Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

Physical Review A

Two-atom fluorescence spectrum with dipole interaction and finite detuning

J. G. Cordes, Winston Roberts

Published Jun 1, 1984• 5 citations
Publisher

Abstract

The exact fluorescence spectrum for two atoms in a monochromatic driving field is analyzed. The dipole-dipole interaction is treated in the small-sample approximation, and finite detuning from the atomic resonance is also allowed for. The terms dominating the high-field spectrum are given explicitly, as well as a Lorentzian decomposition valid for the case of well-separated peaks.

DOI
10.1103/physreva.29.3437

Related papers

Two-atom resonance fluorescence

Marek Kuś, K. Wódkiewicz

Resonance-fluorescence power spectrum of two-level atoms driven by a strong monochromatic laser field is discussed, taking into account effects due to the dipole-dipole interaction between the atoms. For two atoms confined to a region smaller than the wavelength of the driving field, we predict significant deviations of the power spectrum from the single-atom case. The two-atom spectrum is nonsymmetric, the wing peaks are shifted from their Rabi-frequency positions, and additional maxima may appear.

Physical Review A•Feb 1, 1981•39 citations

Analytical solution for the two-atom fluorescence spectrum with finite detuning

J. G. Cordes, Calum E. MacAulay

The two-atom fluorescence spectrum with finite detuning is calculated analytically. For large field strengths, a Lorentzian decomposition is presented which exhibits the presence of two-component peaks at the central peak and at the Rabi sidebands; thus finite detuning destroys the proportionality to the one-atom spectrum. The analytical solution for the incoherent part of the spectrum is also obtained and a peculiarity of its weak-field behavior is pointed out.

Physical Review A•Sep 1, 1982•12 citations

Two-atom resonance fluorescence

Constantine Mavroyannis

The excitation spectrum arising from the interaction between two identical atoms (molecules), one of which is excited in the presence of a resonant strong electromagnetic field (pump field), is investigated. The excitation spectrum is found to consist of those describing the symmetric and antisymmetric modes, respectively. The form of both spectra depends on the relation between the distance $R$ separating the atoms and the wavelength $\ensuremath{\lambda}$ of the transition from the ground state to the excited state. For $R<\ensuremath{\lambda}$, and when certain conditions prevail, the spectral function for the symmetric modes consists of three Lorentzian lines describing the central peak and the two sidebands whose radiative widths are equal to ${\ensuremath{\gamma}}_{0}$, $\frac{3{\ensuremath{\gamma}}_{0}}{2}$, and $\frac{3{\ensuremath{\gamma}}_{0}}{2}$, which are twice the corresponding ones arising from an isolated single atom interacting with the pump field. For the antisymmetric modes the central peak has a $\ensuremath{\delta}$-function distribution indicating the stability of the mode in question, while, when certain conditions are satisfied, the two sidebands are described by Lorentzian lines each having a radiative width of the order of $\frac{{\ensuremath{\gamma}}_{0}}{2}$, which is equal to the natural linewidth for a photon spontaneously emitted from an isolated atom. For both the symmetric and antisymmetric modes, the dipole-dipole interaction between the atoms brings about small energy shifts. For $R>\ensuremath{\lambda}$, apart from the small energy shifts caused by the dipole-dipole interaction, the spectral functions for symmetric and antisymmetric modes are similar to that for the single atom interacting with the pump field.

Physical Review A•Jul 1, 1978•70 citations

Collective atomic effects in resonance fluorescence: Dipole-dipole interaction

Helen S. Freedhoff

The resonance fluorescence of a two-atom system interacting collectively with an intense driving field is studied. The first-order dispersion forces, or dipole-dipole interaction, between the atoms is included as well. The scattered-light spectrum is found to differ considerably from the single-atom spectrum even for very intense driving fields, in direct contrast with the results obtained by Agarwal et al., who studied the two-atom system but neglected the dipole-dipole interaction. The effects of collective scattering are calculated on the fluorescence spectra of idealized beams of atoms moving with uniform velocity, for a number of different number densities $〈N〉$.

Physical Review A•Mar 1, 1979•58 citations

Effect of Detuning on Squeezing in Two-atom Resonance Fluorescence

Thomas Richter

The exact steady-state solution is presented for the reduced atomic density operator describing the cooperative resonance fluorescence from a system of two atoms separated by an arbitrary distance in an off-resonance laser field, with the dipole-dipole near-field interaction between the atoms included. It is shown that the destructive effect of the dipole-dipole interaction on the formation of squeezing in two-atom resonance fluorescence found recently by Ficek et al. can be compensated to a very large extent by an appropriate choice of the detuning between the laser frequency and the single-atom transition frequency.

Optica Acta International Journal of Optics•Sep 1, 1984•8 citations

Two-atom resonance fluorescence including the dipole-dipole interaction

R. D. Griffin, Samuel M. Harris

The spectrum of resonance fluorescence and the second-order correlation function are calculated for a system of two identical two-level cooperative systems interacting via the dipole-dipole interaction. The results are valid for arbitrary incident-field strengths and for atomic separations much less than the resonant wavelength. The intensity of the sidebands at the Rabi frequency is diminished by the dipole interaction, whereas that of the sidebands at twice the Rabi frequency is enhanced. Both the cooperative behavior and the dipole-dipole interaction act to diminish the photon antibunching, as shown by the second-order correlation function.

Physical Review A•Mar 1, 1982•29 citations
The exact fluorescence spectrum for two atoms in a monochromatic driving field is analyzed. The dipole-dipole interaction is treated in the small-sample approximation, and finite detuning from the atomic resonance is also allowed for. The terms dominating the high-field spectrum are given explicitly, as well as a Lorentzian decomposition valid for the case of well-separated peaks.
Resonance-fluorescence power spectrum of two-level atoms driven by a strong monochromatic laser field is discussed, taking into account effects due to the dipole-dipole interaction between the atoms. For two atoms confined to a region smaller than the wavelength of the driving field, we predict significant deviations of the power spectrum from the single-atom case. The two-atom spectrum is nonsymmetric, the wing peaks are shifted from their Rabi-frequency positions, and additional maxima may appear.
The excitation spectrum arising from the interaction between two identical atoms (molecules), one of which is excited in the presence of a resonant strong electromagnetic field (pump field), is investigated. The excitation spectrum is found to consist of those describing the symmetric and antisymmetric modes, respectively. The form of both spectra depends on the relation between the distance RRR separating the atoms and the wavelength $\ensuremath{\lambda}$ of the transition from the ground state to the excited state. For $R<\ensuremath{\lambda}$, and when certain conditions prevail, the spectral function for the symmetric modes consists of three Lorentzian lines describing the central peak and the two sidebands whose radiative widths are equal to ${\ensuremath{\gamma}}_{0}$, $\frac{3{\ensuremath{\gamma}}_{0}}{2}$, and $\frac{3{\ensuremath{\gamma}}_{0}}{2}$, which are twice the corresponding ones arising from an isolated single atom interacting with the pump field. For the antisymmetric modes the central peak has a $\ensuremath{\delta}$-function distribution indicating the stability of the mode in question, while, when certain conditions are satisfied, the two sidebands are described by Lorentzian lines each having a radiative width of the order of $\frac{{\ensuremath{\gamma}}_{0}}{2}$, which is equal to the natural linewidth for a photon spontaneously emitted from an isolated atom. For both the symmetric and antisymmetric modes, the dipole-dipole interaction between the atoms brings about small energy shifts. For $R>\ensuremath{\lambda}$, apart from the small energy shifts caused by the dipole-dipole interaction, the spectral functions for symmetric and antisymmetric modes are similar to that for the single atom interacting with the pump field.
The resonance fluorescence of a two-atom system interacting collectively with an intense driving field is studied. The first-order dispersion forces, or dipole-dipole interaction, between the atoms is included as well. The scattered-light spectrum is found to differ considerably from the single-atom spectrum even for very intense driving fields, in direct contrast with the results obtained by Agarwal et al., who studied the two-atom system but neglected the dipole-dipole interaction. The effects of collective scattering are calculated on the fluorescence spectra of idealized beams of atoms moving with uniform velocity, for a number of different number densities 〈N〉〈N〉〈N〉.
The exact steady-state solution is presented for the reduced atomic density operator describing the cooperative resonance fluorescence from a system of two atoms separated by an arbitrary distance in an off-resonance laser field, with the dipole-dipole near-field interaction between the atoms included. It is shown that the destructive effect of the dipole-dipole interaction on the formation of squeezing in two-atom resonance fluorescence found recently by Ficek et al. can be compensated to a very large extent by an appropriate choice of the detuning between the laser frequency and the single-atom transition frequency.
The spectrum of resonance fluorescence and the second-order correlation function are calculated for a system of two identical two-level cooperative systems interacting via the dipole-dipole interaction. The results are valid for arbitrary incident-field strengths and for atomic separations much less than the resonant wavelength. The intensity of the sidebands at the Rabi frequency is diminished by the dipole interaction, whereas that of the sidebands at twice the Rabi frequency is enhanced. Both the cooperative behavior and the dipole-dipole interaction act to diminish the photon antibunching, as shown by the second-order correlation function.