Flow induced bistable anchoring switching in nematic liquid crystals

A hydrodynamically controlled switching of orientations of a nematic bistable surface anchoring is observed. A viscous torque moves surface lines between domains corresponding to bistable anchoring. An observed threshold for this viscous torque is attributed to relative spatial inhomogeneities of surface energy (∼10^-2).     

Disclinations dynamics in confined nematic liquid crystals: strong anchoring

We have investigated the dynamics of pair annihilation of disclination lines in strong anchoring. This work is based on the Frank free energy. The director angle, φ(x, y, z), is obtained by the continuous theory. We show that the form of the viscous force in a confined nematic liquid crystal and in strong anchoring is a function of the initial distance between the two disclination lines. The asymptotic velocity, v _asy, is also a function of the initial distance. Our theoretical result on the asymptotic velocity is in good agreement with previous experimental results.     

Disclinations dynamics in confined nematic liquid crystals: strong anchoring

We have investigated the dynamics of pair annihilation of disclination lines in strong anchoring. This work is based on the Frank free energy. The director angle, φ(x, y, z), is obtained by the continuous theory. We show that the form of the viscous force in a confined nematic liquid crystal and in strong anchoring is a function of the initial distance between the two disclination lines. The asymptotic velocity, v _asy, is also a function of the initial distance. Our theoretical result on the asymptotic velocity is in good agreement with previous experimental results.     

Orientation and anchoring effects in stretched polymer dispersed nematic liquid crystals

The induction of liquid crystal orientation through mechanical stretching was investigated for polymer dispersed liquid crystals (PDLCs) by means of infrared dichroism. Using a nematic liquid crystal BL006 and polyacrylic acid as the polymer matrix, it was possible to stretch the PDLC films with BL006 in either the isotropic or the nematic phase. After cooling the films under strain to room temperature, the molecular orientation of BL006 was found to be much higher for films that contained isotropic liquid droplets of BL006 at the time of stretching than for films that had nematic droplets. Stretching PDLC films with isotropic droplets results in no molecular orientation, but the orientation is induced during the subsequent cooling when BL006 goes through the isotropic-to-nematic phase transition. Interestingly for PAA/BL006, the nematic director orients along the long axes of the elongated droplets despite liquid crystal anchoring perpendicular to the polymer interface.     

Orientation and anchoring effects in stretched polymer dispersed nematic liquid crystals

The induction of liquid crystal orientation through mechanical stretching was investigated for polymer dispersed liquid crystals (PDLCs) by means of infrared dichroism. Using a nematic liquid crystal BL006 and polyacrylic acid as the polymer matrix, it was possible to stretch the PDLC films with BL006 in either the isotropic or the nematic phase. After cooling the films under strain to room temperature, the molecular orientation of BL006 was found to be much higher for films that contained isotropic liquid droplets of BL006 at the time of stretching than for films that had nematic droplets. Stretching PDLC films with isotropic droplets results in no molecular orientation, but the orientation is induced during the subsequent cooling when BL006 goes through the isotropic-to-nematic phase transition. Interestingly for PAA/BL006, the nematic director orients along the long axes of the elongated droplets despite liquid crystal anchoring perpendicular to the polymer interface.     

Influence of weak anchoring on flow instabilities in nematic liquid crystals

We analyse the homogeneous instabilities in a nematic liquid crystal subjected to plane steady Couette or Poiseuille flow in the case when the director is prealigned perpendicular to the flow plane taking into account weak anchoring at the confining surfaces. The critical shear rate decreases for decreasing anchoring strength and goes to zero in the limit of torque-free boundary conditions. For Poiseuille flow two types of instability arise depending on the values of the azimuthal (W _a) and polar (W _p) surface anchoring strengths. The critical line in (W _a,W _p) space which separates the two instabilities regimes is obtained.     

Influence of weak anchoring on flow instabilities in nematic liquid crystals

We analyse the homogeneous instabilities in a nematic liquid crystal subjected to plane steady Couette or Poiseuille flow in the case when the director is prealigned perpendicular to the flow plane taking into account weak anchoring at the confining surfaces. The critical shear rate decreases for decreasing anchoring strength and goes to zero in the limit of torque-free boundary conditions. For Poiseuille flow two types of instability arise depending on the values of the azimuthal (W_a) and polar (W_p) surface anchoring strengths. The critical line in (W_a,W_p) space which separates the two instabilities regimes is obtained.     

A statistical model for transitions in nematic liquid crystals

The two-lattice model of Lennard-Jones and Devonshire has been modified and applied to the study of the transition from the nematic to the isotropic phase. We have used the concept of external degrees of freedom for molecules introduced by Prigogine and applied to the case of chain liquids.     

Electric field effects in nematic layers with weak boundary anchoring

The stationary states induced by an electric field in nematic layers with weak boundary anchoring are described by means of the Taylor expansion method based on catastrophe theory. The planar, twisted and supertwisted structures are considered. The analysis is extended to materials with negative dielectric anisotropy. Several types of behaviour are found. The possibility of switching between twisted and homeotropic states is suggested.     

Slow relaxation processes in nematic liquid crystals at weak surface anchoring

We present new results of experimental investigations of azimuthal director reorientation dynamics for a nematic liquid crystal on solid substrates. Two types of substrate with weak anchoring were studied: glass/polystyrene and glass/UV-activated dye. Slow and fast relaxation processes were observed in both cases under the action of a strong 'in-plane' electric field. The slow surface reorientation and memory effects were controlled by two parameters: the electric voltage and the excitation time. It was established that the increase of the excitation time results in a slowing of the relaxation of the system to the initial state after turning off the electric field. A phenomenological model of a gliding of easy axes is proposed to explain the slow relaxation process.     

New method for measuring polar anchoring energy of nematic liquid crystals

A new method for measuring a polar anchoring energy of nematic liquid crystals (LCs) is proposed. A variation of LC tilt angle on the surface with an applied electrical field was determined by a reflective method. The twisted LC cell configuration was selected to compensate a contribution of the induced birefringence in the reflective spectra. The electrical field controlled reflectance was used to analyse the potential form of the polar anchoring energy and to define the anchoring strength. The proposed method is applicable for 2–5 μm thick LC cells.     

Temperature induced anchoring transition in nematic liquid crystals with two-fold degenerate alignment

The two-fold degenerate alignment of nematic liquid crystals provided by obliquely evaporated SiOx layers was studied as a function of temperature. A temperature induced anchoring transition from tilted to planar alignment with more than 80 degrees between their preferred directions was found. The director in the two-fold degenerate region seems to follow a circular sector from the uniform tilted to the uniform planar anchoring, as the temperature increases. The anchoring transition is reversible and reveals the existing coupling between the azimuthal and polar angles of the preferred directions of alignment. The applicability of the two-fold degenerate alignment and related anchoring transitions of nematic liquid crystals for devices is briefly discussed.     

Effect of carbon nanotubes on phase transitions of nematic liquid crystals

Phase diagrams of multi‐wall carbon nanotube (MWNT)/nematic liquid crystal (E7) and buckminsterfullerene (C₆₀‐I _h)/nematic liquid crystal (E7) binary systems have been investigated by means of polarizing optical microscopy and differential scanning calorimetry. It was found that the isotropic–nematic phase transition temperature (T _NI) of the liquid crystal component was enhanced by the incorporation of MWNT within a small composition gap. A chimney‐type phase diagram can be identified in the MWNT/E7 mixture over a narrow range of ～0.1–0.2% MWNT concentration. Upon substituting the nanotubes with isotropic fillers such as fullerene, the (C₆₀‐I _h)/E7 blend showed no discernible change of T _NI in the same concentration range of the chimney of the MWNT/E7 mixture, suggesting a significant contribution of anisotropy (or the aspect ratio) of the nanotubes to the entropy of the system containing liquid crystal molecules. This enhanced T _NI phenomenon may be attributed to anisotropic alignment of liquid crystal molecules along the carbon nanotube bundles.     

Effect of carbon nanotubes on phase transitions of nematic liquid crystals

Phase diagrams of multi-wall carbon nanotube (MWNT)/nematic liquid crystal (E7) and buckminsterfullerene (C₆₀-I _h)/nematic liquid crystal (E7) binary systems have been investigated by means of polarizing optical microscopy and differential scanning calorimetry. It was found that the isotropic-nematic phase transition temperature (T _NI) of the liquid crystal component was enhanced by the incorporation of MWNT within a small composition gap. A chimney-type phase diagram can be identified in the MWNT/E7 mixture over a narrow range of ∼0.1-0.2% MWNT concentration. Upon substituting the nanotubes with isotropic fillers such as fullerene, the (C₆₀-I _h)/E7 blend showed no discernible change of T _NI in the same concentration range of the chimney of the MWNT/E7 mixture, suggesting a significant contribution of anisotropy (or the aspect ratio) of the nanotubes to the entropy of the system containing liquid crystal molecules. This enhanced T _NI phenomenon may be attributed to anisotropic alignment of liquid crystal molecules along the carbon nanotube bundles.     

Invited Lecture. Experimental studies of the anchoring energy of nematic liquid crystals

An analysis is given of experimental techniques for measuring the anchoring energy, W, of nematic liquid crystals with solid surfaces. Two novel methods for measuring W in homeotropically oriented samples are discussed. The first is based on the stabilization of the flexoelectric distortion by a magnetic field. In the second the thickness dependence of the phase delay for the light beam transmitted through a wedge-form cell with the hybrid orientation of a nematic should be measured. New experimental data on thickness and temperature dependences of the anchoring energy for homogeneously oriented 5CB are also presented. The anchoring energy was even measured for thin interface layers in the isotropic phase and its critical behaviour near the N-I transition is also discussed. New data were also obtained for the anchoring energy of nematics at crystalline surfaces.     

The polar anchoring energy of nematic liquid crystals with polyvinylidene fluoride alignment layer

It has been proved that the high dielectric polyvinylidene fluoride (PVDF) could be used as an alignment layer in liquid crystal device. In this paper, the transmittance, pretilt angle and the polar anchoring energy of the substrates with PVDF alignment layer were researched. Theoretical results and the experimental results about the reflectivity R_SS (polarisation-conserving signals) recorded by full-leaky guided mode in liquid crystal technique are analysed to evaluate the anchoring energy of PVDF alignment layer. The result shows that the polar anchoring energy between PVDF alignment layer and liquid crystal molecules is 2.80 × 10^?4 J/m².     

Carbazole nematic liquid crystals

A number of calamitic 2,7-diary-N-alkyl-substituted carbazoles with an enantiotropic nematic phase have been prepared. Branching of the aliphatic chain attached to the nitrogen atom in the carbazole ring leads to significantly lower liquid crystal transition temperatures. These new materials show a lower ionisation potential than fluorene analogues and blue photoluminescence in solution and as thin solid films.     

Highly birefringent nematic and chiral nematic liquid crystals

We report a simple interference method to determine the dispersion of the extraordinary refractive index and birefringence of highly conjugated and coloured nematic liquid crystals used as light-emitting materials in organic electroluminescent devices. The measurements are made in the nematic glass phase at room temperature. The birefringence is highly dispersive and values up to 1.1 are obtained. Chiral groups are incorporated into the end chains giving a chiral nematic liquid crystal with a very wide stopband in the visible region. The Berreman matrix method is used to simulate transmission through the chiral nematic liquid crystal cell using the refractive index parameters obtained experimentally. Excellent agreement between theory and experiment is found.     

Ordering transitions in nematic liquid crystals induced by vesicles captured through ligand-receptor interactions

We report that phospholipid vesicles incorporating ligands, when captured from solution onto surfaces presenting receptors for these ligands, can trigger surface-induced orientational ordering transitions in nematic phases of 4'-pentyl-4-cyanobiphenyl (5CB). Specifically, whereas avidin-functionalized surfaces incubated against vesicles composed of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) were observed to cause the liquid crystal (LC) to adopt a parallel orientation at the surface, the same surfaces incubated against biotinylated vesicles (DOPC and 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-(biotinyl) (biotin-DOPE)) caused the homeotropic (perpendicular) ordering of the LC. The use of a combination of atomic force microscopy (AFM), ellipsometry and quantitative fluorimetry, performed as a function of vesicle composition and vesicle concentration in solution, revealed the capture of intact vesicles containing 1% biotin-DOPE from buffer at the avidin-functionalized surfaces. Subsequent exposure to water prior to contact with the LC, however, resulted in the rupture of the majority of vesicles into interfacial multilayer assemblies with a maximum phospholipid loading set by random close packing of the intact vesicles initially captured on the surface (5.1 ± 0.2 phospholipid molecules/nm(2)). At high concentrations of biotinylated lipid (>10% biotin-DOPE) in the vesicles, the limiting lipid loading was measured to be 4.0 ± 0.3 phospholipid molecules/nm(2), consistent with the maximum phospholipid loading set by the spontaneous formation of a bilayer during incubation with the biotinylated vesicles. We measured the homeotropic ordering of the LC on the surfaces independently of the initial morphology of the phospholipid assembly captured on the surface (intact vesicle, planar multilayer). We interpret this result to infer the reorganization of the phospholipid bilayers either prior to or upon contact with the LCs such that interactions of the acyl chains of the phospholipid and the LC dominate the ordering of the LC, a conclusion that is further supported by quantitative measurements of the orientation of the LC as a function of the phospholipid surface density (>1.8 molecules/nm(2) is required to cause the homeotropic ordering of the LC). These results and others presented herein provide fundamental insights into the interactions of phospholipid-decorated interfaces with LCs and thereby provide guidance for the design of surfaces on which phospholipid assemblies captured through ligand-receptor recognition can be reported via ordering transitions in LCs.     

Highly birefringent nematic and chiral nematic liquid crystals

We report a simple interference method to determine the dispersion of the extraordinary refractive index and birefringence of highly conjugated and coloured nematic liquid crystals used as light‐emitting materials in organic electroluminescent devices. The measurements are made in the nematic glass phase at room temperature. The birefringence is highly dispersive and values up to 1.1 are obtained. Chiral groups are incorporated into the end chains giving a chiral nematic liquid crystal with a very wide stopband in the visible region. The Berreman matrix method is used to simulate transmission through the chiral nematic liquid crystal cell using the refractive index parameters obtained experimentally. Excellent agreement between theory and experiment is found.