Self-assembly in mixtures with competing interactions

A binary mixture of particles interacting with spherically-symmetrical potentials leading to microsegregation is studied by theory and molecular dynamics (MD) simulations. We consider spherical particles with equal diameters and volume fractions. Motivated by the mixture of oppositely charged particles with different adsorption preferences immersed in a near-critical binary solvent, we assume short-range attraction long-range repulsion for the interaction between like particles, and short-range repulsion long-range attraction for the interaction between different ones. In order to predict structural and thermodynamic properties of such complex mixtures, we develop a theory combining the density functional and field-theoretical methods. We show that concentration fluctuations in mesoscopic regions lead to a qualitative change of the phase diagram compared to mean-field predictions. Both theory and MD simulations show coexistence of a low-density disordered phase with a high-density phase with alternating layers rich in the first and second components. In these layers, crystalline structure is present in the solid, and absent in the liquid crystals. The density and the degree of order of the ordered phase decrease with increasing temperature, up to a temperature where the theory predicts a narrow two-phase region with increasing density of both phases for increasing temperature. MD simulations show that monocrystals of the solid and liquid crystals have a prolate shape with the axis parallel to the direction of concentration oscillations, and the deviation from the spherical shape increases with increasing periodic order.

Automated summary

The study investigates the interaction between particles in a binary mixture under spherically-symmetrical potentials, leading to microsegregation. Both theory and MD simulations demonstrate coexistence of different phases with varying densities and degrees of order, with the phase diagram showing significant differences from mean-field predictions. The ordered phases exhibit crystalline structures in the solid form, while lacking in the liquid crystals, with a prolate shape noted in monocrystals that deviates from a spherical shape with increasing periodic order.