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Physica A Statistical Mechanics and its Applications

Superradiance and energy transfer within a system of atoms

James P. Stone, Abraham Nitzan, John Ross

Published Jan 1, 1976• 2 citations
Publisher
DOI
10.1016/0378-4371(76)90062-5

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Dicke's superradiance from a gas system of atoms and molecules was described in terms of two-level atoms, i.e., as an assembly of half-spin operators. In this system the magnitude of the total spin, which is called a cooperation number, is conserved at the maximum for the whole radiative process. We will answer in this paper how this superradiance is modified in the crystal in which an excitation can propagate from atom to atom through dipolar interactions. As a prototype of a crystal, we choose a linear chain of two-level atoms. The superradiance master equation of this system can be solved in terms of the exact solution of Lieb, Shultz, and Mattis for the spin system. The first effect is that the emitted frequency shows opposite shifts red and blue, respectively, for the first and second halves of the superradiance pulse, or vice versa, depending upon the sign of the transfer-matrix element of the excitation. The second effect is the appearance of a slow component in the emission tail, which originates from mixture of the states with smaller cooperation numbers or smaller oscillator strength under the transfer of the excitations. These results are demonstrated for a mesoscopic system of linear chains.

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Femtosecond pump-probe studies of atomic hydrogen superfluorescence in flames

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We investigate the excited-state dynamics of hydrogen (H) atoms in flames by using a femtosecond (fs) pump-probe scheme and measuring directional emission signals. An approximately 100-fs pump pulse at 205.1 nm excites H atoms through a two-photon process (n = 3 ←← n = 1), which is followed by detection of the forward emission signals induced by a broadband fs probe pulse near 656 nm. Above a certain threshold, we observe a quadratic dependence of the emission signal on the pump laser energy. Moreover, the linewidth of the forward emission signal varies with the probe delay and the probe laser energy. This behavior can be explained in terms of superradiance. We perform a theoretical analysis and compare the experimental results with the theory, and conclude that, within the conditions of our experiment, the behavior of the atomic system involves atomic coherence, which is produced non-adiabatically and corresponds to a superradiant process. Variations in the duration of the gain time window and lifetime of the excited-state H atoms in flames are explored at different flame conditions (i.e., equivalence ratio and heights above the burner). The fs pump-probe technique demonstrated here can also be extended to characterize the time-resolved population dynamics and the corresponding collisional energy transfer rates for energy levels involved in laser-induced fluorescence detection of H atoms in flames relevant to practical combustion applications.

Applied Physics Letters•May 18, 2020•6 citations
Dicke's superradiance from a gas system of atoms and molecules was described in terms of two-level atoms, i.e., as an assembly of half-spin operators. In this system the magnitude of the total spin, which is called a cooperation number, is conserved at the maximum for the whole radiative process. We will answer in this paper how this superradiance is modified in the crystal in which an excitation can propagate from atom to atom through dipolar interactions. As a prototype of a crystal, we choose a linear chain of two-level atoms. The superradiance master equation of this system can be solved in terms of the exact solution of Lieb, Shultz, and Mattis for the spin system. The first effect is that the emitted frequency shows opposite shifts red and blue, respectively, for the first and second halves of the superradiance pulse, or vice versa, depending upon the sign of the transfer-matrix element of the excitation. The second effect is the appearance of a slow component in the emission tail, which originates from mixture of the states with smaller cooperation numbers or smaller oscillator strength under the transfer of the excitations. These results are demonstrated for a mesoscopic system of linear chains.
In this paper, we study the superradiant decay of an ensemble of inverted two-level atoms embedded into a continuous dielectric and a two-dimensional (2-D) photonic crystal with lateral confinement of the radiation. The nonlinear superradiance pulse characteristics are calculated using a Green's-function-based model. Specifically, we predict fast phase synchronization across the ensemble that builds up a distributed feedback structure responsible for the superradiation anisotropic emission and the directional switching. We show that the transfer of the optical excitation takes place along the Bragg planes and is manifested by strong energy localization.
We investigate the excited-state dynamics of hydrogen (H) atoms in flames by using a femtosecond (fs) pump-probe scheme and measuring directional emission signals. An approximately 100-fs pump pulse at 205.1 nm excites H atoms through a two-photon process (n = 3 ←← n = 1), which is followed by detection of the forward emission signals induced by a broadband fs probe pulse near 656 nm. Above a certain threshold, we observe a quadratic dependence of the emission signal on the pump laser energy. Moreover, the linewidth of the forward emission signal varies with the probe delay and the probe laser energy. This behavior can be explained in terms of superradiance. We perform a theoretical analysis and compare the experimental results with the theory, and conclude that, within the conditions of our experiment, the behavior of the atomic system involves atomic coherence, which is produced non-adiabatically and corresponds to a superradiant process. Variations in the duration of the gain time window and lifetime of the excited-state H atoms in flames are explored at different flame conditions (i.e., equivalence ratio and heights above the burner). The fs pump-probe technique demonstrated here can also be extended to characterize the time-resolved population dynamics and the corresponding collisional energy transfer rates for energy levels involved in laser-induced fluorescence detection of H atoms in flames relevant to practical combustion applications.