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Physical Review

Relaxation Mechanisms in Optical Pumping

F. A. Franz

Published Jan 7, 1966• 30 citations
Publisher

Abstract

The distribution of population in the ground-state sublevels of an optically pumped alkali-metal vapor has been found to be strongly dependent on the mechanism assumed responsible for relaxation. Two modes of optical pumping zero mixing and complete mixing in the excited state, and three modes of alkali relaxation, uniform, Zeeman, and electron randomization, are considered. Calculations of the sublevel relative populations are made in terms of experimentally measurable parameters for all six combinations of pumping and relaxation modes. Optical-pumping transient signals are then used to demonstrate that alkali relaxation due to wall collisions is of the low-frequency "Zeeman" variety, while relaxation due to alkali-rare-gas collisions takes place through randomization of the spin of the alkali valence electron. Equations for the rate of change of the electronic spin polarization are derived for all cases, and are found to be nonexponential, in contrast with the case of an alkali of zero nuclear spin.

DOI
10.1103/physrev.141.105

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Optical Methods of Atomic Orientation and of Magnetic Resonance*

Alfred Kastler

In the optical excitation of atoms with polarized light, producing excited atoms, only some of the Zeeman sublevels of the excited state are actually reached, so that large differences of population can be built up between Zeeman sublevels or between hyperfine structure (hfs) levels. This property can be used to detect radio-frequency resonance in optically excited atomic states. These resonances produce a characteristic change in intensity or in the degree of polarization of the light re-emitted. Zeeman intervals, Stark effects, and hfs intervals can be measured in this manner. (The Stark constant of the 63P1 level of Hg and the electric quadrupole moments of the alkali atoms have been obtained in this way.)The technique of “optical pumping” gives a way to concentrate atoms in some of the Zeeman sublevels of one of the hfs levels of the ground state.Atomic orientation has been obtained with the Na atom, in an atomic beam and in the vapor in equilibrium with the metal. The orientation effects have been studied by detection of radio-frequency resonance signals in the ground state. Orientation can be increased many times by adding a variable pressure of a foreign gas to the pure Na vapor. Because of the coupling between nuclear spin and electron spin, nuclear orientation is produced at the same time as atomic orientation.

Journal of the Optical Society of America•Jun 1, 1957•223 citations
The distribution of population in the ground-state sublevels of an optically pumped alkali-metal vapor has been found to be strongly dependent on the mechanism assumed responsible for relaxation. Two modes of optical pumping zero mixing and complete mixing in the excited state, and three modes of alkali relaxation, uniform, Zeeman, and electron randomization, are considered. Calculations of the sublevel relative populations are made in terms of experimentally measurable parameters for all six combinations of pumping and relaxation modes. Optical-pumping transient signals are then used to demonstrate that alkali relaxation due to wall collisions is of the low-frequency "Zeeman" variety, while relaxation due to alkali-rare-gas collisions takes place through randomization of the spin of the alkali valence electron. Equations for the rate of change of the electronic spin polarization are derived for all cases, and are found to be nonexponential, in contrast with the case of an alkali of zero nuclear spin.
Rate equations for the optical pumping of alkali-metal vapors simultaneously subject to pumping, relaxation in the excited state, and relaxation in the ground state are shown to yield analytic solutions for the alkali-metal electronic and nuclear-spin polarizations in the limit of weak pumping. Nuclear-spin and hyperfine-interaction effects are properly included. Analysis of the double-exponential form of the pumping transient of the ground-state electronic-spin polarization is shown to yield new methods for the measurement of cross sections for collisional relaxation in both the ground and excited states. Formulas are derived that relate relaxation cross sections to experimentally measurable parameters. Formulas describing the influence of nuclear spin on signals obtained from standard depolarization of resonance-radiation experiments also are provided. Ambiguities in earlier optical-pumping experiments and calculations arising from oversimplified descriptions of relaxation processes are discussed.
The relaxation and generation of multipole orientations in a heavy-alkali-metal vapor in the presence of a weak static magnetic field are theoretically studied both for populations and for Zeeman coherences by taking into account the effects on the evolution of the atomic density matrix of the relaxation processes (by alkali-atom--buffer-gas, alkali-atom--alkali-atom with spin exchange and alkali-atom--cell-wall collisions) and of the optical pumping with any light polarization and spectral distribution. The dependence of the stationary-state multipole orientations on the pumping characteristic parameters is numerically analyzed. The detection process of these orientations is also studied.
We present a comprehensive theory of nuclear spin polarization of 3He{}^{3}\mathrm{He}3He and 129Xe{}^{129}\mathrm{Xe}129Xe gases by spin-exchange collisions with optically pumped alkali-metal vapors. The most important physical processes considered are (1) spin-conserving spin-exchange collisions between like or unlike alkali-metal atoms; (2) spin-destroying collisions of the alkali-metal atoms with each other and with buffer-gas atoms; (3) electron-nuclear spin-exchange collisions between alkali-metal atoms and 3He{}^{3}\mathrm{He}3He or 129Xe{}^{129}\mathrm{Xe}129Xe atoms; (4) spin interactions in van der Waals molecules consisting of a Xe atom bound to an alkali-metal atom; (5) optical pumping by laser photons; (6) spatial diffusion. The static magnetic field is assumed to be small enough that the nuclear spin of the alkali-metal atom is well coupled to the electron spin and the total spin is very nearly a good quantum number. Conditions appropriate for the production of large quantities of spin-polarized 3He{}^{3}\mathrm{He}3He or 129Xe{}^{129}\mathrm{Xe}129Xe gas are assumed, namely, atmospheres of gas pressure and nearly complete quenching of the optically excited alkali-metal atoms by collisions with N2{\mathrm{N}}_{2}N2​ or H2{\mathrm{H}}_{2}H2​ gas. Some of the more important results of this work are as follows: (1) Most of the pumping and relaxation processes are sudden with respect to the nuclear polarization. Consequently, the steady-state population distribution of alkali-metal atoms is well described by a spin temperature, whether the rate of spin-exchange collisions between alkali-metal atoms is large or small compared to the optical pumping rate or the collisional spin-relaxation rates. (2) The population distributions that characterize the response to sudden changes in the intensity of the pumping light are not described by a spin temperature, except in the limit of very rapid spin exchange. (3) Expressions given for the radio-frequency (rf) resonance linewidths and areas can be used to make reliable estimates of the local spin polarization of the alkali-metal atoms. (4) Diffusion effects for these high-pressure conditions are mainly limited to thin layers at the cell surface and at internal resonant surfaces generated by radio-frequency magnetic fields when the static magnetic field has substantial spatial inhomogeneities. The highly localized effects of diffusion at these surfaces are described with closed-form analytic functions instead of the spatial eigenmode expansions that are appropriate for lower-pressure cells.
The effect of excited-state mixing on the optical pumping of alkali-metal vapors is considered for the case where the energy separation between the 2P12^{2}P_{\frac{1}{2}}2P21​​ and 2P32^{2}P_{\frac{3}{2}}2P23​​ first excited states is relatively large, allowing the isolation of mixing effects within a particular JJJ level. Two models for the mixing process are proposed, one a random reorientation of the total electronic angular momentum J, and the other a reorientation of J subject to the selection rule $\ensuremath{\Delta}{m}_{J}=0, \ifmmode\pm\else\textpm\fi{}2$. The probabilities for mixing transitions among JJJ-state sublevels have been calculated for an alkali atom of nuclear spin 32\frac{3}{2}23​, and can be used to calculate the optical-pumping transition probabilities for a vapor subject to any degree of excited-state mixing. Several possible experiments suggested by these calculations are discussed.
The effect of the hyperfine interaction on collisional relaxation among Zeeman sublevels is evaluated for a J=32J=\frac{3}{2}J=23​ state coupled to nuclear spins of 32\frac{3}{2}23​, 52\frac{5}{2}25​, and 72\frac{7}{2}27​. Standard depolarization experiments, performed on atoms with hyperfine structure, are discussed in terms of relaxation-probability matrices parametrized in terms of the relative collisional-transition probabilities for a nuclear-spin-zero atom. Experimental results involving D2{D}_{2}D2​ optical pumping of 85Rb^{85}\mathrm{Rb}85Rb and 87Rb^{87}\mathrm{Rb}87Rb are shown to support the approximation of nuclear decoupling in collisional relaxation. The cross sections for electronic collisional relaxation, assuming a van der Waals model for the collisional interaction, are, in units of ${10}^{\ensuremath{-}14}$ cm2{\mathrm{cm}}^{2}cm2, 1.19 (85Rb^{85}\mathrm{Rb}85Rb-He), 1.09 (85Rb^{85}\mathrm{Rb}85Rb-Ne), 2.44 (85Rb^{85}\mathrm{Rb}85Rb-Ar), 1.13 (87Rb^{87}\mathrm{Rb}87Rb-He), 1.03 (87Rb^{87}\mathrm{Rb}87Rb-Ne), and 2.26 (87Rb^{87}\mathrm{Rb}87Rb-Ar).
In the optical excitation of atoms with polarized light, producing excited atoms, only some of the Zeeman sublevels of the excited state are actually reached, so that large differences of population can be built up between Zeeman sublevels or between hyperfine structure (hfs) levels. This property can be used to detect radio-frequency resonance in optically excited atomic states. These resonances produce a characteristic change in intensity or in the degree of polarization of the light re-emitted. Zeeman intervals, Stark effects, and hfs intervals can be measured in this manner. (The Stark constant of the 63P1 level of Hg and the electric quadrupole moments of the alkali atoms have been obtained in this way.)The technique of “optical pumping” gives a way to concentrate atoms in some of the Zeeman sublevels of one of the hfs levels of the ground state.Atomic orientation has been obtained with the Na atom, in an atomic beam and in the vapor in equilibrium with the metal. The orientation effects have been studied by detection of radio-frequency resonance signals in the ground state. Orientation can be increased many times by adding a variable pressure of a foreign gas to the pure Na vapor. Because of the coupling between nuclear spin and electron spin, nuclear orientation is produced at the same time as atomic orientation.