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Cambridge University Press eBooks

Rate equations

J. Donald Rimstidt

Published Nov 7, 2013• 1 citation
Publisher
DOI
10.1017/cbo9781139342773.004

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We derive two different sets of rate equations for sympathetic cooling of harmonically trapped bosons or fermions. The rate equations are obtained from a master equation derived earlier by Lewenstein et al. [Phys. Rev. A 51, 4617 (1995)] by means of decoherence and ergodicity arguments. We show analytically that the thermal equilibrium state is a stationary solution of our rate equation. We present analytical results for the rate coefficients which are needed to solve the rate equations, and we give approximate formulas that permit their computation in practice. We solve the two sets of rate equations numerically and compare the results. The cooling times obtained in both approaches agree very well. The equilibration rates show fair agreement.

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Masers exhibit interesting transient behavior that cannot be completely understood on the basis of the rate equations. The use of the rate equations in most transient analyses is usually justified on a more or less intuitive basis and the implied assumptions are not always clear. In this paper, the macroscopic maser rate equations are derived systematically from the Boltzmann equation for the density matrix of the atomic systems and Maxwell's equations for the radiation fields. When the coherence linewidth (T2−1) of the atomic systems is much larger than the cavity linewidth and the natural linewidth (T1−1) of the atomic emission, and with a WKB approximation, in the lowest order of approximation one obtains the two widely used, coupled first-order nonlinear rate equations of Statz and deMars. On the other hand, if the cavity linewidth is much larger than the atomic linewidths (T1−1 and T2−1), one can use the so-called ``reaction-field principle'' of Anderson and obtain, again, two coupled first-order rate equations; however, only one of the equations is nonlinear. The ranges of validity of both approaches are discussed in some detail.

Journal of Applied Physics•Oct 1, 1963•60 citations
We derive two different sets of rate equations for sympathetic cooling of harmonically trapped bosons or fermions. The rate equations are obtained from a master equation derived earlier by Lewenstein et al. [Phys. Rev. A 51, 4617 (1995)] by means of decoherence and ergodicity arguments. We show analytically that the thermal equilibrium state is a stationary solution of our rate equation. We present analytical results for the rate coefficients which are needed to solve the rate equations, and we give approximate formulas that permit their computation in practice. We solve the two sets of rate equations numerically and compare the results. The cooling times obtained in both approaches agree very well. The equilibration rates show fair agreement.
Starting from the multi-level master equation a non-Markoffian rate equation is derived. Explicit expressions for the transition rates between each pair of atomic levels in this equation are derived at it is shown that these may be interpreted as the sum of one-photon, two-photon,..., etc. transition rates connecting the given pair of levels. The non-Markoffian master equation is exact and so can describe long- or short-time behaviour under monochromatic or broad-band excitation. The exact steady-state solutions are obtained by solving a Markoffian rate equation.
Masers exhibit interesting transient behavior that cannot be completely understood on the basis of the rate equations. The use of the rate equations in most transient analyses is usually justified on a more or less intuitive basis and the implied assumptions are not always clear. In this paper, the macroscopic maser rate equations are derived systematically from the Boltzmann equation for the density matrix of the atomic systems and Maxwell's equations for the radiation fields. When the coherence linewidth (T2−1) of the atomic systems is much larger than the cavity linewidth and the natural linewidth (T1−1) of the atomic emission, and with a WKB approximation, in the lowest order of approximation one obtains the two widely used, coupled first-order nonlinear rate equations of Statz and deMars. On the other hand, if the cavity linewidth is much larger than the atomic linewidths (T1−1 and T2−1), one can use the so-called ``reaction-field principle'' of Anderson and obtain, again, two coupled first-order rate equations; however, only one of the equations is nonlinear. The ranges of validity of both approaches are discussed in some detail.