RESUMEN
The dielectric tensor is a physical descriptor of fundamental light-matter interactions, characterizing anisotropic materials with principal refractive indices and optic axes. Despite its importance in scientific and industrial applications ranging from material science to soft matter physics, the direct measurement of the three-dimensional dielectric tensor has been limited by the vectorial and inhomogeneous nature of light scattering from anisotropic materials. Here, we present a dielectric tensor tomographic approach to directly measure dielectric tensors of anisotropic structures including the spatial variations of principal refractive indices and directors. The anisotropic structure is illuminated with a polarized plane wave with various angles and polarization states. Then, the scattered fields are holographically measured and converted into vectorial diffracted field components. Finally, by inversely solving a vectorial wave equation, the three-dimensional dielectric tensor is reconstructed. Using this approach, we demonstrate quantitative tomographic measurements of various nematic liquid-crystal structures and their fast three-dimensional non-equilibrium dynamics.
Asunto(s)
Cristales Líquidos , Refractometría , Anisotropía , Cristales Líquidos/química , Refractometría/métodos , Tomografía Computarizada por Rayos XRESUMEN
Our study of cholesteric lyotropic chromonic liquid crystals in cylindrical confinement reveals the topological aspects of cholesteric liquid crystals. The double-twist configurations we observe exhibit discontinuous layering transitions, domain formation, metastability, and chiral point defects as the concentration of chiral dopant is varied. We demonstrate that these distinct layer states can be distinguished by chiral topological invariants. We show that changes in the layer structure give rise to a chiral soliton similar to a toron, comprising a metastable pair of chiral point defects. Through the applicability of the invariants we describe to general systems, our work has broad relevance to the study of chiral materials.
RESUMEN
We study the effect of purification and impurities on the self-assembly and phase behavior of lyotropic chromonic liquid crystals (LCLCs). LCLC molecules in water stack to form aggregates; then, the elongated nanoaggregates align to make liquid crystalline phases. Utilizing multiple experimental techniques, we unveil impurities in commercial Sunset Yellow FCF (SSY), a representative LCLC, and how the precipitation-based purification promotes the formation of the aggregates and mesophase. We further explore the roles of intrinsic impurities, i.e., byproducts of the SSY synthesis, whose molecular structures are almost identical to that of SSY but differ only in the number and position of sulfonate groups. Combining quantum chemical calculations of molecular structures and experimental investigation of aggregate structures and phase behavior, we propose that the impurities of the planar shapes behave as planar SSY, i.e., participating in aggregate formation, whereas the nonplanar one disrupts the nematic phase. These results highlight the critical roles of the impurities and deepen our understanding of self-assembled aggregates and their aligned mesophases.
RESUMEN
This corrects the article DOI: 10.1103/PhysRevE.100.012702.
RESUMEN
We investigate how chiral dopants affect the chiral symmetry breaking of lyotropic chromonic liquid crystals (LCLCs) focusing on the double-twist (DT) director configurations in a cylindrical capillary. LCLCs of unusual elastic properties tend to exhibit chiral director configurations under confinement despite the absence of intrinsic chirality. The DT director configuration in a cylindrical cavity with a degenerate planar anchoring, resulting from the large saddle-splay-to-twist elastic modulus ratio, is a representative example. Here we start by reexamining the DT configuration of nematic disodium cromoglycate in a cylindrical capillary and estimate the ratio of saddle splay to bend modulus K_{24}/K_{3}=0.5±0.1. Additionally, we study the DT configurations of the chiral nematic LCLCs with chiral dopants. The DT configuration becomes homochiral when the dopant concentration surpasses the critical concentration. We characterize these chiral DT configurations and provide a theoretical model on their energetics. Finally, we observe how the enantiomeric excess of chiral dopants determines the director configuration when dopants of two different handednesses are mixed.
RESUMEN
This study introduces cylindrical nematic liquid crystal (LC) shells. Shells as confinement can provide soft matter with intriguing topology and geometry. Indeed, in spherical shells of LCs, rich defect structures have been reported. Avoiding the inherent Plateau-Rayleigh instability of cylindrical liquid-liquid interfaces, we realize the cylindrical nematic LC shell by two different methods: the phase separation in the nematic-isotropic coexistence phase and a cylindrical cavity with a glass rod suspended in the middle. Specifically, the director configurations of lyotropic chromonic LCs (LCLCs) in the cylindrical shell and their energetics are investigated theoretically and experimentally. Unusual elastic properties of LCLCs, i.e., a large saddle-splay modulus, and a shell geometry with both concave and convex curvatures, result in a double-twist director configuration.
