Geometrical explanation and scaling of dynamical heterogeneities in glass forming systems

We show how dynamical heterogeneities in glass forming systems emerge as a consequence of the existence of dynamical constraints, and we offer an interpretation of the glass transition as an entropy crisis in trajectory space (space-time) rather than in configuration space. To illustrate our general ideas, we analyze the one-dimensional (d = 1) Fredrickson-Andersen and East models. Dynamics of such dynamically constrained systems are shown to be isomorphic to the statics of ( d + 1)-dimensional dense mixtures of polydisperse noninterpenetrating domains. The domains coincide with arrested regions in trajectory space.     

Space-time phase transitions in driven kinetically constrained lattice models

Kinetically constrained models (KCMs) have been widely used to study and understand the origin of glassy dynamics. These models show an ergodic-nonergodic first-order phase transition between phases of distinct dynamical “activity”. We introduce driven variants of two popular KCMs, the FA model and the (2)-TLG, as models for driven supercooled liquids. By classifying trajectories through their entropy production we prove that driven KCMs display an analogous first-order space-time transition between dynamical phases of finite and vanishing entropy production. We discuss how trajectories with rare values of entropy production can be realized as typical trajectories of a mapped system with modified forces.     

Caging and mosaic length scales in plaquette spin models of glasses

We consider two systems of Ising spins with plaquette interactions. They are simple models of glasses which have dual representations as kinetically constrained systems. These models allow an explicit analysis using the mosaic, or entropic droplet, approach of the random first-order transition theory of the glass transition. We show that the low-temperature states of these systems resemble glassy mosaic states, despite the fact that excitations are localized and that there are no static singularities. By means of finite-size thermodynamics we study a generalized caging effect whereby the system is frozen on short length scales, but free at larger length scales. We find that the freezing length scales obtained from statics coincide with those relevant to dynamic correlations, as expected in the mosaic view. The simple nucleation arguments of the mosaic approach, however, do not give the correct relation between freezing lengths and relaxation times, as they do not capture the transition states for relaxation. We discuss how these results make a connection between the mosaic and the dynamic facilitation views of glass formers.     

Activated aging dynamics and negative fluctuation-dissipation ratios

In glassy materials, aging proceeds at large times via thermal activation. We show that this can lead to negative dynamical response functions and novel and well-defined violations of the fluctuation-dissipation theorem, in particular, negative fluctuation-dissipation ratios. Our analysis is based on detailed theoretical and numerical results for the activated aging regime of simple kinetically constrained models. The results are relevant to a variety of physical situations, such as aging in glass formers, thermally activated domain growth, and granular compaction.     

Dynamic criticality in glass-forming liquids

We propose that the dynamics of supercooled liquids and the formation of glasses can be understood from the existence of a zero-temperature dynamical critical point. To support our proposal, we derive a dynamic field theory for a generic kinetically constrained model, which we expect to describe the dynamics of a supercooled liquid. We study this field theory using the renormalization group (RG). Its long time behavior is dominated by a zero-temperature critical point, which for d>2 belongs to the directed percolation universality class. Molecular dynamics simulations seem to confirm the existence of dynamic scaling behavior consistent with the RG predictions.     

Decoupling of exchange and persistence times in atomistic models of glass formers

With molecular dynamics simulations of a fluid mixture of classical particles interacting with pairwise additive Weeks-Chandler-Andersen potentials, we consider the time series of particle displacements and thereby determine the distributions for local persistence times and local exchange times. These basic characterizations of glassy dynamics are studied over a range of supercooled conditions and were shown to have behaviors, most notably decoupling, similar to those found in kinetically constrained lattice models of structural glasses. Implications are noted.