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Journal of Applied Research and Technology

A laser spectroscopy system with combined absorption, polarization rotation and fluorescence detection to study two photon transitions in atomic rubidium

O López-Hernández, Santiago Hernández-Gómez, F. Ponciano-Ojeda, Cristian Mojica-Casique, Ricardo Colín‐Rodríguez, J. Flores-Mijangos, Daniel Sahagún, F. Ramírez-Martínez, J. Jiménez-Mier

Published Nov 19, 2015• 2 citations
Publisher

Abstract

The design and construction of an experimental system for studying two photon spectroscopy processes in atomic rubidium is presented. It is designed to measure absorption and polarization rotation induced by any of the two laser beams and also the visible fluorescence that results from decay of the excited states. Two home-built diode lasers are used to produce the optical fields that later interact with room temperature rubidium atoms. Using counterpropagating beams allows velocity selection of the groups of atoms that interact with both laser beams. The system was tested in the 5 S?5 P3/2 ?5 Dj ladder energy level configuration of atomic rubidium. Blue fluorescence (420 nm) that results from decay of the intermediate 6Pj states is filtered and then measured with a photomultiplier tube. Absorption and fluorescence spectra provide mutually complementary information about the interaction between the rubidium atoms and the two optical fields. All Rights Reserved © 2015 Universidad Nacional Autónoma de México, Centro de Ciencias Aplicadas y Desarrollo Tecnológico. This is an open access item distributed under the Creative Commons CC License BY-NC-ND 4.0.

DOI
10.1016/j.jart.2015.09.006

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The design and construction of an experimental system for studying two photon spectroscopy processes in atomic rubidium is presented. It is designed to measure absorption and polarization rotation induced by any of the two laser beams and also the visible fluorescence that results from decay of the excited states. Two home-built diode lasers are used to produce the optical fields that later interact with room temperature rubidium atoms. Using counterpropagating beams allows velocity selection of the groups of atoms that interact with both laser beams. The system was tested in the 5 S?5 P3/2 ?5 Dj ladder energy level configuration of atomic rubidium. Blue fluorescence (420 nm) that results from decay of the intermediate 6Pj states is filtered and then measured with a photomultiplier tube. Absorption and fluorescence spectra provide mutually complementary information about the interaction between the rubidium atoms and the two optical fields. All Rights Reserved © 2015 Universidad Nacional Autónoma de México, Centro de Ciencias Aplicadas y Desarrollo Tecnológico. This is an open access item distributed under the Creative Commons CC License BY-NC-ND 4.0.
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.
In this paper, we describe two complementary nonlinear spectroscopy methods which both allow one to achieve Doppler-free spectra of atomic gases. First, saturated absorption spectroscopy is used to investigate the structure of the 5S 1/2 → 5P 3/2 transition in rubidium. Using a slightly modified experimental setup, Doppler-free two-photon absorption spectroscopy is then performed on the 5S 1/2 → 5D 5/2 transition in rubidium, leading to accurate measurements of the hyperfine structure of the 5D 5/2 energy level. In addition, electric dipole selection rules of the two-photon transition are investigated, first by modifying the polarization of the excitation laser, and then by measuring two-photon absorption spectra when a magnetic field is applied close to the rubidium vapour. All experiments are performed with the same grating-feedback laser diode, providing an opportunity to compare different high-resolution spectroscopy methods using a single experimental setup. Such experiments may acquaint students with quantum mechanics selection rules, atomic spectra and Zeeman effect.
Doppler-free optical double-resonance spectroscopy is used to study the 5S1/2 → 5P3/2 → 6Pj (j = 3/2,1/2) excitation sequence in room-temperature rubidium atoms. This involves a 5S1/2 → 5P3/2 electric dipole preparation step followed by the 5P3/2 → 6Pj electric quadrupole excitation. The electric dipole forbidden transitions occur at 911.0 nm (j = 3/2) and 917.5 nm (j = 1/2). Production of atoms in the 6Pj states is detected by observing their direct decay to the ground state through emission of blue photons (λ ≈ 420 nm). A detailed experimental and theoretical study of the dependence on the relative linear polarizations of excitation beams is made. It is shown that specific electric quadrupole selection rules over magnetic quantum numbers are directly related to the relative orientation of the linear polarization of the excitation beams.
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.
The two-photon transition $5S\ensuremath{-}5P\ensuremath{-}5D$ in rubidium vapor is investigated by detecting the fluorescence from the 6P3/26{P}_{3/2}6P3/2​ state when the atomic system is excited by the combined action of a cw diode laser and a frequency comb. The cw laser plays a role as a velocity-selective filter and allows for sub-Doppler spectroscopy over a large spectral range including the 5D3/25{D}_{3/2}5D3/2​ and 5D5/25{D}_{5/2}5D5/2​ states. For a counterpropagating beam configuration, the response of each atomic velocity group is well characterized within the Doppler profile and the excited hyperfine levels are clearly resolved. The contribution of the optical pumping to the direct two-photon process is also revealed. The results are well described in a frequency domain picture by considering the interaction of each velocity group with the cw laser and the modes of the frequency comb.
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.