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Physical Review

Study of the Spin-Relaxation Times and the Effects of Spin-Exchange Collisions in an Optically Oriented Sodium Vapor

L. W. Anderson, Alan T. Ramsey

Published Oct 15, 1963• 82 citations
Publisher

Abstract

The spin-relaxation time of an optically oriented sodium vapor diffusing in a helium or neon buffer gas has been measured and analyzed by the method of Franzen. The diffusion coefficients for sodium in helium and neon are 1.0\ifmmode\pm\else\textpm\fi{}0.3 and 0.50\ifmmode\pm\else\textpm\fi{}0.17 ${\mathrm{cm}}^{2}$/sec, respectively. The disorientation cross sections for sodium colliding with helium and neon are (3\ifmmode\pm\else\textpm\fi{}4)\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}26}$ and (1.8\ifmmode\pm\else\textpm\fi{}0.6)\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}24}$ ${\mathrm{cm}}^{2}$, respectively. The radio-frequency (rf) Zeeman transitions of the sodium atoms in the ground state have been examined. An analysis of the effects of spin-exchange collisions between sodium atoms on the intensities and line shapes of the various Zeeman transitions is presented. From these studies a spin exchange cross section of (1-3)\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}14}$ ${\mathrm{cm}}^{2}$ is estimated for two sodium atoms colliding. The main source of error in this measurement is probably lack of knowledge of the sodium vapor pressure in the sodium-absorption cells.

DOI
10.1103/physrev.132.712

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Effect of Spin-Exchange Collisions on the Optical Orientation of Atomic Sodium

L. W. Anderson, Alan T. Ramsey

The effect of spin-exchange collisions on the state populations obtained in an optically pumped ${\mathrm{Na}}^{23}$ vapor is studied in the limit of low light intensity. These state populations and hence the intensity of the rf Zeeman transitions are found theoretically to depend strongly on the spin-exchange cross sections. The various Zeeman rf transitions are found experimentally to be very different in intensity and this is interpreted as being partially due to spin-exchange collisions. From the intensity of the rf transitions in a magnetic field large enough to separate the six Zeeman components and from the observed relaxation time a spin-exchange cross section for two sodium atoms of $\ensuremath{\pi}{{S}_{0}}^{2}=6\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}14}$ ${\mathrm{cm}}^{2}$ is found.

Physical Review•Dec 15, 1961•14 citations

Spin Relaxation of Optically Aligned Rubidium Vapor

W. Franzen

A new optical method for studying the spin relaxation of optically aligned rubidium vapor is described. In this method, the pumping radiation, consisting of circularly polarized ${D}_{1}$ resonance radiation, is suddenly shut off and then turned on again after a known time interval. The relaxation which takes place during the interval of darkness causes the vapor to become more opaque to the pumping radiation at a rate which is determined by the relaxation time. A large degree of alignment, as well as a relaxation time of about 80 milliseconds, were observed in a closed-off evacuated cylindrical glass cell completely lined, except for $\frac{1}{200}$ of the wall area, with a thin film of tetracontane (${\mathrm{C}}_{40}$${\mathrm{H}}_{82}$). The variation of relaxation time with buffer gas pressure was studied in this cell and in an unlined glass cell. From the observations with the unlined cell, diffusion coefficients for rubidium in neon and argon of 0.31 ${\mathrm{cm}}^{2}$/sec and 0.24 ${\mathrm{cm}}^{2}$/sec, respectively, can be deduced. Observed cross sections for disorientation collisions between aligned ground-state rubidium atoms and neon, argon, krypton, and xenon atoms are 5.2\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}23}$ ${\mathrm{cm}}^{2}$, 3.7\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}22}$ ${\mathrm{cm}}^{2}$, 5.9\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}21}$ ${\mathrm{cm}}^{2}$, and 1.3\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}20}$ ${\mathrm{cm}}^{2}$, respectively. In the evacuated tetracontane-lined cell, the relaxation time decreased by 30% for a tenfold increase in rubidium vapor pressure. An explanation for this relatively weak dependence is suggested. The longest observed relaxation time was approximately 0.4 seconds in a tetracontanelined cell filled with neon to a pressure of 3 cm Hg.

Physical Review•Aug 15, 1959•279 citations

Hyperfine Relaxation of Optically Pumped Rb87 Atoms in Buffer Gases

Maurice Arditi, T. R. Carver

The hyperfine relaxation of a population difference, produced by optical pumping, between the $F=1$ ${m}_{F}=0$ and $F=2$ ${m}_{F}=0$ energy levels of the ground state of ${\mathrm{Rb}}^{87}$, has been studied in cells containing neon, argon, helium, or krypton as a buffer gas. The relaxation times ${T}_{1}$ and ${T}_{2}$ have been measured as a function of the rubidium vapor pressure in the cell. The relaxation rate due to spin exchange in ${\mathrm{Rb}}^{87}$-${\mathrm{Rb}}^{87}$ collisions has been found equal to 65 ${\mathrm{sec}}^{\ensuremath{-}1}$ at 44\ifmmode^\circ\else\textdegree\fi{}C, and the diffusion coefficients of ${\mathrm{Rb}}^{87}$ atoms in He, Ne, and Ar evaluated as 0.6, 0.31, and 0.22 ${\mathrm{cm}}^{2}$ ${\mathrm{sec}}^{\ensuremath{-}1}$, respectively. The cross section for ${\mathrm{Rb}}^{87}$-Ne and ${\mathrm{Rb}}^{87}$-Ar collisions are found to be 1.6\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}22}$ ${\mathrm{cm}}^{2}$ and 9\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}22}$ ${\mathrm{cm}}^{2}$. These values are in general agreement with values previously obtained by other methods. The extrapolated values of $\frac{1}{{T}_{2}}$ for zero vapor pressure of rubidium are 185, 237, and 318 ${\mathrm{sec}}^{\ensuremath{-}1}$ for Ne, He, or Ar, respectively. Relaxations by the pumping light or by the magnetic field inhomogeneities are also discussed.

Physical Review•Nov 2, 1964•38 citations

Rubidium Spin Relaxation in the Rare Gases Under Ultraclean Conditions

F. A. Franz

The spin relaxation of optically pumped rubidium vapor induced by rubidium-rare-gas atomic collisions has been investigated in an ultraclean environment. The experiment was performed under conditions such that the partial pressure of nonrare-gas impurities was less than 1\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}8}$ Torr, and that the time between Rb-Rb spin exchange collisions was short compared to the spin relaxation time. The cross sections (in ${\mathrm{cm}}^{2}$) for disorientation of rubidium were found to be: He, 3.3\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}25}$; Ne, 3.3\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}24}$; Ar, 1.1\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}22}$; Kr, 7.3\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}21}$; Xe, 1.3\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}19}$. The fact that these cross sections are considerably smaller than previously reported values is attributed primarily to the low degree of impurity contamination in the present work. When compared with already existing values for cesium and sodium, the disorientation cross sections of these three alkali metals are seen to have a remarkably similar dependence on buffer-gas atomic number. The new experimental values are also compared with recent theoretical calculations.

Physical Review•Aug 2, 1965•33 citations

Spin Relaxation of Optically Pumped Rubidium Atoms in Molecular Buffer Gases

Robert J. McNeal

Short spin relaxation times for rubidium atoms, oriented by optical pumping, have been observed in the presence of benzene, ammonia, and dimethyl ether buffer gases. The disorientation cross sections of these gases in rubidium are obtained from relaxation times measured in mixtures with molecular nitrogen. The partial pressures of the gases were low compared to the nitrogen pressures in the mixtures, and the diffusion coefficient of rubidium in the mixtures was assumed to be the same as in pure nitrogen. The disorientation cross sections at 55°C are 7±1×10—19 cm2 for benzene, 8±2×10—18 cm2 for ammonia, and 3±1×10—18 cm2 for dimethyl ether. The cross section of carbon monoxide has also been obtained from the longer rubidium spin relaxation time in this gas. These measurements, complicated by a slow reaction of carbon monoxide with liquid rubidium, yield a cross section of 1±0.5×10—22 cm2 for carbon monoxide. The cross sections of ammonia, dimethyl ether, and benzene are much larger than cross sections of other molecular buffer gases. A discussion of the relaxation processes in these gases is given. The large cross sections of polar gases with appreciable dipole moments are found to result from an interaction of the rubidium atoms with the electric field of the polar molecules during a collision. Virtual excitation to the p states of the atom by the electric field gives rise to an interaction of the spin of the valence electron with the orbital angular momentum of the p states. The direct contribution of the magnetic field of the moving polar molecule is also considered and found to be small compared to the electric interaction. The large cross section of benzene is assumed to result from a spin exchange interaction with a charge transfer complex of rubidium and benzene formed in very small amounts. If the assumed complex is responsible for the large benzene cross section, the equilibrium constant for its formation can be calculated from an estimate of the spin exchange cross section.

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Effect of Na–Na spin-exchange collisions on spin relaxation of optically pumped Na in Xe gas

Hou Mei-ying, Bingying Cheng, R. Ju

We report the first detection of the effect of Na–Na spin exchange collisions on spin relaxation of optically pumped Na in Xe gas by studying the relaxation in the "dark" of the variable ⟨ S z ⟩ in a mixture of dense sodium vapor (number density [Na] ~ 10 13 cm −3 ), and buffer gas helium, xenon and nitrogen as a function of [Na] and xenon pressure.

Chinese Physics Letters•Nov 1, 1984•8 citations
The spin-relaxation time of an optically oriented sodium vapor diffusing in a helium or neon buffer gas has been measured and analyzed by the method of Franzen. The diffusion coefficients for sodium in helium and neon are 1.0\ifmmode\pm\else\textpm\fi{}0.3 and 0.50\ifmmode\pm\else\textpm\fi{}0.17 cm2{\mathrm{cm}}^{2}cm2/sec, respectively. The disorientation cross sections for sodium colliding with helium and neon are (3\ifmmode\pm\else\textpm\fi{}4)\ifmmode\times\else\texttimes\fi{}10\ensuremath−26{10}^{\ensuremath{-}26}10\ensuremath−26 and (1.8\ifmmode\pm\else\textpm\fi{}0.6)\ifmmode\times\else\texttimes\fi{}10\ensuremath−24{10}^{\ensuremath{-}24}10\ensuremath−24 cm2{\mathrm{cm}}^{2}cm2, respectively. The radio-frequency (rf) Zeeman transitions of the sodium atoms in the ground state have been examined. An analysis of the effects of spin-exchange collisions between sodium atoms on the intensities and line shapes of the various Zeeman transitions is presented. From these studies a spin exchange cross section of (1-3)\ifmmode\times\else\texttimes\fi{}10\ensuremath−14{10}^{\ensuremath{-}14}10\ensuremath−14 cm2{\mathrm{cm}}^{2}cm2 is estimated for two sodium atoms colliding. The main source of error in this measurement is probably lack of knowledge of the sodium vapor pressure in the sodium-absorption cells.
The effect of spin-exchange collisions on the state populations obtained in an optically pumped Na23{\mathrm{Na}}^{23}Na23 vapor is studied in the limit of low light intensity. These state populations and hence the intensity of the rf Zeeman transitions are found theoretically to depend strongly on the spin-exchange cross sections. The various Zeeman rf transitions are found experimentally to be very different in intensity and this is interpreted as being partially due to spin-exchange collisions. From the intensity of the rf transitions in a magnetic field large enough to separate the six Zeeman components and from the observed relaxation time a spin-exchange cross section for two sodium atoms of $\ensuremath{\pi}{{S}_{0}}^{2}=6\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}14}$ cm2{\mathrm{cm}}^{2}cm2 is found.
A new optical method for studying the spin relaxation of optically aligned rubidium vapor is described. In this method, the pumping radiation, consisting of circularly polarized D1{D}_{1}D1​ resonance radiation, is suddenly shut off and then turned on again after a known time interval. The relaxation which takes place during the interval of darkness causes the vapor to become more opaque to the pumping radiation at a rate which is determined by the relaxation time. A large degree of alignment, as well as a relaxation time of about 80 milliseconds, were observed in a closed-off evacuated cylindrical glass cell completely lined, except for 1200\frac{1}{200}2001​ of the wall area, with a thin film of tetracontane (C40{\mathrm{C}}_{40}C40​H82{\mathrm{H}}_{82}H82​). The variation of relaxation time with buffer gas pressure was studied in this cell and in an unlined glass cell. From the observations with the unlined cell, diffusion coefficients for rubidium in neon and argon of 0.31 cm2{\mathrm{cm}}^{2}cm2/sec and 0.24 cm2{\mathrm{cm}}^{2}cm2/sec, respectively, can be deduced. Observed cross sections for disorientation collisions between aligned ground-state rubidium atoms and neon, argon, krypton, and xenon atoms are 5.2\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}23}$ cm2{\mathrm{cm}}^{2}cm2, 3.7\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}22}$ cm2{\mathrm{cm}}^{2}cm2, 5.9\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}21}$ cm2{\mathrm{cm}}^{2}cm2, and 1.3\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}20}$ cm2{\mathrm{cm}}^{2}cm2, respectively. In the evacuated tetracontane-lined cell, the relaxation time decreased by 30% for a tenfold increase in rubidium vapor pressure. An explanation for this relatively weak dependence is suggested. The longest observed relaxation time was approximately 0.4 seconds in a tetracontanelined cell filled with neon to a pressure of 3 cm Hg.
The hyperfine relaxation of a population difference, produced by optical pumping, between the F=1F=1F=1 mF=0{m}_{F}=0mF​=0 and F=2F=2F=2 mF=0{m}_{F}=0mF​=0 energy levels of the ground state of Rb87{\mathrm{Rb}}^{87}Rb87, has been studied in cells containing neon, argon, helium, or krypton as a buffer gas. The relaxation times T1{T}_{1}T1​ and T2{T}_{2}T2​ have been measured as a function of the rubidium vapor pressure in the cell. The relaxation rate due to spin exchange in Rb87{\mathrm{Rb}}^{87}Rb87-Rb87{\mathrm{Rb}}^{87}Rb87 collisions has been found equal to 65 ${\mathrm{sec}}^{\ensuremath{-}1}$ at 44\ifmmode^\circ\else\textdegree\fi{}C, and the diffusion coefficients of Rb87{\mathrm{Rb}}^{87}Rb87 atoms in He, Ne, and Ar evaluated as 0.6, 0.31, and 0.22 cm2{\mathrm{cm}}^{2}cm2 ${\mathrm{sec}}^{\ensuremath{-}1}$, respectively. The cross section for Rb87{\mathrm{Rb}}^{87}Rb87-Ne and Rb87{\mathrm{Rb}}^{87}Rb87-Ar collisions are found to be 1.6\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}22}$ cm2{\mathrm{cm}}^{2}cm2 and 9\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}22}$ cm2{\mathrm{cm}}^{2}cm2. These values are in general agreement with values previously obtained by other methods. The extrapolated values of 1T2\frac{1}{{T}_{2}}T2​1​ for zero vapor pressure of rubidium are 185, 237, and 318 ${\mathrm{sec}}^{\ensuremath{-}1}$ for Ne, He, or Ar, respectively. Relaxations by the pumping light or by the magnetic field inhomogeneities are also discussed.
The spin relaxation of optically pumped rubidium vapor induced by rubidium-rare-gas atomic collisions has been investigated in an ultraclean environment. The experiment was performed under conditions such that the partial pressure of nonrare-gas impurities was less than 1\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}8}$ Torr, and that the time between Rb-Rb spin exchange collisions was short compared to the spin relaxation time. The cross sections (in cm2{\mathrm{cm}}^{2}cm2) for disorientation of rubidium were found to be: He, 3.3\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}25}$; Ne, 3.3\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}24}$; Ar, 1.1\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}22}$; Kr, 7.3\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}21}$; Xe, 1.3\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}19}$. The fact that these cross sections are considerably smaller than previously reported values is attributed primarily to the low degree of impurity contamination in the present work. When compared with already existing values for cesium and sodium, the disorientation cross sections of these three alkali metals are seen to have a remarkably similar dependence on buffer-gas atomic number. The new experimental values are also compared with recent theoretical calculations.
Short spin relaxation times for rubidium atoms, oriented by optical pumping, have been observed in the presence of benzene, ammonia, and dimethyl ether buffer gases. The disorientation cross sections of these gases in rubidium are obtained from relaxation times measured in mixtures with molecular nitrogen. The partial pressures of the gases were low compared to the nitrogen pressures in the mixtures, and the diffusion coefficient of rubidium in the mixtures was assumed to be the same as in pure nitrogen. The disorientation cross sections at 55°C are 7±1×10—19 cm2 for benzene, 8±2×10—18 cm2 for ammonia, and 3±1×10—18 cm2 for dimethyl ether. The cross section of carbon monoxide has also been obtained from the longer rubidium spin relaxation time in this gas. These measurements, complicated by a slow reaction of carbon monoxide with liquid rubidium, yield a cross section of 1±0.5×10—22 cm2 for carbon monoxide. The cross sections of ammonia, dimethyl ether, and benzene are much larger than cross sections of other molecular buffer gases. A discussion of the relaxation processes in these gases is given. The large cross sections of polar gases with appreciable dipole moments are found to result from an interaction of the rubidium atoms with the electric field of the polar molecules during a collision. Virtual excitation to the p states of the atom by the electric field gives rise to an interaction of the spin of the valence electron with the orbital angular momentum of the p states. The direct contribution of the magnetic field of the moving polar molecule is also considered and found to be small compared to the electric interaction. The large cross section of benzene is assumed to result from a spin exchange interaction with a charge transfer complex of rubidium and benzene formed in very small amounts. If the assumed complex is responsible for the large benzene cross section, the equilibrium constant for its formation can be calculated from an estimate of the spin exchange cross section.