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arXiv:1605.09245 · Optics Letters

Doppler-free spectroscopy on the Cs D_1 line with a dual-frequency laser

Moustafa Abdel Hafiz, Grégoire Coget, Emeric de Clercq, Rodolphe Boudot

Published Jun 22, 2016• 65 citations
arXivHTMLPDF

Abstract

We report on Doppler-free laser spectroscopy in a Cs vapor cell using a dual-frequency laser system tuned on the Cs D1 line. Using counter-propagating beams with crossed linear polarizations, an original sign reversal of the usual saturated absorption dip and large increase in Doppler-free atomic absorption is observed. This phenomenon is explained by coherent population trapping (CPT) effects. The impact of laser intensity and light polarization on absorption profiles is reported in both single-frequency and dual-frequency regimes. In the latter, frequency stabilization of two diode lasers was performed, yielding a beat note fractional frequency stability at the level of 3×10−12 at 1 s averaging time. These performances are about an order of magnitude better than those obtained using a conventional single-frequency saturated absorption scheme.

DOI
10.1364/ol.41.002982

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We report on Doppler-free laser spectroscopy in a Cs vapor cell using a dual-frequency laser system tuned on the Cs D1 line. Using counter-propagating beams with crossed linear polarizations, an original sign reversal of the usual saturated absorption dip and large increase in Doppler-free atomic absorption is observed. This phenomenon is explained by coherent population trapping (CPT) effects. The impact of laser intensity and light polarization on absorption profiles is reported in both single-frequency and dual-frequency regimes. In the latter, frequency stabilization of two diode lasers was performed, yielding a beat note fractional frequency stability at the level of 3×10−12 at 1 s averaging time. These performances are about an order of magnitude better than those obtained using a conventional single-frequency saturated absorption scheme.
We demonstrate a bichromatic Doppler-free spectroscopy of an 87 R b D 1 line by using a dual-frequency, counterpropagating laser field with orthogonal linear polarizations. A reversed Doppler-free resonance dip is observed in the dual-frequency scheme, and a significant improvement of frequency discrimination curve is acquired due to the coherent population trapping (CPT) effect. The influence of the static magnetic field and laser intensity on the spectroscopy is studied in both single- and dual-frequency schemes. After locking the laser frequency to the 87 R b D 1 line in the dual-frequency stabilization scheme, the beat note fractional frequency stability is at the level of 7 × 10 − 12 at 1 s integration time. This technique can be used in various applications, such as CPT atomic clocks, laser spectroscopy, quantum optics, and laser-cooling experiments.
Abstract We report on a global crossover saturated-absorption spectroscopy (SAS) of Cs D 2 transition using a dual-frequency laser field with a frequency difference of less than the Doppler width. With two pairs of dual-frequency laser beams counter-propagating through the vapor cell, the line shape and non-linear features observed in the transmission spectra of the probe beam change with the frequency difference of the dual-frequency laser. The superficially complicated transmission signal includes two sets of common single-frequency SAS and several velocity-selective resonances (VSRs), we call these VSR peaks ‘global crossover SAS’. This phenomenon is explained by VSR effect. The global crossover SAS is formed by the atomic velocity groups resonance with both the initial and modulated laser fields, which are counter-propagated. Moreover, the global crossover SAS dips having the separation of allowed hyperfine transitions move along with the two sets of common single-frequency SAS while the frequency difference of the dual-frequency laser is changed. This indicates a resonance between the velocity shifted pump laser frequency and the velocity shifted probe laser frequency. The results obtained in this system are of great interest for laser spectroscopy. Furthermore, the application of the counter-propagating laser beams in the dual-mode regime increase the number of atoms that effectively interact with the field, hence, this scheme has a potential advantage for laser frequency stabilization.
Sub-Doppler spectroscopy in alkali-metal vapor cells using two counterpropagating dual-frequency laser beams allows the detection of high-contrast sign-reversed natural-linewidth sub-Doppler resonances. Previously, a qualitative theory based on a simplified \ensuremath{\Lambda}-scheme model has been reported to explain underlying physics of this phenomenon. In this paper, an extended theoretical model of dual-frequency sub-Doppler spectroscopy (DFSDS) for the Cs D1{D}_{1}D1​ line is reported. Taking into account the real atomic energy structure, main relaxation processes, and various nonlinear effects, this model describes quantitatively the respective contributions of involved physical processes and predicts main properties (height and linewidth) of the sub-Doppler resonances. Experimental tests are performed with a Cs vapor microfabricated cell and results are found to be in correct agreement with theoretical predictions. Spatial oscillations of the sub-Doppler resonance amplitude with translation of the reflection mirror are highlighted. A beat note between two laser systems, including one stabilized with DFSDS on a Cs vapor microcell, yields a fractional frequency stability of $2\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}12}\phantom{\rule{0.16em}{0ex}}{\ensuremath{\tau}}^{\ensuremath{-}1/2}$ until 10-s averaging time. These results demonstrate that DFSDS could be an interesting approach for the development of a high-performance microcell-based optical frequency reference, with applications in various compact quantum devices.
The detection of narrow and high-amplitude optical resonances in atomic cells is of crucial importance for the development of compact and high-stability lasers or vapor-cell optical references. In this work, using monochromatic light and appropriate polarization settings for the counterpropagating pump and probe beams, we demonstrate the detection of enhanced-absorption sub-Doppler resonances on the D1{D}_{1}D1​ line of the Rb\mathrm{Rb}Rb atom. We report a theoretical model showing that the Zeeman coherence induced between magnetic sublevels---especially in the $F\ensuremath{\rightarrow}{F}^{\ensuremath{'}}=F\ensuremath{-}1$ systems, with FFF and ${F}^{\ensuremath{'}}$ being the hyperfine quantum numbers of the ground and excited states, respectively---plays a key role in the observed enhanced-absorption process. The theoretically predicted behavior matches the experimental observations well. The impact of light polarization, laser intensity, magnetic field, and cell temperature on the Doppler-free resonance features is experimentally investigated. For application, two identical diode lasers are frequency-stabilized onto enhanced-absorption sub-Doppler resonances. The fractional frequency stability of the laser beatnote is measured to be $1.8\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}12}$ at 1s1\phantom{\rule{0.1em}{0ex}}\mathrm{s}1s and $8.4\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}12}$ at 104s{10}^{4}\phantom{\rule{0.1em}{0ex}}\mathrm{s}104s. These results demonstrate the potential of this scheme for the implementation of a compact or even chip-scale optical frequency reference, which might find applications in instrumentation, navigation, and metrology.
The saturated absorption technique is an elegant method widely used in atomic and molecular physics for high-resolution spectroscopy, laser frequency standards and metrology purposes. We have recently discovered that a saturated absorption scheme with a dual-frequency laser can lead to a significant sign reversal of the usual Doppler-free dip, yielding a deep enhanced-absorption spike. In this paper, we report detailed experimental investigations of this phenomenon, together with a full in-depth theoretical description. It is shown that several physical effects can support or oppose the formation of the high-contrast central spike in the absorption profile. The physical conditions for which all these effects act constructively and result in very bright Doppler-free resonances are revealed. Apart from their theoretical interest, results obtained in this manuscript are of great interest for laser spectroscopy and laser frequency stabilization purposes, with applications in laser cooling, matter-wave sensors, atomic clocks or quantum optics.
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.