Volume-stabilized ULH structure for the flexoelectro-optic effect and the phase-shift effect in cholesterics

Flexoelectric coupling gives rise to a linear electro-optic response in cholesterics (flexoelectrooptic effect) with a uniformly lying helix (ULH) structure and this electro-optic effect is strongly reliant on the homogeneity and quality of the texture. The ULH structure, unfortunately, is complicated in itself and may be perturbed by factors such as dielectric coupling, surface/liquid crystal interactions and phase transitions, and often there is a tendency for relaxation into the Grandjean texture (standing helix structure) with time. Hence, in order to exploit the flexoelectro-optic effect in cholesterics any instability of the ULH structure must be ruled out. We have overcome these problems by incorporating a polymer network by means of photopolymerization of a reactive monomer added to the cholesteric. The volume stabilized ULH structure still exhibits the flexoelectro-optic effect, it is stable and it is also retained after heating to the isotropic phase and going back to the cholesteric phase. In addition to the flexoelectro-optic mode, the ULH structure is of interest in an electro-optic mode characterized by a pure phase-shift with no change in amplitude (transmittance). This mode, which has obvious applications in spatial light modulators, optical computing devices and electrically controlled kinoforms and phase holograms working without polarizers, is also briefly discussed.     

Characterization of large tilt-angle flexoelectro-optic switching in chiral nematic liquid crystal devices

The ‘flexoelastic ratio’ is commonly used to characterise the electro-optic behaviour of chiral nematic liquid crystal (LC) devices that exhibit flexoelectro-optic switching. There has been renewed interest in this electro-optic effect of late as new LC materials and mixtures have been developed that exhibit large tilt angles, Ø, of the optic axis (Ø ≥ 45°) whilst maintaining a fast response time (< 1 ms). In this study, we compare the different flexoelastic ratios that are obtained for fixed and variable-pitch chiral nematic LCs for materials with a tilt of the optic axis as large as Ø = ± 45°. We show that for large tilt angles of the optic axis the values for the two different flexoelastic ratios measurably diverge. Of the two ratios, we propose that for large tilt-angle mixtures it is more appropriate to use the flexoelastic ratio that is derived for the case when the pitch of the helix is constrained. In addition, a simple way of determining the ‘pitch-constrained’ flexoelastic ratio is presented that involves identifying the electric field amplitude at the point for which the transmission levels are the same for both positive and negative electric field polarities.     

Ferroelectric, pyroelectric and electro-optic properties of a chiral side chain copolymer with high polarization and a broad C* phase

The synthetic route to a chiral side chain copolymer exhibiting broad smectic phases is described. The copolymer shows a smectic C* phase from below room temperature up to 105°C. Ferroelectric properties of this copolymer are reported as well as results showing electroclinic switching. The pyroelectric effect and the dielectric behaviour of the copolymer are also demonstrated.     

The packing of azobenzene dye moieties and mesogens in polysiloxane copolymers and its impact on the opto-dielectric effect

Broadband dielectric spectroscopy (102-105Hz) is used to study the opto-dielectric effect in statistical polysiloxane copolymers with side groups containing chiral mesogenic units and others containing azobenzene moieties. Below 64 C, the unexposed copolymer is ferroelectric. UV-exposure induces a photoisomerization of the azobenzene to the cis -configuration, and the phase transition, ferroelectric/non-ferroelectric (SC*/SA), is shifted to lower temperatures. In the temperature interval between the phase transition temperatures ferroelectric/nonferroelectric of the exposed and unexposed samples, an opto-dielectric effect is observed. The efficiency of this opto-dielectric switching depends on the packing of the chromophore within the smectic layers.     

Antiferroelectric phase induced by a semi-fluoroalkane positioned at the chiral tail of a molecule

A novel fluorinated chiral liquid crystal material derived from a newly designed optically active semi-perfluorinated alkyl chain in the chiral group, (S)-1-(2,2,3,3,3-pentafluoropropyloxy)-2-propanol, and a non-fluorinated homologue derived from (S)-1-propyloxy-2-propanol, were prepared for comparison of their mesomorphic properties. The investigation of defect textures, switching behaviour and dielectric permmitivity showed that the introduction of a semi-perfluorinated alkyl chain into the chiral tail of the molecule induces formation of an antiferroelectric phase.     

Photochemical tuning of the helical structure of cholesteric liquid crystals by photoisomerization of chiral azobenzenes, and their structural effects

Several chiral azobenzene compounds having different chiral substituents were synthesized. A cholesteric phase was induced by mixing each chiral azobenzene compound with a host non-chiral nematic liquid crystal (E44). The helical twisting power (HTP) as well as the change in HTP by trans-cis photoisomerization of the chiral azobenzene compound was dependent on the structure of the chiral substituents. A compensated nematic phase was induced by combination of E44, a chiral azobenzene compound and a non-photochromic chiral compound. Reversible switching between the compensated nematic phase and cholesteric phase was brought about by trans-cis photoisomerization of the chiral azobenzene compound in the liquid crystalline systems. An azobenzene compound substituted with a menthyl group showed the highest efficiency as the trigger for the switching; this efficiency was related to the compactness of the chiral group substituted within the azobenzene core moiety.     

Molecular and collective relaxations of ferroelectric side chain liquid crystalline polysiloxanes

The influences of mesogenic group chemical structures on dielectric relaxation behavior were investigated for ferroelectric side chain liquid crystalline polymers (FLCPs). The relaxation time and activation energies of the Goldstone mode, α‐, and β‐relaxations decrease with increasing spacer length because of the plasticizer effect of the spacer. Moreover, the relaxation intensity increases with increasing spacer length for FLCPs. An FLCP with a longer spacer length exhibits a higher mesogenic group mobility, and subsequently leads to easier reorientation toward the alternating electrical field. An increase in mesogenic core rigidity results in an increase in the relaxation time and activation energies, and a decrease in the relaxation intensities for the Goldstone mode, α‐, and β‐relaxations. Moreover, the β‐relaxation is suppressed and cannot be observed in the glassy state for FLCPs containing naphthyl biphenylcarboxylate as the mesogenic group. Shorter relaxation time, smaller activation energies, and higher intensity of the α‐, and β‐relaxations were obtained for FLCPs containing chiral moiety with a flexible heptyl alkyl chain. However, the relaxation intensity of the Goldstone mode for FLCPs containing this chiral moiety was smaller than that for FLCPs containing the chiral moiety with a butyl alkyl chain. For FLCPs containing a chiral moiety with two asymmetrical centers, their Goldstone mode relaxation showed larger amplitude. The α‐ and β‐relaxations are suppressed for these FLCPs because of the dense packing and memory effect of the smectic phase. The relationship between the chemical structure of the mesogenic group and dielectric relaxations is discussed in great detail. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 2035–2049, 2006     

Synthesis and mesomorphic properties of chiral liquid crystals derived from ( S )-lactic acid with 3-pentanol

The chiral swallow-tailed liquid crystals, 1-ethylpropyl (R)-2-[4-(4′-alkoxybiphenylcarbonyloxy)-phenoxy]propionates, EPmPBPP (m = 8?12), were prepared by using chiral (S)-lactic acid with 3-pentanol as starting materials. Mesophases and their corresponding transition temperatures were determined by polarizing microscopic textures and DSC. The results showed that all the chiral materials exhibited enantiotropic BP, N*, TGBA*, SmA*, and SmC* phases. Spontaneous polarization, dielectric constant and electro-optical response for the materials in the ferroelectric SmC* phase were investigated. It was noted that the electro-optical response of transmittance versus applied voltage obtained from the ferroelectric phase of material EPmPBPP (m = 10) displayed V-shaped switching, while that of other materials displayed the typical characteristics of ferroelectric hysteresis switching or U-shaped switching.     

A molecular theoretical derivation of the Landau free energy of chiral smectic C liquid crystals

A molecular theoretical derivation of the Landau free energy of chiral smectic C liquid crystals is presented on the basis of a molecular theoretical approach. The excess free energy concerned with the ferroelectric helicoidal structure is derived within a mean field approximation. Several material constants such as the Curie temperature, the elastic constant, the helical pitch, the piezo- and flexoelectric constants and the dielectric susceptibility are expressed in terms of some effective intermolecular interaction parameters between molecules. A molecular theoretical consideration of the chiral smectic C-smectic A transitions is given in comparison with a few previous works. By comparing with some available experimental data for DOBAMBC, effective interaction parameters are numerically estimated.     

Experimental and theoretical study of the influence of a bias electric field on the dielectric properties of the chiral smectic A* phase

The influence of a bias electric field on the temperature and frequency dependence of the soft mode part of the complex dielectric constant of the chiral smectic A* phase has been studied experimentally. It was found that only close to T_S*CS*A does the bias field have any influence on the experimentally determined quantities. Here the relaxation frequency increased with increasing bias field, while the corresponding dielectric strength decreases. We also present a theoretical calculation of the influence of a bias field on the complex dielectric constant of the chiral smectic A* phase which, apart from minor details, is in accordance with the observed behaviour. Finally we discuss how the nature of the electroclinic effect can be correlated with the influence of the bias field on the smectic A* dielectric constant.     

Flexoelectric response at defect sites in nematic inversion walls

Electric field experiments have been carried out on +1 and -1 defects formed in alignment inversion walls, in a planarly aligned nematic phenyl benzoate. The results show that the defects are non-singular in the core and exhibit a flexoelectric response to an applied d.c. or low frequency a.c. field. When the c-director flux lines are circular, as in a +1 defect in a wall parallel to the easy axis, flexoelectro-optic switching characterized by an azimuthal angle variation is observed. When the c-director flux is radial, the response is seemingly through polar angle variations involving no rotation of the extinction brushes due to crossed polarizers. This conclusion follows from the field-induced structural distortions observed at a -1 defect having a combination of radial and tangential c-director fields.     

Synthesis and ferroelectric properties of chiral swallow-tailed liquid crystals derived from (S)-2-[1-(2-ethylbutoxy)]propanol

(S)-2-[1-(2-Ethylbutoxy)]propanol was designed and synthesized as a chiral building block for the preparation of chiral liquid crystals. Its derivatives, the (S)-2-[1-(2-ethylbutoxy)]propyl 4-[4-(4-alkoxyphenyl)phenoyloxy]benzoates, EPmPPB (m = 8-12), were prepared and their mesomorphic phases investigated. The results showed that the chiral materials displayed enantiotropic SmA* and SmC* phases, while those with shorter alkyl chains (m = 8-10) displayed an additional unidentified SmX* phase. The switching current, spontaneous polarization, tilt angle, dielectric constant and electro-optical response for the materials in the ferroelectric SmC* phase were measured. The electro-optic responses of the materials in polyimide film-coated, homogeneously aligned cell exhibit thresholdless, V-shaped switching in the ferroelectric phase.     

Coupling quantum Monte Carlo to a nonlinear polarizable continuum model for spherical solutes

Starting from the nonlinear dielectric response model of Sandberg and Edholm, we derive an analytical expression of the polarization contribution to the solvation free energy in terms of the electronic density of the solute and the dielectric properties of the solvent. The solvent inhomogeneity is taken into account with the use of a smooth switching function whose spacial variation is established on the basis of how the solvent is arranged around the solute. An explicit form of a local potential representing the solvent effect on the solute is thus obtained by functional analysis. This effective potential can be combined with density functional or quantum chemical methods for the quantum mechanical treatment of the solute. Here, we use quantum Monte Carlo techniques for the solute and apply the method to the hydration of atomic ions finding very good agreement with experimental data.     

A chiral lead-free tin(IV)-based halide organic-inorganic semiconductor with dielectric switching and phase transition

Chiral organic-inorganic metal halide semiconductors (OIMHSs) have recently attracted numerous interests due to their unique chirality, structural tunability, and extensive physical properties. However, most reported chiral OIMHSs contain toxic lead, which will be a potential obstacle to their further applications. Herein, we successfully synthesized a novel chiral lead-free tin(IV)-based OIMHS [(R)-3-hydroxyquinuclidinium]₂SnCl₆ ([R-HQ]₂SnCl₆). It exhibits a wide band gap (E_g) of about 4.11 eV. Moreover, [R-HQ]₂SnCl₆ undergoes a phase transition around 330 K (T_c) and shows distinct dielectric switching characteristics with good repeatability. This work enriches the chiral lead-free OIMHS family and stimulates further exploration of chiral lead-free OIMHS switching materials     

New antiferroelectric liquid crystalline materials containing a keto group and two lactate groups

New chiral liquid crystalline materials containing a keto group and two lactate units attached to the mesogenic core have been synthesized and studied. All the new compounds show the paraelectric SmA, ferroelectric SmC* and antiferroelectric SmC*_A phases each over rather broad temperature ranges. The properties of the phases were characterized by DSC, electro-optical and dielectric studies. The spontaneous polarization, tilt angle, helical pitch, and switching times were determined for the polar phases.     

In Situ Controlled Construction of a Hierarchical Supramolecular Chiral Liquid-Crystalline Polymer Assembly

Hierarchical supramolecular chiral liquid-crystalline (LC) polymer assemblies are challenging to construct in situ in a controlled manner. Now, polymerization-induced chiral self-assembly (PICSA) is reported. Hierarchical supramolecular chiral azobenzene-containing block copolymer (Azo-BCP) assemblies were constructed with π–π stacking interactions occurring in the layered structure of Azo smectic phases. The evolution of chirality from terminal alkyl chain to Azo mesogen building blocks and further induction of supramolecular chirality in LC BCP assemblies during PICSA is achieved. Morphologies such as spheres, worms, helical fibers, lamellae, and vesicles were observed. The morphological transition had a crucial effect on the chiral expression of Azo-BCP assemblies. The supramolecular chirality of Azo-BCP assemblies destroyed by 365 nm UV irradiation can be recovered by heating–cooling treatment; this dynamic reversible achiral–chiral switching can be repeated at least five times.     

The influence of chirality on the difference in flexoelectric coefficients investigated in uniform lying helix,Grandjean and twisted nematic structures

Measurements of the difference in flexoelectric coefficients (e ₁ – e ₃), using the sign convention as originally defined by Meyer, are reported from three experiments employing the flexoelectro-optic effect in different geometries. The uniform lying helix (ULH) structure is used to measure the tilt angle of the liquid crystal director with respect to the helix axis for an applied electric field, in order to infer a value for (e ₁ – e ₃). Alternatively, measurements of the flexoelectric difference can be made by considering the transmission through a device with an in-plane electric field aligned in either the Grandjean structure for highly chiral materials, or a twisted nematic (TN) structure for largely achiral materials. The results from the Grandjean and ULH structures show the equivalence of the measurement techniques with helix axis either perpendicular or parallel to the substrates. Further comparison of these results with the measurement from the achiral TN device shows that the difference in flexoelectric coefficients displays no dependence on chirality, demonstrating that flexoelectricity is purely associated with splay and bend director deformations, as expected from symmetry considerations.     

The effect of the biaxial permittivity tensor and tilted layer geometries on the switching of ferroelectric liquid crystals

Using a simple uniform switching model, we investigate the behaviour of the voltage dependent switching time of surface stabilized ferroelectric liquid crystals as a function of the biaxial permittivity tensor and the layer tilt angle. We show that the dielectric biaxiality can markedly effect the response time (τ) of the device and is the origin of the minimum in τ as a function of voltage (V) in tilted layer systems. The dielectric biaxiality should, therefore, be optimized for multiplexing schemes which use the τ—V minimum.     

New antiferroelectric liquid crystalline materials containing a keto group and two lactate groups

New chiral liquid crystalline materials containing a keto group and two lactate units attached to the mesogenic core have been synthesized and studied. All the new compounds show the paraelectric SmA, ferroelectric SmC* and antiferroelectric SmC*_A phases each over rather broad temperature ranges. The properties of the phases were characterized by DSC, electro-optical and dielectric studies. The spontaneous polarization, tilt angle, helical pitch, and switching times were determined for the polar phases.     

In Situ Controlled Construction of a Hierarchical Supramolecular Chiral Liquid‐Crystalline Polymer Assembly

Hierarchical supramolecular chiral liquid‐crystalline (LC) polymer assemblies are challenging to construct in situ in a controlled manner. Now, polymerization‐induced chiral self‐assembly (PICSA) is reported. Hierarchical supramolecular chiral azobenzene‐containing block copolymer (Azo‐BCP) assemblies were constructed with π–π stacking interactions occurring in the layered structure of Azo smectic phases. The evolution of chirality from terminal alkyl chain to Azo mesogen building blocks and further induction of supramolecular chirality in LC BCP assemblies during PICSA is achieved. Morphologies such as spheres, worms, helical fibers, lamellae, and vesicles were observed. The morphological transition had a crucial effect on the chiral expression of Azo‐BCP assemblies. The supramolecular chirality of Azo‐BCP assemblies destroyed by 365 nm UV irradiation can be recovered by heating–cooling treatment; this dynamic reversible achiral–chiral switching can be repeated at least five times.