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Register a new userStatistics of non-affine defect precursors: tailoring defect densities in colloidal crystals using external fields
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Coarse-graining atomic displacements in a solid produces both local affine strains and non-affine fluctuations. Here we study the equilibrium dynamics of these coarse grained quantities to obtain space-time dependent correlation functions. We show how a subset of these thermally excited, non-affine fluctuations act as precursors for the nucleation of lattice defects and suggest how defect probabilities may be altered by an {it experimentally realisable} external field conjugate to the global non-affinity parameter. Our results are amenable to verification in experiments on colloidal crystals using commonly available holographic laser tweezer and video microscopy techniques, and may lead to simple ways of controlling the defect density of a colloidal solid.
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We compute the equilibrium concentration of stacking faults and point defects in polydisperse hard-sphere crystals. We find that, while the concentration of stacking faults remains similar to that of monodisperse hard sphere crystals, the concentration of vacancies decreases by about a factor two. Most strikingly, the concentration of interstitials in the maximally polydisperse crystal may be some six orders of magnitude larger than in a monodisperse crystal. We show that this dramatic increase in interstitial concentration is due to the increased probability of finding small particles and that the small-particle tail of the particle size distribution is crucial for the interstitial concentration in a colloidal crystal.
We study the topology of smectic defects in two and three dimensions. We give a topological classification of smectic point defects and disclination lines in three dimensions. In addition we describe the combination rules for smectic point defects in two and three dimensions, showing how the broken translational symmetry of the smectic confers a path dependence on the result of defect addition.
The influence of an external field acting differently on the two constituents of a binary colloidal mixture performing Brownian dynamics is investigated by computer simulations and a simple theory. In our model, one half of the particles ($A$-particles) are pulled by an external force ${vec F}^{(A)}$ while the other half of them ($B$-particles) are pulled by an external force ${vec F}^{(B)}$. If ${vec F}^{(A)}$ and ${vec F}^{(B)}$ are parallel and the field-free state is a mixed fluid, previous simulations (J. Dzubiella et al, Phys. Rev. E {bf 65} 021402 (2002)) have shown a nonequilibrium pattern formation involving lanes of $A$ or $B$ particles only which are sliding against each other in the direction of the external forces. In this paper, we generalize the situation both to non-parallel external forces and to field-free crystalline states. For non-parallel forces, lane formation is also observed but with an orientation {it tilted} with respect to the external forces. If the field-free state is crystalline, a continuous increase of the parallel external forces yields a novel {it reentrant freezing} behavior: the crystal first melts mechanically via the external force and then recrystallizes into demixed crystalline lanes sliding against each other.
We report on a novel and flexible experiment to investigate the non-equilibrium melting behaviour of model crystals made from charged colloidal spheres. In a slit geometry polycrystalline material formed in a low salt region is driven by hydrostatic pressure up an evolving gradient in salt concentration and melts at large salt concentration. Depending on particle and initial salt concentration, driving velocity and the local salt concentration complex morphologic evolution is observed. Crystal-melt interface positions and the melting velocity are obtained quantitatively from time resolved Bragg- and polarization microscopic measurements. A simple theoretical model predicts the interface to first advance, then for balanced drift and melting velocities to become stationary at a salt concentration larger than the equilibrium melting concentration. It also describes the relaxation of the interface to its equilibrium position in a stationary gradient after stopping the drive in different manners. We further discuss the influence of the gradient strength on the resulting interface morphology and a shear induced morphologic transition from polycrystalline to oriented single crystalline material before melting.
Cholesteric Liquid Crystals (CLCs), subject to externally applied magnetic fields and confined between two parallel planar surfaces with strong homeotropic anchoring conditions, are found to undergo transitions to different types of helicoidal configurations with disclinations. Analytical and numerical studies are performed in order to characterise their properties. In particular, we produce a phase diagram for the transitions from the nematic state to the helicoidal phases in terms of the molecular chirality and the strength of the applied magnetic field.
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