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Modern Physics Letters A

ABSORPTION AND EMISSION PROCESSES IN NONCOMMUTATIVE SPACE

C. Yüce

Published Jul 30, 2006• 0 citations
Publisher

Abstract

Atom-field interaction and absorption, emission of photons in noncommutative space are investigated. We calculate the rate and the directional distribution of the radiation. The modified selection rules which govern allowed and forbidden transitions in noncommutative space are derived.
DOI
10.1142/s0217732306020123

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Radiation can change the energy state of matter via three optical processes: spontaneous emission, absorption and stimulated emission. In spontaneous emission, an excited atomic or molecular state decays to a lower energy state with the emission of a photon of energy equal to the difference in the quantum state energies. Photon absorption is the reverse process, with a photon causing excitation from a lower to an excited quantum state. Stimulated emission was first proposed by Einstein in a paper published in 1917. He attempted to balance spontaneous emission and photon absorption, but could not get the correct balance without the postulated process of stimulated emission (see Section 4.2). With stimulated emission, an excited quantum state is stimulated to decay to a lower quantum state by an impinging photon. The existing photon survives with another identical photon being created (so that energy is conserved). The rates at which radiative transitions occur can be calculated using quantum mechanics. The time-dependent Schrodinger equation is used with the system wavefunction comprising time-varying linear combinations of the two wavefunctions for the lower and upper quantum states. In semi-classical treatments, an atom is treated quantum mechanically with the radiation field treated classically. There is a perturbation in energy associated with, say, the electric field of the radiation interacting with the electric dipole of the atom, though other interactions can be significant if the electric dipole interaction energy is small. In absorption, for example, a differential equation representing the change in ‘weighting’ of the wavefunction from the lower to upper state is obtained. A ‘time constant’ for the speed of change represents the rate of the radiative process. We examine the quantum mechanical nature of radiation absorption in Section 10.1 before discussing (Section 10.3) another important parameter arising with radiative transitions between discrete bound quantum states: the lineshape function. Quantum Theory of the Atom–Radiation Interaction An expression for the Einstein B-coefficient for photo-absorption is derived using quantum mechanics in this section. Einstein determined the detailed balance relationship between the rates of spontaneous emission, photo-absorption and stimulated emission when light interacts with an atom by considering an atomic system of two energy levels which are in equilibrium with a black-body radiation field. We use a semi-classical treatment where the atom is treated quantum mechanically and the radiation field is treated as a classical oscillating electric field.
The collision-induced absorption and emission coefficients for electric-dipole forbidden atomic transitions are calculated for weak radiation fields. The approximations used are valid for $\ensuremath{\hbar}\ensuremath{\omega}$ near $\ensuremath{\hbar}{\ensuremath{\omega}}_{0}$, the atomic energy differences. The example case of $S\ensuremath{-}D$ transitions induced by a spherically symmetric perturber (e.g., a noble-gas atom) is treated in detail and compared to measurements. The case of "radiative collisions," in which both colliding atoms change their state, is included in the theory and is also compared to experiment.
We treat the interaction between an electromagnetic radiation bath and a material system in the semi-classical picture: the radiation is treated according to the Maxwell equations, but the process of emission/absorption is described through the concept of a photon; on the other hand, the material system is modelled according to quantum mechanics, assuming a discrete two-level energy spectrum. This very simple model allows one to elaborate the elementary theory of the absorption/emission coefficients, both for the spontaneous and for the stimulated processes which will be described within the electric dipole approximation. Selection rules for allowed transitions are eventually obtained and the nature of high-order transition is briefly outlined. Finally, a qualitative description of the light amplification by stimulated emission of radiation is presented.
When there exists no external field, physical results should not depend on the choice of quantization axis. This theorem is known as spectroscopic stability and is well established for one photon absorption and emission processes. In two photon absorption by a three level atom one can make the excitation of the top level forbidden if the absorption processes are restricted to one selection rule in Δ M (=+1, 0 or -1). The choice of selection rule assumes relative orientation between the polarization of the radiation field and an external field. If this relative orientation is changed the selection rule would also change and the top level would appear as a final result of two photon absorption . A question is what happens if the external field disappears in the latter case. Would the top level disappear although the selection rule stays unaltered? It is shown that the probability of having the top level disappears when the external field vanishes, confirming the spectroscopic stability and the degree of violation is obtained as a function of the strength of the external field.
So far we have treated the energy levels of an atomic system as stable states with infinite lifetimes. The presence of an electromagnetic field changes this picture. Absorption of photons will excite atoms and ions to higher levels, while stimulated emission will make excited ones decay. Einstein (1917) showed, using purely statistical arguments, that an excited ion will decay through spontaneous emission in the absence of an electromagnetic field. This process can also be derived by using a rigorous quantum electrodynamic treatment, where the field is quantized. In this chapter we start by discussing transitions between atomic levels in a general sense, postulating the operators responsible for the decay. After the first few sections we will concentrate on the most important few multipoles or terms in the expansion of the electromagnetic field. We will introduce a number of different properties describing the transition, and eventually arrive at the measurable transition rate and, directly linked to it, the lifetime of an excited state. We will start, however, with the most basic property, the component strength. Our aim is to arrive at computationally useful expressions as soon as possible. For a more thorough treatment of the theory of radiative transitions we refer to the book by Sobelman (1972). For a brief review of the many factors affecting spectra of atoms, see Martin and Wiese (1996) .