Dynamic relaxation of a liquid cavity under amorphous boundary conditions

Autores
Cavagna, A.; Grigera, Tomás Sebastián; Verrocchio, Paolo
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The growth of cooperatively rearranging regions was invoked long ago by Adam and Gibbs to explain the slowing down of glass-forming liquids. The lack of knowledge about the nature of the growing order, though, complicates the definition of an appropriate correlation function. One option is the point-to-set (PTS) correlation function, which measures the spatial span of the influence of amorphous boundary conditions on a confined system. By using a swap Monte Carlo algorithm we measure the equilibration time of a liquid droplet bounded by amorphous boundary conditions in a model glass-former at low temperature, and we show that the cavity relaxation time increases with the size of the droplet, saturating to the bulk value when the droplet outgrows the point-to-set correlation length. This fact supports the idea that the point-to-set correlation length is the natural size of the cooperatively rearranging regions. On the other hand, the cavity relaxation time computed by a standard, nonswap dynamics, has the opposite behavior, showing a very steep increase when the cavity size is decreased. We try to reconcile this difference by discussing the possible hybridization between mode-coupling theory and activated processes, and by introducing a new kind of amorphous boundary conditions, inspired by the concept of frozen external state as an alternative to the commonly used frozen external configuration.
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas
Materia
Física
Ciencias Exactas
Glass-forming liquids
Cavity relaxation time
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/98087

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network_name_str SEDICI (UNLP)
spelling Dynamic relaxation of a liquid cavity under amorphous boundary conditionsCavagna, A.Grigera, Tomás SebastiánVerrocchio, PaoloFísicaCiencias ExactasGlass-forming liquidsCavity relaxation timeThe growth of cooperatively rearranging regions was invoked long ago by Adam and Gibbs to explain the slowing down of glass-forming liquids. The lack of knowledge about the nature of the growing order, though, complicates the definition of an appropriate correlation function. One option is the point-to-set (PTS) correlation function, which measures the spatial span of the influence of amorphous boundary conditions on a confined system. By using a swap Monte Carlo algorithm we measure the equilibration time of a liquid droplet bounded by amorphous boundary conditions in a model glass-former at low temperature, and we show that the cavity relaxation time increases with the size of the droplet, saturating to the bulk value when the droplet outgrows the point-to-set correlation length. This fact supports the idea that the point-to-set correlation length is the natural size of the cooperatively rearranging regions. On the other hand, the cavity relaxation time computed by a standard, nonswap dynamics, has the opposite behavior, showing a very steep increase when the cavity size is decreased. We try to reconcile this difference by discussing the possible hybridization between mode-coupling theory and activated processes, and by introducing a new kind of amorphous boundary conditions, inspired by the concept of frozen external state as an alternative to the commonly used frozen external configuration.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas2012-05-24info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf1-16http://sedici.unlp.edu.ar/handle/10915/98087enginfo:eu-repo/semantics/altIdentifier/url/https://ri.conicet.gov.ar/11336/81913info:eu-repo/semantics/altIdentifier/url/https://aip.scitation.org/doi/10.1063/1.4720477info:eu-repo/semantics/altIdentifier/issn/0021-9606info:eu-repo/semantics/altIdentifier/doi/10.1063/1.4720477info:eu-repo/semantics/altIdentifier/hdl/11336/81913info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/2.5/ar/Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Argentina (CC BY-NC-SA 2.5)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T11:12:20Zoai:sedici.unlp.edu.ar:10915/98087Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:12:20.315SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Dynamic relaxation of a liquid cavity under amorphous boundary conditions
title Dynamic relaxation of a liquid cavity under amorphous boundary conditions
spellingShingle Dynamic relaxation of a liquid cavity under amorphous boundary conditions
Cavagna, A.
Física
Ciencias Exactas
Glass-forming liquids
Cavity relaxation time
title_short Dynamic relaxation of a liquid cavity under amorphous boundary conditions
title_full Dynamic relaxation of a liquid cavity under amorphous boundary conditions
title_fullStr Dynamic relaxation of a liquid cavity under amorphous boundary conditions
title_full_unstemmed Dynamic relaxation of a liquid cavity under amorphous boundary conditions
title_sort Dynamic relaxation of a liquid cavity under amorphous boundary conditions
dc.creator.none.fl_str_mv Cavagna, A.
Grigera, Tomás Sebastián
Verrocchio, Paolo
author Cavagna, A.
author_facet Cavagna, A.
Grigera, Tomás Sebastián
Verrocchio, Paolo
author_role author
author2 Grigera, Tomás Sebastián
Verrocchio, Paolo
author2_role author
author
dc.subject.none.fl_str_mv Física
Ciencias Exactas
Glass-forming liquids
Cavity relaxation time
topic Física
Ciencias Exactas
Glass-forming liquids
Cavity relaxation time
dc.description.none.fl_txt_mv The growth of cooperatively rearranging regions was invoked long ago by Adam and Gibbs to explain the slowing down of glass-forming liquids. The lack of knowledge about the nature of the growing order, though, complicates the definition of an appropriate correlation function. One option is the point-to-set (PTS) correlation function, which measures the spatial span of the influence of amorphous boundary conditions on a confined system. By using a swap Monte Carlo algorithm we measure the equilibration time of a liquid droplet bounded by amorphous boundary conditions in a model glass-former at low temperature, and we show that the cavity relaxation time increases with the size of the droplet, saturating to the bulk value when the droplet outgrows the point-to-set correlation length. This fact supports the idea that the point-to-set correlation length is the natural size of the cooperatively rearranging regions. On the other hand, the cavity relaxation time computed by a standard, nonswap dynamics, has the opposite behavior, showing a very steep increase when the cavity size is decreased. We try to reconcile this difference by discussing the possible hybridization between mode-coupling theory and activated processes, and by introducing a new kind of amorphous boundary conditions, inspired by the concept of frozen external state as an alternative to the commonly used frozen external configuration.
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas
description The growth of cooperatively rearranging regions was invoked long ago by Adam and Gibbs to explain the slowing down of glass-forming liquids. The lack of knowledge about the nature of the growing order, though, complicates the definition of an appropriate correlation function. One option is the point-to-set (PTS) correlation function, which measures the spatial span of the influence of amorphous boundary conditions on a confined system. By using a swap Monte Carlo algorithm we measure the equilibration time of a liquid droplet bounded by amorphous boundary conditions in a model glass-former at low temperature, and we show that the cavity relaxation time increases with the size of the droplet, saturating to the bulk value when the droplet outgrows the point-to-set correlation length. This fact supports the idea that the point-to-set correlation length is the natural size of the cooperatively rearranging regions. On the other hand, the cavity relaxation time computed by a standard, nonswap dynamics, has the opposite behavior, showing a very steep increase when the cavity size is decreased. We try to reconcile this difference by discussing the possible hybridization between mode-coupling theory and activated processes, and by introducing a new kind of amorphous boundary conditions, inspired by the concept of frozen external state as an alternative to the commonly used frozen external configuration.
publishDate 2012
dc.date.none.fl_str_mv 2012-05-24
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
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dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/98087
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dc.language.none.fl_str_mv eng
language eng
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info:eu-repo/semantics/altIdentifier/url/https://aip.scitation.org/doi/10.1063/1.4720477
info:eu-repo/semantics/altIdentifier/issn/0021-9606
info:eu-repo/semantics/altIdentifier/doi/10.1063/1.4720477
info:eu-repo/semantics/altIdentifier/hdl/11336/81913
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Argentina (CC BY-NC-SA 2.5)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Argentina (CC BY-NC-SA 2.5)
dc.format.none.fl_str_mv application/pdf
1-16
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instname:Universidad Nacional de La Plata
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reponame_str SEDICI (UNLP)
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instname_str Universidad Nacional de La Plata
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institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
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