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A substrate was patterned with two pairs of half-integer strength topological defects, (+½, +½) and (+½, −½). In a sufficiently thick cell, a disclination line runs in an arch above the substrate connecting the two half integer defects within each pair. The director around the disclination line for the like-sign pair must rotate in 3D, whereas for the opposite-sign defect pair the director lies in the xy-plane parallel to the substrate. For a negative dielectric anisotropy nematic, an electric field applied normal to the substrate drives the director into the xy-plane, forcing the arch of the disclination line of the like-sign pair to become extended along the z-axis. For sufficiently large field the arch splits, resulting in two nearly parallel disclination lines traversing the cell from one substrate to the other. The opposite-sign defect pair is largely unaffected by the electric field as the director already already lies in the xy-plane. Experimental results are presented, which are consistent with numerical simulations. 

We present the first preparation and properties of chiral nanocapsules. The chiral shell, a polyurea derivative, was obtained by interfacial emulsion polymerization of L-lysine with polymethylene polyphenyl isocyanate. The chirality of these nanocapsules was manifested by its ability to induce conformational deracemization of liquid crystal. This induced chirality was measured using the “Raynes experiment”, in which the cell’s boundary conditions impose a ±90o rotation of the liquid crystal director from one surface to the other. Both left and right-handed director twist domains appear on cooling from the isotropic to the nematic phase. Owing to the weak induced chirality of the liquid crystal, one sense of director rotation is energetically more favorable and its domain size expands, resulting in curvature of the domain walls. The curvature was measured as a function of capsule concentration, and serves as a metric of the induction of chirality in the surrounding liquid crystal. 

Chiral organosilica particles of size ~200 nm were synthesized from an enantio-pure multi-armed chiral D-maltose organosilane precursor in the absence of co-condensation with an achiral monomer. Two distinct experiments were performed to demonstrate the particles’ ability to induce conformational deracemization of a host liquid crystal. The first involves an electric field-induced tilt of the liquid crystal director in the deracemized smectic-A phase. The other involves domain wall curvature separating left- and right-handed liquid crystal helical pitch domains imposed by the cells’ substrates. The results demonstrate unequivocally that enantio-pure organosilica nanoparticles can be synthesized and can induce chirality in a host. 

Using a Landau–de Gennes approach, we study the impact of confinement topology, geometry and external fields on spatial positioning of nematic topological defects (TDs). In quasi two-dimensional systems we demonstrate that confinement enforced total topological charge m>>1 decays into elementary TDs bearing charge m=1/2. These assemble close to the bounding substrate to enable essentially bulk-like uniform nematic ordering in the central part of a system. This effect is reminiscent of the Faraday cavity phenomenon in electrostatics. We observe that in certain confinement geometries, varying the order parameter correlation length size could trigger global rotation of an assembly of TDs. Finally, we show that an external electric field could be used to drag the boojum finger tip towards a confinement cell interior. Assemblies of TDs could be exploited as traps for appropriate nanoparticles, opening several opportunities for development of functional nanodevices. 

A novel structure was observed below the smectic-A–smectic-C phase transition in a very thin open cell having an air interface above and enforced planar anchoring at the substrate below. The structure appears as periodic dark and light streaks running perpendicular to the oily streaks, which are present in the smectic-A phase [D. Coursault et al., Soft Matter, 2016, 12, 678]. These new streaks, which we call ‘‘soapy streaks’’, form by extending from one oily streak to the next in discrete steps, eliminating optical evidence at visible wavelengths of the oily streaks. At lower temperatures the streaks can undulate and exhibit a sawtooth-like structure; such a structure is chiral in two dimensions. A possible scenario for the origin of these streaks is presented. 

Nematic cells patterned with square arrays of strength m = ±1 topological defects were examined as a function of cell thickness (3 < h < 7.5 μm), temperature, and applied voltage. Thicker cells tend to exhibit an escape or partial escape of the nematic director as a means of mitigating the elastic energy cost near the defect cores, whereas thinner cells tend to favor splitting of the integer defects into pairs of half-integer strength defects. On heating the sample into the isotropic phase and cooling back into the nematic, some apparently split defects can reappear as unsplit integer defects, or vice versa. This is consistent with the system’s symmetry, which requires a first order transition between the two relaxation mechanisms. 

Long time ago, Brochard and de Gennes predicted the possibility of significantly decreasing the critical magnetic feld of the Fredericksz transition (the magnetic Fredericksz threshold) in a mixture of nematic liquid crystals and ferromagnetic particles, the so-called ferronematics. This phenomenon has rarely been measured, usually due to soft homeotropic anchoring induced at the nanoparticle surface. Here we present an optical study of the magnetic Fredericksz transition combined with a light scattering study of the classical nematic liquid crystal, 5CB, doped with 6 nm diameter magnetic and non-magnetic nanoparticles. Surprisingly, for both nanoparticles, we observe at room temperature a net decrease of the threshold field of the Fredericksz transition at low nanoparti cle concentrations, which appears associated with a coating of the nanoparticles by a brush of polydimethylsiloxane copolymer chains inducing planar anchoring of the director on the nanoparticle surface. Moreover the magnetic Fredericksz threshold exhibits non-monotonic behaviour as a function of the nanoparticle concentration for both types of nanoparticles, first decreasing down to a value from 23% to 31% below that of pure 5CB, then increasing with a further increase of nanoparticle concentration. This is interpreted as an aggregation starting at around 0.02 weight fraction that consumes more isolated nanoparticles than those introduced when the concentration is increased above c = 0:05 weight fraction (volume fraction 3:5 x 10^-2). This shows the larger effect of isolated nanoparticles on the threshold with respect to aggregates. From dynamic light scattering measurements we deduced that, if the decrease of the magnetic threshold when the nanoparticle concentration increases is similar for both kinds of nanoparticles, the origin of this decrease is different for magnetic and non-magnetic nanoparticles. For non-magnetic nanoparticles, the behavior may be associated with a decrease of the elastic constant due to weak planar anchoring. For magnetic nanoparticles there are non-negligible local magnetic interactions between liquid crystal molecules and magnetic nanoparticles, leading to an increase of the average order parameter. This magnetic interaction thus favors an easier liquid crystal director rotation in the presence of external magnetic field, able to reorient the magnetic moments of the nanoparticles along with the molecules.