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Optics Letters

Continuous-wave Doppler-free two-photon frequency-modulation spectroscopy in Rb vapor

Werner Zapka, M. D. Levenson, Frank M. Schellenberg, A. C. Tam, Gary C. Bjorklund

Published Jan 1, 1983• 23 citations
Publisher

Abstract

Frequency-modulation spectroscopy was employed successfully to measure the Doppler-free absorption and dispersion signals originating from several two-photon transitions in (85)Rb and (87)Rb. The two-photon cross section of the hyperfine transition 5S(1/2) (F = 2) ? 5D(5/2) (F = 4) in (87)Rb was determined to be sigma((2)) asymptotically equal to 4 x 10(-20) cm(4)/W. The transition isotope shift (TIS) of the transition 5S(1/2) ? 5D(5/2) between (87)Rb and (85)Rb was found to be Deltanu(TIS) = +166 +/- 2 MHz.

DOI
10.1364/ol.8.000027

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Physica Scripta•Sep 1, 1995•73 citations
Frequency-modulation spectroscopy was employed successfully to measure the Doppler-free absorption and dispersion signals originating from several two-photon transitions in (85)Rb and (87)Rb. The two-photon cross section of the hyperfine transition 5S(1/2) (F = 2) ? 5D(5/2) (F = 4) in (87)Rb was determined to be sigma((2)) asymptotically equal to 4 x 10(-20) cm(4)/W. The transition isotope shift (TIS) of the transition 5S(1/2) ? 5D(5/2) between (87)Rb and (85)Rb was found to be Deltanu(TIS) = +166 +/- 2 MHz.
Heterodyne Doppler-free spectroscopy, previously demonstrated on single-photon resonances (heterodyne saturation spectroscopy), has been extended to two-photon transitions in rubidium (5S-5D and 5S-7S). It provides a simple method of observing the two-photon dispersion lineshape directly. The noticeable sensitivity of this absorption technique, which has been used for an optical measurement of the hyperfine structure of the 5D level, is discussed in comparison with that currently obtained in two-photon-induced fluorescence.
Abstract Using a Rb cell and a wavemeter, with a Doppler-free two-photon transition near 993 nm, we have measured the four hyperfine components (two isotopes, Δ F = 0) of the 5S–6S transition, finding the absolute energies of those transitions to a spectral resolution of 0.002 cm −1 = 60 MHz. We find the (87 minus 85) isotope shift of the 5S–6S transition to be +94(12) MHz. Using our single frequency cw laser with focused intensity up to 10 4 W cm −2 at the cell, we find no AC Stark or light shift of the lines at 6 MHz spectral resolution. We find no density shift of the lines at 6 MHz spectral resolution, for a range of Rb atom densities from 3 × 10 11 to 5 × 10 13 atoms/cm 3 .
Doppler-free two-photon absorption spectroscopy was applied to study highly-excited D states of Rb atoms. Using a cw dye laser as an excitation source, transitions from the ground 5S state to nd 2D states (n=11-32) were observed, the ionization energy of the highest state being only 117cm-1. These D doublets are not inverted. The fine structure splittings of these states do not vary as (neff) -3, nor as n-3. The isotope shift of the 85Rb, 87Rb ground states is found to be 160±12MHz. No pressure broadening was observed for these transitions within the instrumental resolution of 15 MHz.
A high-resolution two-photon spectrum of 5S 1/2 → 5P 3/2 → 5D 5/2 transitions in a thermal 85 Rb vapor cell is presented by using an optical frequency comb and a cw laser. The fluorescence of 6P 3/2 → 5S 1/2 spontaneous emission is detected when the cw laser frequency is scanned from the 5S 1/2 ground state to 5P 3/2 hyperfine levels and the optical frequency comb repetition rate is fixed. The hyperfine splittings (F f = 2–5) of the 5D 5/2 excited state are well resolved. The dependences of fluorescence intensities on the cw laser intensity and temperature of 85 Rb vapor cell are studied, respectively. The experimental results are in good agreement with the theoretical analyses.
We report on spectroscopic measurements of the Rb 5 D 5/2 state performed using two-photon excitation with a resonant intermediate state. With the two beams (5 S 1/2 → 5 P 3/2 at 780 nm and 5 P 3/2 → 5 D 5/2 at 776 nm) counterpropagating, the spectra are Doppler-free and the signals are very robust, even in a room temperature vapor. This is due to the near match of the transition wavelengths. The 5 D 5/2 hyperfine constants have been measured and compared to previous determinations. We have also performed the excitation in a sample of laser-cooled atoms and compare these results to those obtained at room temperature. The fact that the 5 P 3/2 → 5 D 5/2 transition is narrow, robust, diode-laser accessible, and relatively immune to AC-Stark shifts, may make it a promising candidate for a frequency reference at 776 nm.