The cooperative spontaneous emission by a fully inverted array of N atoms, interacting with and via the radiation field is studied. The arrays to which this treatment is applicable are symmetric under the exchange of any pair of atoms, including the dipole-dipole interaction in the energy and are confined to a volume with linear dimensions that are small relative to the radiation wavelength. Analytic expressions are obtained for the populations of the levels and the intensity of emission as functions of time, and for the spectrum of the radiation emitted in the cascade to the ground state.
The cooperative spontaneous emission by a fully inverted array of N atoms, interacting with and via the radiation field is studied. The arrays to which this treatment is applicable are symmetric under the exchange of any pair of atoms, including the dipole-dipole interaction in the energy and are confined to a volume with linear dimensions that are small relative to the radiation wavelength. Analytic expressions are obtained for the populations of the levels and the intensity of emission as functions of time, and for the spectrum of the radiation emitted in the cascade to the ground state.
We present a theory of cascade emission from an array of N fixed, ``three-level'' atoms. The total angular momentum of the ground state of each atom is J=0, that of the intermediate state is J=1, and that of the upper state is J=0. The atoms are prepared in a spatially phased superposition of their ground and upper states, collectively sharing a single excitation. We calculate the time-integrated, joint probability distribution for radiation to be emitted in a given direction with a given polarization on each transition and use this joint probability distribution to calculate the time-integrated intensity emitted on each transition. The dipole-dipole interaction between the atoms is taken into account. Analytic expressions are obtained for two atoms and the calculation is then extended formally to an ensemble of N atoms at arbitrary positions. As expected, the radiation emitted on the upper transition is unpolarized and isotropic. However, somewhat surprisingly, we find that for excitation by counterpropagating fields and for nearly equal ground to intermediate and intermediate to upper level transition frequencies, the radiation on the lower transition is also isotropic and unpolarized, provided the atoms are prepared in a fully symmetric state. We also establish conditions for which there can be a phase-matched enhancement of the joint probability density for specific directions of emissions on the upper and lower transitions.
For pt.II see ibid., vol.19, p.2109 (1986). This paper is the third in a theoretical study of subradiance, i.e. the cooperative inhibition of spontaneous emission by a destructive interatomic interference, a phenomenon which has recently been observed. The paper is devoted to the problem of the cooperative spontaneous emission of atomic samples with linear dimensions much smaller than the wavelength of the emitted light. The treatment, which is based on a fully quantum mechanical description of the problem, corroborates the results obtained in a semiclassical treatment by Friedberg and Hartmann (1974). Starting from a master equation describing both the cooperative spontaneous emission and the dipole-dipole interaction, a statistical treatment of the latter is introduced and the corresponding symmetry relaxation is studied. The evolution of the atoms is described in three typical cases that correspond to different sample geometries and/or atomic distributions. In one of these cases, in particular, the symmetry is first conserved and the atoms follow Dicke's predictions for a time. A 'retarded' symmetry breaking then occurs suddenly, near the zero value of the collective energy, as in Friedberg and Hartmann's calculations for a small sphere. With regard to the further evolution of the atoms in this case, which cannot be studied in a semiclassical model, it is shown that the decay rate quickly becomes much smaller than the incoherent decay rate. An unquestionable subradiance phenomenon is thus predicted in this case.
Using the formalism developed earlier, we treat spontaneous emission from a pair of identical two-level atoms A1, A2, whose separation r21 can be comparable to the wavelength $\ensuremath{\lambda}$. We obtain expressions for time-dependent intensities and damping rates with the initial conditions (a) both atoms inverted, (b) prior excitation by a short $\frac{1}{2}\ensuremath{\pi}$ pulse, and (c) only A1 inverted. The results in (a) are compared with those obtained for a model consisting of two initially excited harmonic oscillators O1, O2. The atoms exhibit superradiant behavior, whereas O1, O2 tend to trap radiation. In (a), the intensity pattern $\mathcal{R}(\ensuremath{\theta},t)$ develops lobes in different directions at different times, so that the spatial distribution of photons at time $t\ensuremath{\rightarrow}\ensuremath{\infty}$ is the same as in the independent-atom case ${r}_{21}\ensuremath{\gg}\ensuremath{\lambda}$. For the oscillators, the lobes of $\mathcal{R}(\ensuremath{\theta},t)$ do not change direction, but only become more pronounced as time increases. In (b) and (c), the lobes oscillate back and forth at frequency $2{\ensuremath{\Omega}}_{12}$ corresponding to the shifts $\ifmmode\pm\else\textpm\fi{}{\ensuremath{\Omega}}_{12}$ of the triplet and singlet states due to the ${A}_{1}\ensuremath{-}{A}_{2}$ interaction. The intensity can therefore have a sinusoidal component. Field correlation functions calculated for (a) and (c) show that A2 and A2 radiate simultaneously around the frequencies $\ensuremath{\epsilon}\ifmmode\pm\else\textpm\fi{}{\ensuremath{\Omega}}_{12}$, where $\ensuremath{\epsilon}$ is the single-atom resonant frequency. The spectrum is calculated for case (c), and shows the effects of coherent linewidth enhancement in addition to the frequency shifts.
When atoms are coupled to a common electromagnetic environment, the exchange of photons through dipole-dipole interactions leads to the emergence of cooperative effects. As a particular example, superradiance arises from spontaneous emission when this exchange leads to constructive interference of the emitted photons. Here, we introduce an integrated method for studying cooperative radiation in many-body systems. This method, which allows to study extended systems with arbitrarily large number of particles, can be formulated by an effective, nonlinear, two-atom master equation that describes the dynamics using a closed form which treats single- and many-body terms on an equal footing. We apply this method to a homogeneous gas of initially inverted two-level atoms, and demonstrate the appearance of both superradiance and subradiance, identifying a many-body coherence term as the source of these cooperative effects. We describe the many-body induced broadening -- which is analytically found to scale with the optical depth of the system -- and light shifts, and distinguish spontaneous effects from induced ones. In addition, we theoretically predict the time-dependence of subradiance, and the phase change of the radiated field during the cooperative decay.
The spontaneous emission of a set of N identical two-level atoms interacting with a quantized electromagnetic field is studied. The atoms are assumed to be close together compared to the mean wavelength of the emitted radiation, and their initial state is either a Dicke state or a superposition of the ground and excited state for each atom. Approximate expressions are obtained for transition probabilities, expectation values, and correlations as functions of time. The spontaneous emission for a very large separation of the atoms is also studied. In this case the directional properties of the emitted radiation, as well as the time within which the atoms decay to their ground state, depend on the position of each atom.
Abstract Using Lehmberg's master equation and taking into account dipole‐dipole near‐field interaction the time‐dependent intensity pattern, intensity – and angular correlations of the cooperative spontaneous radiation from an initially fully excited system of three identical two‐level atoms are calculated. The intensity pattern developes lobes in different directions at different times in such a way that contrary to the two‐atom system the spatial distribution of the total number of the emitted photons differs from that of the single‐atom radiation pattern. In particular three atoms placed in proper distances on a straight line emit preferentially their energy along this line. At the beginning of the emission process the probability to find two photons simultaneously in the same (or geometrical equivalent) direction is always highest but in the course of time, contrary to the two‐atom case, it may well happen that the probability of finding two photons in quite different directions becomes more favoured.