The ability to generate regular spatial arrangements of particles is an important technological and fundamental aspect of colloidal science. We showed that colloidal particles confined to a few-micrometer-thick layer of a nematic liquid crystal form two-dimensional crystal structures that are bound by topological defects. Two basic crystalline structures were observed, depending on the ordering of the liquid crystal around the particle. Colloids inducing quadrupolar order crystallize into weakly bound two-dimensional ordered structure, where the particle interaction is mediated by the sharing of localized topological defects. Colloids inducing dipolar order are strongly bound into antiferroelectric-like two-dimensional crystallites of dipolar colloidal chains. Self-assembly by topological defects could be applied to other systems with similar symmetry.
The light scattering and electro-optic response of new material with display potential are investigated. The materials consist of microdroplets of nematic liquid crystals which are spontaneously formed in a solid polymer at the time of its polymerization. Droplet size, spacing, and distribution are readily controlled in these materials to allow optimization of displays based upon electrically controlled light scattering from the liquid crystal droplets. Preliminary experimental and theoretical studies of the light scattering properties show these materials to offer new features suitable for many display applications.
Tying knots and linking microscopic loops of polymers, macromolecules, or defect lines in complex materials is a challenging task for material scientists. We demonstrate the knotting of microscopic topological defect lines in chiral nematic liquid-crystal colloids into knots and links of arbitrary complexity by using laser tweezers as a micromanipulation tool. All knots and links with up to six crossings, including the Hopf link, the Star of David, and the Borromean rings, are demonstrated, stabilizing colloidal particles into an unusual soft matter. The knots in chiral nematic colloids are classified by the quantized self-linking number, a direct measure of the geometric, or Berry's, phase. Forming arbitrary microscopic knots and links in chiral nematic colloids is a demonstration of how relevant the topology can be for the material engineering of soft matter.
The ability to generate regular spatial arrangements of particles on different length scales is one of the central issues of the "bottom-up" approach in nanotechnology. Current techniques rely on single atom or molecule manipulation by the STM, colloidal particle manipulation by laser or optoelectronic tweezers, microfluidics, optofluidics, micromanipulation and classical lithography. Of particular interest is self-assembly, where the pre-determined spatial arrangements of particles, such as 3D photonic crystals, could be realized spontaneously. Dispersions of particles in liquid crystals show several novel classes of anisotropic forces between inclusions, which result in an amazing diversity of self-assembled patterns, such as linear chains and 2D photonic crystals of microspheres. The forces between the particles in nematic colloids are extremely strong and long-range, resulting in several thousand times stronger binding compared to the binding in water based colloids. The mechanisms of self-assembly in nematic colloids are discussed, showing this is a novel paradigm in colloidal science, which can lead to new approaches in colloidal self-assembly for photonic devices.
We present experimental and theoretical study of colloidal interactions in quadrupolar nematic liquid crystal colloids, confined to a thin planar nematic cell. Using the laser tweezers, the particles have been positioned in the vicinity of other colloidal particles and their interactions have been determined using particle tracking video microscopy. Several types of interactions have been analyzed: (i) quadrupolar pair interaction, (ii) the interaction of an isolated quadrupole with a quadrupolar chain, and (iii) the interaction of an isolated quadrupolar colloidal particle with a two-dimensional (2D) quadrupolar crystallite. In all cases, the interactions are of the order of several 100k(B)T for 2 microm particles, which gives rise to relatively stable 2D colloidal crystals. The experimental results are compared to the predictions of Landau-de Gennes theory and we find a relatively good qualitative agreement.
It has been predicted, but never confirmed, that colloidal particles in a nematic liquid crystal could be self-assembled by delocalized topological defects and entangled disclinations. We show experimentally and theoretically that colloidal dimers and 1D structures bound by entangled topological defect loops can indeed be created by locally thermally quenching a thin layer of the nematic liquid crystal around selected colloidal particles. The topological entanglement provides a strong stringlike binding, which is ten thousand times stronger compared to water-based colloids. This unique binding mechanism could be used to assemble resonator optical waveguides and robust chiral and achiral structures of topologically entangled colloids that we call colloidal wires.
Colloidal dispersions in liquid crystals can serve as a soft-matter toolkit for the self-assembly of composite materials with pre-engineered properties and structures that are highly dependent on particle-induced topological defects. Here, we demonstrate that bulk and surface defects in nematic fluids can be patterned by tuning the topology of colloidal particles dispersed in them. In particular, by taking advantage of two-photon photopolymerization techniques to make knot-shaped microparticles, we show that the interplay of the topologies of the knotted particles, the nematic field and the induced defects leads to knotted, linked and other topologically non-trivial field configurations. These structures match theoretical predictions made on the basis of the minimization of the elastic free energy and satisfy topological constraints. Our approach may find uses in self-assembled topological superstructures of knotted particles linked by nematic fields, in topological scaffolds supporting the decoration of defect networks with nanoparticles, and in modelling other physical systems exhibiting topologically analogous phenomena.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.