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Physical Review A

Quantum electrodynamics near an interface

J. M. Wylie, John E. Sipe

Published Sep 1, 1984• 482 citations
Publisher

Abstract

A quantum-mechanical linear-response formalism is used to calculate the frequency shift and lifetime of an excited atom near an arbitrary flat interface. The results depend on the frequency-dependent atom and field susceptibilities, and in the vicinity of an interface can be expressed in terms of the appropriate Fresnel reflection coefficients; the contributions from surface excitations are easily identified. As examples, we consider an atom above a metal and a dielectric waveguide.

DOI
10.1103/physreva.30.1185

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A quantum-mechanical linear-response formalism is used to calculate the frequency shift and lifetime of an excited atom near an arbitrary flat interface. The results depend on the frequency-dependent atom and field susceptibilities, and in the vicinity of an interface can be expressed in terms of the appropriate Fresnel reflection coefficients; the contributions from surface excitations are easily identified. As examples, we consider an atom above a metal and a dielectric waveguide.
A quantum-electrodynamic theory of spontaneous emission in presence of dielectrics and conductors is developed. The theory makes use of the master-equation techniques and the response-function formalism of part I of this series of papers. Various observable entities such as damping coefficients (lifetimes), Lamb shifts, and frequency shifts are related to the appropriate surface-dependent response functions. The results are valid for arbitrary geometries (involving linear dielectrics) and naturally contain, as a special case, the usual results of spontaneous emission in free space. As explicit examples we consider a two-level atom (also the multilevel atom) in presence of a plane dielectric interface and between two conducting plates. Formulas for the shifts and widths are given and their asymptotic behavior for large and short distances is discussed. The behavior when the atom is embedded inside the dielectric is different than when the atom is outside the dielectric. The origin of coherence in the present model is discussed and the coherence effects in this model are contrasted with those in Dicke's model. The results are also compared with those obtained by the image method. Exact expressions for the operator radiation-reaction fields are obtained in terms of the atomic polarization operators and response functions. Approximate results for such fields are also given. The far-zone behavior of the radiation fields is obtained in terms of response functions and the polarization operators. Some of the normally ordered correlation functions are also calculated. The connection of some of the theoretical results with a recent experimental work of Carniglia, Mandel, and Drexhage is discussed. The effect of anisotropy of the dielectric function on the lifetimes as well as on the far-field correlation functions is also considered. Finally the contribution to the shifts and widths due to the excitation of surface polariton modes is computed and the results are compared with those obtained by the quantization of surface polariton field. It is found that such surface modes contribute significantly to widths.
Quantum electrodynamic theory (QED) in the vicinity of macroscopic structures has achieved new importance due to its applicability, particularly in nanotechnology. There are many powerful methods for studying QED near media with diverse properties and geometries. However, applying them to a particular problem generally necessitates extensive numerical calculations. This is not the case for simple systems of high symmetry, in which the electromagnetic field can be quantised by explicit mode expansion, allowing exact analytic calculations. In the present thesis, we calculate the energy-level shift of a ground state atom near a non-dispersive and non-dissipative dielectric slab. The shift is due to the interaction of the atom with electromagnetic field fluctuations, which in turn are affected by the presence of the slab. Thus, a quantisation of the electromagnetic field in the presence of a layered system is required. We derive the field modes, which comprise of a continuous set of travelling modes (with incident, reflected and transmitted parts) and trapped modes, subject to repeated total internal reflection and emerge as an evanescent field outside the slab, they only exist at certain discrete frequencies. The shift is obtained by means of second-order perturbation theory. It splits up naturally into two contributions, due to the different nature of the modes, and a problem arises when we have to add them all. We have come up with a convenient method of summing over all modes, and its validity has been demonstrated by proving the completeness. The calculation of the shift follows as an application of our method. The result is analysed asymptotically for various regions, reducing to simple formulas that can be utilised in recent experiments, in which the thickness of the substrate matters.
We calculate the energy-level shifts of an atom near a dielectric microsphere. With the quantum electrodynamic linear-response formalism and the exact field susceptibility satisfying the boundary conditions, the energy shifts of a ground-state atom are calculated numerically. From the numerical results, in particular, we are able to identify the short-range instantaneous van der Waals interaction energy and the long-range Casimir-Polder retarded interaction energy between two polarizable objects (atom and cavity).
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We develop a microscopic quantum theory of surface plasmon polaritons valid for arbitrary metal-dielectric geometries. Our framework is based on the Power-Zienau-Woolley representation of quantum electrodynamics, which provides an optimal separation between electronic and photonic degrees of freedom and is therefore particularly well suited for constructing quantum descriptions of polaritonic excitations in strongly dispersive media. Within this formulation, the fundamental electronic oscillator is identified as the bulk plasmon mode, which is nonperturbatively coupled to the radiative continuum of free photon modes. This coupling induces a geometry-dependent renormalization of the bulk plasma frequency, giving rise to confined plasmonic resonances. As specific applications, we recover the localized surface plasmon modes of metallic nanoparticles, including radiative frequency shifts and decay, as well as the exact dispersion relation of propagating surface plasmon polaritons at planar interfaces. Our quantum treatment further reveals that light-matter interactions at metal-dielectric interfaces are inherently in the ultrastrong coupling regime. As a result, in the quasistatic limit, the system exhibits unconventional ground-state quantum fluctuations that can be controlled through the refractive index. These results open new intriguing perspectives in the field of quantum plasmonics.