We make a first principle calculation of the fragility index $m$ of a simple liquid using the structure of the supercooled liquid as an input. Using the density functional theory (DFT) of classical liquids, the configurational entropy ${\cal S}_c$ is obtained for low degree of supercooling. We extrapolate this data to estimate the Kauzmann temperature $T_\mathrm{K}$ for the liquid. Using the Adam-Gibbs relation, we link the configurational entropy ${\cal S}_c$ to the relaxation time. The relaxation times are obtained from direct solutions of the equations of fluctuating nonlinear hydrodynamics (FNH). These equations also form the basis of the mode coupling theory (MCT) for glassy dynamics. The fragility index for the supercooled liquid is estimated from analysis of the curves on the Angell plot.
We investigate the influence of space curvature, and of the associated "frustration", on the dynamics of a model glassformer: a monatomic liquid on the hyperbolic plane. We find that the system's fragility, i.e. the sensitivity of the relaxation time to temperature changes, increases as one decreases the frustration. As a result, curving space provides a way to tune fragility and make it as large as wanted. We also show that the nature of the emerging "dynamic heterogeneities", another distinctive feature of slowly relaxing systems, is directly connected to the presence of frustration-induced …
An analysis of diffusion in a supercooled liquid based solely in the density of diffusive directions and the value of energy barriers shows how the potential energy landscape (PEL) approach is capable of explaining the $α$ and $β$ relaxations and the fragility of a glassy system. We find that the $β$ relaxation is directly related to the search for diffusive directions. Our analysis shows how in strong liquids diffusion is mainly energy activated, and how in fragile liquids the diffusion is governed by the density of diffusive directions. We describe the fragile-to-strong crossover as a change…
A low temperature Monte Carlo dynamics of a Keating like oscillator model is used to study the relationship between the nature of glasses from the viewpoint of rigidity, and the strong-fragile behaviour of glass-forming liquids. The model shows that a Phillips optimal glass formation with minimal enthalpic changes is obtained under a cooling/annealing cycle when the system is optimally constrained by the harmonic interactions, i.e. when it is isostatically rigid. For these peculiar systems, the computed fragility shows also a minimum, which demonstrates that isostatically rigid glasses are str…
We analyze results for the Boson Peak from the neutron time of flight spectroscopy data on Ge-As-Se, and Raman spectra data on m-TCP and OTP, using a recent mode coupling model that takes into account the coupling of density fluctuations with vibrational modes in presence of defects in the supercooled state. From the experimental results for different materials we observe that for more fragile systems characterized by increasing fragility parameter m, a slower relaxation of the defect-density correlation is needed to give rise to the observed peak in the spectra.
The term "fragility" describes the rate at which viscosity grows when a supercooled liquid approaches its putative glass transition temperature. The field of glassy materials is actively searching for a structural origin that governs this dynamical slowing down in the supercooled liquid, which occurs without any discernible change in structure. Our work shows clear evidence that growing many-body static amorphous order is intimately correlated with the kinetic fragility of glass-forming liquids. It confirms that the system's dynamical response to temperature is concealed in its micro-structure…
Glass is a microscopically disordered, solid form of matter that results when a fluid is cooled or compressed in such a fashion that it does not crystallise. Almost all types of materials are capable of glass formation -- polymers, metal alloys, and molten salts, to name a few. Given such diversity, organising principles which systematise data concerning glass formation are invaluable. One such principle is the classification of glass formers according to their fragility\cite{fragility}. Fragility measures the rapidity with which a liquid's properties such as viscosity change as the glassy sta…
The rapid rise of viscosity or relaxation time upon supercooling is universal hallmark of glassy liquids. The temperature dependence of the viscosity, however, is quite non universal for glassy liquids and is characterized by the system's "fragility," with liquids with nearly Arrhenius temperature-dependent relaxation times referred to as strong liquids and those with super-Arrhenius behavior referred to as fragile liquids. What makes some liquids strong and others fragile is still not well understood. Here we explore this question in a family of glassy liquids that range from extremely strong…
Super-cooled liquids are characterized by their fragility: the slowing down of the dynamics under cooling is more sudden and the jump of specific heat at the glass transition is generally larger in fragile liquids than in strong ones. Despite the importance of this quantity in classifying liquids, explaining what aspects of the microscopic structure controls fragility remains a challenge. Surprisingly, experiments indicate that the linear elasticity of the glass -- a purely local property of the free energy landscape -- is a good predictor of fragility. In particular, materials presenting a la…
We report the observation of a distinct correlation between the kinetic fragility index $m$ and the reduced Arrhenius crossover temperature $θ_A = T_A/T_g$ in various glass-forming liquids, identifying three distinguishable groups. In particular, for 11 glass-forming metallic liquids, we universally observe a crossover in the mean diffusion coefficient from high-temperature Arrhenius to low-temperature super-Arrhenius behavior at approximately $θ_A \approx 2$ which is in the stable liquid phases. In contrast, for fragile molecular liquids, this crossover occurs at much lower $θ_A \approx 1.4$ …
We obtain monatomic glass formers in simulations by modifying the tetrahedral character in a silicon potential to explore a triple point zone between potentials favoring diamond (dc) and bcc crystals. dc crystallization is always preceded by a polyamorphic transformation of the liquid, and is frustrated when the Kauzmann temperature of the high temperature liquid intersects the liquid-liquid coexistence line. The glass forming liquids are extraordinarily fragile. Our results suggest that Si and Ge liquids may be vitrified at a pressure close to the diamond-beta-tin-liquid triple point.
Using molecular dynamics simulations, we study the slow dynamics of supercooled liquids confined in a random matrix of immobile obstacles. We study the dynamical crossover from glass-like to Lorentz-gas-like behavior in terms of the density correlation function, the mean square displacement, the nonlinear dynamic susceptibility, the non-Gaussian parameter, and the fragility. Cooperative and spatially heterogeneous dynamics are suppressed as the obstacle density increases, which lead to the more Arrhenius-like behavior in the temperature dependence of the relaxation time. Our findings are quali…
We show that the fragility $m$, the steepness of the viscosity and relaxation time close to the vitrification, increases with the degree of elastic softening, i.e. the decrease of the elastic modulus with increasing temperature, in universal way. This provides a novel connection between the thermodynamics, via the modulus, and the kinetics. The finding is evidenced by numerical simulations and comparison with the experimental data of glassformers with widely different fragilities ($33 \le m \le 115$), leading to a fragility-independent elastic master curve extending over eighteen decades in vi…
Dynamical quantities such as the diffusion coefficient and relaxation times for some glass-formers may depend on density and temperature through a specific combination, rather than independently, allowing the representation of data over ranges of density and temperature as a function of a single scaling variable. Such a scaling, referred to as density - temperature (DT) scaling, is exact for liquids with inverse power law (IPL) interactions but has also been found to be approximately valid in many non-IPL liquids. We have analyzed the consequences of DT scaling on the density dependence of the…
Extensive computer simulations are performed for a few model glass-forming liquids in both two and three dimensions to study their dynamics when a randomly chosen fraction of particles are frozen in their equilibrium positions. For all the studied systems, we find that the temperature-dependence of the $α$ relaxation time extracted from an overlap function related to the self part of the density autocorrelation function can be explained within the framework of the Random First Order Transition (RFOT) theory of the glass transition. We propose a scaling description to rationalize the simulation…
A relation between vibrational entropy and particles mean square displacement is derived in super-cooled liquids, assuming that the main effect of temperature changes is to rescale the vibrational spectrum. Deviations from this relation, in particular due to the presence of a Boson Peak whose shape and frequency changes with temperature, are estimated. Using observations of the short-time dynamics in liquids of various fragility, it is argued that (i) if the crystal entropy is significantly smaller than the liquid entropy at $T_g$, the extrapolation of the vibrational entropy leads to the corr…
We theoretically investigate structural relaxation and activated diffusion of glass-forming liquids at different pressures using both the Elastically Collective Nonlinear Langevin Equation (ECNLE) theory and molecular dynamics (MD) simulation. An external pressure restricts local motions of a single molecule within its cage and triggers the slowing down of cooperative mobility. While the ECNLE theory and simulation generally predict a monotonic increase of the glass transition temperature and dynamic fragility with pressure, the simulation indicates a decrease of fragility as pressure above 10…
The mode-coupling theory of the glass transition treats the dynamics of supercooled liquids in terms of two-point density correlation functions. Here we consider a generalized, hierarchical formulation of schematic mode-coupling equations in which the full basis of multipoint density correlations is taken into account. By varying the parameters that control the effective contributions of higher-order correlations, we show that infinite hierarchies can give rise to both sharp and avoided glass transitions. Moreover, small changes in the form of the coefficients result in different scaling behav…
The characterization of the formation mechanisms of amorphous solids is a large avenue for research, since understanding its non-Arrhenius behavior is challenging to overcome. In this context, we present one path toward modeling the diffusive processes in supercooled liquids near glass transition through a class of non-homogeneous continuity equations, providing a consistent theoretical basis for the physical interpretation of its non-Arrhenius behavior. More precisely, we obtain the generalized drag and diffusion coefficients that allow us to model a wide range of non-Arrhenius processes. Thi…
Polydispersity is found to have a significant effect on the potential energy landscape; the the average inherent structure energy with temperature decreases with polydispersity. Increasing polydispersity at fixed volume fraction decreases the glass transition temperature and the fragility of glass formation analogous to the antiplasticization seen in some polymeric melts. An interesting temperature dependent crossover of heterogeneity with polydispersity is observed at low temperature due to the faster build-up of dynamic heterogeneity at lower polydispersity.
For a deeply supercooled liquid just above its glass transition temperature, we present a simple thermodynamic model, where the deeply supercooled liquid is assumed to be a mixture of solid-like and liquid-like micro regions. The mole fraction of the liquid-like regions controls the thermodynamic properties of the supercooled liquid while that of the solid-like regions controls its relaxation time or viscosity. From the universal temperature dependence of the molar excess entropy for the deeply supercooled liquids, we derive the temperature dependence of the mole fraction of the liquid-like re…
The configurational entropy is among the key observables to characterize experimentally the formation of a glass. Physically, it quantifies the multiplicity of metastable states in which an amorphous material can be found at a given temperature, and its temperature dependence provides a major thermodynamic signature of the glass transition, which is experimentally accessible. Measurements of the configurational entropy require, however, some approximations which have often led to ambiguities and contradictory results. Here we implement a novel numerical scheme to measure the configurational en…
We numerically study a nondisordered lattice spin system with a first order liquid-crystal transition, as a model for supercooled liquids and glasses. Below the melting temperature the system can be kept in the metastable liquid phase, and it displays a dynamic phenomenology analogous to fragile supercooled liquids, with stretched exponential relaxation, power law increase of the relaxation time and high fragility index. At an effective spinodal temperature Tsp the relaxation time exceeds the crystal nucleation time, and the supercooled liquid loses stability. Below Tsp liquid properties canno…
The thermodynamics and dynamics of supercooled liquids correlate with their elasticity. In particular for covalent networks, the jump of specific heat is small and the liquid is {\it strong} near the threshold valence where the network acquires rigidity. By contrast, the jump of specific heat and the fragility are large away from this threshold valence. In a previous work [Proc. Natl. Acad. Sci. U.S.A., 110, 6307 (2013)], we could explain these behaviors by introducing a model of supercooled liquids in which local rearrangements interact via elasticity. However, in that model the disorder char…
We perform extensive molecular dynamics simulations of dense liquids composed of bidisperse dimer- and ellipse-shaped particles in 2D that interact via repulsive contact forces. We measure the structural relaxation times obtained from the long-time decay of the self-part of the intermediate scattering function for the translational and rotational degrees of freedom (DOF) as a function of packing fraction ϕ, temperature T, and aspect ratio α. We are able to collapse the ϕand T-dependent structural relaxation times for disks, and dimers and ellipses over a wide range of α, onto a universal scali…
