Cosmology in the laboratory: defect dynamics in liquid crystals

Liquid crystals are remarkably useful for laboratory exploration of the dynamics of cosmologically relevant defects. They are convenient to work with, they allow the direct study of the "scaling solution" for a network of strings, and they provide a model for the evolution of monopoles and texture. Experiments described here support the simple "one-scale" model for cosmic string evolution, as well as some qualitative predictions of string statistical mechanics. The structure of monopoles and their apparent cylindrical but not spherical symmetry is discussed. A particular kind of defect known as texture is described and is shown to have a dynamical instability-it can decay into a monopole-antimonopole pair. This decay process has been observed occurring in the liquid crystal, and studied with numerical simulations.     

Optical activity and ferroelectricity in liquid crystals

Some liquid-crystalline phases of optically active materials are themselves optically active and have dissymmetric structures. The cholesteric phase and smectics C,I, and F have a helical order of their molecules. Plane-polarized light is rotated by the helix, and when the pitch of the helix is comparable to the wavelength of visible light, these phases will reflect irridescent light of a single color. The smectics phases can exhibit ferroelectricity and have been utilized recently in fast-switching light valves. A relation between the microscopic property of molecular configuration and the macroscopic properties of ferroelectricity and the rotation of plane-polarized light is developed.     

Biomolecular interactions at phospholipid-decorated surfaces of liquid crystals

The spontaneous assembly of phospholipids at planar interfaces between thermotropic liquid crystals and aqueous phases gives rise to patterned orientations of the liquid crystals that reflect the spatial and temporal organization of the phospholipids. Strong and weak specific-binding events involving proteins at these interfaces drive the reorganization of the phospholipids and trigger orientational transitions in the liquid crystals. Because these interfaces are fluid, processes involving the lateral organization of proteins (such as the formation of protein- and phospholipid-rich domains) are also readily imaged by the orientational response of the liquid crystal, as are stereospecific enzymatic events. These results provide principles for label-free monitoring of aqueous streams for molecular and biomolecular species without the need for complex instrumentation.     

Complex multicolor tilings and critical phenomena in tetraphilic liquid crystals

T-shaped molecules with a rod-like aromatic core and a flexible side chain form liquid crystal honeycombs with aromatic cell walls and a cell interior filled with the side chains. Here, we show how the addition of a second chain, incompatible with the first (X-shaped molecules), can form honeycombs with highly complex tiling patterns, with cells of up to five different compositions ("colors") and polygonal shapes. The complexity is caused by the inability of the side chains to separate cleanly because of geometric frustration. Furthermore, a thermoreversible transition was observed between a multicolor (phase-separated) and a single-color (mixed) honeycomb phase. This is analogous to the Curie transition in simple and frustrated ferro- and antiferromagnets; here spin flips are replaced by 180° reorientations of the molecules.     

Alignment of liquid crystals with patterned isotropic surfaces

The molecules of a nematic liquid crystal exposed to an isotropic surface adopt a mean tilt relative to the normal but have no in-plane alignment-that is, they are free to have any azimuthal orientation in the surface plane. Pursuing the theoretical suggestion by Meyer that, in spite of this azimuthal degeneracy, spatially inhomogeneous isotropic surfaces combine with liquid crystal elastic anisotropy to produce alignment, we show that a boundary line between two isotropic regions that differ in mean tilt does indeed align the liquid crystal. The boundaries on a patterned surface of distinct isotropic regions thus act as a system of lines that the molecular orientation locally follows. This enables the development of liquid crystal alignment surfaces based on printing or lithographic patterning.     

A self-quenched defect glass in a colloid-nematic liquid crystal composite

Colloidal particles immersed in liquid crystals frustrate orientational order. This generates defect lines known as disclinations. At the core of these defects, the orientational order drops sharply. We have discovered a class of soft solids, with shear moduli up to 10(4) pascals, containing high concentrations of colloidal particles (volume fraction φ ? 20%) directly dispersed into a nematic liquid crystal. Confocal microscopy and computer simulations show that the mechanical strength derives from a percolated network of defect lines entangled with the particles in three dimensions. Such a "self-quenched glass" of defect lines and particles can be considered a self-organized analog of the "vortex glass" state in type II superconductors.     

Self-organized discotic liquid crystals for high-efficiency organic photovoltaics

Self-organization of liquid crystalline and crystalline-conjugated materials has been used to create, directly from solution, thin films with structures optimized for use in photodiodes. The discotic liquid crystal hexa-peri-hexabenzocoronene was used in combination with a perylene dye to produce thin films with vertically segregated perylene and hexabenzocoronene, with large interfacial surface area. When incorporated into diode structures, these films show photovoltaic response with external quantum efficiencies of more than 34 percent near 490 nanometers. These efficiencies result from efficient photoinduced charge transfer between the hexabenzocoronene and perylene, as well as from effective transport of charges through vertically segregated perylene and hexabenzocoronene pi systems. This development demonstrates that complex structures can be engineered from novel materials by means of simple solution-processing steps and may enable inexpensive, high-performance, thin-film photovoltaic technology.     

Surface-driven switching of liquid crystals using redox-active groups on electrodes

Electrochemical control of the oxidation state of ferrocene-decorated electrodes leads to surface-driven changes in the orientations of thermotropic liquid crystals. When the electrodes possess nanometer-scale topography, voltages of 0.0 to 0.3 volts (versus a counter electrode in a two-electrode cell) can drive changes in the orientation of the liquid crystals in the plane and/or out of the plane of the electrodes. Electrodes not supporting ferrocene do not lead to surface-driven orientational transitions. The in-plane transitions are driven by the reorganization of the monolayer of ferrocene upon oxidation of ferrocene to ferrocenium. The out-of-plane transition reflects a dielectric coupling between the liquid crystal and the diffuse part of an electrical double layer that evolves upon oxidation of ferrocene to ferrocenium. These results suggest new ways to couple the orientations of liquid crystals to chemical and electrical stimuli in electro-optical devices and chemical sensors.     

The cosmological kibble mechanism in the laboratory: string formation in liquid crystals

The production of strings (disclination lines and loops) has been observed by means of the Kibble mechanism of domain (bubble) formation in the isotropic-nematic phase transition of the uniaxial nematic liquid crystal 4-cyano-4'-n-pentylbiphenyl. The number of strings formed per bubble is about 0.6. This value is in reasonable agreement with a numerical simulation of the experiment in which the Kibble mechanism is used for the order parameter space of a uniaxial nematic liquid crystal.     

非热电磁生物效应特性与液晶电流体动力不稳定性的对比研究

采用液晶生物膜模型，将非热电磁生物效应与液晶电流体动力不稳定性的特性进行了对比研究，提出非热电磁生物效应的关键机理是液晶生物膜的电流体不稳定性假说。并用此假说对非热电磁生物效应的非线性特性、协同性、相干性、“窗”特性、阈值特性等重要特性都作了很好的解释。     

Principles for measurement of chemical exposure based on recognition-driven anchoring transitions in liquid crystals

The competitive binding of a molecule forming a liquid crystal and a targeted analyte to a common molecular receptor presented at a solid surface possessing nanometer-scale topography is used to trigger an easily visualized surface-driven change in the orientation of a micrometer-thick film of liquid crystal. Diffusion of the targeted analyte from atmosphere to surface-immobilized receptor across the micrometer-thick film of liquid crystal is fast (on the order of seconds), and the competitive interaction of the targeted analyte and liquid crystal with the receptor provides a high level of tolerance to nontargeted species (water, ethanol, acetone, and hexanes). Systems that provide parts-per-billion (by volume) sensitivity to either organoamine or organophosphorus compounds are demonstrated, and their use for imaging of spatial gradients in concentration is reported. This approach does not require complex instrumentation and could provide the basis of wearable personalized sensors for measurement of real-time and cumulative exposure to environmental agents.     

Cerenkov radiation in photonic crystals

In a conventional material, the coherent Cerenkov radiation due to a moving charged particle is associated with a velocity threshold, a forward-pointing radiation cone, and a forward direction of emission. We describe different behavior for the Cerenkov radiation in a photonic crystal. In particular, this radiation is intrinsically coupled with transition radiation and is observable without any threshold. Within one particle-velocity range, we found a radiation pattern with a backward-pointing radiation cone. In another velocity range, backward-propagating Cerenkov radiation can be expected. Potential applications include velocity-sensitive particle detection and radiation generation at selectable frequencies.     

Lipoprotein patterns in acrylamide gel electrophoresis

Lipoproteins of serum stained before electrophoresis gave distinct patterns in acrylamide gel of 3-percent concentration. Samples compared in parallel on gel slabs showed qualitative differences in migration rates of beta-lipoprotein bands.     

Graphite polyhedral crystals

Polyhedral nano- and microstructures with shapes of faceted needles, rods, rings, barrels, and double-tipped pyramids, which we call graphite polyhedral crystals (GPCs), have been discovered. They were found in pores of glassy carbon. They have nanotube cores and graphite faces, and they can exhibit unusual sevenfold, ninefold, or more complex axial symmetry. Although some are giant radially extended nanotubes, Raman spectroscopy and transmission electron microscopy suggest GPCs have a degree of perfection higher than in multiwall nanotubes of similar size. The crystals are up to 1 micrometer in cross section and 5 micrometers in length, and they can probably be grown in much larger sizes. Preliminary results suggest a high electrical conductivity, strength, and chemical stability of GPC.     

Superconductivity in layered structure organometallic crystals

Superconductivity persists in several, layered, transition metal dichalcogenide superconductors when the layers are spread apart to accommodate organic molecules between them. These materials are of interest not only because of their two-dimensional character but also because they may provide a means for examining hypotheses regarding organic molecules and superconductivity.     

Trace element partition coefficient in ionic crystals

Partition coefficient monovalent trace ions between liquids and either solid NaNO(2) or KCl were determined. The isotropic elastic model of ionic crystals was used for calculating the energy change caused by the ionic substitutions. The observed values of partition coefficients in KCl good agreement with calculate values.