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We report experiments that probe the self-assembly of micrometer-size colloids into one-particle-thick, robust, and self-healing membranes. In a magic-angle precessing magnetic field, superparamagnetic spheres experience isotropic pair attraction similar to the van der Waals force between atoms. But the many-body polarization interactions among them steer an ordered aggregation pathway consisting of growth of short chains, cross-linking and network formation, network coarsening, and consolidation of membrane patches. This generic aggregation scenario can be induced in any particles of large enough susceptibility.
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We show that colloidal superstructures could be assembled in mixtures of large and small colloidal particles dispersed in a nematic liquid crystal. Using elastic interaction of small colloidal particles with the disclination lines we succeed to demonstrate how one can decorate with small particles a topological matrix of defect rings and loops formed by an array of large colloidal particles. Our simulations show that this concept of colloidal self-assembly in nematics could be extended down to the nanoscale particles.
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We present experimental and theoretical study of colloidal interactions in quadrupolar nematic liquid crystal colloids, confined to a thin planar nematic cell. Using the laser tweezers, the particles have been positioned in the vicinity of other colloidal particles and their interactions have been determined using particle tracking video microscopy. Several types of interactions have been analyzed: (i) quadrupolar pair interaction, (ii) the interaction of an isolated quadrupole with a quadrupolar chain, and (iii) the interaction of an isolated quadrupolar colloidal particle with a two-dimensional (2D) quadrupolar crystallite. In all cases, the interactions are of the order of several 100k(B)T for 2 microm particles, which gives rise to relatively stable 2D colloidal crystals. The experimental results are compared to the predictions of Landau-de Gennes theory and we find a relatively good qualitative agreement.
RESUMEN
In this Letter, we demonstrate that the symmetry of the elastic interaction between the dipolar and quadrupolar colloidal particles in the nematic liquid crystal leads to a novel variety of 2D nematic "binary" colloidal crystals, which have not been observed in any colloidal system. The dipolar-quadrupolar interaction is highly anisotropic and shows a power-law dependence when the particles approach each other along the director field with a pair-binding energy of the order of several thousands of k(B)T for 4 microm diameter colloids.
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We show that diffraction of visible light from 2D dipolar nematic colloidal crystals can be tuned electrically. When the external electric field of approximately 1 V/microm is applied in a direction perpendicular to the plane of the 2D colloidal crystal, the induced strain is highly anisotropic, and the inter-colloidal spacing changes by as much as 20% along one direction and approximately 2% along the perpendicular one. Although the speed of response is in the range of several seconds, this novel mechanism could provide interesting photonic applications.
Asunto(s)
Coloides/química , Física/métodos , Anisotropía , Cristalización , Electroquímica/métodos , Luz , Modelos Estadísticos , Dióxido de Silicio , Factores de TiempoRESUMEN
It has been predicted, but never confirmed, that colloidal particles in a nematic liquid crystal could be self-assembled by delocalized topological defects and entangled disclinations. We show experimentally and theoretically that colloidal dimers and 1D structures bound by entangled topological defect loops can indeed be created by locally thermally quenching a thin layer of the nematic liquid crystal around selected colloidal particles. The topological entanglement provides a strong stringlike binding, which is ten thousand times stronger compared to water-based colloids. This unique binding mechanism could be used to assemble resonator optical waveguides and robust chiral and achiral structures of topologically entangled colloids that we call colloidal wires.
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We experimentally study the condensed phases of repelling core-softened spheres in two dimensions. The dipolar pair repulsion between superparamagnetic spheres trapped in a thin cell is induced by a transverse magnetic field and softened by suitably adjusting the cell thickness. We scan a broad density range and we materialize a large part of the theoretically predicted phases in systems of core-softened particles, including expanded and close-packed hexagonal, square, chainlike, stripe or labyrinthine, and honeycomb phase. Further insight into their structure is provided by Monte Carlo simulations.
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Coloides/química , Modelos Químicos , MagnetismoRESUMEN
We study the interactions and directed assembly of dipolar nematic colloidal particles in planar nematic cells using laser tweezers. The binding energies for two stable configurations of a colloidal pair with homeotropic surface alignment are determined. It is shown that the orientation of the dipolar colloidal particle can efficiently be controlled and changed by locally quenching the nematic liquid crystal from the laser-induced isotropic phase. The interaction of a single colloidal particle with a single colloidal chain is determined and the interactions between pairs of colloidal chains are studied. We demonstrate that dipolar colloidal chains self-assemble into the two-dimensional (2D) dipolar nematic colloidal crystals. An odd-even effect is observed with increasing number of colloidal chains forming the 2D colloidal crystal.
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The interaction between a colloidal particle and a focused laser beam in a nematic liquid crystal reveals an unusual anisotropic Coulomb-like character. Experiments demonstrate two opposite directions in which the particle is attracted to and repelled from the nematic region deformed by the light-induced director reorientation. In this work we present analytical analysis of such behavior and derive the energy of interaction between colloidal particle and deformed director field. The analytical solution is in good agreement with recent results obtained by computer simulation.
Asunto(s)
Coloides/química , Rayos Láser , Cristales Líquidos/química , Soluciones/química , Simulación por Computador , Cristalización , Interacciones Hidrofóbicas e Hidrofílicas , Matemática , Óptica y Fotónica , Tamaño de la Partícula , Dióxido de Silicio/química , Propiedades de SuperficieRESUMEN
We describe and analyze laser trapping of small colloidal particles in a nematic liquid crystal, where the index of refraction of colloids is smaller compared to the indices of the liquid crystal. Two mechanisms are identified that are responsible for this anomalous trapping: (i) below the optical Fréedericksz transition, the trapping is due to the anisotropic dielectric interaction of the polarized light with the inhomogeneous director field around the colloid, (ii) above the optical Fréedericksz transition, the optical trapping is accompanied by the elasticity-mediated interaction between the optically distorted region of a liquid crystal and the colloid. In the majority of the experiments, the trapping above the Fréedericksz transition is highly anisotropic. Qualitative agreement is found with a numerical analysis, considering the nematic director elastic distortion, dielectric director-light field coupling and optical repulsion due to low refraction index colloid in high index surroundings.
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We show that, contrary to intuition, small (< or =1 microm) transparent particles can be trapped and manipulated in a nematic liquid crystal using an intense laser beam, although their index of refraction is lower than both refractive indices of the surrounding birefringent fluid. Two mechanisms are identified that are responsible for this anomalous trapping: (i) surface-induced distortion of the birefringent media around the particle, creating a high-index "cloud" around the colloid, and (ii) laser-induced distortion or (partial) melting of a nematic, creating a ghost colloid.