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Annals of Physics

Master Equation for an Oscillator Coupled to the Electromagnetic Field

G. W. Ford, John T. Lewis, Robert F. O’Connell

Published Dec 1, 1996• 33 citations
Publisher
DOI
10.1006/aphy.1996.0137

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Microscopic open quantum physics

In this chapter, we derive quantum master equations with explicit, microscopic coefficients, for the systems of interest of a superradiant semiconductor structure: the active electrons, the electromagnetic field, and the optical crystal vibrations. These vibrations determine an important retardation in the field propagation (refractive index), and a spectrum splitting (the Raman effect). For the active electrons we consider three environmental systems: the quasi-free electrons/holes of the conduction regions, the crystal lattice vibrations excited by electron transitions, and the free electromagnetic field. For the electromagnetic field, we consider the absorption by coupling to the conduction electrons/holes, and to the optical vibrations of the crystal, while these vibrations are damped by coupling with the valence electron transitions to thermally released states. For the electron-field coupling we consider the potential derived in chapter 2 from the Lorentz force, while the momentum difference is supposed to be taken by the crystal lattce. For the coupling of the crystal vibrations to the electromagnetic field and electron transitions we consider potentials obtained from the momentum conservation. For the active electrons, we find a quantum master equation with a Markovian term describing correlated transitions with the environmental particles, and a non-Markovian term given by the self-consistent field of the environmental particles. Since the dissipative environment of the electromagnetic field is contained inside the quantization volume of this field, which is taken as a unit volume, its quantum master equation includes a dissipative term of a space integral form. For the field mean values, the dissipation integral, of propagation through the dissipative environment, can be divided in two parts: an integral from the initial coordinate up to the boundary of the quantum uncertainty region, taken for a coherent wave, which describes dephasing, and an integral over the uncertainty region, which describes absorption. Similar equations are obtained for the optical vibration field. When the vibrational field is eliminated from these equations, we obtain a frequency splitting, corresponding to the Raman effect, and an absorption rate, including the absorption of the electromagnetic waves by conduction electrons/holes, and the absorption of the vibrational waves by the valence electrons, excited by the crystal deformations in the thermally released states.

BENTHAM SCIENCE PUBLISHERS eBooks•Dec 17, 2014•0 citations
We perform a first-principles derivation of the general master equation to study the non-Markovian dynamics of a two-level atom (2LA) interacting with an electromagnetic field (EMF). We use the influence functional method, which can incorporate the full back reaction of the field on the atom, while adopting Grassmannian variables for the 2LA and the coherent-state representation for the EMF. We find exact master equations for the cases of a free quantum field and a cavity field in the vacuum. In response to the search for mechanisms to preserve maximal coherence in quantum computations in ion trap prototypes, we apply these equations to analyze the decoherence of a 2LA in an EMF, and find that decoherence time is close to relaxation time. This is at variance with the claims by authors who studied the same system but used a different coupling model. We explain the source of difference and argue that, contrary to common belief, the EMF, when resonantly coupled to an atom, does not decohere it as efficiently as a bath does on a quantum Brownian particle. The master equations for non-Markovian dynamics derived here are expected to be useful for exploring new regimes of 2LAEMF interaction, which is becoming physically important experimentally.
In this chapter, we derive quantum master equations with explicit, microscopic coefficients, for the systems of interest of a superradiant semiconductor structure: the active electrons, the electromagnetic field, and the optical crystal vibrations. These vibrations determine an important retardation in the field propagation (refractive index), and a spectrum splitting (the Raman effect). For the active electrons we consider three environmental systems: the quasi-free electrons/holes of the conduction regions, the crystal lattice vibrations excited by electron transitions, and the free electromagnetic field. For the electromagnetic field, we consider the absorption by coupling to the conduction electrons/holes, and to the optical vibrations of the crystal, while these vibrations are damped by coupling with the valence electron transitions to thermally released states. For the electron-field coupling we consider the potential derived in chapter 2 from the Lorentz force, while the momentum difference is supposed to be taken by the crystal lattce. For the coupling of the crystal vibrations to the electromagnetic field and electron transitions we consider potentials obtained from the momentum conservation. For the active electrons, we find a quantum master equation with a Markovian term describing correlated transitions with the environmental particles, and a non-Markovian term given by the self-consistent field of the environmental particles. Since the dissipative environment of the electromagnetic field is contained inside the quantization volume of this field, which is taken as a unit volume, its quantum master equation includes a dissipative term of a space integral form. For the field mean values, the dissipation integral, of propagation through the dissipative environment, can be divided in two parts: an integral from the initial coordinate up to the boundary of the quantum uncertainty region, taken for a coherent wave, which describes dephasing, and an integral over the uncertainty region, which describes absorption. Similar equations are obtained for the optical vibration field. When the vibrational field is eliminated from these equations, we obtain a frequency splitting, corresponding to the Raman effect, and an absorption rate, including the absorption of the electromagnetic waves by conduction electrons/holes, and the absorption of the vibrational waves by the valence electrons, excited by the crystal deformations in the thermally released states.