Polyamorphism in Glassy Network Materials

TL;DR

This paper introduces a microscopic model to study polyamorphism in network liquids, linking thermodynamic anomalies and glassy dynamics, with implications for understanding water-like phase transitions near the glass transition.

Contribution

It presents a simple microscopic model that captures the interplay of polyamorphism and glassy properties, applying RFOT theory to reveal nucleation kinetics near the phase transition.

Findings

The model exhibits a liquid-liquid phase transition tunable relative to the glass transition.

Water-like thermodynamic anomalies are connected to glassy kinetic behaviors.

Nanonucleation leads to small domains and nonclassical nucleation kinetics predicted by RFOT.

Abstract

One dramatic feature of network liquids is the emergence at low temperatures and high pressures of polyamorphism, where multiple distinct liquid phases are accessed in a single material. Polyamorphism can arise from the competition between distinct local inherent structures corresponding to bonded and nonbonded ordering. Thermal bond breaking thus can lead to a phase transition often accompanied by thermodynamic anomalies away from the transition itself, such as the familiar density maximum in water at atmospheric pressure and $4^\circ$ C. Water exhibits network interactions in the form of hydrogen bonding between water molecules. The polyamorphic transition in water, however, is difficult to study due to the rapid crystallization of supercooled water and due to glassy effects at low temperatures. In the present work, we propose a simple microscopic model where the glassy and thermodynamic properties are both calculated directly from the microscopic potentials. The model contains a liquid-liquid phase transition, which, after tuning the microscopic parameters, may be located either above, near, or below the glass transition. By applying the Random First Order Transition theory of the glass transition to this simple microscopic model, we shine light on the interplay of polyamorphism and glassy properties in network liquids. We show the connection between the thermodynamic water-like anomalies and corresponding anomalies in the glassy kinetics. The analysis unveils key details on the way glassy dynamics modifies the phase transition kinetics. When the parameters of the model are tuned to produce a phase diagram resembling that of water, the liquid-liquid phase transformation near $T_g$ occurs via ``nanonucleation'', resulting in extremely small domains sizes and nonclassical nucleation kinetics which are predicted from the RFOT theory.