Crystallization of hard-sphere glasses

We study by molecular dynamics the interplay between arrest and crystallization in hard spheres. For state points in the plane of volume fraction ($0.54 \leq phi \leq 0.63$) and polydispersity ($0 \leq s \leq 0.085$), we delineate states that spontaneously crystallize from those that do not. For noncrystallizing (or precrystallization) samples we find isodiffusivity lines consistent with an ideal glass transition at $\phi_g \approx 0.585$, independent of $s$. Despite this, for $s<0.05$, crystallization occurs at $\phi > \phi_g$. This happens on time scales for which the system is aging, and a diffusive regime in the mean square displacement is not reached; by those criteria, the system is a glass. Hence, contrary to a widespread assumption in the colloid literature, the occurrence of spontaneous crystallization within a bulk amorphous state does not prove that this state was an ergodic fluid rather than a glass.Comment: 4 pages, 3 figure

Strain versus stress in a model granular material: a Devil's staircase

The series of equilibrium states reached by disordered packings of rigid, frictionless discs in two dimensions, under gradually varying stress, are studied by numerical simulations. Statistical properties of trajectories in configuration space are found to be independent of specific assumptions ruling granular dynamics, and determined by geometry only. A monotonic increase in some macroscopic loading parameter causes a discrete sequence of rearrangements. For a biaxial compression, we show that, due to the statistical importance of such events of large magnitudes, the dependence of the resulting strain on stress direction is a Levy flight in the thermodynamic limit.Comment: REVTeX, 4 pages, 5 included PostScript figures. New version altered throughout text, very close to published pape

Crystallization Mechanism of Hard Sphere Glasses

In supercooled liquids, vitrification generally suppresses crystallization. Yet some glasses can still crystallize despite the arrest of diffusive motion. This ill-understood process may limit the stability of glasses, but its microscopic mechanism is not yet known. Here we present extensive computer simulations addressing the crystallization of monodisperse hard-sphere glasses at constant volume (as in a colloid experiment). Multiple crystalline patches appear without particles having to diffuse more than one diameter. As these patches grow, the mobility in neighbouring areas is enhanced, creating dynamic heterogeneity with positive feedback. The future crystallization pattern cannot be predicted from the coordinates alone: crystallization proceeds by a sequence of stochastic micro-nucleation events, correlated in space by emergent dynamic heterogeneity.Comment: 4 pages 4 figures Accepted for publication in Phys. Rev. Lett., April 201

Phase separation and rotor self-assembly in active particle suspensions

Adding a non-adsorbing polymer to passive colloids induces an attraction between the particles via the `depletion' mechanism. High enough polymer concentrations lead to phase separation. We combine experiments, theory and simulations to demonstrate that using active colloids (such as motile bacteria) dramatically changes the physics of such mixtures. First, significantly stronger inter-particle attraction is needed to cause phase separation. Secondly, the finite size aggregates formed at lower inter-particle attraction show unidirectional rotation. These micro-rotors demonstrate the self assembly of functional structures using active particles. The angular speed of the rotating clusters scales approximately as the inverse of their size, which may be understood theoretically by assuming that the torques exerted by the outermost bacteria in a cluster add up randomly. Our simulations suggest that both the suppression of phase separation and the self assembly of rotors are generic features of aggregating swimmers, and should therefore occur in a variety of biological and synthetic active particle systems.Comment: Main text: 6 pages, 5 figures. Supplementary information: 5 pages, 4 figures. Supplementary movies available from httP://www.pnas.org/lookup/suppl/doi:10.1073/pnas.1116334109/-/DCSupplementa

Coexistence and Phase Separation in Sheared Complex Fluids

We demonstrate how to construct dynamic phase diagrams for complex fluids that undergo transitions under flow, in which the conserved composition variable and the broken-symmetry order parameter (nematic, smectic, crystalline, etc.) are coupled to shear rate. Our construction relies on a selection criterion, the existence of a steady interface connecting two stable homogeneous states. We use the (generalized) Doi model of lyotropic nematic liquid crystals as a model system, but the method can be easily applied to other systems, provided non-local effects are included.Comment: 4 pages REVTEX, 5 figures using epsf macros. To appear in Physical Review E (Rapid Communications

Two-Dimensional Copolymers and Exact Conformal Multifractality

We consider in two dimensions the most general star-shaped copolymer, mixing random (RW) or self-avoiding walks (SAW) with specific interactions thereof. Its exact bulk or boundary conformal scaling dimensions in the plane are all derived from an algebraic structure existing on a random lattice (2D quantum gravity). The multifractal dimensions of the harmonic measure of a 2D RW or SAW are conformal dimensions of certain star copolymers, here calculated exactly as non rational algebraic numbers. The associated multifractal function f(alpha) are found to be identical for a random walk or a SAW in 2D. These are the first examples of exact conformal multifractality in two dimensions.Comment: 4 pages, 2 figures, revtex, to appear in Phys. Rev. Lett., January 199

Non--Newtonian viscosity of interacting Brownian particles: comparison of theory and data

A recent first-principles approach to the non-linear rheology of dense colloidal suspensions is evaluated and compared to simulation results of sheared systems close to their glass transitions. The predicted scenario of a universal transition of the structural dynamics between yielding of glasses and non-Newtonian (shear-thinning) fluid flow appears well obeyed, and calculations within simplified models rationalize the data over variations in shear rate and viscosity of up to 3 decades.Comment: 6 pages, 2 figures; J. Phys. Condens. Matter to be published (Jan. 2003

Plastic energies in layered superconductors

We estimate the energy cost associated with two pancake vortices colliding in a layered superconductor. It is argued that this energy sets the plastics energy scale and is the analogue of the crossing energy for vortices in the continuum case. The starting point of the calculation is the Lawrence-Doniach version of the Ginzburg-Landau free energy for type-II superconductors. The magnetic fields considered are along the c-direction and assumed to be sufficiently high that the lowest Landau level approximation is valid. For Bi-2212, where it is know that layering is very important, the results are radically different from what would have been obtained using a three-dimensional anisotropic continuum model. We then use the plastic energy for Bi-2212 to successfully explain recent results from Hellerqvist {\em et al.}\ on its longitudinal resistance.Comment: 5 Pages Revtex, 4 uuencoded postscript figure

Statistical Mechanics of Stress Transmission in Disordered Granular Arrays

We give a statistical-mechanical theory of stress transmission in disordered arrays of rigid grains with perfect friction. Starting from the equations of microscopic force and torque balance we derive the fundamental equations of stress equilibrium. We illustrate the validity of our approach by solving the stress distribution of a homogeneous and isotropic array.Comment: 4 pages, to be published in PR