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Optics Express

Single-resonance optical pumping spectroscopy and application in dressed-state measurement with atomic vapor cell at room temperature

Qiangbing Liang, Baodong Yang, Tiancai Zhang, Junmin Wang

Published Jun 9, 2010• 4 citations
Publisher

Abstract

By monitoring the transmission of probe laser beam (also served as coupling laser beam) which is locked to a cycling hyperfine transition of cesium D(2) line, while pumping laser is scanned across cesium D(1) or D(2) lines, the single-resonance optical pumping (SROP) spectra are obtained with atomic vapor cell. The SROP spectra indicate the variation of the zero-velocity atoms population of one hyperfine fold of ground state, which is optically pumped into another hyperfine fold of ground state by pumping laser. With the virtue of Doppler-free linewidth, high signal-to-noise ratio (SNR), flat background and elimination of crossover resonance lines (CRLs), the SROP spectra with atomic vapor cell around room temperature can be employed to measure dressed-state splitting of ground state, which is normally detected with laser-cooled atomic sample only, even if the dressed-state splitting is much smaller than the Doppler-broaden linewidth at room temperature.

DOI
10.1364/oe.18.013554

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The spectra of cesium 6P3/2 - 8S1/2 excited-state transition have been obtained using double resonance optical-pumping (DROP) technique in a room-temperature vapor cell, and have shown a much better signal-to-noise ratio (SNR) compared with that using the traditional optical-optical double resonance (OODR) method. Furthermore, the line-width of DROP spectra is obviously narrowed by electromagnetically-induced transparency (EIT) effect in cesium 6S1/2 F=4 - 6P3/2 F'=5 - 8S1/2 F''=4 transitions. Finally, such DROP spectrum of 6P3/2 F'=5 - 8S1/2 F''=4 transition with a high SNR and a narrow line-width is applied into frequency stabilization of a 795 nm external-cavity diode laser, and the residual frequency fluctuation is ~ 600 kHz within 500 s.

Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE•Oct 8, 2010•1 citation
By monitoring the transmission of probe laser beam (also served as coupling laser beam) which is locked to a cycling hyperfine transition of cesium D(2) line, while pumping laser is scanned across cesium D(1) or D(2) lines, the single-resonance optical pumping (SROP) spectra are obtained with atomic vapor cell. The SROP spectra indicate the variation of the zero-velocity atoms population of one hyperfine fold of ground state, which is optically pumped into another hyperfine fold of ground state by pumping laser. With the virtue of Doppler-free linewidth, high signal-to-noise ratio (SNR), flat background and elimination of crossover resonance lines (CRLs), the SROP spectra with atomic vapor cell around room temperature can be employed to measure dressed-state splitting of ground state, which is normally detected with laser-cooled atomic sample only, even if the dressed-state splitting is much smaller than the Doppler-broaden linewidth at room temperature.
Two schemes of Doppler-free high-resolution velocity-selective optical-pumping atomic spectroscopy, named single-resonance optical pumping (SROP) and double-resonance optical pumping (DROP), are performed and characterized with room-temperature cesium vapor cells. Due to velocity-selective optical pumping from one hyperfine fold of ground state to another via one-photon excitation in SROP or cascade two-photon excitation in DROP and decay processes thereafter, the atomic population variation of one hyperfine fold of ground state is indicated by SROP and DROP spectra by using of the transmission of the probe laser which is usually frequency locked to a cycling hyperfine transition. As a result, SROP and DROP spectra often have flat background and higher signal-to-noise ratio. Therefore, SROP and DROP spectra are very useful for measurement of the dressed-state splitting of ground state with an alkali atomic vapor cell, precise measurement of hyperfine splitting of alkali atomic excited states, frequency references for laser frequency stabilization, two-color MOT, and so on.
We demonstrate the single-photon excitation spectra of cesium Rydberg atoms by means of a Doppler-free purely all-optical detection with a room-temperature vapor cell and a 319 nm ultra-violet (UV) laser. We excite atoms directly from 6S1/2 ground state to 71P3/2 Rydberg state with a narrow-linewidth 319 nm UV laser. The detection of Rydberg states is performed by monitoring the absorption of an 852 nm probe beam in a V-type three-level system. With a strong coupling light, we observe the Autler-Townes (AT) doublet, and the dependences of the separation and linewidths on the coupling intensity are experimentally investigated, which is consistent with the prediction based on the dressed state theory. Moreover, the AT splitting can be used to measure the Rabi frequency. In an external magnetic field, the Rydberg spectra of nondegenerate Zeeman sublevels are demonstrated. The splitting of the spectrum is of great significance for studying the characteristics of Rydberg atoms.
Two-color polarization spectroscopy (TCPS) of cesium 6S1/2-6P3/2-8S1/2 (852.3 nm + 794.6 nm) ladder-type system in a room-temperature vapor cell are investigated. The frequency of 852.3 nm laser used as a pump beam is locked on one of the hyperfine transitions between the ground state 6S1/2 and excited state 6P3/2 by the saturated absorption spectroscopy technique, which can populate some atoms on the 6P3/2 excited state and induce anisotropy in the atomic medium. The frequency of 794.6 nm laser serving as a probe beam is scanned across the whole 6P3/2→8S1/2 transition to ascertain this anisotropy, and thus the TCPS is obtained. In experiment, we measure and analyse the influence of frequency detuning of 852.3 nm pump laser on TCPS, and especially reveal that some of hyperfine energy levels of intermediate excited state 6P3/2, which has no direct interaction with the 852.3 nm pump laser, are also populated by a small fraction of atoms with a specific speed in the direction of pump laser beam due to Doppler effect, so they also have contribution to the TCPS when the 794.6 nm probe laser is scanned to the resonance transition line between the 6P3/2 and 8S1/2 states after the Doppler frequency shift has been considered. In addition, we prove that the atomic coherence like electromagnetically induced transparency effect obviously results in a narrower line width of TCPS in the case of counter-propagating experimental configuration than that in the case of pump beam co-propagating with the probe beam in the Cs vapor cell. Finally, we apply the TCPS with dispersive shaped feature to frequency stabilization with no modulation, and the frequency fluctuations of 794.6 nm laser are ～0.5 MHz and ～9.2 MHz for the frequency-locking and free running in ～225 s, respectively. The above research work is expected to play a role in precisely measuring the atomic energy level structure and its related hyperfine structure constant (magnetic dipole and electric quadrupole coupling constants), and also in stabilizing the laser frequency to the excited state transition especially for the optical fiber communication, two-color laser cooling/trapping neutral atoms, optical filter, etc.
We have shown earlier that hyperfine spectroscopy in a vapor cell using co-propagating pump-probe beams has many advantages over the usual technique of saturated-absorption spectroscopy using counter-propagating beams. The main advantages are the absence of crossover resonances, the appearance of the signal on a flat (Doppler-free) background, and the higher signal-to-noise ratio of the primary peaks. Interaction with non-zero-velocity atoms causes additional peaks, but only one of them appears within the primary spectrum. We first illustrate the advantages of this technique for high-resolution spectroscopy by studying the D2D_2D2​ line of Rb. We then use an acousto-optic modulator (AOM) for frequency calibration to make precise hyperfine-interval measurements in the first excited P3/2P_{3/2}P3/2​ state of 85,87^{85,87}85,87Rb and 133^{133}133Cs.
We demonstrate a single-photon Rydberg excitation spectroscopy of cesium (Cs) atoms in a room-temperature vapor cell. Cs atoms are excited directly from 6S1/2 ground state to nP3/2 (n = 70 - 100) Rydberg states with a 318.6 nm ultraviolet (UV) laser,and Rydberg excitation spectra are obtained by transmission enhancement of a probe beam resonant to Cs 6S1/2, F = 4 - 6P3/2, F' = 5 transition as partial population on F = 4 ground state are transferred to Rydberg state .Analysis reveals that the observed spectra are velocity-selective spectroscopy of Rydberg state, from which the amplitude and linewidth influenced by lasers'Rabi frequency have been investigated. Fitting to energies of Cs nP3/2 (n = 70 -100) states, the determined quantum defect is 3.56671(42). The demodulated spectra can also be employed as frequency references to stabilize the UV laser frequency to specific Cs Rydberg transition.
The spectra of cesium 6P3/2 - 8S1/2 excited-state transition have been obtained using double resonance optical-pumping (DROP) technique in a room-temperature vapor cell, and have shown a much better signal-to-noise ratio (SNR) compared with that using the traditional optical-optical double resonance (OODR) method. Furthermore, the line-width of DROP spectra is obviously narrowed by electromagnetically-induced transparency (EIT) effect in cesium 6S1/2 F=4 - 6P3/2 F'=5 - 8S1/2 F''=4 transitions. Finally, such DROP spectrum of 6P3/2 F'=5 - 8S1/2 F''=4 transition with a high SNR and a narrow line-width is applied into frequency stabilization of a 795 nm external-cavity diode laser, and the residual frequency fluctuation is ~ 600 kHz within 500 s.