How to steer active colloids up a vertical wall.

An important challenge in active matter lies in harnessing useful global work from entities that produce work locally, e.g., via self-propulsion.

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.

Aging or DEAD: Origin of the non-monotonic response to weak self-propulsion in active glasses.

Among amorphous states, glass is defined by relaxation times longer than the observation time. This nonergodic nature makes the understanding of glassy systems an involved topic, with complex aging effects or responses to further out-of-equilibrium external drivings. In this respect, active glasses made of self-propelled particles have recently emerged as a stimulating systems, which broadens and challenges our current understanding of glasses by considering novel internal out-of-equilibrium degrees of freedom.

Two-dimensional numerical model of Marangoni surfers: From single swimmer to crystallization.

We numerically study the dynamics of an ensemble of Marangoni surfers in a two-dimensional and unconfined space. The swimmers are modeled as Gaussian sources of surfactant generating surface tension gradients and are shown to follow the Marangoni flow filtered at their spatial scale in the lubrication regime, an unstable situation leading to spontaneous motion as soon as the Marangoni effect is intense enough. As the system is fully unconstrained, it is possible to study the various dynamical regimes from single swimmer, two-body interaction, to the many-particles case characterized by an efficient particle dispersion.

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.

Nonmonotonic behavior in dense assemblies of active colloids.

We study experimentally a sediment of self-propelled Brownian particles with densities ranging from dilute to ergodic supercooled to nonergodic glass to nonergodic polycrystal. In a companion paper, we observe a nonmonotonic response to activity of relaxation of the nonergodic glass state: a dramatic slowdown when particles become weakly self-propelled, followed by a speedup at higher activities. Here we map ergodic supercooled states to standard passive glassy physics, provided a monotonic shift of the glass packing fraction and the replacement of the ambient temperature by the effective temperature.

Active Glass: Ergodicity Breaking Dramatically Affects Response to Self-Propulsion.

We study experimentally the response of a dense sediment of Brownian particles to self-propulsion. We observe that the ergodic supercooled liquid relaxation is monotonically enhanced by activity. By contrast the nonergodic glass shows an order of magnitude slowdown at low activities with respect to the passive case, followed by fluidization at higher activities.

Flow-induced shift of the Donnan equilibrium for ultra-sensitive mass transport measurement through a single nanochannel.

Despite mass flow being arguably the most elementary transport associated with nanofluidics, its measurement still constitutes a significant bottleneck for the development of this promising field. Here, we investigate how a liquid flow perturbs the ubiquitous enrichment-or depletion-of a solute inside a single nanochannel. Using fluorescence correlation spectroscopy to access the local solute concentration, we demonstrate that the initial enrichment-the so-called Donnan equilibrium-is depleted under flow, thus revealing the underlying mass transport.

Self-propulsion of symmetric chemically active particles: Point-source model and experiments on camphor disks.

Solid undeformable particles surrounded by a liquid medium or interface may propel themselves by altering their local environment. Such nonmechanical swimming is at work in autophoretic swimmers, whose self-generated field gradient induces a slip velocity on their surface, and in interfacial swimmers, which exploit unbalance in surface tension. In both classes of systems, swimmers with intrinsic asymmetry have received the most attention but self-propulsion is also possible for particles that are perfectly isotropic.

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.

Structural and cooperative length scales in polymer gels.

Understanding the relationship between the material structural details, the geometrical confining constraints, the local dynamical events and the global rheological response is at the core of present investigations on complex fluid properties. In the present article, this problem is addressed on a model yield stress fluid made of highly entangled polymer gels of Carbopol which follows at the macroscopic scale the well-known Herschel-Bulkley rheological law. First, performing local rheology measurements up to high shear rates ([Formula: see text] s)and under confinement, we evidence unambiguously the breakdown of bulk rheology associated with cooperative processes under flow.

Carbon membranes for efficient water-ethanol separation.

We demonstrate, on the basis of molecular dynamics simulations, the possibility of an efficient water-ethanol separation using nanoporous carbon membranes, namely, carbon nanotube membranes, nanoporous graphene sheets, and multilayer graphene membranes. While these carbon membranes are in general permeable to both pure liquids, they exhibit a counter-intuitive "self-semi-permeability" to water in the presence of water-ethanol mixtures. This originates in a preferred ethanol adsorption in nanoconfinement that prevents water molecules from entering the carbon nanopores.

Velocity Condensation for Magnetotactic Bacteria.

Magnetotactic swimmers tend to align along magnetic field lines against stochastic reorientations. We show that the swimming strategy, e.g.

Anomalous capillary filling and wettability reversal in nanochannels.

This work revisits capillary filling dynamics in the regime of nanometric to subnanometric channels. Using molecular dynamics simulations of water in carbon nanotubes, we show that for tube radii below one nanometer, both the filling velocity and the Jurin rise vary nonmonotonically with the tube radius. Strikingly, with fixed chemical surface properties, this leads to confinement-induced reversal of the tube wettability from hydrophilic to hydrophobic for specific values of the radius.

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.

[Optimal permeability of aquaporins: a question of shape?].

Aquaporins are transmembrane proteins, ubiquitous in the human body. Inserted into the cell membranes, they play an important role in filtration, absorption and secretion of fluids. However, the excellent compromise between selectivity and permeability of aquaporins remains elusive.

Large permeabilities of hourglass nanopores: from hydrodynamics to single file transport.

In fluid transport across nanopores, there is a fundamental dissipation that arises from the connection between the pore and the macroscopic reservoirs. This entrance effect can hinder the whole transport in certain situations, for short pores and/or highly slipping channels. In this paper, we explore the hydrodynamic permeability of hourglass shape nanopores using molecular dynamics (MD) simulations, with the central pore size ranging from several nanometers down to a few Angströms.

How a "pinch of salt" can tune chaotic mixing of colloidal suspensions.

Efficient mixing of colloids, particles or molecules is a central issue in many processes. It results from the complex interplay between flow deformations and molecular diffusion, which is generally assumed to control the homogenization processes. In this work we demonstrate on the contrary that despite fixed flow and self-diffusion conditions, the chaotic mixing of colloidal suspensions can be either boosted or inhibited by the sole addition of a trace amount of salt as a co-mixing species.

Optimizing water permeability through the hourglass shape of aquaporins.

The ubiquitous aquaporin channels are able to conduct water across cell membranes, combining the seemingly antagonist functions of a very high selectivity with a remarkable permeability. Whereas molecular details are obvious keys to perform these tasks, the overall efficiency of transport in such nanopores is also strongly limited by viscous dissipation arising at the connection between the nanoconstriction and the nearby bulk reservoirs. In this contribution, we focus on these so-called entrance effects and specifically examine whether the characteristic hourglass shape of aquaporins may arise from a geometrical optimum for such hydrodynamic dissipation.

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.

Probing the fluctuation-dissipation theorem in a Perrin-like experiment.

In this Letter, we present a new experimental approach to investigate the effective temperature concept as a generalization of the fluctuation-dissipation theorem (FDT) for nonequilibrium systems. Simultaneous measurements of diffusion coefficient and sedimentation velocity of heavy colloids, embedded in a Laponite clay suspension, are performed with a fluorescence-recovery-based setup. This nonperturbative dual measurement, performed at a single time in a single sample, allows for a direct application of the FDT to the tracer velocity observable.

Sedimentation and effective temperature of active colloidal suspensions.

In this Letter, we investigate experimentally the nonequilibrium steady state of an active colloidal suspension under gravity field. The active particles are made of chemically powered colloids, showing self propulsion in the presence of an added fuel, here hydrogen peroxide. The active suspension is studied in a dedicated microfluidic device, made of permeable gel microstructures.

Colloidal motility and pattern formation under rectified diffusiophoresis.

In this Letter, we characterize experimentally the diffusiophoretic motion of colloids and lambda-DNA toward higher concentration of solutes, using microfluidic technology to build spatially and temporally controlled concentration gradients. We then demonstrate that segregation and spatial patterning of the particles can be achieved from temporal variations of the solute concentration profile. This segregation takes the form of a strong trapping potential, stemming from an osmotically induced rectification mechanism of the solute time-dependent variations.

Wetting controls separation of inertial flows from solid surfaces.

We investigate the flow of liquids around solid surfaces in the inertial regime, a situation commonly encountered with the so-called "teapot effect", the annoying tendency for a liquid to trickle down the outside of a receptacle after pouring. We demonstrate that surface wettability is an unexpected key factor in controlling flow separation and trickling, the latter being completely suppressed in the limit of superhydrophobic substrates. This unforeseen coupling is rationalized in terms of an inertial-capillary adhesion framework, which couples inertial flows to surface wettability effects.