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arXiv:1807.11430 · Physical Review A

Time-dependent resonance interaction energy between two entangled atoms under nonequilibrium conditions

Giuseppe Fiscelli, Roberta Palacino, Roberto Passante, Lucia Rizzuto, Salvatore Spagnolo, Wenting Zhou

Published Oct 15, 2018• 3 citations
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Abstract

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 $t=R/c$ ($R$ 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.

DOI
10.1103/physreva.98.042506

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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.
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Abstract We consider the resonance interaction energy between two identical entangled atoms, where one is in the excited state and the other in the ground state. They interact with the quantum electromagnetic field in the vacuum state and are placed in a photonic-bandgap environment with a dispersion relation quadratic near the gap edge and linear for low frequencies, while the atomic transition frequency is assumed to be inside the photonic gap and near its lower edge. This problem is strictly related to the coherent resonant energy transfer between atoms in external environments. The analysis involves both an isotropic three-dimensional model and the one-dimensional case. The resonance interaction asymptotically decays faster with distance compared to the free-space case, specifically as 1/r2 compared to the 1/r free-space dependence in the three-dimensional case, and as 1/r compared to the oscillatory dependence in free space for the one-dimensional case. Nonetheless, the interaction energy remains significant and much stronger than dispersion interactions between atoms. On the other hand, spontaneous emission is strongly suppressed by the environment and the correlated state is thus preserved by the spontaneous-decay decoherence effects. We conclude that our configuration is suitable for observing the elusive quantum resonance interaction between entangled 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.
We apply the DDC formalism [proposed by Dalibard, Dupont-Roc and Cohen-Tannoudji] to study the average rate of change of energy of two identical two-level atoms interacting with the vacuum massless scalar field in synchronized motion along stationary trajectories. By separating the contributions of vacuum fluctuations and atomic radiation reaction, we first show that for the two-atom system initially prepared in the factorizable eigenstates ∣gAgB⟩|{g}_{A}{g}_{B}⟩∣gA​gB​⟩ and ∣eAeB⟩|{e}_{A}{e}_{B}⟩∣eA​eB​⟩, where ggg and eee represent the ground state and the excited state of a single atom, respectively, both vacuum fluctuations and atomic radiation reaction contribute to the average rate of change of energy of the two-atom system, and the contribution of vacuum fluctuations is independent of the interatomic separation while that of atomic radiation reaction is dependent on it. This is contrary to the existing results in the literature where vacuum fluctuations are interatomic-separation dependent. However, if the two-atom system is initially prepared in the unfactorizable symmetric/antisymmetric entangled state, the average rate of change of energy of the two-atom system is never perturbed by the vacuum fluctuations, but is totally a result of the atomic radiation reaction. We then consider two special cases of motion of the two-atom system, which is initially prepared in the symmetric/antisymmetric entangled state, i.e., synchronized inertial motion and synchronized uniform acceleration. In contrast to the average rate of change of energy of a single uniformly accelerated atom, the average rate of change of energy of the uniformly accelerated two-atom system is nonthermal-like. The effects of noninertial motion on the transitions of states of the two correlated atoms are also discussed.
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