Elastic anomalies in glasses: the string theory understanding in the case of Glycerol and Silica

Abstract

We present an implementation of the analytical string theory recently applied to the description of glasses. These are modeled as continuum media with embedded elastic string heterogeneities, randomly located and randomly oriented, which oscillate around a straight equilibrium position with a fundamental frequency depending on their length. The existence of a length distribution reflects then in a distribution of oscillation frequencies which is responsible for the Boson Peak in the glass density of states. Previously, it has been shown that such a description can account for the elastic anomalies reported at frequencies comparable with the Boson Peak. Here we start from the generalized hydrodynamics to determine the dynamic correlation function $S(k,\omega)$ associated with the coherent, dispersive and attenuated, sound waves resulting from a sound-string interference. Once the vibrational density of states has been measured, we can use it for univocally fixing the string length distribution inherent to a given glass. The density-density correlation function obtained using such distribution is strongly constrained, and able to account for the experimental data collected on two prototypical glasses: glycerol and silica. The obtained string length distribution is compatible with the typical size of elastic heterogeneities previously reported for silica and supercooled liquids, and the atomic motion associated to the string dynamics is consistent with the soft modes recently identified in large scale numerical simulations as non-phonon modes responsible for the Boson Peak. The theory is thus in agreement with the most recent advances in the understanding of the glass specific dynamics and offers an appealing simple understanding of the microscopic origin of the latter, while raising new questions on the universality or material-specificity of the string distribution properties.