1,178 research outputs found

    Ordering dynamics of blue phases entails kinetic stabilization of amorphous networks

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    The cubic blue phases of liquid crystals are fascinating and technologically promising examples of hierarchically structured soft materials, comprising ordered networks of defect lines (disclinations) within a liquid crystalline matrix. We present the first large-scale simulations of their domain growth, starting from a blue phase nucleus within a supercooled isotropic or cholesteric background. The nucleated phase is thermodynamically stable; one expects its slow orderly growth, creating a bulk cubic. Instead, we find that the strong propensity to form disclinations drives the rapid disorderly growth of a metastable amorphous defect network. During this process the original nucleus is destroyed; re-emergence of the stable phase may therefore require a second nucleation step. Our findings suggest that blue phases exhibit hierarchical behavior in their ordering dynamics, to match that in their structure.Comment: 11 pages, 5 figures, 2 supplementary figures, 2 supplementary tables, accepted by PNA

    Colloidal Jamming at Interfaces: a Route to Fluid-bicontinuous Gels

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    Colloidal particles or nanoparticles, with equal affinity for two fluids, are known to adsorb irreversibly to the fluid-fluid interface. We present large-scale computer simulations of the demixing of a binary solvent containing such particles. The newly formed interface sequesters the colloidal particles; as the interface coarsens, the particles are forced into close contact by interfacial tension. Coarsening is dramatically curtailed, and the jammed colloidal layer seemingly enters a glassy state, creating a multiply connected, solid-like film in three dimensions. The resulting gel contains percolating domains of both fluids, with possible uses as, for example, a microreaction medium

    Thermodynamics of Blue Phases In Electric Fields

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    We present extensive numerical studies to determine the phase diagrams of cubic and hexagonal blue phases in an electric field. We confirm the earlier prediction that hexagonal phases, both 2 and 3 dimensional, are stabilized by a field, but we significantly refine the phase boundaries, which were previously estimated by means of a semi-analytical approximation. In particular, our simulations show that the blue phase I -- blue phase II transition at fixed chirality is largely unaffected by electric field, as observed experimentally.Comment: submitted to Physical Review E, 7 pages (excluding figures), 12 figure

    Nonequilibrium steady states in sheared binary fluids

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    We simulate by lattice Boltzmann the steady shearing of a binary fluid mixture undergoing phase separation with full hydrodynamics in two dimensions. Contrary to some theoretical scenarios, a dynamical steady state is attained with finite domain lengths Lx,yL_{x,y} in the directions (x,y)x,y) of velocity and velocity gradient. Apparent scaling exponents are estimated as Lx∼γ˙−2/3L_{x}\sim\dot{\gamma}^{-2/3} and Ly∼γ˙−3/4L_{y}\sim\dot{\gamma}^{-3/4}. We discuss the relative roles of diffusivity and hydrodynamics in attaining steady state.Comment: 4 pages, 3 figure

    Binary fluids under steady shear in three dimensions

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    We simulate by lattice Boltzmann the steady shearing of a binary fluid mixture with full hydrodynamics in three dimensions. Contrary to some theoretical scenarios, a dynamical steady state is attained with finite correlation lengths in all three spatial directions. Using large simulations we obtain at moderately high Reynolds numbers apparent scaling expon ents comparable to those found by us previously in 2D. However, in 3D there may be a crossover to different behavior at low Reynolds number: accessing this regime requires even larger computational resource than used here.Comment: 4 pages, 3 figure

    Bulk rheology and microrheology of active fluids

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    We simulate macroscopic shear experiments in active nematics and compare them with microrheology simulations where a spherical probe particle is dragged through an active fluid. In both cases we define an effective viscosity: in the case of bulk shear simulations this is the ratio between shear stress and shear rate, whereas in the microrheology case it involves the ratio between the friction coefficient and the particle size. We show that this effective viscosity, rather than being solely a property of the active fluid, is affected by the way chosen to measure it, and strongly depends on details such as the anchoring conditions at the probe surface and on both the system size and the size of the probe particle.Comment: 12 pages, 10 figure
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