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arXiv:2405.14911

Saturated absorption spectroscopy and frequency locking of DBR laser on the D2 transition of rubidium atoms

Davood Razzaghi, Ali Motazedifard, Marzieh Akbari, Seyed Ahmad Madani, Masoud Yousefi, A. Allahi, Ghazal Mehrabanpajooh, Mohsen Shokrolahi, Asgari, Hamid, Z. Riazi

Published May 23, 2024• 1 citation
arXivHTMLPDF

Abstract

In this paper, we experimentally report the saturated absorption spectroscopy (SAS) and frequency locking (FL) of a narrow-band DBR laser with 0.5MHz linewidth on the LD2-transition of Rb atoms.
DOI
10.48550/arxiv.2405.14911

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Abstract An experiment on the saturated absorption spectroscopy (SAS) of 87Rb-D2 line is performed using the Laguerre–Gaussian (LG) beam as structured light. The theoretical simulation of which is done by considering a four-level atom-laser coupled system. The theoretically simulated spectra fairly match with the experimentally observed spectra. The line-width narrowing behavior of both the observed hyperfine and crossover resonances in the Doppler-broadened probe absorption spectra is attributed by the spatially dependent Rabi frequency of the pump LG beam irrespective of the characteristics of the probe beam. The results also illustrated that the narrowing behavior of the line shapes of the hyperfine structure using the LG beam is universal in nature, i.e. irrespective of hyperfine or crossover transitions. This structured light-induced narrowing of line-width of the sub-Doppler hyperfine and crossover resonances can be utilized for high-precision laser frequency locking at a particular hyperfine or crossover transition. Moreover, a significant narrowing of hyperfine and crossover resonances with the variation of the orbital angular momentum (OAM) number of the LG beam shows that the generated SAS signal can be manipulated by using the OAM of the structured light as a control knob.
In recent years, much work has been done in experimental studies to frequency lock laser diodes to atomic or molecular resonances.1 By such techniques it is possible to improve greatly the laser frequency stability and to define precisely its nominal value. For laser sources operating in the 0.8-μm range, rubidium is the preferred specie and each isotope offers two resonance lines, one at 780 nm (D2 line) and one at 795 nm (D1 line). Both linear and saturated absorption have been used, and laser frequency charcteristics are published.2,3
Precise laser stabilization is a fundamental aspect of modern metrology, directly influencing the accuracy of fundamental measurements in fields such as high-precision metrology, atomic sensor applications, and quantum technologies. Saturation absorption spectroscopy (SAS) is one of the most effective techniques for achieving high spectral stability, as it enables laser frequencies to be locked to atomic resonances. This technique exploits the nonlinear interaction between a weaker probe beam and a stronger pump beam within a rubidium (Rb) atomic vapor cell. By eliminating Doppler broadening, SAS allows well-defined hyperfine transitions to be resolved, providing a reliable optical frequency reference. This study aims to optimize laser frequency stabilization using the SAS technique by investigating the effects of laser light polarization, atomic vapor cell temperature, and pump-probe power adjustments. Polarization-dependent selection rules influence transition probabilities, thereby affecting spectral contrast and frequency stability. Additionally, atomic density variations, which depend on the vapor cell temperature, influence signal strength and linewidth, necessitating precise temperature control for optimal performance. Furthermore, the pump power must be sufficient to induce saturation without excessive power broadening, while the probe power must remain low enough to prevent spectral line distortion. By optimizing polarization, temperature, and power parameters, the stabilization of the Rb atomic laser can be enhanced, leading to improved reproducibility and consistency in high-precision measurements. SAS-based laser stabilization is particularly crucial for atomic sensor applications and quantum technologies, where highly stable, narrow-linewidth lasers are essential for precision measurements. Applications such as atomic magnetometers, gyroscopes, and inertial navigation systems depend on precisely stabilized lasers for optimal performance. By enhancing the reliability of laser frequency stabilization, this work contributes to the advancement of next-generation atomic sensors with improved sensitivity and stability.
We demonstrate a simple technique to lock the frequency of a laser to an atomic transition with a new technique of subnatural linewidth spectroscopy. The coupled rubidium system exhibits an enhanced absorption spectrum of the probe beam with a subnatural linewidth. Compared with other techniques with an additional laser, our scheme only utilizes a single laser, which will be locked. The observed spectroscopic linewidth is down to about 3.5 MHz. The laser frequency fluctuation is about 226 kHz after locking on. The demonstrated scheme offers a convenient and low-cost technique for laser frequency stabilization and related precision measurements.
We present and analyze a bichromatic version of the well-known saturation absorption spectroscopy technique used to stabilize lasers to atomic resonances without Doppler broadening. We show that the spectroscopic properties can be transferred between two transitions at very different wavelengths by spectral hole burning in a Doppler-broadened atomic ensemble. Specifically, we demonstrate that this technique can be used to stabilize a laser to the D1 line of Rb87 by obtaining a saturation absorption spectrum with a strong pump laser stabilized to the D2 line. This allows for more freedom in the choice of the probe laser frequency offsets compared to conventional saturation absorption spectroscopy. We compare our experimental results to an analytical model and numerical results based on rate equations.