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Physical Review A

Spontaneous emission near an absorbing dielectric surface

Michael S. Yeung, T. Kenneth Gustafson

Published Dec 1, 1996• 100 citations
Publisher

Abstract

The lifetime of an excited atom near an absorbing dielectric surface is calculated from an exact solution of a microscopic Hamiltonian model, which includes the effects of dispersion, local-field correction, and near-field Coulomb interaction. Results for the total decay rate are shown to be in excellent agreement with those based on classical electromagnetic theory and to yield the well-known result for the rate of nonradiative energy transfer in the limit of very small distance from the surface. \textcopyright{} 1996 The American Physical Society.

DOI
10.1103/physreva.54.5227

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The lifetime of an excited atom near an absorbing dielectric surface is calculated from an exact solution of a microscopic Hamiltonian model, which includes the effects of dispersion, local-field correction, and near-field Coulomb interaction. Results for the total decay rate are shown to be in excellent agreement with those based on classical electromagnetic theory and to yield the well-known result for the rate of nonradiative energy transfer in the limit of very small distance from the surface. \textcopyright{} 1996 The American Physical Society.
Decay of an excited molecule ~atom! has been considered in an absorbing dielectric. The decay rate has been derived calculating the total rate of excitation transfer to the surrounding species. The contribution due to the far-zone energy transfer yields the rate of photon emission in the absorbing medium. The analysis is based on a microscopic QED theory of energy transfer in condensed phases. As a result, effects due to discreteness of the medium ~such as the local field effects! are reflected intrinsically in the decay rates. The microscopic approach supports the previous introduction of the local field factors on a phenomenological basis.
Decay of an excited molecule (atom) has been considered in an absorbing dielectric. The decay rate has been derived calculating the total rate of excitation transfer to the surrounding species. The contribution due to the far-zone energy transfer yields the rate of photon emission in the absorbing medium. The analysis is based on a microscopic QED theory of energy transfer in condensed phases. As a result, effects due to discreteness of the medium (such as the local field effects) are reflected intrinsically in the decay rates. The microscopic approach supports the previous introduction of the local field factors on a phenomenological basis.
Spontaneous decay of an excited atom near a dispersing and absorbing microsphere of given complex permittivity that satisfies the Kramers-Kronig relations is studied, with special emphasis on a Drude-Lorentz permittivity. Both the whispering gallery field resonances below the band gap (for a dielectric sphere) and the surface-guided field resonances inside the gap (for a dielectric or a metallic sphere) are considered. Since the decay rate mimics the spectral density of the sphere-assisted ground-state fluctuation of the radiation field, the strengths and widths of the field resonances essentially determine the feasible enhancement of spontaneous decay. In particular, strong enhancement can be observed for transition frequencies within the interval in which the surface-guided field resonances strongly overlap. When material absorption becomes significant, then the highly structured emission pattern that can be observed when radiative losses dominate, reduces to that of a strongly absorbing mirror. Accordingly, nonradiative decay becomes dominant. In particular, if the distance between the atom and the surface of the microsphere is small enough, the decay becomes purely nonradiative.
We have calculated the effect of material absorption on the rate of spontaneous emission by an embedded atom using a macroscopic Green-function approach and a microscopic Hamiltonian method that includes reservoir damping. When local field effects are neglected, the free-space emission rate is modified by the real part of the refractive index at the transition frequency of the embedded atom. Local field effects are introduced via a local field correction factor. This modification of the spontaneous emission rate generalizes a well-known result for transparent media and is of crucial importance in assessing the degree of inhibition of spontaneous emission for frequencies close to the resonances of the dielectric.
Starting from the quantized version of Maxwell's equations for the electromagnetic field in an arbitrary linear Kramers-Kronig dielectric, the Heisenberg equations of motion for a two-level atom resonantly coupled to the radiation field in the presence of dispersive and absorbing dielectric bodies are derived. The theory is applied to the problem of spontaneous decay of excited atoms in absorbing media. The decay rate is calculated for the (Glauber-Lewenstein) real-cavity model, and a comparison with the recently studied (Clausius-Mosotti) virtual-cavity model [S. Scheel, L. Kn\"oll, D.-G. Welsch, and S. M. Barnett, Phys. Rev. A 60, 1590 (1999)] is given. It is shown that owing to nonradiative decay associated with absorption, the rate of spontaneous decay sensitively depends on the cavity radius, particularly when the atomic transition frequency approaches an absorption band of the medium. Only when the effect of absorption is fully disregarded, is the familiar local-field correction factor recovered.
We present calculations of the rates of decay of an excited atom embedded in an absorbing dielectric. Decay can occur by spontaneous emission into transverse radiative modes of the electromagnetic field and by Joule heating via longitudinal coupling of the atom to the dielectric. The spontaneous emission (transverse) decay rate is modified in a dielectric, being the free-space rate multiplied by the real part of the refractive index at the transition frequency of the atom. There is a further modification due to the difference between the macroscopic dielectric field and the local field at the position of the atom. In addition there is a longitudinal decay rate which is proportional to the imaginary part of the dielectric constant and therefore vanishes in non-absorbing media. We derive expressions for each of these rates of decay and discuss the physical mechanisms leading to them.