We report experimental studies on the temperature dependence of equilibrium separation of a pair of nematic boojum colloids. The interparticle separation is linearly proportional to the elastic anisotropy and the orientation angle with respect to the rubbing direction. The latter result is in agreement with the recent prediction of computer simulations. We prepared two-dimensional colloidal crystals assisted by a laser tweezer and measured the temperature dependence of the lattice parameters. We observe a structural transition in boojum colloidal crystal across the N-SmA transition. The structural transition is mediated by the transformation of boojum defects into focal conic lines across the phase transition. The hexagonal close pack structure of the colloidal crystal in the SmA phase could be useful for designing photonic crystal.

We observe that topological defects in nematic colloids are strongly influenced by the elasticity and onset of smectic layering across the nematic (N) to smectic-A (SmA) phase transition. When approaching the SmA phase from above, the nematic hyperbolic hedgehog defect that accompanies a spherical colloidal inclusion is transformed into a focal conic line in the SmA phase. This phase transformation has a strong influence on the pairwise colloidal interaction and is responsible for a structural transition of two-dimensional colloidal crystals. The pretransitional behavior of the point defect is supported by Landau-de Gennes Q-tensor modeling accounting for the increasing elastic anisotropy.

Colloidal self-assembly has been one of the major driving themes in material science to obtain functional and advanced optical materials with complex architecture. Most of the nematic colloids reported so far are based on the optically isotropic spherical microparticles. We study organic single crystal micro-sheets and investigate their orientation, interaction and directed assembly in a nematic liquid crystal. The micro-sheets induce planar surface anchoring of the liquid crystal. The elasticity mediated pair interaction of micro-sheets shows quadrupolar characteristics. The average orientation angle of the micro-sheets in a planar cell and the angle between two micro-sheets in a homeotropic cell are supported by the Landau-de Gennes Q-tensor modeling. The self-assembly of the micro-sheets is assisted by a laser tweezer to form larger two-dimensional structures which have the potential for application of colloids in photonics.

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Liquid crystals (LCs) form an extremely rich range of self-assembled topological structures with artificially or naturally created topological defects. Some of the main applications of LCs are various optical and photonic devices, where compared to their solid-state counterparts, soft photonic systems are fundamentally different in terms of unique properties such as self-assembly, self-healing, large tunability, sensitivity to external stimuli, and biocompatibility. Here we show that complex tunable microlasers emitting structured light can be generated from self-assembled topological LC superstructures containing topological defects inserted into a thin Fabry–Pérot microcavity. The topology and geometry of the LC superstructure determine the structuring of the emitted light by providing complex three-dimensionally varying optical axis and order parameter singularities, also affecting the topology of the light polarization. The microlaser can be switched between modes by an electric field, and its wavelength can be tuned with temperature. The proposed soft matter microlaser approach opens directions in soft matter photonics research, where structured light with specifically tailored intensity and polarization fields could be designed and implemented.

We report experimental studies on the Saturn ring defect associated with a spherical microparticle across the nematic (N) to smectic-A (SmA) phase transition. We observe that the director distortion around the microparticle changes rapidly with temperature. The equilibrium interparticle separation and the angle between two quadrupolar particles in the N phase are larger than those of the SmA phase. They are almost independent of the temperature in both phases, except for a discontinuous jump at the transition. We assembled a few particles using a laser tweezer to form a two-dimensional colloidal crystal in the N phase. The lattice structure of the crystal dissolves irreversibly across the N-SmA phase transition. The results on the pretransitional behavior of the defect are supported by the Landau-de Gennes Q-tensor modeling.

We prepared nanocomposites of a nematic liquid crystal and nanofibers of a conducting polymer (polyaniline). All the nanocomposites exhibit a discontinuous surface anchoring transition from planar to homeotropic in the nematic phase on a perfluoropolymer coated surface with a thermal hysteresis (≈ 5.3 °C). We observe a relatively large bistable conductivity and demonstrate a light driven switching of conductivity and dielectric constant in dye doped nanocomposites in the thermal hysteresis (bistable) region. The experimental results have been explained based on the reorientation of the nanofibers driven by the anchoring transition of the nematic liquid crystal. We show a significant enhancement of the bistable temperature range (≈ 13 °C) by an appropriate choice of compound in the binary system.

We report experimental studies on 2D colloidal crystals of dimers stabilized by vortex-like defects in planar nematic and π/2 twisted nematic cells. The dimers are prepared and self-assembled using a laser tweezer. We study the effect of temperature and electric field on the lattice parameters of the colloidal crystals. The lattice parameters vary with the temperature in the nematic phase and a discontinuous structural change is observed at the nematic to smectic-A phase transition. In the nematic phase, we observed a large change in the lattice parameters (≃30%) by applying an external electric field perpendicular to the plane of the 2D crystals. The idea and the active control of the lattice parameters could be useful for designing tunable colloidal crystals.