Christophe Blanc

Ordering nano- and microparticles assemblies with liquid crystals

Besides nanostructured materials, individual particles are key elements for nanosciences. The structuring properties of liquid crystals (LCs) are appealing to assemble them, to organize them on substrates or to design functional composites. We present here an overview on particles/LC systems, the size of the dispersed particles being larger than the typical LC length. We first summarize the large number of advances made these last 10 years concerning microparticles assemblies. We then discuss the evolution of the relevant interactions between nanoparticles (NPs) dispersed in LCs when their size decreases from micrometers to nanometers. Various NPs assemblies obtained, either in LC bulk, at interfaces or within LC distorted areas or topological defects are then reported and discussed. Finally, we consider the recent possibilities to use NPs as building elements of complex fluids. We discuss accordingly the LC phases, which can be obtained with pure inorganic NPs in concentrated solution, as well as the self-assemblies which can be obtained when NPs are covered by organic mesogenic ligands.

Anisotropic Thin Films of Single-Wall Carbon Nanotubes from Aligned Lyotropic Nematic Suspensions

Lyotropic nematic aqueous suspensions of single-wall carbon nanotubes can be uniformly aligned in thin cells by shearing. Homogeneous anisotropic thin films of nanotubes can be prepared by drying the nematic. Optical transmission between parallel or crossed polarizers is measured and described in order to estimate the dichroic ratio. The order parameter is measured using polarized Raman spectroscopy and found to be quite weak due to entanglement of the nanotubes and/or to an intrinsic viscoelastic behavior of the nanotube suspensions.

Brownian diffusion of a partially wetted colloid

The dynamics of colloidal particles at interfaces between two fluids plays a central role in microrheology, encapsulation, emulsification, biofilm formation, water remediation and the interface-driven assembly of materials. Common intuition corroborated by hydrodynamic theories suggests that such dynamics is governed by a viscous force lower than that observed in the more viscous fluid. Here, we show experimentally that a particle straddling an air/water interface feels a large viscous drag that is unexpectedly larger than that measured in the bulk. We suggest that such a result arises from thermally activated fluctuations of the interface at the solid/air/liquid triple line and their coupling to the particle drag through the fluctuation-dissipation theorem. Our findings should inform approaches for improved control of the kinetically driven assembly of anisotropic particles with a large triple-line-length/particle-size ratio, and help to understand the formation and structure of such arrested materials.

Dispersion and orientation of single-walled carbon nanotubes in a chromonic liquid crystal

A post-synthesis alignment of individual single-walled carbon nanotubes (SWCNTs) is desirable for translating their unique anisotropic properties to a macroscopic scale. Here, we demonstrate excellent dispersion, orientation and concomitant-polarised photoluminescence of SWCNTs in a nematic chromonic liquid crystal. The methods to obtain stable suspension are described, and order parameters of the liquid crystal matrix and of the nanotubes are measured independently.

Behavior of colloidal particles at a nematic liquid crystal 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. The energy profile is discussed in terms of capillary and elastic interactions. Finally, we detail the mechanisms that control the formation of a hexagonal lattice and analyze the role of gravity for curved interfaces.

Liquid Crystallinity and Dimensions of Surfactant-Stabilized Sheets of Reduced Graphene Oxide

Graphene oxide (GO) flakes dissolved in water can spontaneously form liquid crystals. Liquid crystallinity presents an opportunity to process graphene materials into macroscopic assemblies with long-range ordering, but most graphene electronic functionalities are lost in oxidation treatments. Reduction of GO allows recovering functionalities and makes reduced graphene oxide (RGO) of greater interest. Unfortunately, chemical reduction of GO generally results in the aggregation of the flakes, with no liquid crystallinity observed. We report in the present work liquid crystals made of RGO. The addition of surfactants in appropriate conditions is used to stabilize the RGO flakes against aggregation maintaining their ability to form water-based liquid crystals. Structural and thermodynamical studies allow the dimensions of the flakes to be deduced. It is found that the thickness and diameter of RGO flakes are close to that of neat GO flakes.

Toward organization of cyano-bridged coordination polymer nanoparticles within an ionic liquid crystal.

Size controlled cyano-bridged coordination polymer nanoparticles Mn1.5[Cr(CN)6] have been synthesized and organized at the nanolevel by using the room temperature ionic liquid crystal (ILC) C12-MIMBF4. The as-obtained material was studied by transmission electron microscopy (TEM), differential scanning calorimetry (DSC), optical microscopy, and X-ray diffraction. These analyses reveal the presence of a long-range organization of cyano-bridged nanoparticles at the nanoscale level within the ILC phase. The magnetic study of these nanoparticles reveals an appearance of a nanocluster-glass-like regime caused by magnetostatic interactions between neighboring nanoparticles. The properties of these organized nanoparticles have been compared with the properties of nanoparticles of the same composition and stoichiometry obtained and randomly dispersed into the isotropic IL C10-MIMBF4.

Liquid crystals of carbon nanotubes and graphene

Liquid crystal ordering is an opportunity to develop novel materials and applications with spontaneously aligned nanotubes or graphene particles. Nevertheless, achieving high orientational order parameter and large monodomains remains a challenge. In addition, our restricted knowledge of the structure of the currently available materials is a limitation for fundamental studies and future applications. This paper presents recent methodologies that have been developed to achieve large monodomains of nematic liquid crystals. These allow quantification and increase of their order parameters. Nematic ordering provides an efficient way to prepare conductive films that exhibit anisotropic properties. In particular, it is shown how the electrical conductivity anisotropy increases with the order parameter of the nematic liquid crystal. The order parameter can be tuned by controlling the length and entanglement of the nanotubes. In the second part of the paper, recent results on graphene liquid crystals are reported. The possibility to obtain water-based liquid crystals stabilized by surfactant molecules is demonstrated. Structural and thermodynamic characterizations provide indirect but statistical information on the dimensions of the graphene flakes. From a general point of view, this work presents experimental approaches to optimize the use of nanocarbons as liquid crystals and provides new methodologies for the still challenging characterization of such materials.

Phonon Heat Conduction in Corrugated Silicon Nanowires Below the Casimir Limit

The thermal conductance of straight and corrugated monocrystalline silicon nanowires has been measured between 0.3 K and 5 K. It is demonstrated that the corrugation strongly reduces the thermal transport by reducing the mean free path of the phonons. The experimental averaged mean free path is remarkably smaller than the smaller diameter of the nanowire, evidencing a phonon thermal transport reduced below the Casimir limit. Monte Carlo simulations highlight that this effect can be attributed to significant multiple scattering of ballistic phonons occurring on the corrugated surfaces. This result suggests an original approach to transforming a monocrystalline material into a phonon glass.

Radar Scan Matching SLAM Using the Fourier-Mellin Transform

This paper is concerned with the Simultaneous Localization And Mapping (SLAM) problem using data obtained from a microwave radar sensor. The radar scanner is based on Frequency Modulated Continuous Wave (FMCW) technology. In order to meet the needs of radar image analysis complexity, a trajectoryoriented EKF-SLAM technique using data from a 360. field of view radar sensor has been developed. This process makes no landmark assumptions and avoids the data association problem. The method of egomotion estimation makes use of the Fourier-Mellin Transform for registering radar images in a sequence, from which the rotation and translation of the sensor motion can be estimated. In the context of the scan-matching SLAM, the use of the Fourier-Mellin Transform is original and provides an accurate and efficient way of computing the rigid transformation between consecutive scans. Experimental results on real-world data are presented.