Determination of the zeta potential for highly charged colloidal suspensions

We compute the electrostatic potential at the surface, or zeta potential $\zeta$, of a charged particle embedded in a colloidal suspension using a hybrid mesoscopic model. We show that for weakly perturbing electric fields, the value of $\zeta$ obtained at steady state during electrophoresis is statistically indistinguishable from $\zeta$ in thermodynamic equilibrium. We quantify the effect of counterions concentration on $\zeta$. We also evaluate the relevance of the lattice resolution for the calculation of $\zeta$ and discuss how to identify the effective electrostatic radius.Comment: 8 pages, 3 figures with 2 panel

Separation of suspended particles by arrays of obstacles in microfluidic devices

The stochastic transport of suspended particles through a periodic pattern of obstacles in microfluidic devices is investigated by means of the Fokker-Planck equation. Asymmetric arrays of obstacles have been shown to induce the continuous separation of DNA molecules of different length. The analysis presented here of the asymptotic distribution of particles in a unit cell of these systems shows that separation is only possible in the presence of a driving force with a non-vanishing normal component at the surface of the solid obstacles. In addition, vector separation, in which different species move, in average, in different directions within the device, is driven by differences on the force acting on the various particles and not by differences in the diffusion coefficient. Monte-Carlo simulations performed for different particles and force fields agree with the numerical solutions of the Fokker-Planck equation in the periodic system

Velocity fluctuations and hydrodynamic diffusion in sedimentation

We study non-equilibrium velocity fluctuations in a model for the sedimentation of non-Brownian particles experiencing long-range hydrodynamic interactions. The complex behavior of these fluctuations, the outcome of the collective dynamics of the particles, exhibits many of the features observed in sedimentation experiments. In addition, our model predicts a final relaxation to an anisotropic (hydrodynamic) diffusive state that could be observed in experiments performed over longer time ranges.Comment: 7 pages, 5 EPS figures, EPL styl

Correlated dynamics of inclusions in a supported membrane

The hydrodynamic theory of heterogeneous fluid membranes is extended to the case of a membrane adjacent to a solid substrate. We derive the coupling diffusion coefficients of pairs of membrane inclusions in the limit of large separation compared to the inclusion size. Two-dimensional compressive stresses in the membrane make the coupling coefficients decay asymptotically as $1/r^2$ with interparticle distance $r$. For the common case, where the distance to the substrate is of sub-micron scale, we present expressions for the coupling between distant disklike inclusions, which are valid for arbitrary inclusion size. We calculate the effect of inclusions on the response of the membrane and the associated corrections to the coupling diffusion coefficients to leading order in the concentration of inclusions. While at short distances the response is modified as if the membrane were a two-dimensional suspension, the large-distance response is not renormalized by the inclusions.Comment: 15 page

The Electric Double Layer Structure Around Charged Spherical Interfaces

We derive a formally simple approximate analytical solution to the Poisson-Boltzmann equation for the spherical system via a geometric mapping. Its regime of applicability in the parameter space of the spherical radius and the surface potential is determined, and its superiority over the linearized solution is demonstrated.Comment: 7 pages, 5 figure

Investigation of qq-dependent dynamical heterogeneity in a colloidal gel by x-ray photon correlation spectroscopy

We use time-resolved X-Photon Correlation Spectroscopy to investigate the slow dynamics of colloidal gels made of moderately attractive carbon black particles. We show that the slow dynamics is temporally heterogeneous and quantify its fluctuations by measuring the variance $\chi$ of the instantaneous intensity correlation function. The amplitude of dynamical fluctuations has a non-monotonic dependence on scattering vector $q$, in stark contrast with recent experiments on strongly attractive colloidal gels [Duri and Cipelletti, \textit{Europhys. Lett.} \textbf{76}, 972 (2006)]. We propose a simple scaling argument for the $q$-dependence of fluctuations in glassy systems that rationalizes these findings.Comment: Final version published in PR

Self-assembly of the simple cubic lattice with an isotropic potential

Conventional wisdom presumes that low-coordinated crystal ground states require directional interactions. Using our recently introduced optimization procedure to achieve self-assembly of targeted structures (Phys. Rev. Lett. 95, 228301 (2005), Phys. Rev. E 73, 011406 (2006)), we present an isotropic pair potential $V(r)$ for a three-dimensional many-particle system whose classical ground state is the low-coordinated simple cubic (SC) lattice. This result is part of an ongoing pursuit by the authors to develop analytical and computational tools to solve statistical-mechanical inverse problems for the purpose of achieving targeted self-assembly. The purpose of these methods is to design interparticle interactions that cause self-assembly of technologically important target structures for applications in photonics, catalysis, separation, sensors and electronics. We also show that standard approximate integral-equation theories of the liquid state that utilize pair correlation function information cannot be used in the reverse mode to predict the correct simple cubic potential. We report in passing optimized isotropic potentials that yield the body-centered cubic and simple hexagonal lattices, which provide other examples of non-close-packed structures that can be assembled using isotropic pair interactions.Comment: 16 pages, 12 figures. Accepted for publication in Physical Review

Electrophoresis of a polyelectrolyte through a nanopore

A hydrodynamic model for determining the electrophoretic speed of a polyelectrolyte through a nanopore is presented. It is assumed that the speed is determined by a balance of electrical and viscous forces arising from within the pore and that classical continuum electrostatics and hydrodynamics may be considered applicable. An explicit formula for the translocation speed as a function of the pore geometry and other physical parameters is obtained and is shown to be consistent with experimental measurements on DNA translocation through nanopores in silicon membranes. Experiments also show a weak dependence of the translocation speed on polymer length that is not accounted for by the present model. It is hypothesized that this is due to secondary effects that are neglected here.Comment: 5 pages, 2 column, 2 figure

Surface-mediated attraction between colloids

We investigate the equilibrium properties of a colloidal solution in contact with a soft interface. As a result of symmetry breaking, surface effects are generally prevailing in confined colloidal systems. In this Letter, particular emphasis is given to surface fluctuations and their consequences on the local (re)organization of the suspension. It is shown that particles experience a significant effective interaction in the vicinity of the interface. This potential of mean force is always attractive, with range controlled by the surface correlation length. We suggest that, under some circumstances, surface-induced attraction may have a strong influence on the local particle distribution

Structure of a liquid crystalline fluid around a macroparticle: Density functional theory study

The structure of a molecular liquid, in both the nematic liquid crystalline and isotropic phases, around a cylindrical macroparticle, is studied using density functional theory. In the nematic phase the structure of the fluid is highly anisotropic with respect to the director, in agreement with results from simulation and phenomenological theories. On going into the isotropic phase the structure becomes rotationally invariant around the macroparticle with an oriented layer at the surface.Comment: 10 pages, 6 figues. Submitted to Phys. Rev.