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Photon Exchange Between a Pair of Nonidentical Atoms with Two Forms of Interactions

Shahram Mohammad-Mehdi Golshan

Published May 1, 1987• 0 citations
OpenAlex

Abstract

A pair of nonidentical two-level atoms, separated by a fixed distance R, interact through photon exchange. The system is described by a state vector which is assumed to be a superposition of four "essential states": (1) the first atom is excited, the second one is in the ground state, and no photon is present, (2) the first atom is in its ground state, the second one is excited, and no photon is present, (3) both atoms are in their ground states and a photon is present, and (4) both atoms are excited and a photon is also present. The system is initially in state (1). The probabilities of each atom being excited are calculated for both the minimally-coupled interaction and the multipolar interaction in the electric dipole approximation. For the minimally-coupled interaction Hamiltonian, the second atom has a probability of being instantaneously excited, so the interaction is not retarded. For the multipolar interaction Hamiltonian, the second atom is not excited before the retardation time, which agrees with special relativity. For the minimally-coupled interaction the nonphysical result occurs because the unperturbed Hamiltonian is not the energy operator in the Coulomb gauge. For the multipolar Hamiltonian in the electric dipole approximation the unperturbed Hamiltonian is the energy operator. An active view of unitary transformations in nonrelativistic quantum electrodynamics is used to derive transformation laws for the potentials of the electromagnetic field and the static Coulomb potential. For a specific choice of unitary transformation the transformation laws for the potentials are used in the minimally-coupled second-quantized Hamiltonian to obtain the multipolar Hamiltonian, which is expressed in terms of the quantized electric and magnetic fields.

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A pair of nonidentical two-level atoms, separated by a fixed distance R, interact through photon exchange. The system is described by a state vector which is assumed to be a superposition of four "essential states": (1) the first atom is excited, the second one is in the ground state, and no photon is present, (2) the first atom is in its ground state, the second one is excited, and no photon is present, (3) both atoms are in their ground states and a photon is present, and (4) both atoms are excited and a photon is also present. The system is initially in state (1). The probabilities of each atom being excited are calculated for both the minimally-coupled interaction and the multipolar interaction in the electric dipole approximation. For the minimally-coupled interaction Hamiltonian, the second atom has a probability of being instantaneously excited, so the interaction is not retarded. For the multipolar interaction Hamiltonian, the second atom is not excited before the retardation time, which agrees with special relativity. For the minimally-coupled interaction the nonphysical result occurs because the unperturbed Hamiltonian is not the energy operator in the Coulomb gauge. For the multipolar Hamiltonian in the electric dipole approximation the unperturbed Hamiltonian is the energy operator. An active view of unitary transformations in nonrelativistic quantum electrodynamics is used to derive transformation laws for the potentials of the electromagnetic field and the static Coulomb potential. For a specific choice of unitary transformation the transformation laws for the potentials are used in the minimally-coupled second-quantized Hamiltonian to obtain the multipolar Hamiltonian, which is expressed in terms of the quantized electric and magnetic fields.
Two nonidentical two-level atoms are separated by a fixed distance R. The probabilities of the atoms being excited are calculated for both the A\ensuremath{\cdot}p interaction and the E\ensuremath{\cdot}r interaction in the electric dipole approximation. For the A\ensuremath{\cdot}p interaction the second atom has a nonvanishing probability of being excited for times t<R/c, and so the interaction is not retarded. For the E\ensuremath{\cdot}r interaction the second atom has zero probability of being excited for times t<R/c, and so the interaction is completely retarded. Reasons for the difference are discussed.
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.
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.
We investigate (non-relativistic) atomic systems interacting with quantum electromagnetic field (QEF). The resulting model describes spontaneous emission of light from a two-level atom surrounded by various initial states of the QEF. We assume that the quantum field interacts with the atom via the standard, minimal-coupling Hamiltonian, with the A2 term neglected. We also assume that there will appear at most single excitations (photons). By conducting the analysis on a general level we allow for an arbitrary initial state of the QEF (which can be for instance: the vacuum, the ground state in a cavity, or the squeezed state). We derive a Volterra-type equation which governs the time evolution of the amplitude of the excited state. The two-point function of the initial state of the QEF, integrated with a combination of atomic wavefunctions, forms the kernel of this equation.
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.