Open Access Kent State (OAKS)

The salient feature of liquid crystal elastomers and networks is strong coupling between orientational order and mechanical strain. Orientational order can be changed by a wide variety of stimuli, including the presence of moisture. Changes in the orientation of constituents give rise to stresses and strains, which result in changes in sample shape. We have utilized this effect to build soft cellulose-based motor driven by humidity. The motor consists of a circular loop of cellulose film, which passes over two wheels. When humid air is present near one of the wheels on one side of the film, with drier air elsewhere, rotation of the wheels results. As the wheels rotate, the humid film dries. The motor runs so long as the difference in humidity is maintained. Our cellulose liquid crystal motor thus extracts mechanical work from a difference in humidity.

X-ray scattering measurements have been carried out for free-standing, thick . monodomain films of the orthogonal hexatic-B phase. From Fourier analysis of X-scans, 6n-fold-symmetry order parameters were determined and proved to fulfill the scaling relation C6n = C6n+lambdan(n-1). The temperature behavior of C6 and lambda was found nonuniversal when comparing homologues, PIR5 and PIR7, differing in their range of the hexatic phase. The hexatic order parameter varies with the critical exponents 0.25, 0.20 (+/- 0.03), respectively. For comparison results for compound RFL6, of other homologue series, are presented.

The three-dimensional optical anisotropy of photo-buffed dye-doped polymer films and the resulting orientation imparted to a liquid crystal in contact are probed using total internal reflection. Although the linearly polarized writing light generates a uniaxial distribution of dye molecules, the polymer films are biaxial, a result of symmetry breaking by the film surface.

The displacement field around an isolated elementary dislocation in a medium with one-dimensional periodicity is established experimentally. The system studied is a cholesteric fingerprint texture with a macroscopic (∼10 μm) periodicity. The characteristic elastic length is smaller than the “interlayer” distance. As a result, the experimental dislocation profile deviates from the classic pattern predicted by the linear elastic theory but fits well with the recently suggested nonlinear theory of dislocation [Phys. Rev. E 59, R4752 (1999)].

We have observed an interesting pattern evolution of cholesteric liquid crystals during the homeotropic-focal conic transition in a dispersed polymer network. From the electrical field induced homeotropic state, if the field is:reduced to an appropriate bias level focal conics grow at a constant speed, being an open or compact structure depending on the field strength. When the field is increased, these patterns change to ramified structures. We phenomenologically explained the observation.

We employ the fluorescent confocal polarizing microscopy to image edge dislocations in cholesteric liquid crystals. Surface anchoring at the bounding plates determines the structure and behavior of defects. Two types of plates set in-plane director orientation but differ in the type of associated anchoring potentials. Plates with strong polar anchoring and nonzero azimuthal anchoring repel the dislocations, while plates with weak polar anchoring and no azimuthal anchoring allow the dislocations to escape through the boundary. To explain the results, we propose a coarse-grained model of cholesteric anchoring.

We apply experimental technique based on the combination of methods dealing with principal refractive indices and absorption coefficients to study the photoinduced three-dimensional (3D) orientational order in the films of liquid crystalline (LC) azopolymers. The technique is used to identify 3D orientational configurations of trans azobenzene chromophores and to characterize the degree of ordering in terms of order parameters. We study two types of LC azopolymers which form structures with preferred in-plane and out-of-plane alignment of azochromophores, respectively. Using irradiation with the polarized light of two different wavelengths, we find that the kinetics of photoinduced anisotropy can be dominated by either photoreorientation (angular redistribution of trans chromophores) or photoselection (angular selective trans-cis isomerization) mechanisms depending on the wavelength. At the early stages of irradiation, the films of both azopolymers are biaxial. This biaxiality disappears on reaching a state of photosaturation. In the regime of photoselection, the photosaturated state of the film is optically isotropic. But, in the case of the photoreorientation mechanism, anisotropy of this state is uniaxial with the optical axis dependent on the preferential alignment of azochromophores. We formulate the phenomenological model describing the kinetics of photoinduced anisotropy in terms of the isomer concentrations and the order parameter tensor. We present the numerical results for absorption coefficients that are found to be in good agreement with the experimental data. The model is also used to interpret the effect of changing the mechanism with the wavelength of the pumping light.

We have studied the optical and electrical properties of two bent-core substances with an azo linkage in their cores. Pump-probe laser studies, direct textural observations, and spectrophotometric recordings show an initial decrease of light transmission, which at larger light intensities (similar to 1 mW/mm(2)) is followed by a bleaching. Simultaneously the electrical properties (electric conductivity, antiferroelectric polarization, switching threshold, and switching time) decreased monotonically with increasing light intensities. The monotonic decrease of electrical properties indicates that the darkening and bleaching have the same origin, namely, the photochemical isomerization of the azo linkage from the trans to the cis isomer. The material with cis isomer has a lower clearing point and phase separates from the trans-rich domains. Initially the size of the separated isotropic domains is below the visible range, which causes increased scattering. As the size of the isotropic domains increase the scattering disappears and the transmittance becomes the average of the transmittances in the polar tilted smectic and isotropic phases.

We applied ellipsometry to study the distribution of azobenzene fragments in the films of two types of comblike polymers with azobenzene moieties in the side chains before and after ultraviolet ~UV! light irradiation. The polymer with an alkyl chain at the end of the azobenzene fragment forms structures with preferred homeotropic alignment of the fragments. Irradiation of this polymer with nonpolarized UV light at normal incidence induces a homeotropic alignment of azobenzene fragments. Oblique irradiation induces tilted structures. Polarized UV light irradiation at normal beam incidence induces biaxial structures with a fanlike distribution of azobenzene fragments and preferably out-of-plane alignment. The polymer with polar nitro group at the end of the azobenzene moiety shows preferential in-plane orientation. The degenerate in-plane alignment is retained for normal irradiation with nonpolarized UV light. Excitation with polarized light provides highly ordered in-plane alignment of the azobenzene fragments perpendicular to the UV light polarization. Re-orientation of the fragments under a second UV exposure with orthogonal polarization involves out-of-plane rotation of the fragments.

Null-transmission ellipsometry and depolarized light microscopy have been performed on free-standing films of three achiral banana-shaped compounds in the B2 phase. Our results support a two-layer unit cell previously proposed to explain the observed antiferroelectricity in thin films and bulk samples. We have studied thicker films than previously reported and have found no deviations in the film structure from the earlier findings. Moreover, we can determine the layer spacing, the molecular tilt from the layer normal, and the three principal indices of refraction in the molecular reference frame.