An Exploration of Hyperfine Structure of Rubidium Within The 5P 3/2 Excited-State Using Saturated Absorption Spectroscopy

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An Exploration of Hyperfine Structure of Rubidium Within The 5P 3/2 Excited-State Using Saturated Absorption Spectroscopy
Trieu N. Le
Elina M. van Kempen
Priyanka M. Rupasinghe
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One of the laser-based spectroscopy techniques, the Saturated Absorption Specrroscopy (SAS), was performed to observe the hyperfine energy levels of rubidium 5P_{3/2} excited state. Two low-power beams at 780.24 nm produced by an external-cavity diode laser (ECDL) were sent through a vapor cell containing 85Rb and 87Rb. Another strong (high-power) beam from the same laser crosses one of the two beams in the opposite direction through the vapor cell. With atoms absorbing more energy from this strong beam, the low-power beam then shows less absorption, while the laser is scanning through the 5S_{1/2} (Ground) -> 5P_{3/2} atomic transition. By directing the two low-power beams transmitted through the vapor cell at a differential photodiode, atomic spectra corresponding to the hyperfine transitions were collected. Analysis of these spectra resulted in a precise measurement of the ratios of the hyperfine energy splittings of rubidium 5P_{3/2} state. These ratios were found to be DeltaF_{34}/DeltaF_{23} = 1:93 +/- 0.04 and DeltaF_{23}/DeltaF_{12} = 1:71 +/- 0.02, for ^{85}Rb and ^{87}Rb respectively, and agree very well with the expected values of 1.90 and 1.70.
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An Exploration of Hyperfine Structure of Rubidium Excited State Using Saturated Absorption Spectroscopy Trieu N. Le 1 , Elina M. van Kempen 1 , Priyanka M. Rupasinghe 1 1 Department of Physics, State University of New York at Oswego, Oswego, NY 13126, U.S.A In direct absorption optical spectroscopy, the Doppler broadening of spectral lines often prevents us from studying the hyperfine structure of an atom [ 1 ] . With Saturated Absorption Spectroscopy (SAS), this effect can be overcome and can be used to precisely study the finest energy splittings within an atom [ 2 ] . In the SAS setup, two low power beams produced by an external cavity diode laser is sent through a vapor cell containing rubidium while another strong (high power) beam from the same laser crosses one of the two beams in the opposite direction through the vapor cell . With atoms absorbing more photons from this strong beam, the low power beam then shows less absorption while the laser is scanning through the transition . By directing the two low power beams at a differential photodiode, an atomic spectrum corresponding to the hyperfine energy levels can be obtained . Using this technique, here, we measured the hyperfine energy splitting ratios of the first excited state of rubidium using the transition at 780 . 24 nm . The hyperfine splitting ratio in was found to be 1 . 93 ± 0 . 04 with a percent difference of 1 . 6 % with the theoretical value . Similarly, the ratio in was found to be of 1 . 71 ± 0 . 02 with a percent difference of 0 . 6 % with the theoretical value . All error bars above represent only the statistical error . [ 1 ] John Brandenberger . Doppler free spectroscopy, Nov 2012 . [ 2 ] University of Florida Department of Physics . Saturated absorption spectroscopy , Jan 2020 . [ 3 ] V Jacques, B Hingant , et al . Nonlinear spectroscopy of rubidium : an undergraduate experiment . European Journal of Physics, 30 ( 5 ) : 921 934 ,Aug 2009 . Introduction Energy Level S tructure of Rb Experiment On an optic table, t he laser beam from the ECDL first passes through a variable attenuator and is then reflected towards the beam splitter . The beam splitter directs two low power beams (Beams A and B) through the rubidium vapor cell . The strong beam (Beam C), which passes through the beam splitter, is reflected using several mirrors to cross one of the low power beams, Beam B, in the opposition direction . The two low power beams, after going through the vapor cell, are directed towards a differential photodiode and cross converging lenses to have a focus on the photodiode . Results Data Analysis Conclusion Saturated Absorption Through s aturated absorption spectroscopy, the hyperfine splitting energy levels from transition in rubidium were observed carefully . The use of both hyperfine level peaks and crossover peaks increased the statistical precision of the results . References Rubidium has two major isotopes : and . T he split between 5 S and 5 P orbitals is part of the fine structure level and can be identified by L S coupling (electron orbital and spin interaction) scheme with notation . When the strong beam crosses one of the two low power beams, the direct absorption spectra associated with two beams are different . One is a direct absorption spectrum (yellow) and the other shows the direct absorption with saturated absorption features (Blue) . Due to the electron spin and nuclear spin interaction, the fine structure levels are split into hyperfine energy levels as shown in the figure 1 . Hyperfine energy levels are characterized by the total angular momentum quantum number F which is t he sum of electron angular momentum J (L+S) and the nuclear spin angular momentum I . F has allowed values between , in integer steps [ 3 ] . When ground state atoms are in resonance with the strong beam they absorb more photons from that beam and as a result, the direct absorption signal from the crossed low power beam shows less absorption at those frequencies (Blue) . This is called the burning in the direct absorption dip . The hole burning can occur at hyperfine transition frequencies as well as at exactly in the middle of those frequencies due to the Doppler effect caused transitions (cross over resonance) . Twenty sets of saturated absorption for were collected using LabVIEW and analyzed using MATLAB . is height of peaks, is the position of peak on the x axis and is the half width at half maximum Figure 1: Hyperfine structure of rubidium for two isotopes Figure 2 : Direct absorption spectrum (yellow) and direct absorption spectrum with hole burning effect (blue ) . Figure 3 : The raw data, absorption spectra observed on an oscilloscope . D irect absorption spectrum with burning hole effect (yellow) . Saturated absorption spectrum (blue) is the difference signal between direct absorption and direct absorption with burning hole Figure 4: Apparatus set up The raw data were fitted to Lorentzian line shapes (equation on the right) and a linear function to adjust the base line . Figure 5 , 6 : The fitted saturated absorption spectrum for ( left ) Notice that the three of the peaks for each isotope represent hyperfine transitions and the other three are crossover peaks . Figure 7 shows the histogram of hyperfine splitting ratio values determined from and by analyzing 85 Rb spectra . Figure 7 : Histogram of the ratio for Future Work In a future study, we will capture the saturated absorption spectrum along with the Fabry Perot cavity spectra . This will allow us to establish a linearized frequency axis and hence determine the hyperfine energy splittings explicitly . Acknowledgement This project was supported by a Scholarly and Creative Activity Grant (SUNY Oswego). Special thanks to Dr. Priyanka Rupasinghe who supervised this research.