Stimulated optical forces offer a simple and efficient method for providing optical forces far in excess of the saturated radiative force. The bichromatic force, using a counterpropagating pair of two-color beams, has so far been the most effective o
f these stimulated forces for deflecting and slowing atomic beams. We have numerically studied the evolution of a two-level system under several different bichromatic and polychromatic light fields, while retaining the overall geometry of the bichromatic force. New insights are gained by studying the time-dependent trajectory of the Bloch vector, including a better understanding of the remarkable robustness of bi- and polychromatic forces with imbalanced beam intensities. We show that a four-color polychromatic force exhibits great promise. By adding new frequency components at the third harmonic of the original bichromatic detuning, the force is increased by nearly 50% and its velocity range is extended by a factor of three, while the required laser power is increased by only 33%. The excited-state fraction, crucial to possible application to molecules, is reduced from 41% to 24%. We also discuss some important differences between polychromatic forces and pulse trains from a high-repetition-rate laser.
By combining a recent precise measurement of the ionization energy of $^{87}$Rb with previous measurements of electronic and hyperfine structure, an accurate value for the $^{85}textrm{Rb}-^{87}textrm{Rb}$ isotope shift of the 5$^2S_{1/2}$ ground sta
te can be determined. In turn, comparison with additional spectroscopic data makes it possible for the first time to evaluate isotope shifts for the low-lying excited states, accurate in most cases to about 1 MHz. In a few cases, the specific mass shift contribution can be determined in addition to the total shift. This information is particularly useful for spectroscopic analysis of transitions to Rydberg states, and for tests of atomic theory.
