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Oxford University Press eBooks

The absorption and stimulated emission of radiation

Alan Corney

Published Oct 5, 2006• 0 citations
Publisher

Abstract

Starting from the absorption of radiation by a classical electron oscillator, Einstein's A and B coefficients for spontaneous and stimulated transitions are introduced. Stimulated transition rates are derived by time-dependent perturbation theory. Relations between the Einstein B coefficients and oscillator strengths are also determined. The atomic frequency response for stimulated transitions is explained.

DOI
10.1093/acprof:oso/9780199211456.003.0009

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•Nov 1, 2015•0 citations
Starting from the absorption of radiation by a classical electron oscillator, Einstein's A and B coefficients for spontaneous and stimulated transitions are introduced. Stimulated transition rates are derived by time-dependent perturbation theory. Relations between the Einstein B coefficients and oscillator strengths are also determined. The atomic frequency response for stimulated transitions is explained.
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 phenomena which are principally responsible for the interaction of radiation with matter in everyday life are absorption and spontaneous emis­ sion. Light falling on matter is absorbed, leaving atoms in excited states which spontaneously emit radiation with a spread of frequency inversely proportional to the decay time. The situation is modified when the atomic decay times are sufficiently long and the radiation sufficiently intense, for then radiation may fall on excited atoms, resulting in stimulated emission rather than absorption. We saw in Chap. 2 that this third process was required to obtain the Planck blackbody radiation law in Einstein’s derivation. It is stimulated emission which enables an atomic medium to amplify incident radiation, and therefore is an essential ingredient in light amplifiers and oscillators. In fact, the word LASER is an acronym for Light Amplification by Stimulated Emission of Radiation.
Relations described by Einstein connecting the rates of spontaneous emission, stimulated emission, and absorption of radiation by an atomic system in free space are generalized to apply to broadband spectra of quantized systems dilutely distributed in a dielectric medium. Although the gross features of the broadband emission and absorption spectra can be qualitatively different (especially at low temperatures), the various spectra are connected at any specific frequency by simple expressions. For a two-level system imbedded in a medium at temperature TTT, typical equations connecting stimulated-emission and absorption cross sections $\ensuremath{\sigma}(\ensuremath{\omega})$ to the rate $f(\ensuremath{\omega})$ of spontaneous emission of photons per unit solid angle per unit frequency interval are: ${\ensuremath{\sigma}}_{e}(\ensuremath{\omega})={\ensuremath{\sigma}}_{a}(\ensuremath{\omega})\mathrm{exp}[\frac{\ensuremath{\hbar}(\ensuremath{\mu}\ensuremath{-}\ensuremath{\omega})}{\mathrm{kT}}]=f(\ensuremath{\omega}){(\frac{2\ensuremath{\pi}c}{\ensuremath{\omega}n})}^{2}$, where $\ensuremath{\hbar}\ensuremath{\mu}$ is a temperature-dependent excitation potential and nnn is the index of refraction of the host material.
The basic phenomena of interaction between atoms and e.m. fields can be discussed in some detail without the need of a detailed model of the atom. Absorption and stimulated emission of radiation can be explained satisfactorily by the theory, where a classical electromagnetic wave provides a time-dependent perturbation to the energy of the atomic electrons. Laser radiation appears to a very good approximation to be a classical travelling wave of well-defined amplitude and phase. The radiation produced by a continuous laser is a good approximation to a coherent state. For conventional sources of radiation, the interaction energy is small compared with the energy an electron possesses by virtue of the attraction to the atomic nucleus, so perturbation theory produces quite acceptable results. The quantum mechanical analogy to the distortion of the classical charge cloud is given by the writing down of a general state function for the system, Ψ.
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) .