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Measuring the Hyperfine Splittings of Lowest Energy Atomic Transitions in Rubidium

Benjamin Graber

Published Jan 1, 2015• 0 citations

Abstract

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.

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Comparison of absorption, fluorescence, and polarization spectroscopy of atomic rubidium

Seth Ashman, C. Stifler, Joaquín Romero

An ongoing spectroscopic investigation of atomic rubidium utilizes a two-photon, single-laser excitation process. Transitions accessible with our tunable laser include 5P1/2 (F ′ ) ← 5S1/2 (F) and 5P3/2 (F ′ ) ← 5S1/2 (F). The laser is split into a pump and probe beam to allow for Doppler-free measurements of transitions between hyperfine levels. The pump and probe beams are overlapped in a counter-propagating geometry and the laser frequency scans over a transition. Absorption, fluorescence and polarization spectroscopy techniques are applied to this basic experimental setup. The temperature of the vapor cell and the power of the pump and probe beams have been varied to explore line broadening effects and signal-to-noise of each technique. This humble setup will hopefully grow into a more robust experimental arrangement in which double resonance, two-laser excitations are used to explore hyperfine state changing collisions between rubidium atoms and noble gas atoms. Rb-noble gas collisions can transfer population between hyperfine levels, such as 5P3/2 (F ′ = 3) Collision ←− 5P3/2 (F ′ = 2), and the probe beam couples 7S1/2 (F ′′ = 2) ← 5P3/2 (F ′ = 3). Polarization spectroscopy signal depends on the rate of population transfer due to the collision as well as maintaining the orientation created by the pump laser. Fluorescence spectroscopy relies only on transfer of population due to the collision. Comparison of these techniques yields information regarding the change of the magnetic sublevels, mF , during hyperfine state changing collisions.

Bulletin of the American Physical Society•Jun 11, 2015•0 citations

Single-Photon-Level Sub-Doppler Pump-Probe Spectroscopy of Rubidium

Paul Burdekin, Samuele Grandi, Rielly Newbold +3 more

We propose and demonstrate pump-probe spectroscopy of rubidium absorption that reveals the sub-Doppler hyperfine structure of the ${}^{5}{\mathrm{S}}_{1/2}\ensuremath{\leftrightarrow}{}^{5}{\mathrm{P}}_{3/2}$ (${\mathrm{D}}_{2}$) 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 $\mathrm{Rb}$ 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.

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Hyperfine spectroscopy using co-propagating pump-probe beams

Alok K. Singh, Sapam Ranjita Chanu, Dipankar Kaundilya +1 more

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 $D_2$ line of Rb. We then use an acousto-optic modulator (AOM) for frequency calibration to make precise hyperfine-interval measurements in the first excited $P_{3/2}$ state of $^{85,87}$Rb and $^{133}$Cs.

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Doppler-free spectroscopy of rubidium atoms driven by a control laser

Zheng Tan, Xiuchao Zhao, Yong Cheng +5 more

A scheme of Doppler-free spectroscopy is experimentally demonstrated with a co-propagating control laser locking to an atomic hyperfine transition, and the differential transmission of the probe and the reference laser is detected. Crossover resonances are eliminated by selecting the class of atoms with zero velocity in the direction of beam propagation. In addition, the sub-Doppler spectrum experiences optical gain compared to the conventional saturated-absorption spectrum as a result of optical pumping.

Frontiers of Physics•Jul 7, 2011•0 citations

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J.E. Navarro-Navarrete, A. Díaz-Calderón, L M Hoyos-Campo +4 more

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.

arXiv:1906.07114•Jun 17, 2019•2 citations

Measurement and analysis of Rb-D_2 saturated absorption

Lian-Lian Zhang

Two beams generated by a semiconductor laser propagate in opposite directions in the experiment. The weak laser beam serves as probe light, and the other strong as pump light. They pass through the rubidium cell together. After eliminating the Doppler background, the hype-fine saturated absorption spectrum of Rb-D2 line is observed. The influence of the pump power and the probe power on saturated absorption can be observed while changing the temperature of rubidium cell.

Physics Experimentation•Jan 1, 2008•0 citations

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.

An ongoing spectroscopic investigation of atomic rubidium utilizes a two-photon, single-laser excitation process. Transitions accessible with our tunable laser include 5P1/2 (F ′ ) ← 5S1/2 (F) and 5P3/2 (F ′ ) ← 5S1/2 (F). The laser is split into a pump and probe beam to allow for Doppler-free measurements of transitions between hyperfine levels. The pump and probe beams are overlapped in a counter-propagating geometry and the laser frequency scans over a transition. Absorption, fluorescence and polarization spectroscopy techniques are applied to this basic experimental setup. The temperature of the vapor cell and the power of the pump and probe beams have been varied to explore line broadening effects and signal-to-noise of each technique. This humble setup will hopefully grow into a more robust experimental arrangement in which double resonance, two-laser excitations are used to explore hyperfine state changing collisions between rubidium atoms and noble gas atoms. Rb-noble gas collisions can transfer population between hyperfine levels, such as 5P3/2 (F ′ = 3) Collision ←− 5P3/2 (F ′ = 2), and the probe beam couples 7S1/2 (F ′′ = 2) ← 5P3/2 (F ′ = 3). Polarization spectroscopy signal depends on the rate of population transfer due to the collision as well as maintaining the orientation created by the pump laser. Fluorescence spectroscopy relies only on transfer of population due to the collision. Comparison of these techniques yields information regarding the change of the magnetic sublevels, mF , during hyperfine state changing collisions.

We propose and demonstrate pump-probe spectroscopy of rubidium absorption that reveals the sub-Doppler hyperfine structure of the ${}^{5}{\mathrm{S}}_{1/2}\ensuremath{\leftrightarrow}{}^{5}{\mathrm{P}}_{3/2}$ (

{\mathrm{D}}_{2}

) 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

\mathrm{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.

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

D_2

line of Rb. We then use an acousto-optic modulator (AOM) for frequency calibration to make precise hyperfine-interval measurements in the first excited

P_{3/2}

state of

^{85,87}

Rb and

^{133}

Cs.

A scheme of Doppler-free spectroscopy is experimentally demonstrated with a co-propagating control laser locking to an atomic hyperfine transition, and the differential transmission of the probe and the reference laser is detected. Crossover resonances are eliminated by selecting the class of atoms with zero velocity in the direction of beam propagation. In addition, the sub-Doppler spectrum experiences optical gain compared to the conventional saturated-absorption spectrum as a result of optical pumping.

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

^{133}

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.