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dc.contributor.author
Maldonado, Abel Sebastián
dc.contributor.author
Cabeza, Gabriela Fernanda
dc.contributor.author
Ramos, Susana Beatriz
dc.date.available
2022-04-08T12:50:17Z
dc.date.issued
2019
dc.identifier.citation
Thermodynamic properties of Pt nanoclusters: an ab initio study; Simposio Latinoamericano de Física del Estado Sólido XXIII; San Carlos de Bariloche; Argentina; 2018; 110-110
dc.identifier.uri
http://hdl.handle.net/11336/154727
dc.description.abstract
Nanoparticles (NPs) and subnanometer clusters exhibit novel physical andchemical properties that differ significantly from their counterpart bulkmaterials. This is mainly originatedfrom the large fraction of subordinated atoms at the surface for NP of small sizes.Concerning thermodynamic properties, in spite of the fact that a large amountof research has been performed, there are still fundamental questions not yetresolved since in general the conventional thermodynamic knowledge of macroscopic metals does notapply for these nanoscopic systems. As thesize of the NPs is reduced, anomalous behaviors have been reported in theirthermodynamic properties, such as deviations from the Debye law of the specificheat and negative thermal expansion [[1],[2]].The Debyetemperature is a fundamental property, since it is closely related to changesin the vibrational properties and specific heat. For Pt NPs capped with PVP-k30the Debye temperature (QD) wasmeasured by the extended X-ray absorption finestructure (EXAFS) technique leading to values higher than for the bulk [[3]].On the other side for small subnanometer Pt NPs (of approximately 0.9 ± 0.2 nm and Navg ~16 atoms) supported on Al2O3 experimental studies based on scanning transmissionelectron microscopic (STEM) and X-ray absorptionspectroscopy exhibit marked contractions of thePt-Pt bond distances with respect to bulk values, and a negative thermalexpansion of these interatomic distances [[4]].In principle, in both works, the surface atom contraction and the interactionof the Pt atoms with capping molecules or support, both enhanced because of thenanosized dimensions of the NP, were indicated as possible reasons to explainthese anomalous thermodynamic properties. Motivatedby these experimental findings, and, as a first step to investigate theseproblems, in this work we calculate the thermodynamic properties of isolated PtNPs for sizes between 13-55 atoms. By considering isolated NPs, we expect toshed some light on the problem by considering only the intrinsic effects of thesmall dimension of NPs. We first determine their equilibrium geometries, tofurther evaluate their vibrational density of states (VDOS), the specific heatand the Debye temperature. The explicit thermal evolution of the averageinteratomic distances is determined at various temperatures by developing abinitio molecular dynamics. We find that the relaxed interatomic distances arereduced with respect to the bulk ones, in agreement with the experiments. The VDOSare very different from the bulk ones, with the presence of discrete states,which give rise to deviations from the typical Debye model of the specific heatat constant volume and low temperatures. Estimations of the Debye temperatureindicate values lower that those calculated for the solid.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Centro Atómico Bariloche
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
NANOCLUSTERS
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DFT
dc.subject
Pt
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PROPERTIES
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Física Atómica, Molecular y Química
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Ciencias Físicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Thermodynamic properties of Pt nanoclusters: an ab initio study
dc.type
info:eu-repo/semantics/publishedVersion
dc.type
info:eu-repo/semantics/conferenceObject
dc.type
info:ar-repo/semantics/documento de conferencia
dc.date.updated
2022-03-16T19:17:33Z
dc.journal.pagination
110-110
dc.journal.pais
Argentina
dc.journal.ciudad
San Carlos de Bariloche
dc.description.fil
Fil: Maldonado, Abel Sebastián. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte. Instituto de Investigación y Desarrollo en Ingeniería de Procesos, Biotecnología y Energías Alternativas. Universidad Nacional del Comahue. Instituto de Investigación y Desarrollo en Ingeniería de Procesos, Biotecnología y Energías Alternativas; Argentina. Universidad Nacional del Comahue. Facultad de Ingeniería; Argentina
dc.description.fil
Fil: Cabeza, Gabriela Fernanda. Universidad Nacional del Sur. Departamento de Física; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Física del Sur. Universidad Nacional del Sur. Departamento de Física. Instituto de Física del Sur; Argentina
dc.description.fil
Fil: Ramos, Susana Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte. Instituto de Investigación y Desarrollo en Ingeniería de Procesos, Biotecnología y Energías Alternativas. Universidad Nacional del Comahue. Instituto de Investigación y Desarrollo en Ingeniería de Procesos, Biotecnología y Energías Alternativas; Argentina. Universidad Nacional del Comahue. Facultad de Ingeniería; Argentina
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://fisica.cab.cnea.gov.ar/slafes23/abstracts/book-of-abstracts/
dc.conicet.rol
Autor
dc.conicet.rol
Autor
dc.conicet.rol
Autor
dc.coverage
Internacional
dc.type.subtype
Simposio
dc.description.nombreEvento
Simposio Latinoamericano de Física del Estado Sólido XXIII
dc.date.evento
2018-04-10
dc.description.ciudadEvento
San Carlos de Bariloche
dc.description.paisEvento
Argentina
dc.type.publicacion
Book
dc.description.institucionOrganizadora
Centro Atómico Bariloche
dc.description.institucionOrganizadora
Instituto Balseiro
dc.source.libro
Book of abstracts: Simposio Latinoamericano de Física del Estado Sólido XXIII
dc.date.eventoHasta
2018-04-13
dc.type
Simposio
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