9 research outputs found
Colloidal particles at a nematic-isotropic interface: effects of confinement
When captured by a flat nematic-isotropic interface, colloidal particles can
be dragged by it. As a result spatially periodic structures may appear, with
the period depending on a particle mass, size, and interface
velocity~\cite{west.jl:2002}. If liquid crystal is sandwiched between two
substrates, the interface takes a wedge-like shape, accommodating the
interface-substrate contact angle and minimizing the director distortions on
its nematic side. Correspondingly, particles move along complex trajectories:
they are first captured by the interface and then `glide' towards its vertex
point. Our experiments quantify this scenario, and numerical minimization of
the Landau-de Gennes free energy allow for a qualitative description of the
interfacial structure and the drag force.Comment: 7 pages, 9 figure
Zigzag line defects and manipulation of colloids in a nematic liquid crystal in microwrinkle grooves
Spatially confined liquid crystals exhibit non-uniform alignment, often accompanied by self-organised topological defects of non-trivial shape in response to imposed boundary conditions and geometry. Here we show that a nematic liquid crystal, when confined in a sinusoidal microwrinkle groove, exhibits a new periodic arrangement of twist deformations and a zigzag line defect. This periodic ordering results from the inherent liquid crystal elastic anisotropy and the antagonistic boundary conditions at the flat liquid crystal–air and the curved liquid crystal–groove interfaces. The periodic structure can be tuned by controlling the groove geometry and the molecular chirality, which demonstrates the importance of boundary conditions and introduced asymmetry for the engineering of topological defects. Moreover, the kinks in the zigzag defects can trap small particles, which may afford a new method for manipulation of colloids. Our system, which uses easily fabricated microwrinkle grooves, provides a new microfabrication method based on the arrangement of controllable defects
KP1 acceleration scheme for inner iterations consistent with the weighted diamond differencing scheme for the transport equation in three-dimensional geometry
Structural nanotechnology of nucleic acids: Designing “Liquid” and “Rigid” DNA nanoconstructions
Topological defects in liquid crystals as templates for molecular self-assembly
Topological defects in liquid crystals (LCs) have been widely used to organize colloidal dispersions and template polymerization, leading to a range of assemblies, elastomers and gels. However, little is understood about molecular-level assembly processes within defects. Here, we report that nanoscopic environments defined by LC topological defects can selectively trigger processes of molecular self-assembly. By using fluorescence microscopy, cryogenic transmission electron microscopy and super-resolution optical microscopy, we observed signatures of molecular self-assembly of amphiphilic molecules in topological defects, including cooperativity, reversibility and controlled growth. We also show that nanoscopic o-rings synthesized from Saturn-ring disclinations and other molecular assemblies templated by defects can be preserved by using photocrosslinkable amphiphiles. Our results reveal that, in analogy to other classes of macromolecular templates such as polymer-surfactant complexes, topological defects in LCs are a versatile class of three-dimensional, dynamic and reconfigurable templates that can direct processes of molecular self-assembly