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Journal of Physics B Atomic Molecular and Optical Physics

The effect of frequency-mismatched spontaneous emission on atom-field entanglement

John R. Schaibley, P. R. Berman

Published Jun 8, 2012• 5 citations
Publisher

Abstract

A Schrödinger representation approach is used to calculate the atom-field dynamics following spontaneous emission by an atom in its excited state to a superposition of its two ground-state sublevels, in the case where the frequency separation of the ground-state sublevels is large compared to the excited-state decay rate. The emitted radiation is incident on a broadband photodetector. Using a relatively simple model for the photodetector, we show how a measurement of a photo-signal leaves the atom in a coherent superposition of the two ground states. The relative phase between the two ground-state amplitudes can be interpreted in terms of the temporal phase acquired in the time interval between spontaneous emission (viewed as a quantum jump process) and detection. Alternatively, the phase can be associated with a spatial phase of the entangled atom-field system; the source atom is projected into a state containing this spatial phase when the emitted photon is detected.

DOI
10.1088/0953-4075/45/12/124020

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A Schrödinger representation approach is used to calculate the atom-field dynamics following spontaneous emission by an atom in its excited state to a superposition of its two ground-state sublevels, in the case where the frequency separation of the ground-state sublevels is large compared to the excited-state decay rate. The emitted radiation is incident on a broadband photodetector. Using a relatively simple model for the photodetector, we show how a measurement of a photo-signal leaves the atom in a coherent superposition of the two ground states. The relative phase between the two ground-state amplitudes can be interpreted in terms of the temporal phase acquired in the time interval between spontaneous emission (viewed as a quantum jump process) and detection. Alternatively, the phase can be associated with a spatial phase of the entangled atom-field system; the source atom is projected into a state containing this spatial phase when the emitted photon is detected.
The spontaneous emission of a set of NNN 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.
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This paer is concerned with the spontaneous-emision rate of two two-level atoms which have different resonance frequencies and whose spatial separation is much smaller than the corresponding mean resonance wavelength. The total radiation rate of such an atom pair is calculated completely quantum mechanically as a function of time. Explicit results are given for various values of the frequeny difference and the following initial states of the atomic system: (a) both atoms in the excited state, (b) one taom in the excited state the other in the ground state, (c) a symmetric combination of those states, (d) an antisymmetric combination of those states, and product states where each atom is in an equal superposition of its ground and excited states, for which the expectation values of the dipole moments are nonzero and may be considered to be osicillating (e) in phase, (f) in opposite phae, and (g) in random phase. Oscillations are found to appear in the radiation rate in all cases when the frequency difference becomes larger than a certain critical value, viz., the mean half-width of the atomic resonance lines. The oscillations are especially pronounced for the initial atomic states (c), (d), (e), and (f), which exhibit superradiance and radiation trapping. For example, for atoms in the antisymmetric state (d), for which the radiation from two identical atoms is zero (completely self-trapped), a pair of nonidentical atoms begins radiating and even oscillates into the superradiant region at times.
The role of the collective antisymmetric state in entanglement creation by spontaneous emission in a system of two non-overlapping two-level atoms has been investigated. Populations of the collective atomic states and the Wootters entanglement measure (concurrence) for two sets of initial atomic conditions are calculated and illustrated graphically. Calculations include the dipole-dipole interaction and a spatial separation between the atoms that the antisymmetric state of the system is included throughout even for small interatomic separations. It is shown that spontaneous emission can lead to a transient entanglement between the atoms even if the atoms were prepared initially in an unentangled state. It is found that the ability of spontaneous emission to create transient entanglement relies on the absence of population in the collective symmetric state of the system. For the initial state of only one atom excited, entanglement builds up rapidly in time and reaches a maximum for parameter values corresponding roughly to zero population in the symmetric state. On the other hand, for the initial condition of both atoms excited, the atoms remain unentangled until the symmetric state is depopulated. A simple physical interpretation of these results is given in terms of the diagonal states of the density matrix of the system. We also study entanglement creation in a system of two non-identical atoms of different transition frequencies. It is found that the entanglement between the atoms can be enhanced compared to that for identical atoms, and can decay with two different time scales resulting from the coherent transfer of the population from the symmetric to the antisymmetric state. In addition, it was found that a decaying initial entanglement between the atoms can display a revival behaviour.
The Markov model of spontaneous emission of an atom localized in a spatial region with a broadband electromagnetic field with zero photon density is considered in the conditions of coupling of the electromagnetic field with the broadband field of a neighboring space. The evolution operator of the system and the kinetic equation for the atom are obtained. It is shown that the field coupling constant affects the rate of spontaneous emission of the atom, but is not manifested in the atomic frequency shift. The analytic expression for the radiative decay constant for the atom is found to be analogous in a certain sense to the expression for the decay constant for a singly excited localized ensemble of identical atoms in the conditions when the effect of stabilization of its excited state by the Stark interaction with the vacuum broadband electromagnetic field is manifested. The model is formulated based on quantum stochastic differential equations of the non- Wiener type and the generalized algebra of the Ito differential of quantum random processes.
In photodissociation of a homonuclear diatomic molecule, conservation of linear and angular momenta requires that each atomic fragment follow identical but oppositely directed trajectories with respect to the molecular center of mass. For certain values of the incident photon energy, one of the atoms will be electronically excited while the other will be in its ground state. When a detector records the undispersed fluorescence from the decay of the excited atom it cannot distinguish which trajectory the excited atom followed and hence whether the photon possesses a blue or red Doppler shift corresponding to recoil towards or away from the detector. According to the principle of superposition in quantum mechanics, the wave function of the photon must be a sum over two paths corresponding to emission from an excited atom in either of the two recoil directions. Detection of such photons gives rise to an interference between the probability amplitudes for the two paths that is manifested in the output from the photodetector as a beat frequency. Since photodissociation of an ensemble of molecules gives rise to a distribution of recoil directions relative to the electric vector of the incident radiation, a range of beat frequencies must be present in the detected signal. This paper gives a calculation of expected output voltage waveforms from a photodetector viewing atomic fluorescence excited by molecular photodissociation. Expressions are given for partial Fourier transforms of the photodetector signals. The results show that the shape of the voltage waveforms depends strongly on the asymmetry parameter for recoil of the photofragments and on whether or not the magnetic sublevels of the excited atomic state are created in a coherent superposition.