Lyotropic nematic liquid crystals: interplay between a small twist elastic constant and chirality effects under confined geometries

Abstract

There are two classes of liquid crystals (LCs): Thermotropic LCs where the organic molecule represents the anisotropically shaped mesogen and lyotropic LCs, where the mesogens are nonspherical supramolecular assemblies dispersed in a solvent. Various kinds of lyotropic nematic liquid crystals (LLCs) exist, differing in shape and composition of the aggregates: Chromonic, polymeric or micellar LLCs.However, micellar LLCs are the most ubiquitous kind of LLCs, occurring in soaps and biological systems. Although these nematic lyotropics are so different, they exhibitcontrary to thermotropic nematics -spontaneous reflection symmetry breaking under confinement. We discuss spontaneous mirror symmetry breaking under capillary confinement for a standard micellar N D phase and give a detailed director field structure of the twisted polar configuration. Furthermore, we measure for the first time a complete set of viscoelastic properties of a micellar nematic LLC, finding a small twist elastic constant K 22 , which is at least one order of magnitude smaller than K 11 and K 33 . As demonstrated by the following work, a small K 22 and therefore spontaneous mirror symmetry breaking under confinement is rather the rule than the exception in lyotropic nematics and constitutes a unique difference between lyotropic and typical thermotropic nematics, for which the well-known one-constant approximation holds.