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Relation Between Configurational Entropy and Relaxation Dynamics of Glass-Forming Systems under Volume and Temperature Reduction (Articolo in rivista)
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- Label
- Relation Between Configurational Entropy and Relaxation Dynamics of Glass-Forming Systems under Volume and Temperature Reduction (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Alternative label
Capaccioli, S.; Prevosto, D.; Lucchesi, M.; Amirkhani, M.; Rolla, P.A. (2009)
Relation Between Configurational Entropy and Relaxation Dynamics of Glass-Forming Systems under Volume and Temperature Reduction
in Journal of non-crystalline solids
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Capaccioli, S.; Prevosto, D.; Lucchesi, M.; Amirkhani, M.; Rolla, P.A. (literal)
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- ISI Web of Science (WOS) (literal)
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- Dipartimento di Fisica, Università di Pisa, Largo B. Pontecorvo 3, I-56127 Pisa, Italy
INFM-CNR, PolyLab, Largo B. Pontecorvo 3, I-56127 Pisa, Italy (literal)
- Titolo
- Relation Between Configurational Entropy and Relaxation Dynamics of Glass-Forming Systems under Volume and Temperature Reduction (literal)
- Abstract
- The structural relaxation dynamics of two molecular glass-forming systems have been analyzed by
means of dielectric spectroscopy, under cooling and compression conditions. The relation of the dynamic
slowing down with the reduction of the configurational entropy, SC, as predicted by Adam and Gibbs (AG),
was also investigated. As SC is not directly accessible by experiments, it was estimated, following a common
procedure in literature, from the excess entropy Sexc of the supercooled liquid with respect to the
crystal, determined from calorimetric and expansivity measurements over the same TP range of dynamics
investigation. The AG relation, predicting linear dependence between the logarithmic of structural
relaxation time and the reciprocal of the product of temperature with configurational entropy, was successfully
tested. Actually, a bilinear relation between Sexc and SC was found, with different proportionality
factors in isothermal and isobaric conditions. Using such results, we derived an equation for predicting
the pressure dependence of the glass transition temperature, in good accordance with the experimental
values in literature. (literal)
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