2,941 research outputs found

    Density controls the kinetic stability of ultrastable glasses

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    We use a swap Monte Carlo algorithm to numerically prepare bulk glasses with kinetic stability comparable to that of glass films produced experimentally by physical vapor deposition. By melting these systems into the liquid state, we show that some of our glasses retain their amorphous structures longer than 10^5 times the equilibrium structural relaxation time. This exceptional kinetic stability cannot be achieved experimentally for bulk materials. We perform simulations at both constant volume and constant pressure to demonstrate that the density mismatch between the ultrastable glass and the equilibrium liquid accounts for a major part of the observed kinetic stability.Comment: 7 Pages, 6 Figures. Figures 4b) and 5b) updated, revisions to text to improve discussion, missing page numbers added to references, typos correcte

    Can the jamming transition be described using equilibrium statistical mechanics?

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    When materials such as foams or emulsions are compressed, they display solid behaviour above the so-called `jamming' transition. Because compression is done out-of-equilibrium in the absence of thermal fluctuations, jamming appears as a new kind of a nonequilibrium phase transition. In this proceeding paper, we suggest that tools from equilibrium statistical mechanics can in fact be used to describe many specific features of the jamming transition. Our strategy is to introduce thermal fluctuations and use statistical mechanics to describe the complex phase behaviour of systems of soft repulsive particles, before sending temperature to zero at the end of the calculation. We show that currently available implementations of standard tools such as integral equations, mode-coupling theory, or replica calculations all break down at low temperature and large density, but we suggest that new analytical schemes can be developed to provide a fully microscopic, quantitative description of the jamming transition.Comment: 8 pages, 6 figs. Talk presented at Statphys24 (July 2010, Cairns, Australia

    Nonequilibrium dynamics and fluctuation-dissipation relation in a sheared fluid

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    The nonequilibrium dynamics of a binary Lennard-Jones mixture in a simple shear flow is investigated by means of molecular dynamics simulations. The range of temperature investigated covers both the liquid, supercooled and glassy states, while the shear rate covers both the linear and nonlinear regimes of rheology. The results can be interpreted in the context of a nonequilibrium, schematic mode-coupling theory developed recently, which makes the theory applicable to a wide range of soft glassy materials. The behavior of the viscosity is first investigated. In the nonlinear regime, strong shear-thinning is obtained. Scaling properties of the intermediate scattering functions are studied. Standard `mode-coupling properties' of factorization and time-superposition hold in this nonequilibrium situation. The fluctuation-dissipation relation is violated in the shear flow in a way very similar to that predicted theoretically, allowing for the definition of an effective temperature Teff for the slow modes of the fluid. Temperature and shear rate dependencies of Teff are studied using density fluctuations as an observable. The observable dependence of Teff is also investigated. Many different observables are found to lead to the same value of Teff, suggesting several experimental procedures to access Teff. It is proposed that tracer particle of large mass may play the role of an `effective thermometer'. When the Einstein frequency of the tracers becomes smaller than the inverse relaxation time of the fluid, a nonequilibrium equipartition theorem holds. This last result gives strong support to the thermodynamic interpretation of Teff and makes it experimentally accessible in a very direct way.Comment: Version accepted for publication in Journal of Chemical Physic

    A random walk description of the heterogeneous glassy dynamics of attracting colloids

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    We study the heterogeneous dynamics of attractive colloidal particles close to the gel transition using confocal microscopy experiments combined with a theoretical statistical analysis. We focus on single particle dynamics and show that the self part of the van Hove distribution function is not the Gaussian expected for a Fickian process, but that it reflects instead the existence, at any given time, of colloids with widely different mobilities. Our confocal microscopy measurements can be described well by a simple analytical model based on a conventional continuous time random walk picture, as already found in several other glassy materials. In particular, the theory successfully accounts for the presence of broad tails in the van Hove distributions that exhibit exponential, rather than Gaussian, decay at large distance.Comment: 13 pages, 5 figs. Submitted to special issue "Classical and Quantum Glasses" of J. Phys.: Condens. Matter; v2: response to refere

    The role of attractive forces in viscous liquids

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    We present evidence from computer simulation that the slowdown of relaxation of a standard Lennard-Jones glass-forming liquid and that of its reduction to a model with truncated pair potentials without attractive tails is quantitatively and qualitatively different in the viscous regime. The pair structure of the two models is however very similar. This finding, which appears to contradict the common view that the physics of dense liquids is dominated by the steep repulsive forces between atoms, is characterized in detail, and its consequences are explored. Beyond the role of attractive forces themselves, a key aspect in explaining the differences in the dynamical behavior of the two models is the truncation of the interaction potentials beyond a cutoff at typical interatomic distance. This leads us to question the ability of the jamming scenario to describe the physics of glass-forming liquids and polymers.Comment: 13 pages, 12 figure

    Identification of Known SSO in CU4 Object Processing

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    3 p.International audienceThe identification of known solar system objects (SSO) that will be observed by Gaia is a key point of the solar system object processing pipeline (CU4.SSO). It aims to associate the provisional tag assigned to observations of probably solar system objects to already known targets. At the time Gaia flies, it can be estimated that about 600,000 solar system objects (mainly small solar system objects) will be known and characterized by an orbit accurate enough to make their identification almost certain

    Shear localization in a model glass

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    Using molecular dynamics simulations, we show that a simple model of a glassy material exhibits the shear localization phenomenon observed in many complex fluids. At low shear rates, the system separates into a fluidized shear-band and an unsheared part. The two bands are characterized by a very different dynamics probed by a local intermediate scattering function. Furthermore, a stick-slip motion is observed at very small shear rates. Our results, which open the possibility of exploring complex rheological behavior using simulations, are compared to recent experiments on various soft glasses.Comment: 4 pages, 4 figures (5 figure files

    A critical test of the mode-coupling theory of the glass transition

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    The mode-coupling theory of the glass transition predicts the time evolution of the intermediate scattering functions in viscous liquids on the sole basis of the structural information encoded in two-point density correlations. We provide a critical test of this property and show that the theory fails to describe the qualitatively distinct dynamical behavior obtained in two model liquids characterized by very similar pair correlation functions. Because we use `exact' static information provided by numerical simulations, our results are a direct proof that some important information about the dynamics of viscous liquids is not captured by pair correlations, and is thus not described by the mode-coupling theory, even in the temperature regime where the theory is usually applied.Comment: 7 pages, 5 figures

    Jamming transitions in amorphous packings of frictionless spheres occur over a continuous range of volume fractions

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    We numerically produce fully amorphous assemblies of frictionless spheres in three dimensions and study the jamming transition these packings undergo at large volume fractions. We specify four protocols yielding a critical value for the jamming volume fraction which is sharply defined in the limit of large system size, but is different for each protocol. Thus, we directly establish the existence of a continuous range of volume fraction where nonequilibrium jamming transitions occur. However, these jamming transitions share the same critical behaviour. Our results suggest that, even in the absence of partial crystalline ordering, a unique location of a random close packing does not exist, and that volume fraction alone is not sufficient to describe the properties of jammed states.Comment: 5 pages, 3 fig

    Front-mediated melting of ultrastable glasses

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    Ultrastable vapor-deposited glasses display uncommon material properties. Most remarkably, upon heating they are believed to melt via a liquid front that originates at the free surface and propagates over a mesoscopic crossover length, before crossing over to bulk melting. We combine swap Monte Carlo with molecular dynamics simulations to prepare and melt isotropic amorphous films of unprecedendtly high kinetic stability. We are able to directly observe both bulk and front melting, and the crossover between them. We measure the front velocity over a broad range of conditions, and a crossover length scale that grows to nearly 400400 particle diameters in the regime accessible to simulations. Our results disentangle the relative roles of kinetic stability and vapor deposition in the physical properties of stable glasses.Comment: 7 pages, 6 figures; accepted for publication in Phys. Rev. Let
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