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arXiv:0902.3115 · European Journal of Physics

Nonlinear spectroscopy of rubidium: an undergraduate experiment

V. Jacques, B Hingant, A. Allafort, M Pigeard, Jean-François Roch

Published Jul 8, 2009• 22 citations
arXivHTMLPDF

Abstract

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.

DOI
10.1088/0143-0807/30/5/001

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Oxford University Press eBooks•Nov 1, 2015•0 citations
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.
We describe an experiment for investigating the 5S1∕2→5D5∕2 two-photon transition in rubidium using a single grating-feedback diode laser operating at 778.1nm (385THz). Continuous tuning of the laser frequency over 4GHz allows for the clear resolution of the Doppler-free spectral features and allows accurate measurement of the hyperfine ground-state splitting. A direct comparison between Doppler-broadened and Doppler-free spectral features is possible because both are distinctly evident in the two-photon spectra. By independently modifying the polarization state of the two laser fields, the impact of electric dipole selection rules on the two-photon transition spectra is investigated. This experiment is a valuable addition to the advanced undergraduate laboratory because it uses much of the same equipment as the single-photon saturated absorption spectroscopy experiment performed on the 5S1∕2→5P3∕2 transition in rubidium (λ=780.24nm) and provides students with an opportunity to investigate characteristics of atomic spectra not evident in the single-photon experiment.
Heterodyne Doppler-free spectroscopy, previously demonstrated on single-photon resonances (heterodyne saturation spectroscopy), has been extended to two-photon transitions in rubidium (5S-5D and 5S-7S). It provides a simple method of observing the two-photon dispersion lineshape directly. The noticeable sensitivity of this absorption technique, which has been used for an optical measurement of the hyperfine structure of the 5D level, is discussed in comparison with that currently obtained in two-photon-induced fluorescence.
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.
Using an external cavity-tuned diode laser in Doppler-free saturation spectroscopy, we are able to resolve the weak-field Zeeman splittings in the hyperfine levels of the rubidium D1 line. The number of lines observed in the Zeeman structure of rubidium and their measured energy-level splittings are as expected from theory. The measured amplitudes of the saturated-absorption signals, crossover resonances, and velocity-selective optical pumping signals are used in the analysis of various theories concerning saturated-absorption spectroscopy.
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.
Experiments using relatively inexpensive tunable diode lasers are used to study high-resolution absorption spectroscopy in alkali vapors. Direct absorption spectra for cesium and rubidium show adsorption profiles that are Doppler-broadened. A second experiment demonstrates saturated adsorption spectroscopy to remove Doppler broadening in atomic spectroscopy for rubidium atoms in a cell at room temperature. Lamb dips are seen in the Doppler-broadened profiles. Finally a third experiment is described which demonstrate Doppler-free two photon spectroscopy for rubidium vapour. All of these experiments were historical stepping stones toward the creation of a Bose–Einstein condensate.