Isotope study of the nonlinear pressure shifts of $^{85}$Rb and $^{87}$Rb hyperfine resonances in Ar, Kr, and Xe buffer gases

TL;DR

This study investigates the nonlinear pressure shifts of hyperfine resonances in rubidium isotopes caused by buffer gases, revealing discrepancies with previous theories and improving models for practical atomic clock applications.

Contribution

It introduces a refined quantum mechanical model that accurately fits nonlinear pressure shifts for both rubidium isotopes across different buffer gases.

Findings

Nonlinear pressure shifts observed in $^{85}$Rb and $^{87}$Rb are similar to previous results but show discrepancies with existing theories.

Including dipolar-hyperfine interactions in the model improves the fit to experimental data.

Shifts in He and N$_2$ buffer gases are linear with pressure, contrasting with noble gases.

Abstract

Measurements of the 0--0 hyperfine resonant frequencies of ground-state $^{85}$Rb atoms show a nonlinear dependence on the pressure of the buffer gases Ar, Kr, and Xe. The nonlinearities are similar to those previously observed with $^{87}$Rb and $^{133}$Cs and presumed to come from alkali-metal--noble-gas van der Waals molecules. However, the shape of the nonlinearity observed for Xe conflicts with previous theory, and the nonlinearities for Ar and Kr disagree with the expected isotopic scaling of previous $^{87}$Rb results. Improving the modeling alleviates most of these discrepancies by treating rotation quantum mechanically and considering additional spin interactions in the molecules. Including the dipolar-hyperfine interaction allows simultaneous fitting of the linear and nonlinear shifts of both $^{85}$Rb and $^{87}$Rb in either Ar, Kr, or Xe buffer gases with a minimal set of shared, isotope-independent parameters. To the limit of experimental accuracy, the shifts in He and N$_2$ were linear with pressure. The results are of practical interest to vapor-cell atomic clocks and related devices.