arXiv subjects

Pablo Barcellona

Publications and source records attributed to Pablo Barcellona.

9 recordsLinked to original sources

arXiv2020

Lateral interatomic dispersion forces

Van der Waals forces between atoms and molecules are universally assumed to act along the line separating them. Inspired by recent works on effects which can propel atoms parallel to a macroscopic surface via the Casimir--Polder force, we predict a lateral van der Waals force between two atoms, one of which is in an excited state with non-zero angular momentum and the other is isotropic and in its ground state. The resulting force acts in the same way as a planetary gear, in contrast to the rack-and-pinion motion predicted in works on the lateral Casimir--Polder force in the analogous case, for which the force predicted here is the microscopic origin. We illustrate the effect by predicting the trajectories of an excited caesium in the vicinity of ground-state rubidium, finding behaviour qualitatively different to that if lateral forces are ignored.

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arXiv2019

Medium-assisted van der Waals dispersion interactions involving chiral molecules

The van der Waals dispersion interaction between two chiral molecules in the presence of arbirary magnetoelectric media is derived using perturbation theory. To be general, the molecular polarisabilities are assumed to be of electric, paramagnetic and diamagnetic natures and the material environment is considered to possess a chiral electromagnetic response. The derived formulas of electric-chiral, paramagnetic-chiral, diamagnetic-chiral and chiral-chiral interaction potentials when added to the previously obtained contributions in literature, form a complete set of dispersion interaction formulas. We present them in a unified form making use of electric--magnetic duality. As an application, the case of two anisotropic molecules in free space is considered where we drive the retarded and non-retarded limits with respect to intermolecular distance.

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arXiv2017

Lateral Casimir-Polder forces by breaking time-reversal symmetry

We examine the lateral Casimir-Polder force acting on a circular rotating emitter near a dielectric plane surface. As the circular motion breaks time-reversal symmetry, the spontaneous emission in a direction parallel to the surface is in general anisotropic. We show that a lateral force arises which can be interpreted as a recoil force because of this asymmetric emission. The force is an oscillating function of the distance between the emitter and the surface, and the lossy character of the dielectric strongly influences the results in the near-field regime. The force exhibits also a population-induced dynamics, decaying exponentially with respect to time on timescales of the inverse of the spontaneous decay rate. We propose that this effect could be detected measuring the velocity acquired by the emitter, following different cycles of excitation and thermalisation. Our results are expressed in terms of the Green's tensor and can therefore easily be applied to more complex geometries.

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arXiv2017

Manipulating the Coulomb interaction: A Green's function perspective

We present a unified framework for studying Coulomb interactions in arbitrary environments using macroscopic quantum electrodynamics on the basis of the electromagnetic Green's function. Our theory can be used to derive the Coulomb potential of a single charged particle as well as that between two charges in the presence of media, bodies and interfaces of arbitrary shapes. To demonstrate this, we reproduce the well-known screened Coulomb force, account for local-field effects and consider new cases such as a dielectric cavity and a conducting plate with a hole.

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arXiv2017

Enhanced chiral discriminatory van der Waals interactions mediated by chiral surfaces

We predict a discriminatory interaction between a chiral molecule and an achiral molecule which is mediated by a chiral body. To achieve this, we generalize the van der Waals interaction potential between two ground-state molecules with electric, magnetic and chiral response to non-trivial environments. The force is evaluated using second-order perturbation theory with an effective Hamiltonian. Chiral media enhance or reduce the free interaction via many-body interactions, making it possible to measure the chiral contributions to the van der Waals force with current technology. The van der Waals interaction is discriminatory with respect to enantiomers of different handedness and could be used to separate enantiomers. We also suggest a specific geometric configuration where the electric contribution to the van der Waals interaction is zero, making the chiral component the dominant effect.

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arXiv2017

Van der Waals interactions between excited atoms in generic environments

We consider the the van der Waals force involving excited atoms in general environments, constituted by magnetodielectric bodies. We develop a dynamical approach studying the dynamics of the atoms and the field, mutually coupled. When only one atom is excited, our dynamical theory suggests that for large distances the van der Waals force acting on the ground-state atom is monotonic, while the force acting in the excited atom is spatially oscillating. We show how this latter force can be related to the known oscillating Casimir--Polder force on an excited atom near a (ground-state) body. Our force also reveals a population-induced dynamics: for times much larger that the atomic lifetime the atoms will decay to their ground-states leading to the van der Waals interaction between ground-state atoms.

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arXiv2016

Dynamical Casimir-Polder force between an excited atom and a conducting wall

We consider the dynamical atom-surface Casimir-Polder force in the non-equilibrium configuration of an atom near a perfectly conducting wall, initially prepared in an excited state with the field in its vacuum state. We evaluate the time-dependent Casimir-Polder force on the atom, and find that it shows an oscillatory behavior from attractive to repulsive both in time and in space. We also investigate the asymptotic behavior in time of the dynamical force and of related local field quantities, showing that the static value of the force, as obtained by a time-independent approach, is recovered for times much larger than the timescale of the atomic self-dressing, but smaller than the atomic decay time. We then discuss the evolution of global quantities such as atomic and field energies, and their asymptotic behavior. We also compare our results for the dynamical force on the excited atom with analogous results recently obtained for an initially bare ground-state atom. We show that new relevant features are obtained in the case of an initially excited atom, for example much larger values of the dynamical force with respect to the static one, allowing for an easier way to single-out and observe the dynamical Casimir-Polder effect.

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arXiv2015

Dynamical Casimir-Polder interaction between a chiral molecule and a surface

We develop a dynamical approach to study the Casimir-Polder force between a initially bare molecule and a magnetodielectric body at finite temperature. Switching on the interaction between the molecule and the field at a particular time, we study the resulting temporal evolution of the Casimir-Polder interaction. The dynamical self-dressing of the molecule and its population-induced dynamics are accounted for and discussed. In particular, we find that the Casimir-Polder force between a chiral molecule and a perfect mirror oscillates in time with a frequency related to the molecular transition frequency, and converges to the static result for large times.

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arXiv2015

A microscopic approach to Casimir and Casimir-Polder forces between metallic bodies

We consider the Casimir-Polder interaction energy between a metallic nanoparticle and a metallic plate, as well as the Casimir interaction energy between two macroscopic metal plates, in terms of the many-body dispersion interactions between their constituents. Expressions for two- and three-body dispersion interactions between the microscopic parts of a real metal are first obtained, both in the retarded and non-retarded limits. These expressions are then used to evaluate, a compare each other, the overall two- and three-body contributions to the macroscopic Casimir-Polder and Casimir force, by summing up the contributions from the microscopic constituents of the bodies (metal nanoparticles), for two geometries: metal nanoparticle/half-space and half-space/half-space, where all the materials are assumed perfect conductors. In the case of nanoparticle/half-space, our results fully agree with those that can be extracted from the corresponding macroscopic results, and explicitly show the non-applicability of the pairwise approximation for the geometry considered. In both cases, we find that, while the overall two-body contribution yields an attractive force, the overall three-body contribution is repulsive. Also, they turn out to be of the same order, consistently with the known nonapplicability of the pairwise approximation. The issue of the rapidity of convergence of the many-body expansion is also briefly discussed.

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