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Journal of Physics B Atomic Molecular and Optical Physics

Triple-resonance method for the detection of hyperfine transitions in heavy-alkali metals

Juan Antonio Vallés, J M Alvarez

Published Feb 28, 1998• 1 citation
Publisher

Abstract

The triple-resonance method for the detection of hyperfine transitions in heavy-alkali metals is studied theoretically. The evolution equations of the reduced fictitious tensorial components of the dressed-atom density matrix in an extended fictitious formalism are determined and solved for the stationary state. Illustrative numerical examples of dressed-caesium are included. Previously unexplained triple-resonance experiments on rubidium and caesium are interpreted in detail.

DOI
10.1088/0953-4075/31/4/016

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The triple-resonance method for the detection of hyperfine transitions in heavy-alkali metals is studied theoretically. The evolution equations of the reduced fictitious tensorial components of the dressed-atom density matrix in an extended fictitious formalism are determined and solved for the stationary state. Illustrative numerical examples of dressed-caesium are included. Previously unexplained triple-resonance experiments on rubidium and caesium are interpreted in detail.
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A set of operators, which act on the eigenstates of the atomic Hamiltonian in the presence of a partial I-J decoupling in a way analogous to the way the usual irreducible tensor operators act on the eigenstates of the total angular momentum, is introduced. Starting from these operators a set of operators, analogous to Haroche's pseudotensor operators, is obtained for the dressed-atom Hilbert space. They are thus particularly suitable to the theoretical treatment of the Delta m F >1 multiple quantum transitions within the Zeeman levels of a hyperfine state of an alkali atom. As an example, this treatment is applied to a system having a 'fictitious' spin F=1, and it is shown that the contribution of the single and multiple quantum transitions to the multipole components of the dressed-atom density matrix is separated.
Simple and efficient λ-method and λ/2-method (λ is the resonant wavelength of laser radiation) based on a nanometric-thickness cell filled with rubidium (Rb) are implemented to study the splitting of hyperfine transitions of an Rb85 and Rb87D1 line in an external magnetic field in the range of B=0.5–0.7 T. It is experimentally demonstrated from 20 (12) Zeeman transitions allowed at low B-field in Rb85 (Rb87) spectra in the case of σ+ polarized laser radiation, only 6 (4) remain at B>0.5 T, caused by decoupling of the total electronic momentum J and the nuclear spin momentum I (hyperfine Paschen–Back regime). The expressions derived in the frame of completely uncoupled basis (J,mJ;I,mI) describe the experimental results extremely well for Rb85 transitions at B>0.6 T (that is a manifestation of hyperfine Paschen–Back regime). A remarkable result is that the calculations based on the eigenstates of the coupled (F,mF) basis, which adequately describe the system for a low magnetic field, also predict reduction of the number of transition components from 20 to 6 for Rb85 and from 12 to 4 for Rb87 spectrum at B>0.5 T. Also, the Zeeman transition frequency shifts, frequency intervals between the components and their slope versus B, are in agreement with the experiment.
We study the hyperfine spectrum of atoms of 87Rb^{87}\mathrm{Rb}87Rb dressed by a radio-frequency field and present experimental results in three different situations: freely falling atoms, atoms trapped in an optical dipole trap, and atoms in an adiabatic radio-frequency dressed shell trap. In all cases, we observe several resonant sidebands spaced (in frequency) at intervals equal to the dressing frequency, corresponding to transitions enabled by the dressing field. We theoretically explain the main features of the microwave spectrum using a semiclassical model in the low-field limit and the rotating-wave approximation for alkali-metal-like species, in general, and 87Rb^{87}\mathrm{Rb}87Rb atoms, in particular. As a proof of concept, we demonstrate how the spectral signal of a dressed atomic ensemble enables an accurate determination of the dressing configuration and the probing microwave field.
A compact source which produces atomic alkali-metal beams in individual hyperfine sublevels has been developed. The methods are demonstrated with 23Na^{23}\mathrm{Na}23Na atoms. Initially nearly all atoms are transferred into one hyperfine sublevel (∣F,mF〉=∣2,2〉|F, {m}_{F}〉=|2, 2〉∣F,mF​〉=∣2,2〉) by a double-resonance technique using laser optical pumping and rf transitions. Subsequently the other hyperfine sublevels can be populated selectively by an adiabatic high-frequency transition. The hyperfine sublevel populations are determined by laser-induced fluorescence spectroscopy in a magnetic field.
We develop a theoretical treatment of polarization spectroscopy and use it to make predictions about the general form of polarization spectra in the alkali-metal atoms. Using our model, we generate theoretical spectra for the D2D2D2 transitions in 87Rb^{87}\mathrm{Rb}87Rb, 85Rb^{85}\mathrm{Rb}85Rb, and 133Cs^{133}\mathrm{Cs}133Cs. Experiments demonstrate that the model accurately reproduces spectra of transitions from the upper hyperfine level of the ground state only. Among these, the closed transition $F\ensuremath{\rightarrow}{F}^{\ensuremath{'}}=F+1$ dominates, with a steep gradient through line center ideally suited for use as a reference in laser locking.