Abstract

A fundamental problem of glass transition is to explain the jump of heat capacity at the glass transition temperature TgT_g without asserting the existence of a distinct solid glass phase. This problem is also common to other disordered systems, including spin glasses. We propose that if TgT_g is defined as the temperature at which the liquid stops relaxing at the experimental time scale, the jump of heat capacity at TgT_g follows as a necessary consequence due to the change of system's elastic, vibrational and thermal properties. In this picture, we discuss time-dependent effects of glass transition, and identify three distinct regimes of relaxation. Our approach explains widely observed logarithmic increase of TgT_g with the quench rate and the correlation of heat capacity jump with liquid fragility.

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