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Abstract We study an integral expression that is encountered in some classical spin models of magnetism. The idea is to calculate the key integral that represents the building block for the expression of the partition function of these models. The general calculation allows one to have a better look at the internal structure of the quantity of interest which, in turn, may lead to potentially new useful insights. We find out that application of two different approaches to solve the problem in a general-case scenario leads to an interesting integral formula involving modified Bessel functions of the first kind which appears to be new. We performed Monte Carlo simulations to verify the correctness of the integral formula obtained. Additional numerical integration tests lead to the same result as well. The approach under consideration, when generalized, leads to a linear integral equation that might be of interest to numerical studies of classical spin models of magnetism that rely on the well-established transfer-matrix formalism. 

We consider a nanosystem consisting of two coplanar uniformly charged nanodisks that are coupled via Coulomb forces. Such a model represents a typical situation encountered in two-dimensional semiconductor quantum dot systems of electrons. We provide an exact integral expression for the interaction energy between the two coplanar nanodisks as a function of their separation distance. It is found that the difference between a standard Coulomb potential and the current one has features reminiscent of a Lennard-Jones interaction potential. The results derived can be useful to understand formation of clusters and/or aggregates in systems of coplanar charged nanodisks that contain electrons. 

It has now become evident that interplay between internal anisotropy parameters (such as electron mass anisotropy and/or anisotropic coupling of electrons to the substrate) and electron-electron correlation effects can create a rich variety of possibilities especially in quantum Hall systems. The electron mass anisotropy or material substrate effects (for example, the piezoelectric effect in GaAs) can lead to an effective anisotropic interaction potential between electrons. For lack of knowledge of realistic ab-initio potentials that may describe such effects, we adopt a phenomenological approach and assume that an anisotropic Coulomb interaction potential mimics the internal anisotropy of the system. In this work we investigate the emergence of liquid crystalline order at filling factor ν = 1/6 of the lowest Landau level, a state very close to the point where a transition from the liquid to the Wigner solid happens. We consider small finite systems of electrons interacting with an anisotropic Coulomb interaction potential and study the energy stability of an anisotropic liquid crystalline state relative to its isotropic Fermi-liquid counterpart. Quantum Monte Carlo simulation results in disk geometry show stabilization of liquid crystalline order driven by an anisotropic Coulomb interaction potential at all values of the interaction anisotropy parameter studied.