Abstract
A fundamental problem of glass transition is to explain the jump of heat capacity at the glass transition temperature 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 is defined as the temperature at which the liquid stops relaxing at the experimental time scale, the jump of heat capacity at 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 with the quench rate and the correlation of heat capacity jump with liquid fragility.
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