13T11:52:43Z-
dc.date.issued2023-12-19-
dc.identifier.issn03603199-
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/2180-
dc.description.abstractMolybdenum disulfide (MoS2) is considered promising noble metal-free catalysts for the hydrogen evolution reaction (HER). Whereas the bulk MoS2 does not exhibit significant activity, the catalytic properties of various nanostructures are noticeable. Therefore we synthesized flower-like molybdenum disulfide with the simple, one-step hydrothermal method. To enhance the catalytic activity of the material, low-energy ion irradiation is employed. As-prepared MoS2 is irradiated with hydrogen and carbon ions of various energies (20–40 keV) and fluences (1014-1017 ion/cm2). Our results show that irradiation has beneficial influence on MoS2 catalytic activity toward hydrogen evolution reaction. By producing morphological changes and defects in the structure, ion irradiation also impacts the conductivity of the material, which shows predominant effect on hydrogen evolution. The increase of current density at an overpotential of 300 mV with hydrogen ion irradiation is even 6 times higher than for as-synthesized catalyst.en_US
dc.relation.ispartofInternational Journal of Hydrogen Energyen_US
dc.subjectElectrocatalysten_US
dc.subjectHydrogen evolution reactionen_US
dc.subjectIon irradiationen_US
dc.subjectMolybdenum disulfideen_US
dc.titleImprovement of MoS<inf>2</inf> electrocatalytic activity for hydrogen evolution reaction by ion irradiationen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.ijhydene.2023.06.178-
dc.identifier.scopus2-s2.0-85164495419-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85164495419-
dc.relation.firstpage38676en_US
dc.relation.lastpage38685en_US
dc.relation.issue98en_US
dc.relation.volume48en_US
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
crisitem.author.orcid0000-0001-7836-4574-
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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