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arXiv:1906.07114

Doppler-free saturation of the cascade fluorescence that follows excitation of the $5s \to 6p $ transition in atomic rubidium

J.E. Navarro-Navarrete, A. Díaz-Calderón, L M Hoyos-Campo, F. Ponciano-Ojeda, J. Flores-Mijangos, F. Ramírez-Martínez, J. Jiménez-Mier

Published Jun 17, 2019• 2 citations
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Abstract

We present an experimental scheme that produces Doppler-free spectra of the $5s \to 6p $ second resonance transition in atomic rubidium. The experiment uses the saturation of the cascade fluorescence that occurs when thermal rubidium atoms interact with two counterpropagating $420 $ nm laser beams of comparable intensity. Part of the excited atomic population goes through the $5p_{3/2}$ level which then decays by emission of $780$ nm photons. Narrow dips appear in this otherwise broad $780$ nm fluorescence, which allows resolution of the $6p_{3/2}$ hyperfine structure. A rate equation model is used to interpret the spectra. It is also shown that these narrow peaks can be used to lock the frequency of the $420 $ nm laser. Using a second beam modulated in frequency produces three sets of spectra with known frequency spacings that can be used to perform an all-optical measurement of the hyperfine splittings of the $6p_{3/2} $ manifold in rubidium.

DOI
10.48550/arxiv.1906.07114

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We present an experimental scheme that produces Doppler-free spectra of the 5s→6p5s \to 6p 5s→6p second resonance transition in atomic rubidium. The experiment uses the saturation of the cascade fluorescence that occurs when thermal rubidium atoms interact with two counterpropagating 420420 420 nm laser beams of comparable intensity. Part of the excited atomic population goes through the 5p3/25p_{3/2}5p3/2​ level which then decays by emission of 780780780 nm photons. Narrow dips appear in this otherwise broad 780780780 nm fluorescence, which allows resolution of the 6p3/26p_{3/2}6p3/2​ hyperfine structure. A rate equation model is used to interpret the spectra. It is also shown that these narrow peaks can be used to lock the frequency of the 420420 420 nm laser. Using a second beam modulated in frequency produces three sets of spectra with known frequency spacings that can be used to perform an all-optical measurement of the hyperfine splittings of the 6p3/26p_{3/2} 6p3/2​ manifold in rubidium.
An advanced undergraduate experiment to study the 5P3/2→6P3/2 electric quadrupole transition in rubidium atoms is presented. The experiment uses two external cavity diode lasers, one operating at the D2 rubidium resonance line and the other built with commercial parts to emit at 911 nm. The lasers produce the 5s→5p→6p excitation sequence in which the second step is the forbidden transition. Production of atoms in the 6P3/2 state is observed by detection of the 420 nm fluorescence that results from electric dipole decay into the ground state. Lines whose widths are significantly narrower than the Doppler width are used to study the hyperfine structure of the 6P3/2 state in rubidium. The spectra illustrate characteristics unique to electric dipole forbidden transitions, like the electric quadrupole selection rules; they are also used to show general aspects of two-color laser spectroscopy such as velocity selection and hyperfine pumping.
Abstract We present the first evidence of excitation of the 5 p 3 / 2 → 6 p 1 / 2 electric dipole-forbidden transition in atomic rubidium. The experiments were done in a rubidium vapor cell using Doppler-free optical–optical double resonance spectroscopy with counter-propagating beams, with a similar scheme to the excitation of the other fine transition 6 p 3/2 in the 6 p J manifold reported in Ponciano-Ojeda et al (2015 Phys. Rev. A 92 042511). The 5 p 3 / 2 → 6 p 1 / 2 dipole-forbidden excitation occurs at a wavelength λ ≈ 917.5 nm. The spectra showed the two main hyperfine states of the 6 p 1/2 manifold, and also resolved up to three satellites that appear due to effects of selection of velocities in thermal rubidium atoms. The polarization dependence of the relative intensities of the hyperfine lines of the decay fluorescence is also investigated. The data show that the individual line intensities and also the total cross-section have a strong dependence on the polarization direction. Experimental data for different polarization configurations of the light beams used in this two-photon spectroscopy are compared with the results of calculations that consider a strong atom-field coupling in the preparation step, followed by a weak electric quadrupole excitation and the blue fluorescence decay emission. Good agreement between experiment and this three-step model is found in the case of linear–linear polarizations, which confirms the results found for the 5 p 3 / 2 → 6 p 3 / 2 forbidden transition. The results presented here complete the information about the 5 p 3/2 → 6 p J electric dipole-forbidden transition in rubidium.
Frequency-modulation (FM) spectroscopy has been performed on the D(2) transitions of rubidium atoms with an AlGaAs diode laser at 780 nm. Doppler-broadened hyperfine-structure transitions of (85)Rb and (87)Rb were resolved with no residual amplitude-modulation-induced background signal by modulating the injection current of the laser diode at a low frequency (20-50 MHz) compared with the Doppler width. To obtain Doppler-free spectra, we combined FM spectroscopy with saturation spectroscopy. The results show that the FM spectroscopy technique is sensitive and should be useful for high-resolution spectroscopy, although the resolution was instrument limited and unusual double peaks were observed.
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The goal of this experiment was to measure the hyperfine energy splittings of the ground to first excited state transitions in rubidium using saturated absorption spectroscopy. Using this technique, we measured these transition energy spectra by taking the difference of two photodiode outputs due to multiple beams of a single laser scanned over a range of frequencies and shone through a cell of Rb vapor. When the laser frequency was resonant with an atomic transition, photons of those frequencies were absorbed, leaving a dip in intensity of the beam measured at the photodiode. One of the two laser beams had its excitations saturated by a more intense, counter-propagating pump beam from the same laser. The pump beam saturated the absorption of the velocity equal zero atoms that the counter-propagating probe beam could have also interacted with due to no Doppler shift. At these frequencies the probe beam experienced less absorption that was measured by a photodiode. The photodiode output was calibrated to the change in frequency of the scanned laser using a Fabry-Pérot interferometer. The output of this interferometer served as a reference for how the laser frequency changed. Final results for the 87Rb F=1 spectrum accounted for the largest error with a maximum of 12.2% deviation from accepted energy spacing values due in part to systematic error. Other spectra measurements were in better agreement, possessing error ranging from 2.1% to 10.1% and some agreeing with accepted values to within our uncertainty.
We propose and demonstrate pump-probe spectroscopy of rubidium absorption that reveals the sub-Doppler hyperfine structure of the ${}^{5}{\mathrm{S}}_{1/2}\ensuremath{\leftrightarrow}{}^{5}{\mathrm{P}}_{3/2}$ (D2{\mathrm{D}}_{2}D2​) transitions. The counterpropagating pump and probe lasers are independently tunable in frequency, with the probe operating at the single-photon level. The two-dimensional spectrum measured as the laser frequencies are scanned shows fluorescence, Doppler-broadened absorption dips, and sub-Doppler features. The detuning between the pump and probe lasers allows compensation of the Doppler shift for all atomic velocities in the room-temperature vapor, meaning we observe sub-Doppler features for all atoms in the beam. We detail a theoretical model of the system that incorporates fluorescence, saturation effects, and optical pumping and compare this with the measured spectrum, finding a mean absolute percentage error of 3.11%. This high level of agreement allows us to extract the number density and temperature of the Rb\mathrm{Rb}Rb vapor from the two-dimensional spectrum. In the future this technique could be used as an atomic frequency standard for calibrating and characterising a single-photon or low-light-level source.