Relaxation experiments performed on optically polarized Rb atoms in a rare gas have been previously reported; their detailed interpretation is given below. It is shown that the relaxation governed by the spin-orbit interaction is strongly affected by the formation of chemically unstable Rb-Kr molecules bound by van der Waals forces. Two processes of molecule formation are analyzed: binary resonant collisions leading to metastable states and three-body collisions producing actual bound states. A relaxation model valid for any disorientation probability per single Rb-Kr interaction is developed. Aside from clear evidence for the existence of alkali-rare-gas molecules, the success of the theoretical interpretation of the relaxation experiments yields the equilibrium constant $\mathcal{K}=1.7\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}22}$
cm3/molecule for the reaction Rb+Kr \ensuremath{\rightleftharpoons} Rb-Kr at 300\ifmmode^\circ\else\textdegree\fi{}K, the average lifetime of a Rb-Kr molecule in the gas phase, $\ensuremath{\tau}=0.65\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}7}$ sec, at a krypton pressure of one Torr, and the average spin-orbit coupling constant in a Rb-Kr molecule, $\overline{\ensuremath{\gamma}}{h}^{\ensuremath{-}1}=0.63$ MHz. It is also shown that the spin-orbit potential is predominantly short-range.
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) 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.