Slow dynamics near glass transitions in thin polymer films

Koji Fukao; Yoshihisa Miyamoto

doi:10.1103/PhysRevE.64.011803

paper

Slow dynamics near glass transitions in thin polymer films

arXiv:cond-mat/0012465 · doi:10.1103/PhysRevE.64.011803

Abstract

The $α$ -process (segmental motion) of thin polystyrene films supported on glass substrate has been investigated in a wider frequency range from 10 $^{- 3}$ Hz to 10 $^{4}$ Hz using dielectric relaxation spectroscopy and thermal expansion spectroscopy. The relaxation rate of the $α$ -process increases with decreasing film thickness at a given temperature above the glass transition. This increase in the relaxation rate with decreasing film thickness is much more enhanced near the glass transition temperature. The glass transition temperature determined as the temperature at which the relaxation time of the $α$ -process becomes a macroscopic time scale shows a distinct molecular weight dependence. It is also found that the Vogel temperature has the thickness dependence, i.e., the Vogel temperature decreases with decreasing film thickness. The expansion coefficient of the free volume $α_{f}$ is extracted from the temperature dependence of the relaxation time within the free volume theory. The fragility index $m$ is also evaluated as a function of thickness. Both $α_{f}$ and $m$ are found to decrease with decreasing film thickness.

9 pages, 7 figures, and 2 tables

Slow dynamics near glass transitions in thin polymer films

Abstract

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