Pablo Barcellona

van der Waals interactions between excited atoms in generic environments

We consider 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.

Tuning the collective decay of two entangled emitters by means of a nearby surface

We consider the radiative properties of a system of two identical correlated atoms interacting with the electromagnetic field in its vacuum state in the presence of a generic dielectric environment. We suppose that the two emitters are prepared in a symmetric or antisymmetric superposition of one ground state and one excited state and we evaluate the transition rate to the collective ground state, showing distinctive cooperative radiative features. Using a macroscopic quantum electrodynamics approach to describe the electromagnetic field, we first obtain an analytical expression for the decay rate of the two entangled two-level atoms in terms of the Greens tensor of the generic external environment. We then investigate the emission process when both atoms are in free space and subsequently when a perfectly reflecting mirror is present, showing how the boundary affects the physical features of the superradiant and subradiant emission by the two coupled emitters. The possibility to control and tailor radiative processes is also discussed.

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.

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

We consider the dynamical atom-surface Casimir-Polder force in the nonequilibrium 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 longer than the time scale of the atomic self-dressing but shorter 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.

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 nontrivial 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.

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.

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 Greens 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 multi-layer medium, a dielectric cavity, a conducting wire and a plate with a hole.

Strong van der Waals Adhesion of a Polymer Film on Rough Substrates

We propose that chemically inert polymeric films can enhance van der Waals (vdW) forces in the same way as nanofabrication of biomimetic adhesive materials. For the vdW adhesion of an ethylene-chlorotrifluoroethylene (ECTFE) film on rough metal and dielectric substrates, we present a model that combines microscopic quantum-chemistry simulations of the polymer response functions and the equilibrium monomer-substrate distance with a macroscopic quantum-electrodynamics calculation of the Casimir force between the polymer film and the substrate. We predict adhesive forces up to 2.22 kN/mm2, where the effect is reduced by substrate roughness and for dielectric surfaces.

Body-assisted Casimir-Polder interaction between two chiral molecules

Using second-order perturbation theory with an effective Hamiltonian, we calculate the Casimir-Polder force between two ground-state chiral molecules at zero temperature in the presence of magnetodielectric bodies. In free space, the Casimir-Polder force has a small chiral component depending on both electric and magnetic transitions. With the presence of a material environment we find some configurations where the chiral contribution overcomes the purely electric contribution. We suggest also an highly symmetric configuration where the electric and magnetic contributions of the Casimir-Polder are zero, making the chiral component the dominant contribution. This is achieved via magnetoelectric plates which exhibit chiral properties. The dominant chiral Casimir-Polder force is discriminatory with respect to enantiomers of different handedness.