Hydrodynamics within the Electric Double Layer on slipping surfaces

We show, using extensive Molecular Dynamics simulations, that the dynamics of the electric double layer (EDL) is very much dependent on the wettability of the charged surface on which the EDL develops. For a wetting surface, the dynamics, characterized by the so-called Zeta potential, is mainly controlled by the electric properties of the surface, and our work provides a clear interpretation for the traditionally introduced immobile Stern layer. In contrast, the immobile layer disappears for non-wetting surfaces and the Zeta potential deduced from electrokinetic effects is considerably amplified by the existence of a slippage at the solid substrate.Comment: accepted for publication in Physical Review Letter

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 Angstr{\"o}ms. Surprisingly, we find a very good agreement between MD results and continuum hydrodynamic predictions, even for the smallest systems undergoing single file transport of water. An optimum of permeability is found for an opening angle around 5 degree, in agreement with continuum predictions, yielding a permeability five times larger than for a straight nanotube. Moreover, we find that the permeability of hourglass shape nanopores is even larger than single nanopores pierced in a molecular thin graphene sheet. This suggests that designing the geometry of nanopores may help considerably increasing the macroscopic permeability of membranes

Destabilization of a flow focused suspension of magnetotactic bacteria

Active matter is a new class of material, intrinsically out-of equilibrium with intriguing properties. So far, the recent upsurge of studies has mostly focused on the spontaneous behavior of these systems --in the absence of external constraints or driving--. Yet, many real life systems evolve under constraints, being both submitted to flow and various taxis. In the present work, we demonstrate a new experimental system which opens up the way for quantitative investigations, and discriminating examinations, of the challenging theoretical description of such systems. We explore the behavior of magnetotactic bacteria as a particularly rich and versatile class of driven matter, which behavior can be studied under contrasting and contradicting stimuli. In particular we demonstrate that the competing driving of an orienting magnetic field and hydrodynamic flow lead not only to jetting, but also unveils a new pearling instability. This illustrates new structuring capabilities of driven active matter

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 trace amount of salt as a co-mixing species. Indeed, this shows that local saline gradients can trigger a chemically-driven transport phenomenon, diffusiophoresis, which controls the rate and direction of molecular transport far more efficiently than usual Brownian diffusion. A simple model combining the elementary ingredients of chaotic mixing with diffusiophoretic transport of the colloids allows to rationalize our observations and highlights how small-scale out-of-equilibrium transport bridges to mixing at much larger scales in a very effective way. Considering chaotic mixing as a prototypal building block for turbulent mixing, this suggests that these phenomena, occurring whenever the chemical environment is inhomogeneous, might bring interesting perspective from micro-systems up to large-scale situations, with examples ranging from ecosystems to industrial contexts.Comment: Submitte

Beating the teapot effect

We investigate the dripping of liquids around solid surfaces in the regime of inertial flows, a situation commonly encountered with the so-called "teapot effect". We demonstrate that surface wettability is an unexpected key factor in controlling flow separation and dripping, the latter being completely suppressed in the limit of superhydrophobic substrates. This unforeseen coupling is rationalized in terms of a novel hydro-capillary adhesion framework, which couples inertial flows to surface wettability effects. This description of flow separation successfully captures the observed dependence on the various experimental parameters - wettability, flow velocity, solid surface edge curvature-. As a further illustration of this coupling, a real-time control of dripping is demonstrated using electro-wetting for contact angle actuation.Comment: 4 pages; movies at http://lpmcn.univ-lyon1.fr/~lbocque

Sedimentation of active colloidal suspensions

In this paper, we investigate experimentally the non-equilibrium 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. Both the microdynamics of individual colloids and the global stationary state of the suspension under gravity - density profiles, number fluctuations - are measured with optical microscopy. This allows to connect the sedimentation length to the individual self-propelled dynamics, suggesting that in the present dilute regime the active colloids behave as 'hot' particles. Our work is a first step in the experimental exploration of the out-of-equilibrium properties of artificial active systems.Comment: 4 pages, 4 figure

Sedimentation of self-propelled Janus colloids: polarization and pressure

We study experimentally-using Janus colloids-and theoretically-using Active Brownian Particles- the sedimentation of dilute active colloids. We first confirm the existence of an exponential density profile. We show experimentally the emergence of a polarized steady state outside the effective equilibrium regime, i.e. when v_s is not much smaller than the propulsion speed. The experimental distribution of polarization is very well described by the theoretical prediction with no fitting parameter. We then discuss and compare three different definitions of pressure for sedimenting particles: the weight of particles above a given height, the flux of momentum and active impulse, and the force density measured by pressure gauges