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Journal of the Optical Society of America B

Production and diagnosis of a highly spin-polarized Na beam

Gregory W. Schinn, Xianming L. Han, Alan Gallagher

Published Jan 1, 1991• 12 citations
Publisher

Abstract

We describe optically pumping a beam of sodium atoms to >96% mS and >92% mS, mI state selection. (We have accurately measured the population of every mS, mI state in the optically pumped beam.) For the optical pumping both ground hyperfine states are pumped, using single-mode cw dye-laser radiation tuned to the 3S1/2–3P1/2 transition that is phase modulated in a LiTaO3 crystal to produce first-order sidebands at approximately the 1772-MHz hyperfine splitting of the ground state. The z-directed optical pumping is performed in a z-directed magnetic field of ~5 G. The state-selected atoms then move, in ~1 cm, into an ~200 G, z-directed field. The downstream probe laser beam is scanned through the 3S1/2 (mS, mI) → 3P3/2 (mS′, mI) transitions, which are spectroscopically resolved at 200 G, and the fluorescence intensities portray the residual populations in each of the eight 3S1/2 states.

DOI
10.1364/josab.8.000169

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Physical Review A•Mar 1, 1977•31 citations
We describe optically pumping a beam of sodium atoms to >96% mS and >92% mS, mI state selection. (We have accurately measured the population of every mS, mI state in the optically pumped beam.) For the optical pumping both ground hyperfine states are pumped, using single-mode cw dye-laser radiation tuned to the 3S1/2–3P1/2 transition that is phase modulated in a LiTaO3 crystal to produce first-order sidebands at approximately the 1772-MHz hyperfine splitting of the ground state. The z-directed optical pumping is performed in a z-directed magnetic field of ~5 G. The state-selected atoms then move, in ~1 cm, into an ~200 G, z-directed field. The downstream probe laser beam is scanned through the 3S1/2 (mS, mI) → 3P3/2 (mS′, mI) transitions, which are spectroscopically resolved at 200 G, and the fluorescence intensities portray the residual populations in each of the eight 3S1/2 states.
A highly polarized 23Na^{23}\mathrm{Na}23Na atomic beam is produced by optical pumping with the use of either a multimode cw dye laser or a single-mode ring dye laser followed by a double-passed acousto-optic modulator. Electron-spin polarizations of 0.72 to 0.90 are obtained.
All magnetometers using alkali atoms rely on the monochromatic light driving the optical pumping process in the D1 or D2 line to create spin-polarized atoms. In the study of a sodium (Na) magnetometer, we find that 23Na exhibits the same hyperfine structure as exhibited by the 87Rb atom but differs from Rb in terms of level splitting. The narrowly split hyperfine levels of the 23Na 3P3/2 excited state are comparable to its natural broadening (9.8 MHz). We have modeled the nearly unresolved hyperfine structure as a partially resolved multilevel system in which the absorption at each photon detuning will induce adjacent allowed transition pathways simultaneously. Thus, the corresponding optical pumping processes of 23Na and 87Rb are governed by similar rate equations but result in different redistributed populations. By numerically solving the rate equations, we demonstrate that optically pumped 23Na has a much smaller spin polarization than that of 87Rb because the population imbalances between the ground state Zeeman levels of 23Na are very small. The inefficient optical pumping can explain why Na magnetometers are not studied extensively. The investigation into the optical pumping process of 23Na is helpful in preparing a highly spin-polarized atomic medium and optimizing the sensitivity of Na magnetometers.
Circularly polarized laser beams propagating through sodium vapor and tuned to the buffer gas broadened atomic D1 transition can optically pump sodium atoms into a nonabsorbing groundstate. The corresponding groundstate populations depend on the intensity distribution, the polarization and the magnetic fields. They lead to refractive index gradients along as well as transverse to the laser beam propagation direction and therefore modify the light path giving rise to a number of nonlinear spatiotemporal intensity and polarization pattern creating processes.
We have used two-photon absorption from counterpropagating laser beams of different frequencies to measure Stark shifts and splittings of the 62S6^{2}S62S, 72S7^{2}S72S, 82S8^{2}S82S, 52D5^{2}D52D, and 62D6^{2}D62D states in sodium. Beams from a fixed-frequency, single-mode Ar+{\mathrm{Ar}}^{+}Ar+ laser and a tunable, single-frequency cw dye laser were focussed into a coarse sodium atomic beam and the fluorescence was monitored. The collimation of the atomic beam reduced the residual Doppler width inherent in using two different frequencies. Using the two lasers allowed two-photon transitions to be observed at frequencies unattainable with the dye laser alone, and enhanced the transition rates due to the near resonance of the dye laser with the strong Na $3^{2}S\ensuremath{\rightarrow}3^{2}P$ transition. Our experimental results for the scalar and tensor polarizabilities, ${\ensuremath{\alpha}}_{0}$ and ${\ensuremath{\alpha}}_{2}$, agree with calculations in the Bates and Damgaard Coulomb approximation within 2% for ${\ensuremath{\alpha}}_{0}$ and 9% for ${\ensuremath{\alpha}}_{2}$. As a by-product the hyperfine-interaction constants aaa for the SSS states and the fine-structure intervals $\ensuremath{\delta}\ensuremath{\nu}=\frac{({E}_{\frac{3}{2}}\ensuremath{-}{E}_{\frac{5}{2}})}{h}$ for the DDD states were obtained.