By applying Doppler-free saturated absorption spectroscopy in the regime of high integrated sample absorption, high-contrast Doppler-free laser transmission signals can be obtained as demonstrated in experiments on the sodium D lines. Natural linewidth background-free signals are observed.
Doppler-free saturation spectroscopy in the regime of strong pumping intensities and optically thick atomic samples is investigated experimentally and theoretically. It is shown that a very high signal-to-background ratio can be obtained and, at the same time, subnatural linewidths can be reached. Further contrast and linewidth improvements can be attained by supplementing the primary depleted pumping beam with a second pumping beam. By using the signal beam from a first setup as the pumping beam for a second identical arrangement, extreme values for contrast and linewidth should be attainable.
Saturated absorption spectroscopy linewidths down to half the natural linewidth have been obtained for the sodium D1 transition in a strongly absorbing gas cell. The strong-line-narrowing effect is achieved by using an experimental ``tandem'' approach with two absorbing cells in series, where the saturated absorption output from the first cell is used as an input beam for a saturated absorption measurement in the second cell. A physical interpretation of the line-narrowing mechanism in highly absorbing media is presented, which, among other things, explains why the narrowing effects are different for crossover transitions. It is further argued that in these experiments the line-narrowing effect is caused by optical pumping and can be appropriately described by rate equations. This is different from several other recent papers on high-contrast transmission spectroscopy, where full Bloch vector models were necessary to fully describe the line shapes. Here a rate equation model, which includes two spatial dimensions, is developed, and reasonable agreement is obtained between experimental and theoretical data. \textcopyright{} 1996 The American Physical Society.
The utilization of atomic or molecular spectroscopy for frequency locking of single-frequency laser to improve laser frequency stability plays an important role in the experimental investigation of optically pumped atomic magnetometers, atomic clocks, laser cooling and trapping of atoms, etc. We have experimentally demonstrated a technique for frequency stabilization of a single-frequency laser employing the bright state spectroscopy (BSS) with a rubidium atomic vapor cell. By utilizing the counter-propagating dual-frequency 795 nm laser beams with mutually orthogonal linear polarization and a frequency difference of 6.834 GHz, which is equal to the hyperfine splitting of rubidium-87 ground state 5S1/2, an absorption-enhanced signal with narrow linewidth at the center of Doppler-broadened transmission spectroscopy is observed when continuous scanning the laser frequency over rubidium-87 D1 transition. This is the so-called BSS. Amplitude of the absorption-enhanced signal in the BSS is much larger compared with the conventional saturation absorption spectroscopy (SAS). The relationship between linewidth and amplitude of the BSS signal and laser beam intensity has been investigated. This high-contrast absorption-enhanced BSS signal has been employed for the laser frequency stabilization. The experimental results show that the frequency stability is 4.4×10−11 with an integration time of 40 s, near one order of magnitude better than that for using the SAS.