arXiv subjects

Suzanne Lafon

Publications and source records attributed to Suzanne Lafon.

4 recordsLinked to original sources

arXiv2026

Light-driven active phase separation and droplet division

Phase separation organizes matter across scales, yet how it operates under sustained energy input remains poorly understood. Experimental approaches to driven phase separation have largely relied on chemically fueled systems, in which reaction fluxes are intrinsically coupled to fuel consumption and reaction-network complexity. Here we show that continuous molecular switching alone is sufficient to generate active phase behavior in a minimal two-phase system. Using light-responsive DNA-azobenzene coacervates confined in microfluidic droplets, we modulate intermolecular interactions with spatiotemporal precision and quantitatively track phase separation dynamics under illumination. Light-driven azobenzene isomerization controls both thermodynamics and kinetics, setting phase boundaries and regulating dissolution and nucleation rates. Under single-wavelength illumination that couples forward and backward isomerization into a dynamic photostationary state, coarsening is arrested and micron-sized coacervates are stabilized. When the two photoisomerization pathways are driven independently, spatially unbalanced reaction fluxes generate sustained interfacial instabilities, including surface undulations, budding, and division. These behaviors arise from a physical coupling between reaction kinetics and phase separation, without chemical fuels or biochemical regulation. Our results show that non-equilibrium phase behavior is governed by how opposing reaction fluxes are imposed, establishing reversible molecular switching as a minimal route to active materials from equilibrium building blocks.

cond-mat.soft↗

arXiv2023

Near surface concentration profile of sheared semi-dilute polymer solutions

Controlling the structure of polymer solutions near a solid surface is crucial for many industrial processes, as it significantly impacts solution flow and influences slip at the interface. To date, only a few techniques have been developed to experimentally investigate this type of interface at the nanometric scale of solid/liquid interaction. In this study, we probe the interface between a smooth sapphire surface and a semi-diluted polystyrene solution, using neutron reflectivity. A special setup for flow measurements under shear has been designed and optimized. Our results show that, at rest, polymer chains are globally depleted from the solid surface. Contrary to common assumptions, some polystyrene chains do adsorb onto the wall. Under flow conditions, we experimentally demonstrate that the depletion layer remains stable, a finding that has been hypothesized but only vaguely confirmed in the literature.

cond-mat.soft↗

arXiv2022

Flow driven control of pulse width in excitable media

Models of pulse formation in nerve conduction have provided manifold insight not only into neuronal dynamics but also the non-linear dynamics of pulse formation in general. Recent observation of neuronal electro-chemical pulses also driving mechanical deformation of the tubular neuronal wall and thereby generating ensuing cytoplasmic flow now question the impact of flow on the electro-chemical dynamics of pulse formation. We, here, theoretically investigate the classical Fitzhugh-Nagumo model now accounting for advective coupling between the pulse propagator typically describing membrane potential and here triggering mechanical deformations and, thus, governing flow magnitude, and the pulse controller, a chemical species advected with the ensuing fluid flow. Employing analytical calculations and numerical simulations we find, that advective coupling allows for a linear control of pulse width while leaving pulse velocity unchanged. We therefore uncover an independent control of pulse width by fluid flow coupling.

nlin.PS↗

arXiv2022

Giant slip length at a supercooled liquid-solid interface

The effect of temperature on friction and slip at the liquid-solid interface has attracted attention over the last twenty years, both numerically and experimentally. However, the role of temperature on slip close to the glass transition has been less explored. Here, we use molecular dynamics to simulate a bi-disperse atomic fluid, which can remain liquid below its melting point (supercooled state), to study the effect of temperature on friction and slip length between the liquid and a smooth apolar wall, in a broad range of temperatures. At high temperatures, an Arrhenius law fits well the temperature dependence of viscosity, friction and slip length. In contrast, when the fluid is supercooled, the viscosity becomes super-Arrhenian, while interfacial friction can remain Arrhenian or even drastically decrease when lowering the temperature, resulting in a massive increase of the slip length. We rationalize the observed superlubricity by the surface crystallization of the fluid, and the incommensurability between the structures of the fluid interfacial layer and of the wall. This study calls for experimental investigation of the slip length of supercooled liquids on low surface energy solids.

cond-mat.soft↗