Steady rigid-body rotation of cholesteric droplets and their dumbbell-shaped aggregates driven by heat flux along the helical axes.

We investigated the steady unidirectional rotation of cholesteric (Ch) droplets driven by a heat flux. The droplets coexisted with the isotropic (Iso) phase and possessed a helical molecular arrangement. When a heat flux was transported along the helical axis, the droplets and their dumbbell-shaped aggregates exhibited steady rigid rotation.

2D Photopolymerization of Liquid Crystalline Langmuir Monolayers: In Situ Observation by Reflected Polarizing Microscopy.

Photopolymerization of Langmuir monolayers composed of bifunctional acrylic liquid crystalline (LC) compounds was observed in situ by polarizing optical microscopy. In a dark state, monolayers of the LC compounds formed at an air-water or liquid-liquid interface exhibited liquid-like fluidity and in-plane optical anisotropy because of the coherent molecular tilt from the surface normal. Irradiated by UV light, the in-plane anisotropy and the liquid fluidity gradually disappeared with time, indicating the formation of the polymerized monolayers.

Heat-Driven Rigid-Body Rotation of a Mixture of Cholesteric Liquid Crystal Droplets and Colloids.

We show that cholesteric (Ch) liquid crystal droplets with cylindrically symmetric orientation dispersing in an isotropic (Iso) phase exhibited unidirectional rotation under a heat flux along the symmetry axis. By introducing colloidal particle adhesive to the Ch droplet surface, we traced the translational motion of the colloids and found that the colloids rotated unidirectionally around the center of each Ch droplet. The director configuration of the droplets was not distorted either spatially or temporally, while the colloids rotated constantly.

A thermomechanical coupling in cholesteric liquid crystals: Unidirectional rotation of double-twist cylinders driven by heat flux.

We made aggregates of cholesteric liquid crystalline Cylinders with Double-Twist orientational structure (DTC) and investigated their rigid-body rotation under a temperature gradient, focusing on how the rotational speed should depend on the cylinder size. The experimental results showed that the angular velocity of the DTC aggregates linearly increased with the height of the cylinders and was inversely proportional to the base area. With a phenomenological equation, we analyzed the torque caused by the heat flux and its balance with the viscous friction, and found that the simple analysis well explained the size-dependence of the rotation of the DTC aggregates.

Formation and dynamics of the aggregates of cholesteric double-twist cylinders.

We succeeded in driving the unidirectional rigid-body rotation of cholesteric (Ch) double-twist cylinder (DTC) droplets under a heat flux along the cylindrical symmetry axis. To directly observe the rigid-body rotation of DTC droplets, in each of which the center of the rotation and the symmetry axis of the structure correspond, we fabricated DTC aggregates that comprise several DTCs with intact structures. Given a steady heat flux, the DTC aggregates metastabilized by the shape and the surface anchoring show a unidirectional rigid-body rotation with a constant angular velocity.

Formation of Concentric Silica Nanogrooves Guided by the Curved Surface of Silica Particles.

The flexible control of nanopatterns by a bottom-up process at the nanometer scale is essential for nanofabrication with a finer pitch. We have previously reported that for the fabrication of linear nanopatterns with sub-5 nm periodicity on Si substrates the outermost surfaces of assembled micelles facing the substrates can be replicated with soluble silicate species generated from the Si substrates under basic conditions. In this study, concentrically arranged nanogrooves with a sub-5 nm periodicity were prepared on Si substrates by replicating the outermost surfaces of bent micelles guided by silica particles.

Unidirectional rotation of cholesteric droplets driven by UV-light irradiation.

We investigated the novel photo-induced dynamics of azobenzene-doped cholesteric (Ch) droplets coexisting with the isotropic (Iso) phase. When the hemispherical Ch droplets initially stuck to glass substrates were irradiated by UV-light, they were parted from the substrates due to the surface disordering caused by the photo-isomerization of azobenzene. Then, the spherical droplets floating in the Iso phase exhibited an unexpected motion - a continuous and unidirectional rotation along the light propagation direction.

Induced smectic phases of stoichiometric liquid crystal mixtures.

We revealed the detailed structures of induced smectic liquid crystal (LC) phases composed of a binary mixture of charge-transfer (CT) LC substances. Although neither of the constituents had highly ordered smectic phases, the mixture exhibited smectic-E (SmE) or smectic-B (SmB) phases when mixed at ratios of 1 : 1 and 2 : 3, respectively. The results of polarized optical microscopy, differential scanning calorimetry, X-ray diffraction, and infrared spectroscopy indicated that the induced smectic phases were stabilized by an exquisite balance between the CT interactions, dipolar interactions, and excluded volume effects.

Stability of a double twisted structure in spherical cholesteric droplets.

We found for the first time the stabilization of a double twisted structure in cholesteric liquid crystals confined to small spherical droplets under weak anchoring conditions. The direct observation of the droplets using a polarized microscope revealed the physical properties of the structure. The experimental results showed that the stability of the double twisted structure is determined by the relationship between the helical pitch length and the droplet size.

Director/barycentric rotation in cholesteric droplets under temperature gradient.

When a chiral liquid crystal is given a transport current, a unidirectional molecular motion is known to take place, which is called the Lehmann effect. In this paper, we study the mysterious heat-current-driven Lehmann effect using two types of hemispherical cholesteric droplets using polarizing, reflecting, confocal and fluorescent microscopies. Both the droplets, coexisting with the isotropic phase and contacting on a glass substrate, are characterized by the concavo-convex modulated surface and the inside orientational helix.

Non-equilibrium dynamics of 2D liquid crystals driven by transmembrane gas flow.

Free-standing films composed of several layers of chiral smectic liquid crystals (SmC*) exhibited unidirectional director precession under various vapor transfers across the films. When the transferred vapors were general organic solvents, the precession speed linearly depended on the momentum of the transmembrane vapors, where the proportional constant was independent of the kind of vapor. In contrast, the same SmC* films under water transfer exhibited precession in the opposite direction.

Orientational correlations in two-dimensional liquid crystals studied by molecular dynamics simulation.

Orientational correlations in Langmuir monolayers of nematic and smectic-C liquid crystal (LC) phases are investigated by molecular dynamics simulation. In both phases, the orientational correlation functions decay algebraically yet with the different exponents of 1.9 and 0.

Theoretical modeling of photo-induced wave propagation in liquid-crystalline Langmuir monolayers.

A phenomenological model of wave propagation in photo-excited liquid-crystalline Langmuir monolayers is constructed. The spontaneous splay deformation of the liquid-crystalline order and the anisotropy of photo-excitation of molecules are taken into account in this model. Numerical simulations of the model well reproduce qualitative features of the wave propagation phenomenon observed in recent experiments.

Generation, propagation, and switching of orientational waves in photoexcited liquid-crystalline monolayers.

Photoinduced orientational waves in illuminated liquid-crystalline monolayers is one of the most remarkable far-from-equilibrium phenomena that systems of soft condensed matter exhibit. We model this behavior from a phenomenological point of view, taking the anisotropic photoexcitation of molecules into account. Numerical simulations as well as theoretical analyses of the model reveal that the intricate interplay between the spontaneous splay deformation of the liquid-crystalline order and the anisotropy of the photoexcitation can lead to the generation and propagation of orientational waves.

Anisotropy of alkyl chains of azobenzene molecules at the air/water interface observed by sum-frequency vibrational spectroscopy.

Surface-specific sum-frequency vibrational spectroscopy has been used to study the structure of alkyl chains of azobenzene molecules at the air/water interface. The results show that the alkyl chains are well aligned before UV irradiation and protruding out of the surface with a certain distribution. Although the alkyl chains become less ordered by UV irradiation following dynamical motion due to cis-trans isomerization of the azobenzene core, the alkyl chains show anisotropy in the direction perpendicular to that of the azobenzene core by linearly polarized UV irradiation.

Coherent collective precession of molecular rotors with chiral propellers.

Successful attempts to manufacture synthetic molecular motors have recently been reported. However, compared with natural systems such as motor proteins, synthetic motors are smaller molecules and are therefore subject to thermal fluctuations that prevent them from performing any useful function. A mechanism is needed to amplify the single molecular motion to such a level that it becomes distinguishable from the thermal background.