arXiv subjects
Publications and source records attributed to A. de Candia.
We study the dynamical behavior of a lattice model of glass former on a random graph, where no corrections to the mean field description are expected. We find that the behavior of dynamical correlation functions and dynamical susceptibility are consistent with the quantitative predictions of the Mode Coupling Theory of the glass transition.
We present a systematic study of dynamical heterogeneity in a model for permanent gels, upon approaching the gelation threshold. We find that the fluctuations of the self intermediate scattering function are increasing functions of time, reaching a plateau whose value, at large length scales, coincides with the mean cluster size and diverges at the percolation threshold. Another measure of dynamical heterogeneities, i.e. the fluctuations of the self-overlap, displays instead a peak and decays to zero at long times. The peak, however, also scales as the mean cluster size. Arguments are given for this difference in the long time behavior. We also find that non-Gaussian parameter reaches a plateau in the long time limit. The value of the plateau of the non-Gaussian parameter, which is connected to the fluctuations of diffusivity of clusters, increases with the volume fraction and remains finite at percolation threshold.
We study the formation of a colloidal gel by means of Molecular Dynamics simulations of a model for colloidal suspensions. A slowing down with gel-like features is observed at low temperatures and low volume fractions, due to the formation of persistent structures. We show that at low volume fraction the dynamic susceptibility, which describes dynamic heterogeneities, exhibits a large plateau, dominated by clusters of long living bonds. At higher volume fraction, where the effect of the crowding of the particles starts to be present, it crosses over towards a regime characterized by a peak. We introduce a suitable mean cluster size of clusters of monomers connected by "persistent" bonds which well describes the dynamic susceptibility.
We compare the slow dynamics of irreversible gels, colloidal gels, glasses and spin glasses by analyzing the behavior of the so called non-linear dynamical susceptibility, a quantity usually introduced to quantitatively characterize the dynamical heterogeneities. In glasses this quantity typically grows with the time, reaches a maximum and then decreases at large time, due to the transient nature of dynamical heterogeneities and to the absence of a diverging static correlation length. We have recently shown that in irreversible gels the dynamical susceptibility is instead an increasing function of the time, as in the case of spin glasses, and tends asymptotically to the mean cluster size. On the basis of molecular dynamics simulations, we here show that in colloidal gelation where clusters are not permanent, at very low temperature and volume fractions, i.e. when the lifetime of the bonds is much larger than the structural relaxation time, the non-linear susceptibility has a behavior similar to the one of the irreversible gel, followed, at higher volume fractions, by a crossover towards the behavior of glass forming liquids.
In colloidal suspensions, the competition between attractive and repulsive interactions gives rise to a rich and complex phenomenology. Here, we study the equilibrium phase diagram of a model system using a DLVO interaction potential by means of molecular dynamics simulations and a thermodynamical approach. As a result, we find tubular and lamellar phases at low volume fraction. Such phases, extremely relevant for designing new materials, may be not easily observed in the experiments because of the long relaxation times and the presence of defects.
We study the structure and the dynamics in the formation of irreversible gels by means of molecular dynamics simulation of a model system where the gelation transition is due to the random percolation of permanent bonds between neighboring particles. We analyze the heterogeneities of the dynamics in terms of the fluctuations of the intermediate scattering functions: In the sol phase close to the percolation threshold, we find that this dynamical susceptibility increases with the time until it reaches a plateau. At the gelation threshold this plateau scales as a function of the wave vector $k$ as $k^{η-2}$, with $η$ being related to the decay of the percolation pair connectedness function. At the lowest wave vector, approaching the gelation threshold it diverges with the same exponent $γ$ as the mean cluster size. These findings suggest an alternative way of measuring critical exponents in a system undergoing chemical gelation.
By means of molecular dynamics, we study a model system for colloidal suspensions where the interaction is based on a competition between attraction and repulsion. At low temperatures the relaxation time $τ$ first increases as a power law as a function of the volume fraction $ϕ$ and then, due to the finite lifetime of the bonded structures, it deviates from this critical behavior. We show that colloidal gelation at low temperatures and low volume fractions is crucially related to the formation of spanning long living cluster. Besides agreeing with experimental findings in different colloidal systems, our results shed new light on the different role played by the formation of long living bonds and the crowding of the particles in colloidal structural arrest.
In order to study analytically the nature of the jamming transition in granular material, we have considered a cavity method mean field theory, in the framework of a statistical mechanics approach, based on Edwards' original idea. For simplicity we have applied the theory to a lattice model and a transition with exactly the same nature of the glass transition in mean field models for usual glass formers is found. The model is also simulated in three dimensions under tap dynamics and a jamming transition with glassy features is observed. In particular two step decays appear in the relaxation functions and dynamic heterogeneities resembling ones usually observed in glassy systems. These results confirm early speculations about the connection between the jamming transition in granular media and the glass transition in usual glass formers, giving moreover a precise interpretation of its nature.
In the framework of schematic hard spheres lattice models for granular media we investigate the phenomenon of the ``jamming transition''. In particular, using Edwards' approach, by analytical calculations at a mean field level, we derive the system phase diagram and show that ``jamming'' corresponds to a phase transition from a ``fluid'' to a ``glassy'' phase, observed when crystallization is avoided. Interestingly, the nature of such a ``glassy'' phase turns out to be the same found in mean field models for glass formers.
We study a model for the gel degradation by an enzyme, where the gel is schematized as a cubic lattice, and the enzyme as a random walker, that cuts the bonds over which it passes. The model undergoes a (reverse) percolation transition, which for low density of enzymes falls in a universality class different from random percolation. In particular we have measured a gel fraction critical exponent beta=1.0+-0.1, in excellent agreement with experiments made on the real system.
In the framework of schematic hard spheres lattice models we discuss Edwards' Statistical Mechanics approach to granular media. As this approach appears to hold here to a very good approximation, by analytical calculations of Edwards' partition function at a mean field level we derive the system phase diagram and show that ``jamming'' corresponds to a phase transition from a ``fluid'' to a ``glassy'' phase, observed when crystallization is avoided. The nature of such a ``glassy'' phase turns out to be the same found in mean field models for glass formers. In the same context, we also briefly discuss mixing/segregation phenomena of binary mixtures: the presence of fluid-crystal phase transitions drives segregation as a form of phase separation and, within a given phase, gravity can also induce a kind of ``vertical'' segregation, usually not associated to phase transitions.
Experiments of in vitro formation of blood vessels show that cells randomly spread on a gel matrix autonomously organize to form a connected vascular network. We propose a simple model which reproduces many features of the biological system. We show that both the model and the real system exhibit a fractal behavior at small scales, due to the process of migration and dynamical aggregation, followed at large scale by a random percolation behavior due to the coalescence of aggregates. The results are in good agreement with the analysis performed on the experimental data.
We study a lattice model with two body interactions that reproduces in three-dimensions many features of structural glasses, like cage effect and vanishing diffusivity. While having a crystalline state at low temperatures, it does not crystallize when quenched, even at the slowest cooling rate used, which makes it suitable to study the glass transition. We study the model on the Bethe lattice as well, and find a scenario typical of p-spin models, as in the Biroli Mezard model.
A thorough numerical investigation of the slow dynamics in the d=1 random field Ising model in the limit of an infinite ferromagnetic coupling is presented. Crossovers from the preasymptotic pure regime to the asymptotic Sinai regime are investigated for the average domain size, the autocorrelation function and staggered magnetization. By switching on an additional small random field at the time tw the linear off equilibrium response function is obtained, which displays as well the crossover from the nontrivial behavior of the d=1 pure Ising model to the asymptotic behavior where it vanishes identically.
We perform large scale simulations of the frustrated Ising lattice gas, a three-dimensional lattice model of a structural glass, using the parallel tempering technique. We evaluate the spin and density overlap distributions, and the corresponding non-linear susceptibilities, as a function of the chemical potential. We then evaluate the relaxation functions of the spin and density self-overlap, and study the behavior of the relaxation times. The results suggest that the spin variables undergo a transition very similar to the one of the Ising spin glass, while the density variables do not show any sign of transition at the same chemical potential. It may be that the density variables undergo a transition at a higher chemical potential, inside the phase where the spins are frozen.
We study the Blume-Emery-Griffiths spin glass model in presence of an attractive coupling between real replicas, and evaluate the effective potential as a function of the density overlap. We find that there is a region, above the first order transition of the model, where metastable states with a large density overlap exist. The line where these metastable states appear should correspond to a purely dynamical transition, with a breaking of ergodicity. Differently from what happens in p-spin glasses, in this model the dynamical transition would not be the precursor of a 1-step RSB transition, but (probably) of a full RSB transition.
In cond-mat/0002074 Ricci-Tersenghi et al. find two linear regimes in the fluctuation-dissipation relation between density-density correlations and associated responses of the Frustrated Ising Lattice Gas. Here we show that this result does not seem to correspond to the equilibrium quantities of the model, by measuring the overlap distribution P(q) of the density and comparing the FDR expected on the ground of the P(q) with the one measured in the off-equilibrium experiments.
We investigate the crossover properties of the frustrated percolation model on a two-dimensional square lattice, with asymmetric distribution of ferromagnetic and antiferromagnetic interactions. We determine the critical exponents nu, gamma and beta of the percolation transition of the model, for various values of the density of antiferromagnetic interactions pi in the range 0 0.