We demonstrate a variety of ordered patterns, including hexagonal structures and chains, formed by colloidal particles (droplets) at the free surface of a nematic liquid crystal (LC). The surface placement introduces a new type of particle interaction as compared to particles entirely in the LC bulk. Namely, director deformations caused by the particles lead to distortions of the interface and thus to capillary attraction. The elastic-capillary coupling is strong enough to remain relevant even at the micron-scale when its buoyancy-capillary counterpart becomes irrelevant.
We propose a general approach to the description of the long-ranged elastic interaction in the nematic colloids, based on the symmetry breaking of the director field. The type of the far-field interaction between particles immersed in a nematic host is determined by the way the symmetry is broken in the near-field region around the colloidal particle. This is caused both by the particle's shape and the anchoring at the surface. If the director field near the particle has a set of three symmetry planes, the far-field interaction falls off as d(-5) with d being the distance between particles. If one symmetry plane is absent, a dipolar moment perpendicular to it is allowed and yields dipole-dipole interactions, which decays as d(-3). If both the horizontal and vertical mirror symmetries are broken (it is equivalent to the case when the nonzero torque moment is applied to the particle by the nematic liquid crystal), the particles are shown to attract each other following the Coulomb law. We propose a simple method for the experimental observation of this Coulomb attraction. The behavior of colloid particles in curved director fields is analyzed. Quadrupolar particles with planar anchoring are shown to be attracted toward the regions with high splay deformations, while quadrupoles with homeotropic anchoring are depleted from such regions. When there are many colloidal particles in the nematic solvent, the distortions of the director from all of them are overlapped and lead to the exponential screening in the elastic pair interaction potential. This is a many-body interaction effect. This screening is essential in the real dense colloid systems, such as ferronematics--suspensions of magnetic cylindrical grains in the nematic liquid crystal. External magnetic field induces an elastic Yukawa attraction between them. We apply this attraction to the explanation of the cellular texture in magnetically doped liquid crystals.
Outermost occupied electron shells of chemical elements can have symmetries resembling that of monopoles, dipoles, quadrupoles and octupoles corresponding to filled s-, p-, d- and f-orbitals. Theoretically, elements with hexadecapolar outer shells could also exist, but none of the known elements have filled g-orbitals. On the other hand, the research paradigm of ‘colloidal atoms' displays complexity of particle behaviour exceeding that of atomic counterparts, which is driven by DNA functionalization, geometric shape and topology and weak external stimuli. Here we describe elastic hexadecapoles formed by polymer microspheres dispersed in a liquid crystal, a nematic fluid of orientationally ordered molecular rods. Because of conically degenerate boundary conditions, the solid microspheres locally perturb the alignment of the nematic host, inducing hexadecapolar distortions that drive anisotropic colloidal interactions. We uncover physical underpinnings of formation of colloidal elastic hexadecapoles and describe the ensuing bonding inaccessible to elastic dipoles, quadrupoles and other nematic colloids studied previously.
We apply the method developed [Chernyshuk and Lev, Phys. Rev. E 81, 041701 (2010)] for theoretical investigation of colloidal elastic interactions between axially symmetric particles in the confined nematic liquid crystal near one wall and in the nematic cell with thickness L. Both cases of homeotropic and planar director orientations are considered. Particularly, dipole-dipole, dipole-quadrupole, and quadrupole-quadrupole interactions of the one particle with the wall and within the nematic cell are found as well as corresponding two particle elastic interactions. A set of results has been predicted: The effective power of repulsion between two dipole particles at height h near the homeotropic wall is reduced gradually from inverse 3 to 5 with an increase of dimensionless distance r / h; near the planar wall, the effect of dipole-dipole isotropic attraction is predicted for large distances r > r(dd) = 4.76 h; maps of attraction and repulsion zones are crucially changed for all interactions near the planar wall and in the planar cell; and one dipole particle in the homeotropic nematic cell was found to be shifted by the distance δ(eq) from the center of the cell. The proposed theory fits very well with experimental data for the confinement effect of elastic interaction between spheres in the homeotropic cell [Vilfan et al., Phys. Rev. Lett. 101, 237801 (2008)] in the range 1-1000 kT. The influence of the K(24) and K(13) terms as well as connection with other theoretical approaches are discussed.
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