Molecular mobility in driven monomeric and polymeric glasses

TL;DR

This paper reveals a universal relation for microscopic structural relaxation time in monomeric glasses under shear, and discusses how this relation breaks down in polymeric glasses, providing a framework for analyzing mobility in glassy materials.

Contribution

It introduces a universal relation for structural relaxation time in monomeric glasses under shear and explains its breakdown in polymeric glasses, offering a new analytical framework.

Findings

Universal relation between stress, shear rate, and relaxation time in monomeric glasses.

Decoupling of stress and relaxation time in polymeric glasses during strain hardening.

Framework for analyzing mobility measurements in various glassy materials.

Abstract

We show that in monomeric supercooled liquids and glasses that are plastically flowing at a constant shear stress $\sigma$ while being deformed with strain rate $\dot{\epsilon}$, the microscopic structural relaxation time $\tau_{\rm str}$ is given by the universal relation $\sigma/G_\infty\dot{\epsilon}$ with $G_\infty$ a modulus. This equality holds for all rheological regimes from temperatures above the glass transition all the way to the athermal limit, and arises from the competing effects of elastic loading and viscous dissipation. In macromolecular (polymeric) glasses, however, the stress decouples from this relaxation time and $\tau_{\rm str}$ is in fact further reduced even though $\sigma$ rises during glassy strain hardening. We develop expressions to capture both effects and thus provide a framework for analyzing mobility measurements in glassy materials.