Structural Origin of Dynamic Heterogeneity in Supercooled Liquids.

Abstract

As a liquid is supercooled toward the glass transition point, its dynamics slow significantly, provided that crystallization is avoided. With increased supercooling, the particle dynamics become more spatially heterogeneous, a phenomenon known as dynamic heterogeneity. Since its discovery, this characteristic of metastable supercooled liquids has garnered considerable attention in glass science. However, the precise physical origins of dynamic heterogeneity remain elusive and widely debated. In this perspective, we examine the relationship between dynamic heterogeneity and structural order, based on numerical simulations of fragile liquids with isotropic potentials and strong liquids with directional interactions. We demonstrate that angular ordering, arising from many-body steric interactions, plays a crucial role in the slow dynamics and dynamic cooperativity of fragile liquids. Additionally, we explore how the growth of static order correlates with slower dynamics. In fragile liquids exhibiting super-Arrhenius behavior, the spatial extent of regions with high angular order grows upon cooling, and the sequential propagation of particle rearrangements within these ordered regions increases the activation energy for particle motion. In contrast, strong liquids with spatially constrained local ordering display a distinct "two-state" dynamic characteristic, marked by a transition between two Arrhenius-type behaviors. We argue that dynamic heterogeneity, irrespective of a liquid's fragility, arises from underlying structural order, with its spatial extent determined by static ordering. This perspective aims to deepen our understanding of the interplay between structural and dynamic properties in metastable supercooled liquids.