Dynamics of colloidal particles with capillary interactions

We investigate the dynamics of colloids at a fluid interface driven by attractive capillary interactions. At submillimeter length scales, the capillary attraction is formally analogous to two-dimensional gravity. In particular it is a non-integrable interaction and it can be actually relevant for collective phenomena in spite of its weakness at the level of the pair potential. We introduce a mean-field model for the dynamical evolution of the particle number density at the interface. For generic values of the physical parameters the homogeneous distribution is found to be unstable against large-scale clustering driven by the capillary attraction. We also show that for the instability to be observable, the appropriate values for the relevant parameters (colloid radius, surface charge, external electric field, etc.) are experimentally well accessible. Our analysis contributes to current studies of the structure and dynamics of systems governed by long-ranged interactions and points towards their experimental realizations via colloidal suspensions.Comment: Matches version accepted for publication. New refs. added, misprints corrected in figs.6,8,9,1

Current Conservation in the Covariant Quark-Diquark Model of the Nucleon

The description of baryons as fully relativistic bound states of quark and glue reduces to an effective Bethe-Salpeter equation with quark-exchange interaction when irreducible 3-quark interactions are neglected and separable 2-quark (diquark) correlations are assumed. This covariant quark-diquark model of baryons is studied with the inclusion of the quark substructure of the diquark correlations. In order to maintain electromagnetic current conservation it is then necessary to go beyond the impulse approximation. A conserved current is obtained by including the coupling of the photon to the exchanged quark and direct ``seagull'' couplings to the diquark structure. Adopting a simple dynamical model of constituent quarks and exploring various parametrisations of scalar diquark correlations, the nucleon Bethe-Salpeter equation is solved and the proton and neutron electromagnetic form factors are calculated numerically. The resulting magnetic moments are still about 50% too small, the improvements necessary to remedy this are discussed. The results obtained in this framework provide an excellent description of the electric form factors (and charge radii) of the proton, up to a photon momentum transfer of 3.5GeV^2, and the neutron.Comment: 30 Pages, LaTeX2e, revised version, minor modifiactions to the text, some phrases eliminated, some remarks adde

Onset of anomalous diffusion in colloids confined to quasi-monolayers

It has been recently shown that a colloidal monolayer, e.g., formed at a fluid interface or by means of a suitable confining potential, exhibits anomalous collective diffusion. This is a consequence of the hydrodynamic interactions mediated by the three-dimensional (3D) ambient fluid when the particles are confined to reside on a two-dimensional (2D) manifold. We study theoretically and with numerical simulations the crossover from normal to anomalous diffusion as the particles are, in real systems, confined by a 3D external potential and thus have the possibility to fluctuate out of the 2D manifold, thus forming actually a quasi-monolayer.Comment: 13 pages, 9 figure

Solid phase properties and crystallization in simple model systems

We review theoretical and simulational approaches to the description of equilibrium bulk crystal and interface properties as well as to the nonequilibrium processes of homogeneous and heterogeneous crystal nucleation for the simple model systems of hard spheres and Lennard-Jones particles. For the equilibrium properties of bulk and interfaces, density functional theories employing fundamental measure functionals prove to be a precise and versatile tool, as exemplified with a closer analysis of the hard sphere crystalliquid interface. A detailed understanding of the dynamic process of nucleation in these model systems nevertheless still relies on simulational approaches. We review bulk nucleation and nucleation at structured walls and examine in closer detail the influence of walls with variable strength on nucleation in the Lennard-Jones fluid. We find that a planar crystalline substrate induces the growth of a crystalline film for a large range of lattice spacings and interaction potentials. Only a strongly incommensurate substrate and a very weakly attractive substrate potential lead to crystal growth with a non-zero contact angle

Theory of capillary-induced interactions beyond the superposition approximation

Within a general theoretical framework we study the effective, deformation-induced interaction between two colloidal particles trapped at a fluid interface in the regime of small deformations. In many studies, this interaction has been computed with the ansatz that the actual interface configuration for the pair is given by the linear superposition of the interface deformations around the single particles. Here we assess the validity of this approach and compute the leading term of the effective interaction for large interparticle separation beyond this so-called superposition approximation. As an application, we consider the experimentally relevant case of interface deformations owing to the electrostatic field emanating from charged colloidal particles. In mechanical isolation, i.e., if the net force acting on the total system consisting of the particles plus the interface vanishes, the superposition approximation is actually invalid. The effective capillary interaction is governed by contributions beyond this approximation and turns out to be attractive. For sufficiently small surface charges on the colloids, such that linearization is strictly valid, and at asymptotically large separations, the effective interaction does not overcome the direct electrostatic repulsion between the colloidal particles.Comment: Minor typos correcte

Solvent-mediated interactions between nanoparticles at fluid interfaces

We investigate the solvent mediated interactions between nanoparticles adsorbed at a liquid-vapor interface in comparison to the solvent mediated interactions in the bulk liquid and vapor phases of a Lennard-Jones solvent. Molecular dynamics simulation data for the latter are in good agreement with results from integral equations in the reference functional approximation and a simple geometric approximation. Simulation results for the solvent mediated interactions at the interface differ markedly from the interactions of the particles in the corresponding bulk phases. We find that at short interparticle distances the interactions are considerably more repulsive than those in either bulk phase. At long interparticle distances we find evidence for a long-ranged attraction. We discuss these observations in terms of interfacial interactions, namely, the three-phase line tension that would operate at short distances, and capillary wave interactions for longer interparticle distances.Comment: 22 pages, 6 figure