Anomalous ionic transport in tunable angstrom-size water films on silica.

Liquid and ionic transport through nanometric structures is central to many phenomena, ranging from cellular exchanges to water resource management or green energy conversion. While pushing down toward molecular scales progressively unveils novel transport behaviors, reaching ultimate confinement in controlled systems remains challenging and has often involved 2D Van der Waals materials. Here, we propose an alternative route which circumvents demanding nanofabrication steps, partially releases material constraints, and offers continuously tunable molecular confinement.

Microscopic Origins of the Viscosity of a Lennard-Jones Liquid.

Unlike crystalline solids or ideal gases, transport properties remain difficult to describe from a microscopic point of view in liquids, whose dynamics result from complex energetic and entropic contributions at the atomic scale. Two scenarios are generally proposed: one represents the dynamics in a fluid as a series of energy-barrier crossings, leading to Arrhenius-like laws, while the other assumes that atoms rearrange themselves by collisions, as exemplified by the free volume model. To assess the validity of these two views, we computed, using molecular dynamics simulations, the transport properties of the Lennard-Jones fluid and tested to what extent the Arrhenius equation and the free volume model describe the temperature dependence of the viscosity and of the diffusion coefficient at fixed pressure.

Interfacial Characterization of Ruthenium-Based Amphiphilic Photosensitizers.

Nonreactive surfactant molecules have long been used and characterized for a wide range of applications in industries, life science, and everyday life. Recently, new types of functional amphiphilic molecules have emerged that bear another function, for example, a light-absorbing action, or catalytic properties. However, the surfactant properties of these molecules remain to date essentially unknown.

Electrokinetic sweeping of colloids at a reactive magnesium oxide interface.

Investigating the electrokinetic (EK) response in the vicinity of interfaces has regained interest due to the development of new membrane based processes for energy harvesting or soil depollution. However, the case of reactive interfaces, ubiquitous in these processes, remains scarcely explored. Here we experimentally investigate the EK response of a model interface between an aqueous electrolyte and a bulk MgO crystal surface (100), for different pH.

Generation and stability of cement soap films.

Foaming a cementitious suspension is a complex process that involves many multiscale chemical, physical and dynamical mechanisms. As a first step, we investigate here experimentally the possibility of withdrawing a single liquid soap film from a suspension of cement. We then determine the film lifetime and if particles are entrained or not.

Rupture of granular rafts: effects of particle mobility and polydispersity.

Reversible encapsulation of liquid materials is a technical challenge in many applications such as for the transport and controlled delivery of active ingredients. In contrast to most state-of-the-art processes, capillary adsorbed solid particles can achieve chemical-reaction-free encapsulation by forming dense rafts which isolate the liquid from its surroundings. While the production conditions of such capsules have been characterized, the control of the armor robustness remains poorly described and understood.

Electroosmosis near surfactant laden liquid-air interfaces.

Generation of an electroosmostic (EO) flow near a liquid-gas interface covered with ionic surfactants is experimentally investigated. A combination of microscopic flow measurements with a molecular characterization of the interface by second harmonic generation (SHG) shows that under an electrical forcing, although a liquid flow is generated below the free surface, the surfactants remain immobile. The zeta potential was then determined and compared to the surfactant surface coverage.

Electrokinetic transport in liquid foams.

Investigating electrokinetic transport in a liquid foam is at the confluence of two well developed research areas. On one hand, the study of electrokinetic flows (i.e.

Bending modulus of bidisperse particle rafts: Local and collective contributions.

The bending modulus of air-water interfaces covered by a monolayer of bidisperse particles is probed experimentally under quasistatic conditions via the compression of the monolayer, and under dynamical conditions studying capillary-wave propagation. Simple averaging of the modulus obtained solely with small or large particles fails to describe our data. Indeed, as observed in other configurations for monodisperse systems, bidisperse rafts have both a granular and an elastic character: chain forces and collective effects must be taken into account to fully understand our results.

Two types of Cassie-to-Wenzel wetting transitions on superhydrophobic surfaces during drop impact.

Despite the fact that superhydrophobic surfaces possess useful and unique properties, their practical application has remained limited by durability issues. Among those, the wetting transition, whereby a surface gets impregnated by the liquid and permanently loses its superhydrophobicity, certainly constitutes the most limiting aspect under many realistic conditions. In this study, we revisit this so-called Cassie-to-Wenzel transition (CWT) under the broadly encountered situation of liquid drop impact.

Surface conductivity measurements in nanometric to micrometric foam films.

Foam films (a liquid lamella in air covered by surfactants) are tools of choice for nanofluidic characterization as they are intrinsically nanometric. Their size is indeed fixed by a balance between external pressure and particular molecular interactions in the vicinity of interfaces. To probe the exact nature of these interfaces, different characterizations can be performed.

Ultra-sensitive flow measurement in individual nanopores through pressure--driven particle translocation.

A challenge for the development of nanofluidics is to develop new instrumentation tools, able to probe the extremely small mass transport across individual nanochannels. Such tools are a prerequisite for the fundamental exploration of the breakdown of continuum transport in nanometric confinement. In this letter, we propose a novel method for the measurement of the hydrodynamic permeability of nanometric pores, by diverting the classical technique of Coulter counting to characterize a pressure-driven flow across an individual nanopore.

Thermodynamic and mechanical timescales involved in foam film rupture and liquid foam coalescence.

Recent advances in the coalescence in liquid foams are reviewed, with a special focus on the multiscale structure of foams. Studies concerning the stability of isolated foam films, on the one hand, and the coalescence process in macroscopic foams, on the other hand, are not always in good agreement. This discrepancy reveals that two routes can induce coalescence in a foam.

Anomalous ζ potential in foam films.

Electrokinetic effects offer a method of choice to control flows in micro- and nanofluidic systems. While a rather clear picture of these phenomena exists now for the liquid-solid interfaces, the case of liquid-air interfaces remains largely unexplored. Here, we investigate at the molecular level electrokinetic transport in a liquid film covered with ionic surfactants.

Oil repartition in a foam film architecture.

The propagation and distribution of oil inside the aqueous network of a foam is investigated in the case where oil can invade the foam without breaking it. The oil is injected into an elementary foam architecture of nine foam films and four vertices obtained by plunging a cubic frame in a foaming solution. The frame is then deformed to trigger a film switching (topological rearrangement named T1) and oil redistribution through this process is reported.

Giant osmotic energy conversion measured in a single transmembrane boron nitride nanotube.

New models of fluid transport are expected to emerge from the confinement of liquids at the nanoscale, with potential applications in ultrafiltration, desalination and energy conversion. Nevertheless, advancing our fundamental understanding of fluid transport on the smallest scales requires mass and ion dynamics to be ultimately characterized across an individual channel to avoid averaging over many pores. A major challenge for nanofluidics thus lies in building distinct and well-controlled nanochannels, amenable to the systematic exploration of their properties.

Soft nanofluidic transport in a soap film.

We investigate experimentally the electrokinetic properties of soft nanofluidic channels that consist in soap films with nanometric thickness, covered with charged surfactants. Both the electric and fluidic responses of the system are measured under an applied voltage drop along the film. The electric field is shown to induce an electro-osmotic hydrodynamic flow in the film.

Large apparent electric size of solid-state nanopores due to spatially extended surface conduction.

Ion transport through nanopores drilled in thin membranes is central to numerous applications, including biosensing and ion selective membranes. This paper reports experiments, numerical calculations, and theoretical predictions demonstrating an unexpectedly large ionic conduction in solid-state nanopores, taking its origin in anomalous entrance effects. In contrast to naive expectations based on analogies with electric circuits, the surface conductance inside the nanopore is shown to perturb the three-dimensional electric current streamlines far outside the nanopore in order to meet charge conservation at the pore entrance.

Transport of long neutral polymers in the semidilute regime through a protein nanopore.

We investigate the entrance of single poly(ethylene glycol) chains into an α-hemolysin channel. We detect the frequency and duration of the current blockades induced by large neutral polymers, where chain radius is larger than pore diameter. In the semidilute regime, these chains pass only if the monomer concentration is larger than a well-defined threshold.

A flux monitoring method for easy and accurate flow rate measurement in pressure-driven flows.

We propose a low-cost and versatile method to measure flow rate in microfluidic channels under pressure-driven flows, thereby providing a simple characterization of the hydrodynamic permeability of the system. The technique is inspired by the current monitoring method usually employed to characterize electro-osmotic flows, and makes use of the measurement of the time-dependent electric resistance inside the channel associated with a moving salt front. We have successfully tested the method in a micrometer-size channel, as well as in a complex microfluidic channel with a varying cross-section, demonstrating its ability in detecting internal shape variations.

Strain-induced yielding in bubble clusters.

We study how shearing clusters of two or four bubbles induces bubble separation or topological rearrangement. The critical deformation at which this yielding occurs is measured as a function of shear rate, liquid composition, and liquid content in the cluster. We establish a geometrical yield criterion in the quasistatic case on the basis of these experimental data as well as simulations.

How topological rearrangements and liquid fraction control liquid foam stability.

The stability of foam is investigated experimentally through coalescence events. Instability (coalescence) occurs when the system is submitted to external perturbations (T1) and when the liquid amount in the film network is below a critical value. Microscopically, transient thick films are observed during film rearrangements.

First steps in the spreading of a liquid droplet.

We describe the first steps of spreading of a liquid droplet brought in contact with a solid that it wets completely. Usually, it is assumed that the dynamics of the droplet results from a balance between the spreading forces and viscosity. But before this classical stage, inertia resists to the motion, which leads to a very different dynamic law.