Au nanoparticles in blue phase LCs: Towards "soft" nanocrystals

Blue phases (BPs), a distinct class of liquid crystals (LCs) with 3D periodic ordering of double twist cylinders involving orthogonal helical director twists, have been theoretically studied as potential templates for tunable colloidal crystals. In this project, we explore the spontaneous formation of thermally reversible, cubic crystal nanoparticle (NP) assemblies in BPs. The NPs assemble by selectively migrating to periodic strong trapping sites in the BP disclination lines. This presents an interesting opportunity to develop novel dynamic optical materials.

Gardens of smectic flowers: Towards "smart" microlenses

A self-assembly of microlenses on a curved interface can be obtained by pinning smectic liquid crystals around a micropillar with appropriate boundary conditions. This hierarchical structure of microlenses, with variable focal lengths from a few micrometers to a few tens of micrometers, is similar to an insect's compound eye; the lenses are reconfigurable with temperature and sensitive to light polarization.

Effect of the light polarization on the smectic lenses. 

Effect of the temperature on the smectic lenses.

Migration of particles at curved nematic interfaces

In this research, we develop new means of directing colloids at an interface to assemble into complex configurations by exploiting defects in a liquid crystal (LC). Through confinement of a nematic LC over a topographically patterned surface, we demonstrate the formation of defects at precise locations in the LC bulk. These defects source elastic distortion fields that guide the assembly of colloids constrained to the LC–air interface. 

Creation of a defect loop around a micropost in an oriented nematic liquid crystal. 

The defect created in bulk, can be used to direct assembly of particles at the interface. 

Assembly of anisotropic particles in oriented nematic liquid crystals

Microbullet particles, cylinders with one blunt and one spherical end, offer a novel platform to study the effects of anisotropy and curvature on colloidal assembly in complex fluids. Here, we disperse microbullets in 5CB nematic liquid crystal (NLC) cells and form oriented elastic dipoles with a nematic point defect located near the curved end. This feature allows us to study particle interactions as a function of dipole alignment. By careful control of the surface anchoring at the particle surface and the confining boundaries, we study the interactions and assembly of microbullets under various conditions. 

When microbullets with homeotropic surface anchoring are dispersed in a planar cell, parallel dipoles form linear chains parallel to the director, while antiparallel dipoles orient side-to-side. 

In a homeotropic cell, particles rotate to orient their long axis parallel to the director. When so aligned, parallel dipoles repel and form 2D ordered assemblies with hexagonal symmetry that ripen over time owing to attraction between antiparallel neighbors. 

The anchoring conditions inside the cell can be altered by application of an electrical field, allowing us to flip microbullets to orient parallel to the director, an effect driven by an elastic torque. 

Confinement of liquid crystals into spherical geometries

A nematic coating could be used to create a valency for spherical colloidal particles through the functionalization of nematic topological defects. Experimental realizations however question the complex behaviour of solid particles and defects embedded in such a nematic spherical shell. In order to address the related topological and geometrical issues, we have studied micrometer-sized silica beads trapped in nematic shells. We show how the coupling between capillarity and nematic elasticity offers new ways to control the valence and directionality of shells.

Dripping mode: nematic double emulsions

Jetting mode: nematic double emulsions

Assembly of spherical particles at an air/nematic interface

We examine the behavior of spherical silica particles trapped at an air–nematic liquid crystal interface. When a strong normal anchoring is imposed, the beads spontaneously form various structures depending on their area density and the nematic thickness. Using optical tweezers, we determine the pair potential and explain the formation of these patterns. 

Particles form hexagonal structures at an air-nematic interface with homeotropic anchoring. 

Particles at a thin air-nematic interface form linear chains along the easy axis of the nematic film. 

Disclinations in nematics are high trapping cites for colloidal particles.