Colloidal particles, which are ubiquitous, have become ideal testing grounds for the structural glass transition (SGT) theories. In these systems glassy behavior is manifested as the density of the particles is increased. Thus, soft colloidal particles with varying degree of softness capture diverse glass forming properties, observed normally in molecular glasses. By performing Brownian dynamics simulations for a binary mixture of micron-sized charged colloidal suspensions, known to form Wigner glasses, we show that by tuning the softness of the potential, achievable by changing the monovalent salt concentration, there is a continuous transition between fragile to strong behavior. Remarkably, this is found in a system where the well characterized potential between the colloidal particles is isotropic. We also show that the predictions of the random first order transition (RFOT) theory quantitatively describes the universal features such as the growing correlation length, $ξ\sim (ϕ_K/ϕ- 1)^{-ν}$ with $ν= 2/3$ where $ϕ_K$, the analogue of the Kauzmann temperature, depends on the salt concentration. As anticipated by the RFOT predictions, we establish a causal relationship between the growing correlation length and a steep increase in the relaxation time and dynamic heterogeneity. The broad range of fragility observed in Wigner glasses is used to draw analogies with molecular glasses. The large variations in the fragility is found only when the temperature dependence of the viscosity is examined for a large class of diverse glass forming materials. In sharp contrast, this is vividly illustrated in a single system that can be experimentally probed. Our work also shows that the RFOT predictions are accurate in describing the dynamics over the entire density range, regardless of the fragility of the glasses, implying that the physics describing the SGT is universal.
In this note I present a simplified version of the recent computation (Mezard and Parisi 1998, 1999) of the properties of glasses in the low temperature phase in the framework of the replica theory, using an extension of the tools used in liquid theory. I will only consider here the case of the internal energy at T=0, which can be studied in a simple way without introducing replicas.
Glass formers are in general classified as strong or fragile depending on whether their relaxation rates follow Arrhenius or super-Arrhenius temperature dependence. There are however notable exceptions such as water, which exhibit a fragile-to-strong (FTS) transition and behave as fragile and strong respectively at high and low temperatures. In this work, the FTS transition is studied using a distinguishable-particle lattice model previously demonstrated to be capable of simulating both strong and fragile glasses [Phys. Rev. Lett. 125, 265703 (2020)]. Starting with a bimodal pair-interaction d…
A disordered spin model suitable for studying inverse freezing in fragile glass-forming systems is introduced. The model is a microscopic realization of the ``random-first order'' scenario in which the glass transition can be either continuous or discontinuous in thermodynamic sense. The phase diagram exhibits a first-order transition line between two fluid phases terminating at a critical point. When the interacting degrees of freedom are entropically favoured an inverse static glass transition and a double inverse dynamic freezing appear.
We perform kinetic Monte Carlo simulations of a distinguishable-particle lattice model of structural glasses with random particle interactions. By varying the interaction distribution and the average particle hopping energy barrier, we obtain an extraordinarily wide range of kinetic fragility. A stretching exponent, characterizing structural relaxation, is found to decrease with the kinetic fragility in agreement with experiments. The most fragile glasses are those exhibiting low hopping barriers and, more importantly, dramatic drops of entropies upon cooling toward the glass transition temper…
The specific heat capacity $c_v$ of glass formers undergoes a hysteresis when subjected to a cooling-heating cycle, with a larger $c_v$ and a more pronounced hysteresis for fragile glasses than for strong ones. Here, we show that these experimental features, including the unusually large magnitude of $c_v$ of fragile glasses, are well reproduced by kinetic Monte Carlo and equilibrium study of a distinguishable particle lattice model (DPLM) incorporating a two-state picture of particle interactions. The large $c_v$ in fragile glasses is caused by a dramatic transfer of probabilistic weight from…
We investigate the Kovacs (or crossover) effect in facilitated $f$-spin models of glassy dynamics. Although the Kovacs hump shows a behavior qualitatively similar for all cases we have examined (irrespective of the facilitation parameter $f$ and the spatial dimension $d$), we find that the dependence of the Kovacs peak time on the temperature of the second quench allows to distinguish among different microscopic mechanisms responsible for the glassy relaxation (e.g. cooperative vs defect diffusion). We also analyze the inherent structure dynamics underlying the Kovacs protocol, and find that t…
Non-reversing relaxation enthalpies (DHnr) at glass transitions Tg(x) in the PxGexSe1-2x ternary display wide, sharp and deep global minima (~ 0) in the 0.09 < x < 0.145 range, within which Tgs become thermally reversing. In this reversibility window, glasses are found not to age, in contrast to aging observed for fragile glass compositions outside the window. Thermal reversibility and lack of aging seem to be paradigms of self-organization which molecular glasses share with protein structures which repetitively and reversibly change conformation near Tg and the folding temperature respectivel…
Microscopic relaxation timescales are estimated from the autocorrelation functions obtained by dynamic light scattering experiments for Laponite suspensions with different concentrations ($C_{L}$), added salt concentrations ($C_{S}$) and temperatures ($T$). It has been shown in an earlier work [Soft Matter, 10, 3292-3300 (2014)] that the evolutions of relaxation timescales of colloidal glasses can be compared with molecular glass formers by mapping the waiting time ($t_{w}$) of the former with the inverse of thermodynamic temperature ($1/T$) of the latter. In this work, the fragility parameter…
We image local structural rearrangements in soft colloidal glasses under small periodic perturbations induced by thermal cycling. Local structural entropy $S_{2}$ positively correlates with observed rearrangements in colloidal glasses. The high $S_{2}$ values of the rearranging clusters in glasses indicate that fragile regions in glasses are structurally less correlated, similar to structural defects in crystalline solids. Slow-evolving high $S_{2}$ spots are capable of predicting local rearrangements long before the relaxations occur, while fluctuation-created high $S_{2}$ spots best correlat…
Within the shoving model of the glass transition, the relaxation time and the viscosity are related to the local cage rigidity. This approach can be extended down to the atomic-level in terms of the interatomic interaction, or potential of mean-force. We applied this approach to both real metallic glass-formers and model Lennard-Jones glasses. The main outcome of this analysis is that in metallic glasses the thermal expansion contribution is mostly independent of composition and is uncorrelated with the interatomic repulsion: as a consequence, the fragility increases upon increasing the intera…
Vapor deposition of molecules on a substrate often results in glassy materials of high kinetic stability and low enthalpy. The extraordinary properties of such glasses are attributed to high rates of surface diffusion during sample deposition, which makes it possible for constituents to find a configuration of much lower energy on a typical laboratory time scale1,2,7. The exact structure of the resulting phase is often assumed to be identical to that obtained by aging of ordinary glass over exceedingly long times. Using Fast Scanning Calorimetry technique, we show that out-of-equilibrium relax…
In these lectures I will review the approach to glasses based on the replica formalism. Many of the physical ideas are very similar to those of older approaches. The replica approach has the advantage of describing in an unified setting both the behaviour near the dynamic transition (mode coupling transition) and near the equilibrium transition (Kauzman transition) that is present in fragile glasses. The replica method may be used to solve simple mean field models, providing explicit examples of systems that may be studied analytically in great details and behave similarly to the experiments. …
The enhancement of surface diffusion (DS) over the bulk (DV) in metallic glasses (MGs) is well documented and likely to strongly influence the properties of glasses grown by vapor deposition. Here, we use classical molecular dynamics simulations to identify different factors influencing the enhancement of surface diffusion in MGs. MGs have a simple atomic structure and belong to the category of moderately fragile glasses that undergo pronounced slowdown of bulk dynamics with cooling close to the glass transition temperature (Tg). We observe that DS exhibits a much more moderate slowdown compar…
Glass-forming liquids are broadly classified as being fragile or strong, depending on the deviation from Arrhenius behavior of their relaxation times. A fragile to strong crossover is observed or inferred in liquids like water and silica, and more recently also in metallic glasses and phase change alloys, leading to the expectation that such a crossover is more widely realised among glass formers. We investigate computationally the well-studied Kob-Andersen model, accessing temperatures well below the mode coupling temperature $T_{MCT}$. We find that relaxation times exhibit a crossover in dyn…
Dense soft glasses show strong collective caging behavior at sufficiently low temperatures. Using molecular dynamics simulations of a model glass former, we show that the incorporation of activity or self-propulsion, f0, can induce cage breaking and fluidization, resulting in a disappearance of the glassy phase beyond a critical f0 . The diffusion coefficient crosses over from being strongly to weakly temperature dependent as f0 is increased. In addition, we demonstrate that activity induces a crossover from a fragile to a strong glass and a tendency for clustering of active particles. Our res…
The fragility of a glassforming liquid characterizes how rapidly its relaxation dynamics slow down with cooling. The viscosity of strong liquids follows an Arrhenius law with a temperature-independent barrier height to rearrangements responsible for relaxation, whereas fragile liquids experience a much faster increase in their dynamics, suggesting a barrier height that increases with decreasing temperature. Strong glassformers are typically network glasses, while fragile glassformers are typically molecular or hard-sphere-like. As a result of these differences at the microscopic level, strong …
In two-dimensional (2D) systems, the melting from a solid to an isotropic liquid can occur via an intermediate phase that retains orientational order. However, in 2D superconducting vortex lattices, the effect of orientational correlations on transport, and their interplay with disorder remain open questions. Here we study a 2D weakly pinned vortex system in amorphous MoGe films over an extensive range of temperatures ($\bm{T}$) and perpendicular magnetic fields ($\bm{H}$) using linear and nonlinear transport measurements. We find that, at low fields, the resistivity obeys the Vogel-Fulcher-Ta…
We study dynamical heterogeneity and growing dynamical lengthscales in two kinetically constrained models, namely, the one- and two-vacancy assisted triangular lattice gases. One of the models is a strong glassformer and the other is a fragile glassformer. Both exhibit heterogeneous dynamics with broadly distributed timescales as seen in the distribution of persistence times. We show that the Stokes-Einstein relation is violated, to a greater degree in the fragile glassformer, and show how this violation is related to dynamic heterogeneity. We extract dynamical lengthscales from structure fact…
Fragility, quantifying the rapidity of variation of relaxation times, is analysed for a series of model glass formers, which differ in the softness of their interparticle interactions. In an attempt to rationalize experimental observations in colloidal suspensions that softer interactions lead to stronger (less fragile) glass formers, we study the variation of relaxation dynamics with density, rather than temperature, as a control parameter. We employ density temperature scaling, analyzed in recent studies, to address the question. We find that while employing inverse density in place of tempe…
Thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) particles of a nearly constant swelling ratio and with polydispersity indices (PDIs) varying over a wide range (7.4% - 48.9%) are synthesized to study the effects of polydispersity on the dynamics of suspensions of soft PNIPAM colloidal particles. The PNIPAM particles are characterized using dynamic light scattering (DLS) and scanning electron microscopy (SEM). The zero shear viscosity ($η_{0}$) data of these colloidal suspensions, estimated from rheometric experiments as a function of the effective volume fraction $ϕ_{eff}$ of the suspensi…
