To verify the status of the divergence K» term in the elastic theory of liquid crystals we study submicron films placed onto an isotropic fluid substrate in the Langmuir trough (Langmuir liquid crystal, LLC). The upper and lower surfaces favor normal and tangential molecular orientation, respectively. The periodic domain phase is observed in a nematic LLC. The dependence of the periodicity L of the domains vs film thickness h can be explained only if the elastic energy is accompanied by divergence terms with nonzero constants K» and K24. It is found that for 5CB K» =-0.2Kl].

Thin submicron and micron films of liquid crystals placed between two isotropic media represent a particular example of confined systems. Such films can be prepared on the surface of glycerin or other liquids, In comparison with Langmuir monolayers, these films are macroscopically thick to involve the liquid crystalline order in the interplay between molecular structure and macroscopic organization. At the same time, the films are thin enough for such a strong competition between surface and bulk properties that transitional in-plane symmetry is spontaneously violated and a number of patterns appear: stripe domains, square lattices, strings, high strength defects and so on. We show that these structures are governed by the divergence (or “sufacelike”) K13 and K24 terms in the nematic free energy which have been ignored for decades. We also show that both terms can be included in the standard elasiticty theory without contradictions with the basic idea of the nematic phase. The one-dimensional confinement makes the films a unique object of investigation: although the phenomena observed are attributed to the vertical confinement, their manifestation is detected in a non-restricted film plane.

We formulate a numerical method for predicting the tensorial linear response of a rigid, asymmetrically charged body to an applied electric field. This prediction requires calculating the response of the fluid to the Stokes drag forces on the moving body and on the countercharges near its surface. To determine the fluid's motion, we represent both the body and the countercharges using many point sources of drag known as stokeslets. Finding the correct flow field amounts to finding the set of drag forces on the stokeslets that is consistent with the relative velocities experienced by each stokeslet. The method rigorously satisfies the condition that the object moves with no transfer of momentum to the fluid. We demonstrate that a sphere represented by 1999 well-separated stokeslets on its surface produces flow and drag force like a solid sphere to one-percent accuracy. We show that a uniformly-charged sphere with 3998 body and countercharge stokeslets obeys the Smoluchowski prediction [1] for electrophoretic mobility when the countercharges lie close to the sphere. Spheres with dipolar and quadrupolar charge distributions rotate and translate as predicted analytically to four percent accuracy or better. We describe how the method can treat general asymmetric shapes and charge distributions. This method offers promise as a way to characterize and manipulate asymmetrically charged colloid-scale objects from biology (eg. viruses) and technology (eg. self-assembled clusters).

Glycerol droplets at a nematic-liquid-crystal-air interface form two different lattices--hexagonal and dense quasihexagonal--which are separated by the energy barrier and can coexist. Director distortions around each droplet form an elastic dipole. The first order transition between the two lattices is driven by a reduction of the dipole-dipole repulsion through reorientation of these dipoles. The elastic-capillary attraction is essential for the both lattices. The effect has a many-body origin.

The interaction between particle-like sources of the nematic director distortions (e.g., colloids, point defects, macromolecules in nematic emulsions) allows for a useful analogy with the electrostatic multipole interaction between charged bodies. In this paper we develop this analogy to the level corresponding to the charge density and consider the general status of the pairwise approach to the nematic emulsions with finite-size colloids. It is shown that the elastic analog of the surface electric charge density is represented by the two transverse director components on the surface imposing the director distortions. The elastic multipoles of a particle are expressed as integrals over the charge density distribution on this surface. Because of the difference between the scalar electrostatics and vector nematostatics, the number of elastic multipoles of each order is doubled compared to that in the electrostatics: there are two elastic charges, two vectors of dipole moments, two quadrupolar tensors, and so on. The two-component elastic charge is expressed via the vector of external mechanical torque applied on the particle. As a result, the elastic Coulomb-like coupling between two particles is found to be proportional to the scalar product of the two external torques and does not directly depend on the particles' form and anchoring. The real-space Green function method is used to develop the pairwise approach to nematic emulsions and determine its form and restrictions. The pairwise potentials are obtained in the familiar form, but, in contrast to the electrostatics, they describe the interaction between pairs (dyads) of the elastic multipole moments. The multipole moments are shown to be uniquely determined by the single-particle director field, unperturbed by other particles. The pairwise approximation is applicable only in the leading order in the small ratio particle size-to-interparticle distance as the next order contains irreducible three-body terms.

An external mechanical torque on colloids immersed in a nematic liquid crystal can induce a Coulomb-like 1/r interaction between them [Lev and Tomchuk, Phys. Rev. E 59, 591 (1999); Lev, ibid. 65, 021709 (2002)]. In this paper we show that the director-mediated Coulomb-like interaction of two colloids is determined by the vectors Gamma perpendicular (1) and Gamma perpendicular (2) of the transverse external torques exerted upon these colloids. We derive the 1/r potential in which the scalar product -(Gamma perpendicular (1) x Gamma perpendicular (2)) of the two torques plays the role of the product of two electrostatic charges. The 1/r interaction is attractive for (Gamma perpendicular (1) x Gamma perpendicular (2))>0 and repulsive for (Gamma perpendicular (1) x Gamma perpendicular (2))<0 ("parallel torques" attract whereas "antiparallel torques" repel each other). The vector of transverse torque determines the two-component "elastic charge" (dyad), which is illustrated by the 1/r2 and 1/r3 terms in the elastic energy (the elastic analogs of the monopole-dipole and dipole-dipole interactions). The general status of the pairwise approach to nematic emulsions is considered in terms of the elastic charge density.

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Active elastomeric liquid crystal particles with initial cylindrical shapes are obtained by means of soft lithography and polymerization in a strong magnetic field. Gold nanocrystals infiltrated into these particles mediate energy transfer from laser light to heat, so that the inherent coupling between the temperature-dependent order and shape allows for dynamic morphing of these particles and well-controlled stable shapes. Continuous changes of particle shapes are followed by their spontaneous realignment and transformations of director structures in the surrounding cholesteric host, as well as locomotion in the case of a nonreciprocal shape morphing. These findings bridge the fields of liquid crystal solids and active colloids, may enable shape-controlled self-assembly of adaptive composites and light-driven micromachines, and can be understood by employing simple symmetry considerations along with electrostatic analogies.