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Physical Review A

Collective-resonance fluorescence in an ideal cavity

H. M. Castro-Beltrán, J. J. Sánchez-Mondragón, S. M. Chumakov

Published Jun 1, 1996• 12 citations
Publisher

Abstract

We study cooperative properties of the emission spectrum of A two-level atoms interacting with a quantized field in a lossless cavity. We show, in a unified treatment, the system anharmonicity, the fine structure, and size of the spectral bands. Further, we show that for an initially inverted atomic system and a thermal cavity field the atomic cooperativity allows the merging of well-defined sidebands, absent in the single-atom case. Thus the cooperativity reduces the destructive effect of the large dispersion of the blackbody photon distribution. For an increasing number of atoms, the central band is split into a doublet. The dip in the doublet is filled when the cavity field is very strong. Also, the extra sidebands have smaller amplitudes than the time-dependent contributions to the spectrum. \textcopyright{} 1996 The American Physical Society.

DOI
10.1103/physreva.53.4420

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We study cooperative properties of the emission spectrum of A two-level atoms interacting with a quantized field in a lossless cavity. We show, in a unified treatment, the system anharmonicity, the fine structure, and size of the spectral bands. Further, we show that for an initially inverted atomic system and a thermal cavity field the atomic cooperativity allows the merging of well-defined sidebands, absent in the single-atom case. Thus the cooperativity reduces the destructive effect of the large dispersion of the blackbody photon distribution. For an increasing number of atoms, the central band is split into a doublet. The dip in the doublet is filled when the cavity field is very strong. Also, the extra sidebands have smaller amplitudes than the time-dependent contributions to the spectrum. \textcopyright{} 1996 The American Physical Society.
We investigate correlations among photons from the components of the resonance fluorescence spectrum of a cooperative system of two-level atoms interacting with a strong field of a single-mode lossless cavity. The properties of the central band are more closely related to the superradiant effect in free space than the sidebands. The central band field has reduced fluctuations and the collective dipole has its largest uncertainty when half the atoms are initially excited. Partial atomic excitation destroys the sub-Poissonian character of the sideband field and leads to a bunching-antibunching transition in the correlation of a sideband photon followed by a central band photon.
The resonance fluorescence spectrum of one and two two-level atoms in an ideal cavity with one resonant mode is investigated as a function of the initial excitation of the system. The analysis is carried out in the Stark representation with respect to the cavity's field and in first-order perturbation theory with respect to the fluorescence field. In the absence of the field of the cavity (n c = 0) and under an initial excitation of one atom only, the spectrum consists of two lines which are symmetrical with respect to ωa. In all other cases the spectrum has a central line at ωa and other lines at ωa ± 2 Ω. The intensity of the higher (ωa ± 4 Ω) harmonics is small and decreases as 1/ 2 c c with increasing n>c. The nonlinearity of the interaction hamiltonian results in the parametric (with respect to the field of the cavity) amplification of the ωa + 2 Ω harmonic and the attenuation of the ωa − 2 Ω harmonic. The stimulated emission of the ωa ± 2 Ω harmonics, vanishing in a strong (n c » 1) field, is shown to exist for two atoms.
We report on the semiclassical solution of the Bloch equations for cooperative resonance fluorescence with collective damping. These equations are shown to be equivalent to the relevant master equation, in the limit of large cooperation number and time scales faster than the one-atom lifetime (reciprocal Einstein AAA coefficient). The resulting spectrum is derived for a coherent driving field of arbitrary intensity. Additional spectral peaks, as well as the central triplet, are predicted above threshold. A physical explanation of the extra peaks is proposed.
By using the method of eigenvalues and eigenstates, the emission and cavity-field spectra of a cascade three-level atom interacting with a single-mode electromagnetic field are studied in both intensity-dependent coupling (IDC) and intensity-independent coupling (IIC) cases. The photon statistics of the field on the spectra are investigated for the initial field in the pure number state, the coherent state and the thermal state. In the resonant case and the strong field limit, the pure-number-state emission spectrum exhibits six peaks and three peaks, respectively, for the IDC case and the IIC case. For a strong initial coherent state field or a strong thermal state field, the central structure of the emission spectrum at the field frequency is a doublet in the IDC case and a singlet in the IIC case. The cavity-field spectrum has three peaks in the IDC case and a single peak in the IIC case in the strong field limit for all of the three kinds of initial fields considered. Results indicate that in the emission spectrum merging of spectral peaks occurs for the IIC case as the initial field becomes stronger while it does not happen for the IDC case.
The nonperturbative theory of the cooperative spontaneous emission from a two level atom trapped in one-dimentional damped nanocavity with a single resonance mode is presented. The time-dependent spectral properties and nonlinear dynamics of a separate photon emission by the micro-molecular-like system "excited atom coupled to a resonance decaying mode" have been analyzed. The investigation has been carried out by solving the Schrödinger equation in the interaction picture with the help of the Green functions method in the Heitler-Ma's form. The formalism was supplemented with the novel algorithm in operating causal singular functions and with fundamentals of the theory of quasi-stationary systems. The proposed theory accounts automatically of both reabsorptions of emitted photon and its simultaneous escaping out of the cavity. Solutions of the wave equation were found without using intermediate virtual states and series expansions. In accordance with the theory of quasi-stationary systems the field of mode decaying exponentially in the empty nanocavity was represented with the Lorenz-shaped packet of stationary photonic states (quasi-modes). The electro-dipolar interaction between the atom and the mode field was adopted to be switched on suddenly. The expressions and plots of emission probabilities spectral densities together with photon emission probability dynamics as functions of time for various ratios Γ/4g of photon escaping rate Γ and coupling constant g are presented. For Γ/4g <1 the transient emission spectrum reveals the presence of two symmetrical side-bands and of the central peak, the latter decaying in time at the rate ∝ Γ/2 so that the final spectrum is a doublet. In this case the photon emission probability is described by decaying oscillations. On the contrary for Γ/4g ≥ 1 the spectrum is a singlet and the emission occurs in exponentially decaying ways.
The emission spectrum of a pair of two-level atoms interacting with a single mode of radiation field in an ideal cavity is investigated, where the interaction of each atom with the field may be different. A general expression for the emission spectrum is presented and the spectrum is studied numerically when the radiation field is initially in the vacuum state, pure number state and squeezed-vacuum state, respectively. The effects of the ratio of two coupling constants (R=g 2 /g 1 ) on the emission spectrum are discussed. In contrast with the spectrum of a one-atom system, the spectrum of a two-atom system is much more complicated. Generally, the emission spectrum shows a 12-peak structure for the vacuum state and 16-peak structure for the pure number state. For the squeezed-vacuum state, it is found that the Rabi splitting is most apparent when R=1.