Tailoring Hot-Carrier Distributions of Plasmonic Nanostructures through Surface Alloying

dc.contributorAalto Universityen
dc.contributor.authorFojt, Jakuben_US
dc.contributor.authorRossi, Tuomas P.en_US
dc.contributor.authorKumar, Priyank V.en_US
dc.contributor.authorErhart, Paulen_US
dc.contributor.departmentDepartment of Applied Physicsen
dc.contributor.groupauthorComputational Electronic Structure Theoryen
dc.contributor.organizationChalmers University of Technologyen_US
dc.contributor.organizationUniversity of New South Walesen_US
dc.descriptionPublisher Copyright: © 2024 The Authors. Published by American Chemical Society
dc.description.abstractAlloyed metal nanoparticles are a promising platform for plasmonically enabled hot-carrier generation, which can be used to drive photochemical reactions. Although the non-plasmonic component in these systems has been investigated for its potential to enhance catalytic activity, its capacity to affect the photochemical process favorably has been underexplored by comparison. Here, we study the impact of surface alloy species and concentration on hot-carrier generation in Ag nanoparticles. By first-principles simulations, we photoexcite the localized surface plasmon, allow it to dephase, and calculate spatially and energetically resolved hot-carrier distributions. We show that the presence of non-noble species in the topmost surface layer drastically enhances hot-hole generation at the surface at the expense of hot-hole generation in the bulk, due to the additional d-type states that are introduced to the surface. The energy of the generated holes can be tuned by choice of the alloyant, with systematic trends across the d-band block. Already low surface alloy concentrations have a large impact, with a saturation of the enhancement effect typically close to 75% of a monolayer. Hot-electron generation at the surface is hindered slightly by alloying, but here a judicious choice of the alloy composition allows one to strike a balance between hot electrons and holes. Our work underscores the promise of utilizing multicomponent nanoparticles to achieve enhanced control over plasmonic catalysis and provides guidelines for how hot-carrier distributions can be tailored by designing the electronic structure of the surface through alloying.en
dc.description.versionPeer revieweden
dc.identifier.citationFojt, J, Rossi, T P, Kumar, P V & Erhart, P 2024, ' Tailoring Hot-Carrier Distributions of Plasmonic Nanostructures through Surface Alloying ', ACS Nano, vol. 18, no. 8, pp. 6398–6405 . https://doi.org/10.1021/acsnano.3c11418en
dc.identifier.otherPURE UUID: 56f4532b-6781-48b9-a2d4-7d543531a4c9en_US
dc.identifier.otherPURE ITEMURL: https://research.aalto.fi/en/publications/56f4532b-6781-48b9-a2d4-7d543531a4c9en_US
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dc.identifier.otherPURE FILEURL: https://research.aalto.fi/files/141127174/Tailoring_Hot-Carrier_Distributions_of_Plasmonic_Nanostructures_through_Surface_Alloying.pdfen_US
dc.publisherAmerican Chemical Society
dc.relation.ispartofseriesACS Nano
dc.relation.ispartofseriesVolume 18, issue 8, pp. 6398–6405
dc.subject.keywordPlasmonic catalysisen_US
dc.subject.keywordTime-dependent density functional theoryen_US
dc.titleTailoring Hot-Carrier Distributions of Plasmonic Nanostructures through Surface Alloyingen
dc.typeA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessäfi