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Degenerate conic anchoring and colloidal elastic dipole-hexadecapole transformations

The defect structure associated with a colloid in a nematic liquid crystal is dictated by molecular orientation at the colloid surface. Perpendicular or parallel orientations to the surface lead to dipole-like or quadrupole-like defect structures. However, the so-called elastic hexadecapole discovered recently, has been assumed to result from a conic anchoring condition. In order to understand it at a fundamental level, a model for this anchoring is introduced here in the context of a Landau-de Gennes free energy functional. We investigate the evolution of defect configurations, as well as colloidal interactions, by tuning the preferred tilt angle (θ e ). The model predicts an elastic dipole whose stability decreases as θ e increases, along with a dipole-hexadecapole transformation, which are confirmed by our experimental observations. Taken together, our results suggest that previously unanticipated avenues may exist for design of self-assembled structures via control of tilt angle.

42 ENGINEERING↗

Hexadecapolar Colloids

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 forbitals. 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. 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 report the ensuing bonding inaccessible to elastic dipoles, quadrupoles and other nematic colloids studied previously.

14 SOLAR ENERGY↗