Decorrelation of the static and dynamic length scales in hard-sphere glass formers.

dc.contributor.author

Charbonneau, Patrick

dc.contributor.author

Tarjus, Gilles

dc.coverage.spatial

United States

dc.date.accessioned

2016-08-03T15:38:40Z

dc.date.issued

2013-04

dc.description.abstract

We show that, in the equilibrium phase of glass-forming hard-sphere fluids in three dimensions, the static length scales tentatively associated with the dynamical slowdown and the dynamical length characterizing spatial heterogeneities in the dynamics unambiguously decorrelate. The former grow at a much slower rate than the latter when density increases. This observation is valid for the dynamical range that is accessible to computer simulations, which roughly corresponds to that accessible in colloidal experiments. We also find that, in this same range, no one-to-one correspondence between relaxation time and point-to-set correlation length exists. These results point to the coexistence of several relaxation mechanisms in the dynamically accessible regime of three-dimensional hard-sphere glass formers.

dc.identifier

http://www.ncbi.nlm.nih.gov/pubmed/23679412

dc.identifier.eissn

1550-2376

dc.identifier.uri

https://hdl.handle.net/10161/12612

dc.language

eng

dc.publisher

American Physical Society (APS)

dc.relation.ispartof

Phys Rev E Stat Nonlin Soft Matter Phys

dc.relation.isversionof

10.1103/PhysRevE.87.042305

dc.title

Decorrelation of the static and dynamic length scales in hard-sphere glass formers.

dc.type

Journal article

duke.contributor.orcid

Charbonneau, Patrick|0000-0001-7174-0821

pubs.author-url

http://www.ncbi.nlm.nih.gov/pubmed/23679412

pubs.begin-page

042305

pubs.declined

2016-08-03T12:40:55.794-0400

pubs.deleted

2016-08-03T12:40:55.807-0400

pubs.issue

4

pubs.organisational-group

Chemistry

pubs.organisational-group

Duke

pubs.organisational-group

Physics

pubs.organisational-group

Trinity College of Arts & Sciences

pubs.publication-status

Published

pubs.volume

87

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