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arXiv:2010.03215 · Physical Review A

Collective spontaneous emission of two entangled atoms near an oscillating mirror

Marta Reina, Michelangelo Domina, Alessandro Ferreri, Giuseppe Fiscelli, Antonio Noto, Roberto Passante, Lucia Rizzuto

Published Mar 22, 2021• 4 citations
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Abstract

We consider the cooperative spontaneous emission of a system of two identical atoms interacting with the electromagnetic field in the vacuum state and in the presence of an oscillating mirror. We assume that the two atoms, one in the ground state and the other in the excited state, are prepared in a correlated (symmetric or antisymmetric) Bell-type state. We also suppose that the perfectly reflecting plate oscillates adiabatically, with the field modes satisfying the boundary conditions at the mirror surface at any given instant, so that the time dependence of the interaction Hamiltonian is entirely enclosed in the instantaneous atom-wall distance. Using time-dependent perturbation theory, we investigate the spectrum of the radiation emitted by the two-atom system, showing how the oscillation of the boundary modifies the features of the emitted spectrum, which exhibits two lateral peaks not present in the case of a static boundary. We also evaluate the transition rate to the collective ground state of the two-atom system in both cases of the superradiant (symmetric) and subradiant (antisymmetric) state. We show that it is modulated in time and that the presence of the oscillating mirror can enhance or inhibit the decay rate compared to the case of atoms in vacuum space or near a static boundary. Our results thus suggest that a dynamical (i.e., time-modulated) environment can offer further possibilities to control and manipulate radiative processes of atoms or molecules nearby, such as the cooperative decay, and strongly indicate a similar possibility for other radiative processes, for example, the resonance interaction and the energy transfer between atoms or molecules.

DOI
10.1103/physreva.103.033710

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We consider the cooperative spontaneous emission of a system of two identical atoms interacting with the electromagnetic field in the vacuum state and in the presence of an oscillating mirror. We assume that the two atoms, one in the ground state and the other in the excited state, are prepared in a correlated (symmetric or antisymmetric) Bell-type state. We also suppose that the perfectly reflecting plate oscillates adiabatically, with the field modes satisfying the boundary conditions at the mirror surface at any given instant, so that the time dependence of the interaction Hamiltonian is entirely enclosed in the instantaneous atom-wall distance. Using time-dependent perturbation theory, we investigate the spectrum of the radiation emitted by the two-atom system, showing how the oscillation of the boundary modifies the features of the emitted spectrum, which exhibits two lateral peaks not present in the case of a static boundary. We also evaluate the transition rate to the collective ground state of the two-atom system in both cases of the superradiant (symmetric) and subradiant (antisymmetric) state. We show that it is modulated in time and that the presence of the oscillating mirror can enhance or inhibit the decay rate compared to the case of atoms in vacuum space or near a static boundary. Our results thus suggest that a dynamical (i.e., time-modulated) environment can offer further possibilities to control and manipulate radiative processes of atoms or molecules nearby, such as the cooperative decay, and strongly indicate a similar possibility for other radiative processes, for example, the resonance interaction and the energy transfer between atoms or molecules.
We investigate the spontaneous emission of one atom placed near an oscillating reflecting plate. We consider the atom modeled as a two-level system, interacting with the quantum electromagnetic field in the vacuum state, in the presence of the oscillating mirror. We suppose that the plate oscillates adiabatically, so that the time-dependence of the interaction Hamiltonian is entirely enclosed in the time-dependent mode functions, satisfying the boundary conditions at the plate surface, at any given time. Using time-dependent perturbation theory, we evaluate the transition rate to the ground-state of the atom, and show that it depends on the time-dependent atom–plate distance. We also show that the presence of the oscillating mirror significantly affects the physical features of the spontaneous emission of the atom, in particular the spectrum of the emitted radiation. Specifically, we find the appearance of two symmetric lateral peaks in the spectrum, not present in the case of a static mirror, due to the modulated environment. The two lateral peaks are separated from the central peak by the modulation frequency, and we discuss the possibility to observe them with actual experimental techniques of dynamical mirrors and atomic trapping. Our results indicate that a dynamical (i.e., time-modulated) environment can give new possibilities to control and manipulate also other radiative processes of two or more atoms or molecules nearby, for example their cooperative decay or the resonant energy transfer.
Abstract 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 Green’s 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.
We analyze radiative processes of a quantum system composed by two identical two-level atoms interacting with a massless scalar field prepared in the vacuum state in the presence of perfect reflecting flat mirrors. We consider that the atoms are prepared in a stationary maximally entangled state. We investigate the spontaneous transitions rates from the entangled states to the collective ground state induced by vacuum fluctuations. In the empty-space case, the spontaneous decay rates can be enhanced or inhibited depending on the specific entangled state and changes with the distance between the atoms. Next, we consider the presence of perfect mirrors and impose Dirichlet boundary conditions on such surfaces. In the presence of a single mirror the transition rate for the symmetric state undergoes a slight reduction, whereas for the antisymmetric state our results indicate a slightly enhancement. Finally, we investigate the effect of multiple reflections by two perfect mirrors on the transition rates.
Spontaneous emission of atoms in free space is modified by the presence of other atoms in close vicinity inducing collective super- and subradiance. For two nearby atoms with a single decay channel the entangled antisymmetric superposition state of the two single excited states will not decay spontaneously. No such excited two-atom dark state exists, if the excited state has two independent optical decay channels of different frequencies or polarizations. However, we show that for an excited atomic state with N-1 independent spontaneous decay channels one can find a highly entangled N-particle dark state, which completely decouples from the vacuum radiation field. It does not decay spontaneously, nor will it absorb resonant laser light. Mathematically, we see that this state is the only such state orthogonal to the subspace spanned by the atomic ground states. Moreover, by means of generic numerical examples we demonstrate that the subradiant behavior largely survives at finite atomic distances including dipole-dipole interactions.
We consider the time-dependent resonance interaction energy between two identical atoms, one in the ground state and the other in an excited state, and interacting with the vacuum electromagnetic field, during a nonequilibrium situation such as the dynamical atomic self-dressing process. We suppose the two atoms prepared in a correlated, symmetric or antisymmetric, state. Since the atoms start from a nonequilibrium conditions, their interaction energy is time dependent. We obtain, at second order in the atom-field coupling, an analytic expression for the time-dependent resonance interaction energy between the atoms. We show that this interaction vanishes when the two atoms are outside the light cone of each other, in agreement with relativistic causality, while it instantaneously settles to its stationary value after time t=R/ct=R/ct=R/c (RRR being the interatomic distance), as obtained in a time-independent approach. We also investigate the time-dependent electric energy density in the space around the two correlated atoms, in both cases of antisymmetric (subradiant) and symmetric (super-radiant) states, during the dressing process of our two-atom system. We show that the field energy density vanishes in points outside the light cone of both atoms, thus preserving relativistic causality. On the other hand, inside the light cone of both atoms, the energy density instantaneously settles to its stationary value. Specifically, for points at equal distance from the two atoms, we find that it vanishes if the two atoms are prepared in the antisymmetric (subradiant) state, while it is enhanced, with respect to the case of atoms in a factorized state, in the symmetric (super-radiant) state. The physical meaning of these results is discussed in detail in terms of interference effects of the field emitted by the two atoms.
We investigate the resonance dipole-dipole interaction energy between two identical atoms, one in the ground state and the other in the excited state, interacting with the electromagnetic field in the presence of a perfectly reflecting plane boundary. The atoms are prepared in a correlated (symmetric or antisymmetric) Bell-type state. Following a procedure due to Dalibard et al. [J. Dalibard et al., J. Phys. (Paris) 43, 1617 (1982); J. Phys. (Paris) 45, 637 (1984)], we separate the contributions of vacuum fluctuations and radiation reaction (source) field to the resonance interaction energy between the two atoms and show that only the source field contributes to the interatomic interaction, while vacuum field fluctuations do not. By considering specific geometric configurations of the two-atom system with respect to the mirror and specific choices of dipole orientations, we show that the presence of the mirror significantly affects the resonance interaction energy and that different features appear with respect to the case of atoms in free space, for example, a change in the spatial dependence of the interaction. Our findings also suggest that the presence of a boundary can be exploited to tailor and control the resonance interaction between two atoms, as well as the related energy transfer process. The possibility of observing these phenomena is also discussed.