Quasi-two-dimensional dispersions of Brownian particles with competitive interactions: phase behavior and structural properties
Abstract
Competing short-range attractive (SA) and long range repulsive (LR) particle interactions can be used to describe three-dimensional charge-stabilized colloid or protein dispersions at low added salt concentrations, as well as membrane proteins with interaction contributions mediated by lipid molecules. Using Langevin dynamics (LD) simulations, we determine the generalized phase diagram, cluster shapes and size distributions of a generic quasi-two-dimensional (Q2D) dispersion of spherical SALR particles confined to in-plane motion inside a bulk fluid. The SA and LR interaction parts are modelled by a generalized Lennard-Jones potential and a screened Coulomb potential, respectively. The microstructures of the detected equilibrium and non-equilibrium Q2D phases are distinctly different from those observed in three-dimensional (3D) SALR systems, by exhibiting different levels of hexagonal ordering. We discuss a thermodynamic perturbation theory prediction for the metastable binodal line of a reference system of particles with SA interactions only, which in the explored Q2D-SALR phase diagram region separates cluster from non-clustered phases. The transition from the high-temperature (small SA) dispersed fluid (DF) phase to the lower-temperature equilibrium cluster (EC) fluid phase is characterised by a low-wavenumber peak height of the static structure factor (corresponding to a thermal correlation length of about twice the particle diameter) featuring a distinctly smaller value (≈1.4) than in 3D SALR systems. With decreasing temperature (increasing SA), the cluster morphology changes from disk-like shapes in the equilibrium cluster phase, to double-stranded anisotropic hexagonal cluster segments formed in a cluster-percolated (CP) gel-like phase. This transition can be quantified by a hexagonal order parameter distribution function. The mean cluster size and coordination number of particles in the CP phase are insensitive to changes in the attraction strength.
- This article is part of the themed collection: Colloidal interactions, dynamics and rheology