Publications by authors named "Frederic Mondiot"

Shaping liquid crystals (LCs) into arrays of defect patterns enables the design of composite materials with new stimuli-responsive properties. Self-assembled defect assemblies that may arise in layered smectic A (SmA) LCs such as focal conic domains (FCDs), exhibit remarkable optical features and abilities for ordering nanoparticles. However, such SmA defect patterns are essentially electrically irreversible, which currently limits their adjustability in a dynamic way.

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We report that assemblies formed by eight oligopeptides at phospholipid-decorated interfaces of thermotropic liquid crystals (LCs) trigger changes in ordering of the LCs that are dependent on the secondary structures of the oligopeptides (as characterized in situ using infrared-visible sum-frequency spectroscopy).

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Article Synopsis
  • The study investigates how tiny particles behave when mixed in a special liquid known as nematic micellar solution, focusing on latex spheres that range from 190 to 780 nanometers in diameter.
  • The results reveal that larger particles tend to form compact clusters or V-shaped structures due to attractive forces, while smaller particles form elongated chains aligned with the liquid's nematic axis.
  • Simulation models suggest that the motion and interactions among the smaller particles change from elastic forces to shorter-range attractions, offering insight into the mechanisms of particle aggregation and highlighting the significance of particle diffusion at very small scales.
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Colloidal particles dispersed in a partially ordered medium, such as a liquid crystal (LC) phase, disturb its alignment and are subject to elastic forces. These forces are long-ranged, anisotropic and tunable through temperature or external fields, making them a valuable asset to control colloidal assembly. The latter is very sensitive to the particle geometry since it alters the interactions between the colloids.

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Common nematic oils, such as 5CB, experience planar anchoring at aqueous interfaces. When these oils are emulsified, this anchoring preference and the resulting topological constraints lead to the formation of droplets that exhibit one or two point defects within the nematic phase. Here, we explore the interactions of adsorbed particles at the aqueous interface through a combination of experiments and coarse-grained modeling, and demonstrate that surface-active particles, driven by elastic forces in the droplet, readily localize to these defect regions in a programmable manner.

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We report the use of liquid crystal (LC)-in-water emulsions for the synthesis of either spherical or non-spherical particles with chemically distinct domains located at the poles of the particles. The approach involves the localization of solid colloids at topological defects that form predictably at surfaces of water-dispersed LC droplets. By polymerizing the LC droplets displaying the colloids at their surface defects, we demonstrate formation of both spherical and, upon extraction of the mesogen, anisotropic composite particles with colloids located at either one or both of the poles.

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We report the experimental observation of anisotropic diffusion of polystyrene particles immersed in a lyotropic liquid crystal with two different anchoring conditions. Diffusion is shown to obey the Stokes-Einstein law for particle diameters ranging from 190 nm up to 2 μm. In the case of prolate micelles, the beads diffuse four times faster along the director than in perpendicular directions, D||/D[Symbol: see text] ≈ 4.

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