The dynamics of supercooled ortho-terphenyl has been studied using photon-correlation spectroscopy (PCS) in the depolarized scattering geometry. The obtained relaxation curves are analyzed according to the mode-coupling theory (MCT) for supercooled liquids. The main results are: i) the observation of the secondary Johari-Goldstein relaxation (beta) that has its onset just at the dynamical crossover temperature TB (T-M > T-B > T-g); ii) the confirmation, of the suggestion of a recent statistical mechanical study, that such a molecular system remains ergodic also below the calorimetric glass-transition temperature T-g. Our experimental data give evidence that the time scales of the primary (alpha) and this secondary relaxations are correlated. Finally a comparison with recent PCS experiments in a colloidal system confirms the primary role of the dynamical crossover in the physics of the dynamical arrest.

On the ergodicity of supercooled molecular glass-forming liquids at the dynamical arrest: the o-terphenyl case

Leone Nancy;Villari Valentina;Micali Norberto;
2014

Abstract

The dynamics of supercooled ortho-terphenyl has been studied using photon-correlation spectroscopy (PCS) in the depolarized scattering geometry. The obtained relaxation curves are analyzed according to the mode-coupling theory (MCT) for supercooled liquids. The main results are: i) the observation of the secondary Johari-Goldstein relaxation (beta) that has its onset just at the dynamical crossover temperature TB (T-M > T-B > T-g); ii) the confirmation, of the suggestion of a recent statistical mechanical study, that such a molecular system remains ergodic also below the calorimetric glass-transition temperature T-g. Our experimental data give evidence that the time scales of the primary (alpha) and this secondary relaxations are correlated. Finally a comparison with recent PCS experiments in a colloidal system confirms the primary role of the dynamical crossover in the physics of the dynamical arrest.
2014
Istituto per i Processi Chimico-Fisici - IPCF
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/264904
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