Crystallization of magnetic dipolar monolayers: a density functional approach
arXiv:0804.3299 · doi:10.1088/0953-8984/20/40/404217
Abstract
We employ density functional theory to study in detail the crystallization of super-paramagnetic particles in two dimensions under the influence of an external magnetic field that lies perpendicular to the confining plane. The field induces non-fluctuating magnetic dipoles on the particles, resulting into an interparticle interaction that scales as the inverse cube of the distance separating them. In line with previous findings for long-range interactions in three spatial dimensions, we find that explicit inclusion of liquid-state structural information on the {\it triplet} correlations is crucial to yield theoretical predictions that agree quantitatively with experiment. A non-perturbative treatment is superior to the oft-employed functional Taylor expansions, truncated at second or third order. We go beyond the usual Gaussian parametrization of the density site-orbitals by performing free minimizations with respect to both the shape and the normalization of the profiles, allowing for finite defect concentrations.
23 pages, 18 figures
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- Vacancy diffusion in colloidal crystals as determined by dynamical density-functional theory and the phase-field-crystal model
- Quasicrystal formation in binary soft matter mixtures
- Density-functional theory for the crystalline phases of a two-dimensional dipolar Fermi gas
- Classical density functional theory for a two-dimensional isotropic ferrogel model with labeled particles
- Density functional theory for the crystallization of two-dimensional dipolar colloidal alloys
- Integral Equation Theory for Pair Correlation Functions in a Crystal
- Freezing of a two dimensional fluid in to a crystalline phase : Density functional approach
- Density functional approach to elastic properties of three-dimensional dipole-spring models for magnetic gels