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arXiv:1804.07928 · OSA Continuum

Low-drift Zeeman shifted atomic frequency reference

Dominic J. Reed, Nikola Šibalić, Daniel J. Whiting, Jorge Douglas Massayuki Kondo, Charles S. Adams, Kevin J. Weatherill

Published Sep 12, 2018• 11 citations

Abstract

We present a simple method for producing a low-drift atomic frequency reference based upon the Zeeman effect. Our Zeeman Shifted Atomic Reference `ZSAR' is demonstrated to have tens of GHz tuning range, limited only by the strength of the applied field. ZSAR uses Doppler-free laser spectroscopy in a thermal vapor where the vapor is situated in a large, static and controllable magnetic field. We use a heated $^{85}$Rb vapor cell between a pair of position-adjustable permanent magnets capable of applying magnetic fields up to 1 T. To demonstrate the frequency reference we use a spectral feature from the Zeeman shifted D1 line in $^{85}$Rb at 795 nm to stabilize a laser to the 7S$_{1/2}$ $\longrightarrow$ 23P$_{1/2}$ transition in atomic cesium, which is detuned by approximately 19 GHz from the unperturbed Rb transition. We place an upper bound on the stability of the technique by measuring a 2.5 MHz RMS frequency difference between the two spectral features over a 24 hour period. This versatile method could be adapted easily for use with other atomic species and the tuning range readily increased by applying larger magnetic fields.

DOI: 10.1364/osac.1.000004

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We present a simple method for producing a low-drift atomic frequency reference based upon the Zeeman effect. Our Zeeman Shifted Atomic Reference `ZSAR' is demonstrated to have tens of GHz tuning range, limited only by the strength of the applied field. ZSAR uses Doppler-free laser spectroscopy in a thermal vapor where the vapor is situated in a large, static and controllable magnetic field. We use a heated

^{85}

Rb vapor cell between a pair of position-adjustable permanent magnets capable of applying magnetic fields up to 1 T. To demonstrate the frequency reference we use a spectral feature from the Zeeman shifted D1 line in

^{85}

Rb at 795 nm to stabilize a laser to the 7S

_{1/2}

\longrightarrow

23P

_{1/2}

transition in atomic cesium, which is detuned by approximately 19 GHz from the unperturbed Rb transition. We place an upper bound on the stability of the technique by measuring a 2.5 MHz RMS frequency difference between the two spectral features over a 24 hour period. This versatile method could be adapted easily for use with other atomic species and the tuning range readily increased by applying larger magnetic fields.

We demonstrate a robust method of stabilizing a diode laser frequency to an atomic transition. This technique employs the Zeeman shift to generate an antisymmetric signal about a Doppler-broadened atomic resonance, and therefore offers a large recapture range as well as high stability. The frequency of a 780-nm diode laser, stabilized to such a signal in Rb, drifted less than 0.5 MHz peak-peak (1 part in 10(9)) in 38 h. This tunable frequency lock can be constructed inexpensively, requires little laser power, rarely loses lock, and can be extended to other wavelengths by use of different atomic species.

We present a simple technique for stabilization of a laser frequency off resonance using the Faraday effect in a heated vapor cell with an applied magnetic field. In particular, we demonstrate stabilization of a 780 nm laser detuned up to 14 GHz from the (85)Rb D(2) 5(2)S(1/2) F = 2 to 5(2)P(3/2) F' = 3 transition. Control of the temperature of the vapor cell and the magnitude of the applied magnetic field allows locking ~6-14 GHz red and blue detuned from the atomic line. We obtain an rms fluctuation of 7 MHz over 1 h without stabilization of the cell temperature or magnetic field.

Rydberg atoms play a pivotal role in the fields of quantum simulation, quantum computing, and quantum sensing, in which the frequency locking and detuning of the laser used to excite the atoms to Rydberg states are crucial. Here, we introduce a novel frequency locking approach for Rydberg lasers at arbitrary frequencies using the Zeeman effect of both DC and AC magnetic fields. The DC magnetic field is used to shift the atomic energy levels, thus altering the frequency locking point, while the AC magnetic field is employed for Zeeman modulation to generate the error signal. This method also enables free tuning of the laser frequency within a sub-hundred MHz range by adjusting the DC magnetic field while maintaining frequency locking.

We describe the so-called "Lambda-Zeeman method" to investigate individual hyperfine transitions between Zeeman sublevels of atoms in an external magnetic field of 0.1 mT - 0.25 T. Atoms are confined in a nanocell with thickness L = Lambda, where Lambda is the resonant wavelength (794 nm or 780 nm for D1 or D2 line of Rb). Narrow resonances in the transmission spectrum of the nanocell are split into several components in a magnetic field; their frequency positions and probabilities depend on the B-field. Possible applications are described, such as magnetometers with nanometric spatial resolution and tunable atomic frequency references.