We study the response of probe particles to weak constant driving in kinetically constrained models of glassy systems, and show that the probe's response can be non-monotonic and give rise to negative differential mobility: increasing the applied force can reduce the probe's drift velocity in the force direction. Oth er significant non-linear effects are also demonstrated, such as the enhancement with increasing force of the probe's fluctuations away from the average path, a phenomenon known in other contexts as giant diffusivity. We show that these res ults can be explained analytically by a continuous-time random walk approximatio n where there is decoupling between persistence and exchange times for local dis placements of the probe. This decoupling is due to dynamic heterogeneity in the glassy system, which also leads to bimodal distributions of probe particle disp lacements. We discuss the relevance of our results to experiments.
The Adam-Gibbs (AG) relation connects the dynamics of a glass-forming liquid to its the thermodynamics via. the configurational entropy, and is of fundamental importance in descriptions of glassy behaviour. The breakdown of the Stokes-Einstein (SEB) relation between the diffusion coefficient and the viscosity (or structural relaxation times) in glass formers raises the question as to which dynamical quantity the AG relation describes. By performing molecular dynamics simulations, we show that the AG relation is valid over the widest temperature range for the diffusion coefficient and not for t…
Supercooled liquids are kinetically trapped materials in which the transition to a thermodynamically more stable state with long-range order is strongly suppressed. To assess the glass-forming abilities of a liquid empirical rules exist, but a comprehensive microscopic picture of devitrification is still missing. Here we study the crystallization of a popular model glass former, the binary Kob-Andersen mixture, in small systems. We perform trajectory sampling employing the population of the locally favored structure as order parameter. While for large population a dynamical phase transition ha…
Heat capacity of B2O3 glass former in a wide temperature region is described well with the intrinsic motions for non-spherical B2O3 molecules, revealing that rather than a conventional network glass former, B2O3 is a typical molecular matter in which the transition from liquid to glass in the system corresponds to the frozen of translational motions for molecules. The finding might provide an opportunity to understand the mysterious glass transition, as well as the intrinsic difference between solids and liquids.
A theory is developed to calculate values of the potential energy barriers to structural relaxation in molecular glass formers from the data of static pair correlation function. The barrier height is shown to increase due to increase in number of the stable bonds a particle forms with its neighbours and energy of each bond as liquids move deeper into the supercooled (super-compressed) region. We present results for a system of hard-spheres and compare calculated values of the structural relaxation time with experimental and simulation results.
In this article we review results of computer simulation of glasses carried out using first principles approaches, notably density functional theory. We start with a brief introduction to this method and compare the pros and cons of this approach with the ones of simulations with classical potentials. This is followed by a discussion of simulation results of various glass-forming systems that have been obtained via ab initio simulations and that demonstrate the usefulness of this approach to understand the properties of glasses on the microscopic level.
Whether the glass transition is caused by an underlying singularity or is a purely kinetic phenomenon is a significant outstanding question. Studying an atomistic glass former, we introduce a sampling method to access temperatures corresponding to dynamical regimes usually hard to reach with computer simulation. We find a peak in the specific heat, which we interpret as a drop in the density of states. We further present evidence of a liquid-liquid transition to a state rich in locally favoured structures related to a recently discovered dynamical phase transition.
We study the nature of the glass transition by cooling model atomistic glass formers at constant rate from a temperature above the onset of glassy dynamics to $T=0$. Motivated by the East model, a kinetically constrained lattice model with hierarchical relaxation, we make several predictions about the behavior of the supercooled liquid as it passes through the glass transition. We then compare those predictions to the results of our atomistic simulations. Consistent with our predictions, our results show that the relaxation time $τ$ of the material undergoes a crossover from super-Arrhenius to…
Using molecular dynamics simulations we investigate the finite-size dependence of the dynamical properties of a diatomic supercooled liquid. The simplicity of the molecule permits us to access the microsecond time scale. We find that the relaxation time decreases simultaneously with the strength of cooperative motions when the size of the system decreases. While the decrease of the cooperative motions is in agreement with previous studies, the decrease of the relaxation time opposes what has been reported to date in monatomic glass formers and in silica. This result suggests the presence of di…
We numerically study the equilibrium relaxation dynamics of a two-dimensional Mari-Kurchan glass model. The tree-like structure of particle interactions forbids both non-trivial structural motifs and the emergence of a complex free-energy landscape leading to a thermodynamic glass transition, while the finite-dimensional nature of the model prevents the existence of a mode-coupling singularity. Nevertheless, the equilibrium relaxation dynamics is shown to be in excellent agreement with simulations performed in conventional glass-formers. Averaged time-correlation functions display a phenomenol…
In a dense colloidal suspension at a volume fraction slightly lower than that of its glass transition, we follow the trajectories of an assembly of tracers over a large time window. We define a local activity, which quantifies the local tendency of the system to rearrange. We determine the statistics of the time and space integrated activity, and we argue that it develops a low activity tail that comes on a par with the onset of glassy behavior and heterogeneous dynamics. These rare events may be interpreted as the reflection of an underlying dynamic phase transition.
We investigate the static and dynamic properties of a weakly polydisperse hard sphere system in the deeply supercooled state, i.e. at densities higher than that corresponding to the mode-coupling transition. The structural analysis reveals the emergence of icosahedral locally favoured structures, previously only found in trace quantities. We present a new approach to probe the shape of dynamically heterogeneous regions, which is insensitive to particle packing effects that can hamper such analysis. Our results indicate that the shape of the dynamically heterogeneous regions changes only weakly…
Amorphous solids under mechanical strains are prone to plastic responses. Recent work showed that in amorphous granular system these plastic events, that are typically quadrupolar in nature, can screen the elastic response. When the density of the quadrupoles is high, the gradients of the quadrupole field act as emergent dipole sources, leading to qualitative changes in the mechanical response, as seen for example in the displacement field. In this paper we examine the effect of screening in classical glass formers. These are made of point particles that interact via binary forces. Both invers…
