Dynamic relaxation of a liquid cavity under amorphous boundary conditions

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...

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Detalles Bibliográficos
Autores principales: Cavagna, A., Grigera, Tomás Sebastián, Verrocchio, Paolo
Formato: Articulo
Lenguaje:Inglés
Publicado: 2012
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/98087
https://ri.conicet.gov.ar/11336/81913
https://aip.scitation.org/doi/10.1063/1.4720477
Aporte de:
id I19-R120-10915-98087
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Física
Ciencias Exactas
Glass-forming liquids
Cavity relaxation time
spellingShingle Física
Ciencias Exactas
Glass-forming liquids
Cavity relaxation time
Cavagna, A.
Grigera, Tomás Sebastián
Verrocchio, Paolo
Dynamic relaxation of a liquid cavity under amorphous boundary conditions
topic_facet Física
Ciencias Exactas
Glass-forming liquids
Cavity relaxation time
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.
format Articulo
Articulo
author Cavagna, A.
Grigera, Tomás Sebastián
Verrocchio, Paolo
author_facet Cavagna, A.
Grigera, Tomás Sebastián
Verrocchio, Paolo
author_sort Cavagna, A.
title Dynamic relaxation of a liquid cavity under amorphous boundary conditions
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
publishDate 2012
url http://sedici.unlp.edu.ar/handle/10915/98087
https://ri.conicet.gov.ar/11336/81913
https://aip.scitation.org/doi/10.1063/1.4720477
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AT grigeratomassebastian dynamicrelaxationofaliquidcavityunderamorphousboundaryconditions
AT verrocchiopaolo dynamicrelaxationofaliquidcavityunderamorphousboundaryconditions
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