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A Jákli

Publications and source records attributed to A Jákli.

At least 19 recordsLinked to original sources

Chirality and polarity transfers between bent-core smectic liquid-crystal substances.

Liquid-crystal phases with both solid and liquid characteristics are unique, since they exhibit chirality on both molecular and mesoscopic levels under special circumstances. We have studied binary composites formed by mixing of a chiral dimer (B-Ch), in which a bent core is covalently linked to a promesogenic cholesterol unit through a flexible spacer, and an achiral bent-core mesogen having two vicinal fluorine atoms (B-2F). The pure materials show smectic phases featuring C2 symmetry. The dimer B-Ch displays conventional chiral smectic C (SmC*) phase with a chirality--induced polarization P(c) approximately 30 nC/cm2, whereas B-2F possesses synclinic and anticlinic antiferroelectric "banana" smectic (SmCP) phase with a relatively high-polarization (P(b)) value of about 900 nC/cm(2). Mixing these two materials we were able to measure P(c), and we have verified that the molecular chirality contributes to the polarization of banana phases only in synclinic configurations.

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Giant flexoelectricity of bent-core nematic liquid crystals.

Flexoelectricity is a coupling between orientational deformation and electric polarization. We present a direct method for measuring the flexoelectric coefficients of nematic liquid crystals (NLCs) via the electric current produced by periodic mechanical flexing of the NLC's bounding surfaces. This method is suitable for measuring the response of bent-core liquid crystals, which are expected to demonstrate a much larger flexoelectric effect than traditional, calamitic liquid crystals. Our results reveal that not only is the bend flexoelectric coefficient of bent-core NLCs gigantic (more than 3 orders of magnitude larger than in calamitics) but also it is much larger than would be expected from microscopic models based on molecular geometry. Thus, bent-core nematic materials can form the basis of a technological breakthrough for conversion between mechanical and electrical energy.

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Critical behavior at the isotropic-to-nematic phase transition in a bent-core liquid crystal.

Magnetic birefringence and dynamic light scattering measurements of orientational order parameter fluctuations at the isotropic-nematic phase transition of a bent-core liquid crystal reveal a pretransitional temperature dependence consistent with the standard Landau-deGennes mean field theory. However, as follows: the transition in the bent-core compound is more weakly first order (TNI-T* approximately 0.4 degrees C), the leading Landau coefficient is approximately 30 times lower, the viscosity associated with nematic order fluctuations is approximately 10 times higher, and the density change is approximately 10 times lower, than typically observed in calamitic (rod-shaped) liquid crystals. One consistent explanation for these anomalies is an optically isotropic phase composed of microscopic complexes or "clusters" of bent-core molecules.

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Nonstandard electroconvection in a bent-core nematic liquid crystal.

We characterize three nonstandard electrohydrodynamic instabilities in nematic liquid crystals composed of bent-core molecules. In addition to their shape, another important attribute of this material is that the anisotropy in the electrical conductivity changes sign as the frequency of the applied electric field changes. These instabilities do not appear to fit within the standard model for electroconvection. The first instability creates a pattern with stripes parallel to the initial director orientation, with a wavelength about equal to the separation of the cell plates. The next is the previously reported prewavy instability. The third instability is optically and dynamically identical to the prewavy instability, but is distinguished by different threshold behavior.

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Electrorotation of colloidal particles in liquid crystals.

We present the first observations of dc electric-field-induced rotational motion of finite particles in liquid crystals. We show that the electrorotation is essentially identical to the well-known Quincke rotation, which in liquid crystals triggers an additional translational motion at higher fields. In the smectic phase the translational motion is confined to the two-dimensional geometry of smectic layers, in contrast to the isotropic and nematic phases, where the particles can move in all three dimensions. We demonstrate that by a proper analysis of the electrorotation, one can determine the in-plane viscosity of smectic liquid crystals. This method needs only a small amount of material, does not require uniform alignment over large areas, and enables probing rheological properties locally.

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Optically isotropic liquid-crystal phase of bent-core molecules with polar nanostructure.

We found that the optically isotropic (I(M)) mesophase observed recently below the nematic phase of the bent-core liquid crystal 4-chlororesorcinol bis[4-(4-n-dodecyloxybenzoyloxy)benzoate] shows ferroelectric-type switching. Polarizing microscopic, electric current, dielectric, and dynamic light scattering studies lead us to propose that the I(M) phase is composed of interconnected orthoconic racemic smectic (Sm-Ca P(F)) nanodomains with random layer orientations. Near the nematic phase, where the polarization can be saturated by electric fields, the system responds in a fashion analogous to the granular structure of a magnetic spin glass--in particular, we observed that the relaxation back to the nonpoled structure follows a similar, inverse logarithmic rule.

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Light-induced changes of optical and electrical properties in bent-core azo compounds.

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 (approximately 1 mW/mm2) 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.

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Glass forming banana-shaped compounds: vitrified liquid crystal states.

The synthesis and physical properties, in particular electro-optic switching behavior, of 3-chloro-biphenyl-3',4-bis[4-[4-(3,7-dimethyloctyloxy)-phenyliminomethyl]] benzoate are reported. The compound exhibits an antiferroelectric tilted smectic liquid crystalline phase (Sm-CP) in a broad temperature range. Below 20 degrees C the sample goes over to a glassy state and no crystallization appears down to -50 degrees C. It is observed that below the glass transition temperature both achiral and chiral structures of the Sm-CP phase can be frozen. Each of them can have three polarization states (two ferroelectric and one antiferroelectric), thus giving six different vitrified textures. This enables atomic force microscopy studies of the different liquid crystalline states and suggests possibilities for electro-optical storage devices.

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Optical studies of the nematic phase of an oxazole-derived bent-core liquid crystal.

Various optical and dynamic light scattering studies have been conducted on the nematic phase of an oxazole-derived bent-core liquid crystal. At optical length scales and in the absence of applied fields, homogeneously aligned samples of this material, which has an oxazole heterocyclic ring in the central core, are found to behave more like a conventional straight-core nematic than a previously investigated ester-based class of bent-core molecules that have a benzene ring as the core linkage between the two arms of the bow-shaped molecule. In particular, the nematic refractive indices of the oxazole compound combine in the standard way [i.e., square root of ((2no2+ne2)/3)] to match the isotropic value throughout the nematic range, and the observed director fluctuation modes have relaxation rates comparable to those of the usual thermotropics. However, polarized light scattering data reveal evidence of weak biaxial fluctuations, and indications of electric-field-induced biaxiality are observed in the refractive index measurements.

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Dielectric relaxation behavior of a liquid crystal showing an unusual type of antiferroelectric-ferroelectric-antiferroelectric phase sequence.

The temperature and frequency dependent dielectric relaxation behavior of a liquid crystalline (S)-(+)-1-methylheptyl 4-[2-(4-alkoxyphenyl) thiophene-5-carbonylthiooxy] benzoate system is reported. Interesting successive antiferroelectric-ferroelectric-antiferroelectric (AF-FE-AF) phase transitions are observed in this system resembling the successive phase transitions observed in crystalline Rochelle salt. The smectic-C* (SmC*) to AF1 phase transition (around 103.0 degrees C) is first order in nature, predicted from the use of Orihara and Ishibashi theory. It is also found that a contribution of the ferroelectric SmC* phase ordering penetrates even in the antiferroelectric AF1 (SmC(*)(A)) and AF2 (SmC(*)(A)) phases very close to the SmC*-AF1 and SmC*-AF2 phase boundaries (critical regions). It is suggested that this type of mixing of AF and FE phases might cause surface induced ferroelectric- or ferroelectric-type ordering near the AF-FE phase transitions. A soft mode with Debye-type dispersion was observed in the SmA phase. The thermal behaviors of dielectric dispersion, absorption, and dielectric strength in different phases are also reported and discussed.

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Unusual sequences of tilted smectic phases in liquid crystals of bent-shape molecules.

The first theoretical description of the experimentally often-observed isotropic-polar smectic phase transitions of symmetric and asymmetric bent-shape molecules is presented. The isotropic-tilted polar smectic phase transition requires a coupling among three types of ordering processes: polar packing, director tilt, and layer ordering. For explaining the unusual triclinic-monoclinic phase transition with the lower symmetry phase at higher temperature, observed in fluoro-containing compounds recently, a mechanism is proposed in which the layer ordering triggers the simultaneous onset of the tilt and polar order.

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Nanophase segregation of nonpolar solvents in smectic liquid crystals of bent-shape molecules.

Electro-optical, calorimetric, x-ray, and dielectric measurements are reported on a mixture containing a bent-core liquid crystal 4-chloro-1,3-phenylinebis [4-(4-n-tetradecyloxyphenyliminomethyl) benzoate] mixed with the nonpolar solvent n-hexadecane (HEX). It is observed that the addition of HEX depresses the isotropic-to-smectic phase transition temperature, but the crystallization temperature does not change considerably. Instead, the texture of the crystalline phase changes and, at sufficiently high concentrations of HEX (>20 wt %), an optically isotropic phase appears. Above 40 wt % HEX concentrations, the mesophase completely disappears and a direct isotropic solid-to-isotropic liquid transition takes place. At increasing HEX concentration, the transition enthalpies, the layer ordering, and the magnitude of the electric polarization decrease. X-ray studies reveal that HEX molecules pack in between the smectic layers, resulting in an increase of the layer spacing by about 3 A. The increase of the layer spacing saturates at 5 wt % of HEX. The phase segregation observed seems to be due to steric interactions between the flexible HEX molecules and the rigid bent cores of the liquid crystal molecules.

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Ferroelectric-chiral-antiferroelectric-racemic liquid crystal phase transition of bent-shape molecules.

Detailed dielectric, polarization current, electro-optical, and textural observations are reported on an asymmetric banana-shaped compound 1,3-biphenylene-bis[4-(3-fluoro-4-octyloxyphenyliminomethyl)benzoate]. The material possesses a chiral-ferroelectric-racemic-antiferroelectric phase transition. Our studies reveal that the higher temperature ferroelectric phase has a polar double-tilted smectic structure, where both the molecular plane and the long axis are tilted with respect to the layer normal. Accordingly, it has a chiral triclinic structure with an out-of-plane polarization component. The lower temperature phase has a monoclinic symmetry, which is higher than that of the higher temperature phase. To our knowledge, among liquid crystals such situations were previously observed only in reentrant phases.

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Piezoelectricity of a ferroelectric liquid crystal with a glass transition.

Pressure-electric (hydrostatic piezoelectric) measurements are reported on bookshelf textures of a ferroelectric smectic-C (Sm C*) liquid crystal with a glass transition. The continuous variation of a partially fluid state to the solid glass enables one to trace how the piezoelectric effect depends on the consistency of the material. It was observed that in the Sm C* samples with poled glass the piezoelectric constants are comparable to conventional piezoelectric crystals and poled piezoelectric polymers. This implies their application possibilities. The magnitude of the piezoelectric constant in the glassy state depends very much on the poling conditions. The studies indicate that there are two counteracting effects, which cancel each other out in the Sm C* phase near the glass transition. Our analysis indicates that the pressure-induced director tilt change has a dominating effect both in the fluid and the glassy Sm C* states.

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Evidence for triclinic symmetry in smectic liquid crystals of bent-shape molecules.

The first experimental evidence for triclinic symmetry of bulk smectic liquid-crystal samples of achiral banana-shaped molecules is presented. This phase corresponds to the so-called Sm-CG phase consisting of biaxial molecules and characterized by two tilt directions with respect to the layer normal: tilt of the molecular plane (clinic) and tilt of the molecular kink direction (leaning). Each smectic layer has a polarization component normal to the smectic layers (C1 symmetry). The observations suggest that the phase tentatively labeled as B7 is identical with the Sm-CG phase.

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Macroscopic chirality of a liquid crystal from nonchiral molecules.

The transfer of chirality from nonchiral polymer networks to the racemic B2 phase of nonchiral banana-shaped molecules is demonstrated. This corresponds to the transfer of chirality from an achiral material to another achiral material. There are two levels of chirality transfers. (a) On a microscopic level the presence of a polymer network (chiral or nonchiral) favors a chiral state over a thermodynamically stable racemic state due to the inversion symmetry breaking at the polymer-liquid crystal interfaces. (b) A macroscopically chiral (enantimerically enriched) sample can be produced if the polymer network has a helical structure, and/or contains chemically chiral groups. The chirality transfer can be locally suppressed by exposing the liquid crystal to a strong electric field treatment.

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Optically induced periodic structures in smectic-C liquid crystals.

We explore periodic structures of smectic-C (SmC) liquid crystals, induced optically by a polarization grating. The studied cells contain a passive surface of rubbed polyimide and an active photosensitive substrate of azo-dye doped polyimide. In a nematic phase the director field can be periodic independent of the angle between the grating vector and the rubbing direction. In the SmA phase periodic structure can be induced only by layer undulations. The SmC behaves similarly to the nematic phase, but the director can rotate only on a cone, which results in a more complex geometry. The periodic pattern is superimposed with four different director and layer structures. In spite of the coexistence of the nonuniform structures the diffraction efficiency is better in the SmC, than in the nematic phase.

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Electric-field-induced chiral separation in liquid crystals.

Recently it was shown that smectic liquid crystal phases formed by achiral banana-shaped molecules are chiral. Films of such phases generally contain both homochiral (consisting of layers of the same chirality) and racemic (the chirality alternates in subsequent layers) domains. So far it has not been clear how to control the overall chirality of the sample. By observing the effects of the application of suitable electric fields, it was noted that chirality of a film of banana shaped molecules was interchanged between homochiral and racemic. We present dielectric, electro-optic, and polarization current measurements on both the racemic and chiral states. The observations indicate that the synclinic states have minimum free energies. The observed dielectric modes can be explained by a simple model assuming that the antiferroelectric state is very weak.

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