Exponential Decay of Correlations in a Model for Strongly Disordered 2D Nematic Elastomers

Lattice Monte-Carlo simulations were performed to study the equilibrium ordering in a two-dimensional nematic system with quenched random disorder. When the disordering field, which competes against the aligning effect of the Frank elasticity, is sufficiently strong, the long-range correlation of the director orientation is found to decay as a simple exponential, Exp[-r/x]. The correlation length {x} itself also decays exponentially with increasing strength of the disordering field. This result represents a new type of behavior, distinct from the Gaussian and power-law decays predicted by some theories.Comment: Latex file (4 pages) + 2 EPS figure

Quasi-long range order in the random anisotropy Heisenberg model

The large distance behaviors of the random field and random anisotropy Heisenberg models are studied with the functional renormalization group in $4-\epsilon$ dimensions. The random anisotropy model is found to have a phase with the infinite correlation radius at low temperatures and weak disorder. The correlation function of the magnetization obeys a power law $<{\bf m}({\bf r}_1) {\bf m}({\bf r}_2)>\sim| {\bf r}_1-{\bf r}_2|^{-0.62\epsilon}$. The magnetic susceptibility diverges at low fields as $\chi\sim H^{-1+0.15\epsilon}$. In the random field model the correlation radius is found to be finite at the arbitrarily weak disorder.Comment: 4 pages, REVTe

Slow stress relaxation in randomly disordered nematic elastomers and gels

Randomly disordered (polydomain) liquid crystalline elastomers align under stress. We study the dynamics of stress relaxation before, during and after the Polydomain-Monodomain transition. The results for different materials show the universal ultra-slow logarithmic behaviour, especially pronounced in the region of the transition. The data is approximated very well by an equation Sigma(t) ~ Sigma_{eq} + A/(1+ Alpha Log[t]). We propose a theoretical model based on the concept of cooperative mechanical resistance for the re-orientation of each domain, attempting to follow the soft-deformation pathway. The exact model solution can be approximated by compact analytical expressions valid at short and at long times of relaxation, with two model parameters determined from the data.Comment: 4 pages (two-column), 5 EPS figures (included via epsfig

Quasi-long-range order in nematics confined in random porous media

We study the effect of random porous matrices on the ordering in nematic liquid crystals. The randomness destroys orientational lang-range order and drives the liquid crystal into a glass state. We predict two glass phases one of which possesses quasi-long-range order. In this state the correlation length is infinite and the correlation function of the order parameter obeys a power dependence on the distance. The small-angle light-scattering amplitude diverges but slower than in the bulk nematic. In the uniaxially strained porous matrices two new phases emerge. One type of strain induces an anisotropic quasi-long-range-ordered state while the other stabilizes nematic long-range order.Comment: 4 pages, Revte

Electro-Mechanical Fredericks Effects in Nematic Gels

The solid nematic equivalent of the Fredericks transition is found to depend on a critical field rather than a critical voltage as in the classical case. This arises because director anchoring is principally to the solid rubbery matrix of the nematic gel rather than to the sample surfaces. Moreover, above the threshold field, we find a competition between quartic (soft) and conventional harmonic elasticity which dictates the director response. By including a small degree of initial director misorientation, the calculated field variation of optical anisotropy agrees well with the conoscopy measurements of Chang et al (Phys.Rev.E56, 595, 1997) of the electro-optical response of nematic gels.Comment: Latex (revtex style), 5 EPS figures, submitted to PRE, corrections to discussion of fig.3, cosmetic change

Soft and non-soft structural transitions in disordered nematic networks

Properties of disordered nematic elastomers and gels are theoretically investigated with emphasis on the roles of non-local elastic interactions and crosslinking conditions. Networks originally crosslinked in the isotropic phase lose their long-range orientational order by the action of quenched random stresses, which we incorporate into the affine-deformation model of nematic rubber elasticity. We present a detailed picture of mechanical quasi-Goldstone modes, which accounts for an almost completely soft polydomain-monodomain (P-M) transition under strain as well as a ``four-leaf clover'' pattern in depolarized light scattering intensity. Dynamical relaxation of the domain structure is studied using a simple model. The peak wavenumber of the structure factor obeys a power-law-type slow kinetics and goes to zero in true mechanical equilibrium. The effect of quenched disorder on director fluctuation in the monodomain state is analyzed. The random frozen contribution to the fluctuation amplitude dominates the thermal one, at long wavelengths and near the P-M transition threshold. We also study networks obtained by crosslinking polydomain nematic polymer melts. The memory of initial director configuration acts as correlated and strong quenched disorder, which renders the P-M transition non-soft. The spatial distribution of the elastic free energy is strongly dehomogenized by external strain, in contrast to the case of isotropically crosslinked networks.Comment: 19 pages, 15 EPS figure

Symmetries and Elasticity of Nematic Gels

A nematic liquid-crystal gel is a macroscopically homogeneous elastic medium with the rotational symmetry of a nematic liquid crystal. In this paper, we develop a general approach to the study of these gels that incorporates all underlying symmetries. After reviewing traditional elasticity and clarifying the role of broken rotational symmetries in both the reference space of points in the undistorted medium and the target space into which these points are mapped, we explore the unusual properties of nematic gels from a number of perspectives. We show how symmetries of nematic gels formed via spontaneous symmetry breaking from an isotropic gel enforce soft elastic response characterized by the vanishing of a shear modulus and the vanishing of stress up to a critical value of strain along certain directions. We also study the phase transition from isotropic to nematic gels. In addition to being fully consistent with approaches to nematic gels based on rubber elasticity, our description has the important advantages of being independent of a microscopic model, of emphasizing and clarifying the role of broken symmetries in determining elastic response, and of permitting easy incorporation of spatial variations, thermal fluctuations, and gel heterogeneity, thereby allowing a full statistical-mechanical treatment of these novel materials.Comment: 21 pages, 4 eps figure

Quasi-long-range order in the random anisotropy Heisenberg model: functional renormalization group in 4-\epsilon dimensions

The large distance behaviors of the random field and random anisotropy O(N) models are studied with the functional renormalization group in 4-\epsilon dimensions. The random anisotropy Heisenberg (N=3) model is found to have a phase with the infinite correlation radius at low temperatures and weak disorder. The correlation function of the magnetization obeys a power law < m(x) m(y) >\sim |x-y|^{-0.62\epsilon}. The magnetic susceptibility diverges at low fields as \chi \sim H^{-1+0.15\epsilon}. In the random field O(N) model the correlation radius is found to be finite at the arbitrarily weak disorder for any N>3. The random field case is studied with a new simple method, based on a rigorous inequality. This approach allows one to avoid the integration of the functional renormalization group equations.Comment: 12 pages, RevTeX; a minor change in the list of reference

Electrical Conductivity of Electrospun Polyaniline and Polyaniline-Blend Fibers and Mats

Submicrometer fibers of polyaniline (PAni) doped with (+)-camphor-10-sulfonic acid (HCSA) and blended with poly(methyl methacrylate) (PMMA) or poly(ethylene oxide) were electrospun over a range of compositions. Continuous, pure PAni fibers doped with HCSA were also produced by coaxial electrospinning and subsequent removal of the PMMA shell polymer. The electrical conductivities of both the fibers and the mats were characterized. The electrical conductivities of the fibers were found to increase exponentially with the weight percent of doped PAni in the fibers, with values as high as 50 ± 30 S/cm for as-electrospun fibers of 100% doped PAni and as high as 130 ± 40 S/cm upon further solid state drawing. These high electrical conductivities are attributed to the enhanced molecular orientation arising from extensional deformation in the electrospinning process and afterward during solid state drawing. A model is proposed that permits the calculation of mat conductivity as a function of fiber conductivity, mat porosity, and fiber orientation distribution; the results agree quantitatively with the independently measured mat conductivities.United States. Army Research Office (Institute for Soldier Nanotechnologies, Contract ARO W911NF-07-D- 0004