Please use this identifier to cite or link to this item: https://physrep.ff.bg.ac.rs/handle/123456789/1312
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dc.contributor.authorLačnjevac, Urošen_US
dc.contributor.authorVasilić, Rastkoen_US
dc.contributor.authorDobrota, Anaen_US
dc.contributor.authorĐurđić, Slađanaen_US
dc.contributor.authorTomanec, Ondřejen_US
dc.contributor.authorZbořil, Radeken_US
dc.contributor.authorMohajernia, Shivaen_US
dc.contributor.authorNguyen, Nhat Truongen_US
dc.contributor.authorSkorodumova, Nataliaen_US
dc.contributor.authorManojlović, Draganen_US
dc.contributor.authorElezović, Nevenkaen_US
dc.contributor.authorPašti, Igoren_US
dc.contributor.authorSchmuki, Patriken_US
dc.date.accessioned2022-09-15T16:19:53Z-
dc.date.available2022-09-15T16:19:53Z-
dc.date.issued2020-11-21-
dc.identifier.issn2050-7488-
dc.identifier.urihttps://physrep.ff.bg.ac.rs/handle/123456789/1312-
dc.description.abstractDeveloping ultraefficient electrocatalytic materials for the hydrogen evolution reaction (HER) with low content of expensive platinum group metals (PGMs) via low-energy-input procedures is the key to the successful commercialization of green water electrolysis technologies for sustainable production of high-purity hydrogen. In this study, we report a facile room-temperature synthesis of ultrafine metallic Ir nanoparticles on conductive, proton-intercalated TiO2 nanotube (H-TNT) arrays via galvanic displacement. A series of experiments demonstrate that a controlled transformation of the H-TNT surface microstructure from neat open-top tubes to disordered nanostripe bundles ("nanograss") is highly beneficial for providing an abundance of exposed Ir active sites. Consequently, for nanograss-engineered composites, outstanding HER activity metrics are achieved even at very low Ir(iii) precursor concentrations. An optimum Ir@TNT cathode loaded with 5.7 μgIr cm-2 exhibits an overpotential of -63 mV at -100 mA cm-2 and a mass activity of 34 A mgIr-1 at -80 mV under acidic conditions, along with excellent catalytic durability and structural integrity. Density functional theory (DFT) simulations reveal that the hydrogen-rich TiO2 surface not only stabilizes the deposited Ir and weakens its H binding strength to a moderate intensity, but also actively takes part in the HER mechanism by refreshing the Ir catalytic sites near the Ir|H-TiO2 interface, thus substantially promoting H2 generation. The comprehensive characterization combined with theory provides an in-depth understanding of the electrocatalytic behavior of H-TNT supported PGM nanoparticles and demonstrates their high potential as competitive electrocatalyst systems for the HER. This journal isen_US
dc.relation.ispartofJournal of Materials Chemistry Aen_US
dc.titleHigh-performance hydrogen evolution electrocatalysis using proton-intercalated TiO<inf>2</inf>nanotube arrays as interactive supports for Ir nanoparticlesen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/d0ta07492f-
dc.identifier.scopus2-s2.0-85096105811-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85096105811-
dc.relation.issue43en_US
dc.relation.volume8en_US
dc.relation.firstpage22773en_US
dc.relation.lastpage22790en_US
item.grantfulltextnone-
item.openairetypeArticle-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
crisitem.author.orcid0000-0003-2476-7516-
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