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420 nm Rb optical frequency standard with short-term frequency stability below 2 × 10 −13

RenPing Sun, WeiHao Zhao, Yu Zhang, Yuan Tian, Hongzhi Liu, 顾思洪, 陈杰华

Published Jul 7, 2026• 1 citation
Publisher

Abstract

We experimentally study the character of saturated absorption spectroscopy (SAS) of the 87 Rb 5 S 1/2 → 6 P 3/2 transition at 420 nm in a miniature cubic glass cell (3 × 3 × 3 mm 3 ). The influences of the laser intensity and cell temperature on the saturated absorption resonance are comprehensively investigated to determine the optimal parameters for a compact stabilized frequency standard. By stabilizing the laser frequency to the optimized SAS signal, a beatnote stability of 2.4 × 10 −13 at 1 s is measured between two identical SAS systems, corresponding to a single-laser stability of 1.7 × 10 −13 at 1 s, assuming equal contribution from each laser. A further analysis of the noise budget reveals that the main contributions of short-term stability arise from the intermodulation effect and the laser frequency noise through the frequency modulation to amplitude modulation (FM-AM) conversion process. Our work provides a promising route toward high-performance miniaturized optical frequency standards based on high-lying excited-state transitions.

DOI
10.1364/oe.605969

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physics.atom-phCross-listedarXiv:2606.30871•Jul 1, 2026•0 citations
We experimentally study the character of saturated absorption spectroscopy (SAS) of the 87 Rb 5 S 1/2 → 6 P 3/2 transition at 420 nm in a miniature cubic glass cell (3 × 3 × 3 mm 3 ). The influences of the laser intensity and cell temperature on the saturated absorption resonance are comprehensively investigated to determine the optimal parameters for a compact stabilized frequency standard. By stabilizing the laser frequency to the optimized SAS signal, a beatnote stability of 2.4 × 10 −13 at 1 s is measured between two identical SAS systems, corresponding to a single-laser stability of 1.7 × 10 −13 at 1 s, assuming equal contribution from each laser. A further analysis of the noise budget reveals that the main contributions of short-term stability arise from the intermodulation effect and the laser frequency noise through the frequency modulation to amplitude modulation (FM-AM) conversion process. Our work provides a promising route toward high-performance miniaturized optical frequency standards based on high-lying excited-state transitions.
This study investigates the application of miniature quantum references within small-scale optical atomic frequency standards, utilizing a diminutive 87 Rb glass cell, dimensions of 6 mm × 6 mm × 6 mm, to establish a quantum frequency standard.By employing the transition spectrum from 5 2 S 1/2 F = 2 to 5 2 P 3/2 F 0 =3, this study successfully demonstrates the development of a compact rubidium atomic optical frequency standard via modulation transfer spectroscopy (MTS).Subsequent to frequency stabilization, the 780 nm clock laser exhibits a linewidth of 6.9 kHz, and its out-of-loop short-term stability reaches 4.1 × 10 -13 @ 1 s, as confirmed through beat frequency analysis.This research not only provides a practical blueprint for the development of small optical atomic frequency standards but also lays down essential groundwork for future advancements in chip-level optical frequency standard technologies.
We implement a compact optical frequency standard scheme with laser frequency locked to the 5 S 1/2 ( F = 2) − 6 P 3/2 ( F ′ = 3) transition of the second excited state of 87 Rb atoms in a 3 mm cubic glass cell, using a Doppler-free saturated absorption spectroscopy. The experimental results show the frequency stability at the level of 2.2 × 10 −12 at 1 s. Furthermore, we conduct an experimental study on the effect of a repump laser on the frequency performance of the saturated absorption spectroscopy optical frequency standard, providing valuable experimental results with reference values for implementing this type of optical atomic clock.
We report on the development and short-term stability characterization of an optical frequency reference based on the spectroscopy of the rubidium two-photon transition at 778 nm in a microfabricated vapor cell. When compared against a 778 nm reference signal extracted from a frequency-doubled cavity-stabilized telecom laser, the short-term stability of the microcell frequency standard is 3.5 ×\times× 10−13^{-13}−13 τ−1/2τ^{-1/2}τ−1/2 until 200~s, in good agreement with a phase noise level of +++ 43 dBrad2^22/Hz at 1~Hz offset frequency. The two main contributions to the short-term stability of the microcell reference are currently the photon shot noise and the intermodulation effect induced by the laser frequency noise. With still a relevant margin of progress, these results show the interest of this spectroscopic approach for the demonstration of high-stability miniaturized optical vapor cell clocks. Such clocks are poised to be highly beneficial for applications in navigation, communications, and metrology.
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 report on the development and short-term stability characterization of an optical frequency reference based on the spectroscopy of the rubidium two-photon transition at 778 nm in a microfabricated vapor cell. When compared against a 778 nm reference signal extracted from a frequency-doubled cavity-stabilized telecom laser, the short-term stability of the microcell frequency standard is 3.5×10−13τ−1/2 until 200 s, in good agreement with a phase noise level of +43dBrad2/Hz at 1 Hz offset frequency. The two main contributions to the short-term stability of the microcell reference are currently the photon shot noise and the intermodulation effect induced by the laser frequency noise. Retaining a relevant margin of progress, these results show the interest of this spectroscopic approach for the demonstration of high-stability miniaturized optical vapor cell clocks. Such clocks are poised to be highly beneficial for applications in navigation, communications, and metrology.
The 5S1/2→6P3/25S_{1/2} \rightarrow 6P_{3/2}5S1/2​→6P3/2​ transition of rubidium at 420420420 nm is a promising candidate for a portable warm-vapor all-optical atomic clock. Despite recent precision spectroscopy studies at 420420420 nm in Rb, an experimental determination of the saturation intensity of this transition has not yet been reported. The saturation intensity is a fundamental parameter that influences the identification of a potential clock transition frequency in terms of optimizing various intensity-dependent parameters and connected systematics. In this work, we report the first experimental measurement of the saturation intensity of the 420420420 nm transition in Rb, obtaining (23.18±0.28)(23.18 \pm 0.28)(23.18±0.28) mW/cm2^22 for the 87^{87}87Rb F=2→F′=3F = 2 \rightarrow F' = 3F=2→F′=3 transition and (25.56±0.37)(25.56 \pm 0.37)(25.56±0.37) mW/cm2^22 for the 85^{85}85Rb F=3→F′=4F = 3 \rightarrow F' = 4F=3→F′=4 transition, in excellent agreement with theoretical predictions. We further investigate the temperature dependence of the Doppler-free Lamb-dip amplitude and linewidth over 59.03 ± 0.3759.03~\pm~0.3759.03 ± 0.37 - 91.20 ± 0.90∘91.20~\pm~0.90^\circ91.20 ± 0.90∘C in a 100100100 mm commercial vapor cell, identifying around 82.02 ± 0.73∘82.02~\pm~ 0.73^\circ82.02 ± 0.73∘C as the optimal operating temperature, where the signal-to-noise ratio of the Lamb-dip amplitude with temperature reaches a maximum and the observed Lamb-dip linewidth exhibits a minimum. We also present precise measurements of the magnetic-dipole (AAA) and electric-quadrupole (BBB) hyperfine constants of the 6P3/26P_{3/2}6P3/2​ state for both isotopes, with the measured values being consistent with previously reported values for the hyperfine constants.