Two-dimensional systems with competing interactions: microphase formation under the effect of a disordered porous matrix

We have investigated the effect of a disordered porous matrix on the cluster microphase formation of a two dimensional system where particles interact via competing interactions. To this end we have performed extensive Monte Carlo simulations and have systematically varied the densities of the fluid and of the matrix as well as the interaction between the matrix particles and between the matrix and fluid particles. Our results provide evidence that the matrix does have a distinct effect on the microphase formation of the fluid particles: as long as the particles interact both among themselves as well as with the fluid particles via a simple hard sphere potential, they essentially reduce the available space, in which the fluid particles form a cluster microphase. On the other hand, if we turn on a long-range tail in the matrix-matrix and in the matrix-fluid interactions, the matrix particles become nucleation centers for the clusters formed by the fluid particles.Comment: 12 pages, 6 figure

Lane-formation vs. cluster-formation in two dimensional square-shoulder systems: A genetic algorithm approach

Introducing genetic algorithms as a reliable and efficient tool to find ordered equilibrium structures, we predict minimum energy configurations of the square shoulder system for different values of corona width $\lambda$. Varying systematically the pressure for different values of $\lambda$ we obtain complete sequences of minimum energy configurations which provide a deeper understanding of the system's strategies to arrange particles in an energetically optimized fashion, leading to the competing self-assembly scenarios of cluster-formation vs. lane-formation.Comment: 5 pages, 6 figure

Freezing of Simple Liquid Metals

Freezing of simple liquid metals and the relative stabilities of competing crystalline solids are investigated using thermodynamic perturbation theory, the interactions between ions being modeled by effective pair potentials derived from pseudopotential theory. The ionic free energy of the solid phase is calculated, to first order in the perturbation potential, using classical density-functional theory and an accurate approximation to the hard-sphere radial distribution function. Free energy calculations for Na, Mg, and Al yield well-defined freezing transitions and structural free energy differences for bcc, fcc, and hcp crystals in qualitative agreement with experiment.Comment: 8 pages, 4 figures, LaTeX with elsart.st

Ordered structures formed by ultrasoft, aspherical particles

We have applied the formalism of classical density functional theory to study the shape and the orientation of the density profiles rho(r) formed by aspherical, ultrasoft particles. For simplicity we have considered particles with an elliptic shape, characterised by an aspect ratio lambda. The rho(r)\u2019s are obtained via the minimisation of the grand-potential functional Omega[rho], for which we have used a mean-field format. The optimisation of Omega[rho] is numerically realised in a free (i.e. unbiased) manner minimising the functional with respect to the density profile, which we have discretised in the unit cell of the lattice on 80^3 grid points. Keeping the temperature fixed and varying the chemical potential and lambda, we have investigated the impact of these parameters on the density profile

Optimized random phase approximations for arbitrary reference systems: extremum conditions and thermodynamic consistence

The optimized random phase approximation (ORPA) for classical liquids is re-examined in the framework of the generating functional approach to the integral equations. We show that the two main variants of the approximation correspond to the addition of the same correction to two different first order approximations of the homogeneous liquid free energy. Furthermore, we show that it is possible to consistently use the ORPA with arbitrary reference systems described by continuous potentials and that the same approximation is equivalent to a particular extremum condition for the corresponding generating functional. Finally, it is possible to enforce the thermodynamic consistence between the thermal and the virial route to the equation of state by requiring the global extremum condition on the generating functional.Comment: 8 pages, RevTe

Self-assembly of DNA-functionalized colloids

Colloidal particles grafted with single-stranded DNA (ssDNA) chains can self-assemble into a number of different crystalline structures, where hybridization of the ssDNA chains creates links between colloids stabilizing their structure. Depending on the geometry and the size of the particles, the grafting density of the ssDNA chains, and the length and choice of DNA sequences, a number of different crystalline structures can be fabricated. However, understanding how these factors contribute synergistically to the self-assembly process of DNA-functionalized nano- or micro-sized particles remains an intensive field of research. Moreover, the fabrication of long-range structures due to kinetic bottlenecks in the self-assembly are additional challenges. Here, we discuss the most recent advances from theory and experiment with particular focus put on recent simulation studies