Molecular theoretic study of Freedericksz transition. Symmetry breaking of oblique axial order

Freedericksz transition, which is usually analyzed by an elastic theory, is studied on the basis of statistical mechanical ground, where nematics with positive dielectric anisotropy in homogeneous anchoring cell is exposed to an electric field in the direction of wall normal. In low temperature region, an oblique axial symmetry breaking occurs, which is nothing but the Freedericksz transition. In high temperature and high field region, biaxial nematic phase with principal axis parallel to the field direction at interior area of the system is proved to appear. A phase diagram on the field versus temperature plane is obtained and compared with the one at a bulk with common biaxial symmetry, where both of electric and magnetic fields are applied in directions perpendicular to each other. In the latter, no symmetry breaking occurs, in contrast with the former case above-mentioned, and the reason why this difference occurs is elucidated.     

Biaxial surface order dynamics in calamitic nematics

Thermotropic nematic materials relax strong distortions by lowering the nematic order: the uniaxial symmetry is broken and is locally replaced by biaxial domains. We investigated the dynamics of the nematic order near a boundary surface of an asymmetric π-cell submitted to an external electric field, close to the electric order reconstruction threshold. An unexpected phenomenon is observed close, but below the threshold: the biaxial order spreads on the surface inducing a consequent bulk topological behaviour equivalent to the splay-bend fast transition allowed by order reconstruction at higher voltage.     

External magnetic field-dependent tricritical points of uniaxial-to-biaxial nematic transition

External magnetic field-dependent behavior of tricritical points of uniaxial–biaxial nematic phase transition in a mixture of prolate and oblate molecules has been studied using the Landau phenomenological theory. Topological classification of phase diagrams in the field-temperature coordinates is performed using a sixth-order term in order parameter tensor. For both prolate and oblate molecules, the tricritical order parameters corresponding to the uniaxial–biaxial increase with the intensity of the external magnetic field. Field-induced paranematic phase has only been reported for prolate molecules, but for oblate molecules, field-induced splitting of the order parameter has been reported.     

Nematic order by disorder in spin-2 Bose-Einstein condensates

We show that quantum and thermal fluctuations in spin-2 Bose-Einstein condensates lift the accidental degeneracy of the mean-field phase diagram. Fluctuations select the uniaxial (square biaxial) nematic state for scattering lengths a4>a2 (a4相似文献   

Deuterium NMR investigation of the biaxial nematic phase in an organosiloxane tetrapode

Deuterium NMR is used to examine the molecular order exhibited by an organosiloxane tetrapode giving the first experimental evidence, using a bulk sample, for the existence of a biaxial nematic phase in this type of compounds. The temperature dependence of the averaged quadrupolar coupling constant and asymmetry parameter was determined in the compound's nematic phase. Two distinct regimes could be identified, one with a vanishing asymmetry parameter corresponding to a uniaxial nematic phase and another with a significant temperature dependent asymmetry parameter, corresponding to a biaxial nematic phase. The high values obtained for the asymmetry parameter at the lower end of the nematic range are well above experimental error and constitute a definite proof of the biaxial nature of the nematic phase exhibited by the studied compound for those temperatures.     

A Hierarchy of Defects in Biaxial Nematics

We study the topological properties of the manifolds which describe uniaxial and biaxial nematics in order to compare and classify all types of bulk and surface defects that can arise in a nematic liquid crystal. We explain how topological charges can be assigned both to isotropic defects in uniaxial nematics and to uniaxial defects in biaxial nematics; we further see how it is possible to distinguish between isolated surface defects and surface defects which extend in the bulk, and between surface defects which can relax in the bulk and defects forced to stay on the surface. Received: 28 November 1994 / Accepted: 30 September 1996     

The elastic anisotropy of nematic elastomers

We examine the robustness of order in nematic elastomers under mechanical strains imposed along and perpendicularly to the director when director rotation is prohibited. In contrast to electric and magnetic fields applied to conventional nematics, mechanical fields are shown theoretically and experimentally to greatly affect the degree of nematic order and related quantities. Unlike in liquid nematics, one can impose fields perpendicular to the director, thereby inducing biaxial order which should be susceptible to experimental detection. Nematic elastomers with unchanging director and degree of order should theoretically have the same elastic moduli for longitudinal and transverse extensions. This is violated when nematic order is permitted to relax in response to strains. Near the transition we predict the longitudinal modulus to be smaller than the transverse modulus; at lower temperatures the converse is true, with a crossover a few degrees below the transition. The differences are ascribed to the different temperature dependence of the stiffness of uniaxial and biaxial order. We synthesised side chain single-crystal nematic polymer networks, performed DSC, X-ray, birefringence, and thermo-mechanical characterisations, and then obtained linear moduli from stress-strain measurements. Received 29 September 2000     

梳型高分子聚合物向列相液晶的相变

本文根据Freiser关于向列相液晶分子相互作用模型,利用平均场理论,建立了梳型高分子聚合物向列相液晶分子的哈密顿量,导出序参数自洽方程,得到各向同性相至单轴向列相以及单轴至双轴向列相的相变,结果表明,当分子主、侧链耦合项中排斥作用及主、侧链中较强向列相场的场强增大时,单轴至双轴向列相相变温度升高,并从一级相变逐渐变为二级相变。 关键词：     

Influence of dipole-dipole correlations on the stability of the biaxial nematic phase in the model bent-core liquid crystal

A molecular theory of biaxial nematic ordering in the system of bent-core molecules has been developed in the two-particle cluster approximation which enables one to take into account short-range polar correlations determined by both electrostatic dipole-dipole interaction and polar molecular shape. All orientational order parameters and short-range correlation functions are calculated numerically as functions of temperature in the uniaxial and in the biaxial nematic phases, and the results are compared with the ones obtained in the mean-field approximation and in the cluster approximation but without taking into consideration the dipole-dipole interaction. It is shown that short-range polar correlations and, in particular, the dipole-dipole correlations dramatically increase the temperature of the transition into the biaxial nematic phase and enhancing its stability range. The results are also very sensitive to the value of the opening angle of a model bent-core molecule.     

Polydispersity stabilizes biaxial nematic liquid crystals

Inspired by the observations of a remarkably stable biaxial nematic phase [van?den?Pol et?al., Phys. Rev. Lett. 103, 258301 (2009)], we investigate the effect of size polydispersity on the phase behavior of a suspension of boardlike particles. By means of Onsager theory within the restricted orientation (Zwanzig) model we show that polydispersity induces a novel topology in the phase diagram, with two Landau tetracritical points in between which oblate uniaxial nematic order is favored over the expected prolate order. Additionally, this phenomenon causes the opening of a huge stable biaxiality regime in between uniaxial nematic and smectic states.     

The formation of biaxial nematic phases in binary mixtures of thermotropic liquid-crystals composed of uniaxial molecules

ABSTRACT

Monte Carlo simulations in the isothermal-isobaric ensemble are used to investigate the formation of an ordered, biaxial nematic phase in a binary mixture of thermotropic liquid crystals. The orientational dependence of the interaction between molecules of each pure component is the same as in the well-known Maier-Saupe model; each pure component of the mixture is therefore capable of forming a uniaxial nematic phase. For the interaction between molecules of different components, we use the same Maier-Saupe model but change the sign of the coupling constant. As a consequence a T-shaped arrangement of these molecules is energetically favoured. The formation of the biaxial phase occurs in two steps. At higher temperatures T, one of the components forms a uniaxial nematic phase whereas the other is in a quasi two-dimensional restricted isotropic liquid state. We develop a simple theoretical model to understand the high degree of (ostensible) nematic order in the latter. At lower T, the second component becomes nematic and then the entire mixture of the two compounds has biaxial symmetry. The biaxial nematic phase does not demix into domains rich in molecules of one or the other species.     

双轴性向列相液晶的相变理论

假设一双轴性向列相液晶分子简单相互作用模型，利用平均场理论，得到从各向同性相至单轴向列相、单轴向列相至双轴向列相的相变. 结果表明，在一定温度范围内，分子形状的非轴对称性可导致系统双轴向列相的产生. 在核磁共振实验中，导出双轴向列相序参数与谱线分裂频率间的一般关系，并讨论序参数测量性的可能性. 关键词： 向列相液晶 相变     

Possible new phase of antagonistic nematogens in a disorienting field

A simple model is proposed for nematogenic molecules that favor perpendicular orientations as well as parallel ones. (Charged rods, for example, show this antagonistic tendency.) When a small disorienting field is applied along z, a low-density phase N- of nematic order parameter S(z)<0 coexists with a dense biaxial nematic N(b). (At zero field, N- becomes isotropic and N(b) uniaxial.) But at stronger fields, a new phase N+4, invariant under pi/2 rotations around the field axis, appears in between N- and N(b). Prospects for finding the N+4 phase experimentally are briefly discussed.     

Uniaxial and biaxial spin nematic phases induced by quantum fluctuations

It is shown that zero point quantum fluctuations completely lift the accidental continuous degeneracy that is found in mean field analysis of quantum spin nematic phases of hyperfine spin-2 cold atoms. The result is two distinct ground states which have higher symmetries: a uniaxial spin nematic and a biaxial spin nematic with dihedral symmetry Dih4. There is a novel first-order quantum phase transition between the two phases as atomic scattering lengths are varied. We find that the ground state of 87Rb atoms should be a uniaxial spin nematic. We note that the energy barrier between the phases could be observable in dynamical experiments.     

Interface in nematics

Summary The structures of the interface between an isotropic liquid and a nematic liquid crystal and also between different uniaxial nematic phases are studied. It is shown that, at a planar orientation in the case of the nematic-isotropic liquid interface and also at a mutually orthogonal orientation of the director in the case of two nematic phases, the interface has the structure of a biaxial nematic liquid crystal. Work presented at the second USSR-Italy Bilateral Meeting on Liquid Crystals held in Moscow, September 15–21, 1988.     

丝状相液晶由表面相互作用产生的相变

导出双轴丝状相液晶在指向矢与易取向轴重合时的表面相互作用能.应用Ritz方法,对半无 界液晶体得出沿表面法向的双轴相(B_c)至沿表面某一轴的双轴相(B_a)的相变.随着表面锚泊强度双轴性部分的增大,B_a的产生机制逐渐由降低温度 转为表面锚泊,因此B_a相可出现在较高温度和较大温度范围内.在表面锚泊强度 单轴性部分α值的一定范围内,增大α值可使B_a在较高温度产生,但α值的进 一步增大则使液晶又从B_α返回B_c相. 关键词： 液晶 相变 表面能     

52Cr spinor condensate: a biaxial or uniaxial spin nematic

We show that the newly discovered 52Cr Bose condensate in zero magnetic field can be a spin nematic of the following kind: a "maximum" polar state, a "colinear" polar state, or a biaxial nematic ferromagnetic state. We also present the phase diagram with a magnetic field in the interaction subspace containing the chromium condensate. It contains many uniaxial and biaxial spin nematic phases, which often but not always break time reversal symmetry, and can exist with or without spontaneous magnetization.     

Tetrahedral Order in Liquid Crystals

We review the impact of tetrahedral order on the macroscopic dynamics of bent-core liquid crystals. We discuss tetrahedral order comparing with other types of orientational order, like nematic, polar nematic, polar smectic, and active polar order. In particular, we present hydrodynamic equations for phases, where only tetrahedral order exists or tetrahedral order is combined with nematic order. Among the latter, we discriminate between three cases, where the nematic director (a) orients along a fourfold, (b) along a threefold symmetry axis of the tetrahedral structure, or (c) is homogeneously uncorrelated with the tetrahedron. For the optically isotropic T_d phase, which only has tetrahedral order, we focus on the coupling of flow with, e.g., temperature gradients and on the specific orientation behavior in external electric fields. For the transition to the nematic phase, electric fields lead to a temperature shift that is linear in the field strength. Electric fields induce nematic order, again linear in the field strength. If strong enough, electric fields can change the tetrahedral structure and symmetry leading to a polar phase. We briefly deal with the T phase that arises when tetrahedral order occurs in a system of chiral molecules. To case (a), defined above, belong (i) the non-polar, achiral, optically uniaxial D2d phase with ambidextrous helicity (due to a linear gradient free energy contribution) and with orientational frustration in external fields, (ii) the non-polar tetragonal S4 phase, (iii) the non-polar, orthorhombic D2 phase that is structurally chiral featuring ambidextrous chirality, (iv) the polar orthorhombic C2v phase, and (v) the polar, structurally chiral, monoclinic C2 phase. Case (b) results in a trigonal C3v phase that behaves like a biaxial polar nematic phase. An example for case (c) is a splay bend phase, where the ground state is inhomogeneous due to a linear gradient free energy contribution. Finally, we discuss some experiments that show typical effects related to the existence of tetrahedral order. A summary and perspective is given.     

Thermotropic biaxial nematic phase in liquid crystalline organo-siloxane tetrapodes

Infrared absorbance measurements have been carried out on two liquid crystalline organo-siloxane tetrapodes. Results unambiguously show the existence of a biaxial nematic phase below a uniaxial nematic phase. The three components of IR absorbance are used to calculate the various order parameters. On cooling, a weak first-order transition from isotropic to nematic is observed, followed by a second-order phase transition to biaxial nematic where the biaxiality parameters are found to be significantly large. Results are supported by observations from conoscopy and texture. Temperature dependences of the order parameters are well explained by the mean-field model for a biaxial phase.