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Physical Review A

Quantum electrodynamics with nonrelativistic sources. II. Maxwell fields in the vicinity of a molecule

Edwin Albert Power, T. Thirunamachandran

Published Nov 1, 1983• 76 citations
Publisher

Abstract

The electromagnetic field operators and the electron field operators for the coupled system governed by the multipolar Hamiltonian are obtained within the Heisenberg picture. Their causal behavior and their relationship to the minimal-coupling forms are discussed. The basic fields of the multipolar theory, namely, the displacement vector and the magnetic field, are calculated up to terms quadratic in the multipole moment sources. The terms linear in the transition moments are the quantum counterparts of the classical fields and do not change the photon occupation number. The quadratic terms have no classical analogs: they act in both the photon and electron occupation-number spaces. It is shown that it is necessary to include these second-order terms in the calculation of the Poynting vector for an emitting dipole, thus demonstrating their role in the transport of radiative energy.

DOI
10.1103/physreva.28.2663

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American Journal of Physics•May 1, 1972•12 citations
The electromagnetic field operators and the electron field operators for the coupled system governed by the multipolar Hamiltonian are obtained within the Heisenberg picture. Their causal behavior and their relationship to the minimal-coupling forms are discussed. The basic fields of the multipolar theory, namely, the displacement vector and the magnetic field, are calculated up to terms quadratic in the multipole moment sources. The terms linear in the transition moments are the quantum counterparts of the classical fields and do not change the photon occupation number. The quadratic terms have no classical analogs: they act in both the photon and electron occupation-number spaces. It is shown that it is necessary to include these second-order terms in the calculation of the Poynting vector for an emitting dipole, thus demonstrating their role in the transport of radiative energy.
The electromagnetic field operators for a chiral (optically active) molecule are calculated in the Heisenberg picture, using the multipolar Hamiltonian. Interactions involving electric-dipole, magnetic-dipole, and electric-quadrupole moments are taken into account. The operators are expanded in powers of moments, and expressions correct to quadratic powers in the moments are given. Comparable contributions from diamagnetic interactions are also presented. The properties of these operators are discussed. Terms that are linear in the moments are found to act in the electron space alone; those quadratic in the moments act in both the electron and photon spaces. The operators are used to calculate the Poynting vector, from which the spontaneous emission rates for magnetic-dipole and electric-quadrupole transitions are obtained. Attention is drawn to the inverse square dependence of the Poynting vector on the distance of the field point from the source. This behavior is shown to be consistent with the requirement of local conservation of energy. The operators are used in the following paper [J. K. Jenkins, A. Salam, and T. Thirunamachandran, Phys. Rev. A 50, 4767 (1994)] to calculate dispersion energies between two optically active molecules.
The quantized electromagnetic field in interaction with nonrelativistic sources, i.e., atoms and molcules, has been the subject of study in the previous papers in this series. The Heisenberg formalism is used to calculate the electric- and magnetic-field operators arising from charges and currents expressed in multipolar form. In this paper, quadratic operators in these fields such as the Thompson energy density and the Poynting vector and their expectation values for specified states are found. The expectation values are, in general, time dependent. For initial conditions given at t=0 it is shown that the fields are causal, i.e., for tr/c the source-dependent fields are zero and the quadratic operators have only their zero-point contributions. For t>r/c they have both time-independent and time-dependent terms. The time-dependent terms, though transient, are shown to obey Poynting's theorem. The steady-state part of the Poynting vector is related to the Einstein coefficients. The corresponding electric-energy density is related to the Casimir-Polder potential for a polarizable test body in the field of the source molecules. Similarly the magnetic-energy density is derived and is used in the calculation of energy shifts. Quadratic operators referring to different field points are also discussed.
The electromagnetic field operators in the Heisenberg picture are found in both the minimal and multipolar forms of nonrelativistic quantum electrodynamics within the electric dipole approximation. These are made up of free- and source-field terms. The free electric- and magnetic-field operators in the two formalisms differ since the creation/annihilation operators are manifestly distinct. Their explicit forms in the Heisenberg picture are given. However, the source fields are formally the same when expressed in terms of dipole moment operators at positive retarded time. The cancellations that lead to this equivalence are presented. In many applications it is necessary to express the operators at retarded time in terms of creation and annihilation operators at the initial time. Explicit expressions for the fields up to second order in terms of the transition dipole moments are given. These enable the formulas for induced dipole moments to be derived within the context of quantum electrodynamics whereas previous derivations have been based on semiclassical electrodynamics.
The relationship between the multipolar and minimal Hamiltonians through a canonical transformation is used to analyze the time dependence of quantum operators in the two formalisms. It is shown that operators dependent on particle position, the vector potential, and their time derivatives have the same time dependence. However, operators such as the photon number and the atomic population number evolve differently in the two cases. Expressions correct to second order in the electric-dipole moments for these are given. The expectation values of the photon number operator are calculated in the two formalisms and are used to predict natural line shapes. These theoretical shapes differ. The observed shape will depend on the particular setup of the experiment involving the radiative decay of an excited atom. A comparison with the theoretical predictions will determine which of the two frameworks is most appropriate to describe the decay. Finally, the energy density of the electromagnetic field in the neighborhood of an atom is calculated within the two formalisms.
Introduction . In the previous chapter we have obtained the form of the coupling between matter and the electromagnetic field. We are thus in a position to treat electrodynamics in the presence of charges and currents. We start by obtaining the Euler-Lagrange equations of the matter-electromagnetic field system. These turn out to be the Maxwell-Lorentz equations, which is a set of coupled equations of motion in which the matter field acts as a source for the electromagnetic field and vice versa. In Section 4.2 we derive the Hamiltonian of the complete system in the Coulomb gauge, and this leads to the so-called minimal coupling Hamiltonian, containing both the electromagnetic potential and the matter-field amplitude. Specializing the nonrelativistic matter field to the case of a neutral atom, consisting of the field of electrons in a static nuclear potential, in Section 4.3 we obtain the atom-photon Hamiltonian in the minimal coupling scheme. Some of the basic processes induced by the atom-photon interaction part of the Hamiltonian are also discussed in this section. This gives us the possibility of introducing at this stage a fundamental simplification of the interaction Hamiltonian, namely the electric dipole approximation. The minimal coupling scheme, however, is not the only possible atom-field coupling.
This paper discusses the quantization of electromagnetic fields interacting with nonrelativistic atoms and molecules in the dipole approximation. Quantizing the field variables D and H and taking the interaction density −ε0−1P·D, we obtain a quantum theory corresponding to classical electrodynamics with no free currents and the induced dipole moments as the only sources of the radiation field. The resulting equations are found to agree with those Power and Zienau obtained from causality requirements. A comparison with the conventional approach is given.