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arXiv:1702.00438 · Physical Review A

Dipole-dipole interaction in cavity QED: The weak-coupling, nondegenerate regime

M. Donaire, J. M. Munõz-Castañeda, Luis Miguel Nieto

Published Oct 24, 2017• 20 citations
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Abstract

We compute the energies of the interaction between two atoms placed in the middle of a perfectly reflecting planar cavity, in the weak-coupling nondegenerate regime. Both inhibition and enhancement of the interactions can be obtained by varying the size of the cavity. We derive exact expressions for the dyadic Green's function of the cavity field which mediates the interactions and apply time-dependent quantum perturbation theory in the adiabatic approximation. We provide explicit expressions for the van der Waals potentials of two polarizable atomic dipoles and the electrostatic potential of two induced dipoles. We compute the van der Waals potentials in three different scenarios: two atoms in their ground states, two atoms excited, and two dissimilar atoms with one of them excited. In addition, we calculate the phase-shift rate of the two-atom wave function in each case. The effect of the two-dimensional confinement of the electromagnetic field on the dipole-dipole interactions is analyzed. This effect depends on the atomic polarization. For dipole moments oriented parallel to the cavity plates, both the electrostatic and the van der Waals interactions are exponentially suppressed for values of the cavity width much less than the interatomic distance, whereas for values of the width close to the interatomic distance, the strength of both interactions is higher than their values in the absence of cavity. For dipole moments perpendicular to the plates, the strength of the van der Waals interaction decreases for values of the cavity width close to the interatomic distance, while it increases for values of the width much less than the interatomic distance with respect to its strength in the absence of cavity. We illustrate these effects by computing the dipole-dipole interactions between two alkali atoms in circular Rydberg states.

DOI
10.1103/physreva.96.042714

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Physical Review A•Sep 21, 2017•13 citations
We compute the energies of the interaction between two atoms placed in the middle of a perfectly reflecting planar cavity, in the weak-coupling nondegenerate regime. Both inhibition and enhancement of the interactions can be obtained by varying the size of the cavity. We derive exact expressions for the dyadic Green's function of the cavity field which mediates the interactions and apply time-dependent quantum perturbation theory in the adiabatic approximation. We provide explicit expressions for the van der Waals potentials of two polarizable atomic dipoles and the electrostatic potential of two induced dipoles. We compute the van der Waals potentials in three different scenarios: two atoms in their ground states, two atoms excited, and two dissimilar atoms with one of them excited. In addition, we calculate the phase-shift rate of the two-atom wave function in each case. The effect of the two-dimensional confinement of the electromagnetic field on the dipole-dipole interactions is analyzed. This effect depends on the atomic polarization. For dipole moments oriented parallel to the cavity plates, both the electrostatic and the van der Waals interactions are exponentially suppressed for values of the cavity width much less than the interatomic distance, whereas for values of the width close to the interatomic distance, the strength of both interactions is higher than their values in the absence of cavity. For dipole moments perpendicular to the plates, the strength of the van der Waals interaction decreases for values of the cavity width close to the interatomic distance, while it increases for values of the width much less than the interatomic distance with respect to its strength in the absence of cavity. We illustrate these effects by computing the dipole-dipole interactions between two alkali atoms in circular Rydberg states.
We establish, within the second quantization method, the general dipole-dipole Hamiltonian interaction of a system of nnn-level atoms. The variational energy surface of the nnn-level atoms interacting with $\ensuremath{\ell}$-mode fields and under the Van Der Waals forces is calculated with respect to the tensorial product of matter and electromagnetic field coherent states. This is used to determine the quantum phase diagram associated with the ground state of the system and quantify the effect of the dipole-dipole Hamiltonian interaction. By considering real induced electric dipole moments, we find the quantum phase transitions for 2- and 3-level atomic systems interacting with one and two modes of the electromagnetic field, respectively. The corresponding order of the transitions is established by means of Ehrenfest classification; for undetermined cases, we propose two procedures: one based on the difference of the expectation value of the Casimir operators of the 2-level subsystems, and another based on maximizing the Bures distance between neighbor variational solutions.
The London-van der Waals potential experienced by an atom under reflection from an atomic mirror is modeled as a quantum dipole-dipole interaction between the atomic dipole induced by the evanescent wave and its image dipole in the dielectric mirror. The quantum dipole-dipole interaction arises from the combined effect of the evanescent field and spontaneous emission. It depends on the electronic structure of the atom and is described by an effective non-Hermitian Hamiltonian that yields dissipative effects under reflection. The analytical expression obtained here preserves the power-law dependence of the static van der Waals interaction at distances close to the wall, but its long-distance behavior reflects that of the evanescent wave.
With the use of second-order perturbation theory in the long-range interatomic interaction for the degenerate states of two Rydberg atoms we have obtained a general formula for the dependence of atomic interaction energy on the interatomic distance R in the presence of the Förster resonance. Inside of the ‘Förster sphere’ ( R < R F ) this dependence transforms to the formula for electric dipole interaction energy Δ E d − d = C 3 / R 3 and for R > R F it transforms to the formula for the van der Waals interaction energy Δ E VdW = − C 6 / R 6 . The van der Waals constant C 6 is represented as an expansion in terms of irreducible components which define the dependence on the interatomic axis orientation relative to the quantisation axis of projections M of the total angular momentum J . The numerical values of the irreducible components of tensor C 6 were calculated for rubidium atoms in the same Rydberg states | nlJM 〉 with large quantum numbers n . We present the calculated resonance interaction energy of two rubidium atoms in the states |43D 5/2 M 〉, whose total energy exceeds by only 8 MHz the total energy of one of the atoms in the state |45P 3/2 M 〉 and of the other in the state |41F 7/2 M 〉.
Abstract We consider the resonant van der Waals (vdW) interaction between two correlated identical two-level atoms (at least one of which being excited) within the framework of macroscopic cavity quantum electrodynamics in linear, dispersing and absorbing media. The interaction of both atoms with the body-assisted electromagnetic field of the cavity is assumed to be strong. Our time-independent evaluation is based on an extended Jaynes–Cummings model. For a system prepared in a superposition of its dressed states, we derive the general form of the vdW forces, using a Lorentzian single-mode approximation. We demonstrate the applicability of this approach by considering the case of a planar cavity and showing the position dependence of Rabi oscillations. We also show that in the limiting case of weak coupling, our results reproduce the perturbative ones for the case where the field is initially in vacuum state while the atomic state is in a superposition of two correlated states sharing one excitation.
Abstract We study many-atom van der Waals (vdW) forces arising from reversible atom–field interactions in cavity quantum electrodynamics by using a dressed-state approximation. In the most general case, a single-mode Dicke model for atoms, sharing an arbitrary number of excitations, placed in an imperfect cavity, has been developed that leads to the vdW potential of such a system. As special cases, we consider the single-excitation Dicke model and also the case of one atom in the presence of multi-photon excitation inside the cavity. In most of the paper, it is assumed that the atoms are distributed symmetrically with respect to the mode structure. This will decouple all asymmetric states, allowing us to ignore them throughout our calculations. The impact of asymmetric states is taken into account for a system wherein one atom, freely placed in a cavity, together with n − 1 equally-coupled atoms, is interacting with the cavity field. By assuming broadened Lorentzian modes instead of sharp ones, the cavity imperfections have been added to the calculations. The position dependence of the effective Rabi frequency is studied for the example of a planar cavity.
The van der Waals coefficient ${C}_{6}(\ensuremath{\theta};nlJM)$ of two like Rydberg atoms in their identical Rydberg states $|nlJM\ensuremath{\rangle}$ is resolved into four irreducible components called scalar Rss{R}_{ss}Rss​, axial (vector) Raa{R}_{aa}Raa​, scalar-tensor RsT=RTs{R}_{sT}={R}_{Ts}RsT​=RTs​, and tensor-tensor RTT{R}_{TT}RTT​ parts in analogy with the components of dipole polarizabilities. The irreducible components determine the dependence of ${C}_{6}(\ensuremath{\theta};nlJM)$ on the angle $\ensuremath{\theta}$ between the interatomic and the quantization axes of atoms. The spectral resolution for the biatomic Green's function with account of the most contributing terms is used for evaluating the components ${R}_{\ensuremath{\alpha}\ensuremath{\beta}}$ of atoms in their Rydberg series of doublet states of the low angular momenta (2S,2P,2D,2F^{2}S, ^{2}P, ^{2}D, ^{2}F2S,2P,2D,2F). The polynomial presentations in powers of the Rydberg-state principal quantum number nnn taking into account the asymptotic dependence ${C}_{6}(\ensuremath{\theta};nlJM)\ensuremath{\propto}{n}^{11}$ are derived for simplified evaluations of irreducible components. Numerical values of the polynomial coefficients are determined for Rb atoms in their n2S1/2,n2P1/2,3/2,n2D3/2,5/2n{\phantom{\rule{0.222222em}{0ex}}}^{2}{S}_{1/2}, n{\phantom{\rule{0.222222em}{0ex}}}^{2}{P}_{1/2,3/2}, n{\phantom{\rule{0.222222em}{0ex}}}^{2}{D}_{3/2,5/2}n2S1/2​,n2P1/2,3/2​,n2D3/2,5/2​, and n2F5/2,7/2n{\phantom{\rule{0.222222em}{0ex}}}^{2}{F}_{5/2,7/2}n2F5/2,7/2​ Rydberg states of arbitrary high nnn. The transformation of the van der Waals interaction law $\ensuremath{-}{C}_{6}/{R}^{6}$ into the dipole-dipole law C3/R3{C}_{3}/{R}^{3}C3​/R3 in the case of close dipole-connected two-atomic states (the F\"orster resonance) is considered and the dependencies on the magnetic quantum numbers MMM and on the angle $\ensuremath{\theta}$ of the constant ${C}_{3}(\ensuremath{\theta};nlJM)$ are determined together with the ranges of interatomic distances RRR, where the transformation appears.