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Journal of the Optical Society of America B

Centimeter-wave spectroscopy of highly excited rubidium atoms

Dieter Meschede

Published Mar 1, 1987• 17 citations
Publisher

Abstract

One- and two-photon transitions between neighboring Rydberg states of rubidium with principal quantum numbers ranging from n = 50 to n = 63 have been studied. From these transition frequencies, corresponding to wavelengths in the centimeter domain, new values for quantum defects and fine- and hyperfine-structure splittings were obtained. The hyperfine structure of the 2S1/2 states was resolved up to n = 59. The data are compared with optically determined spectroscopic parameters, and fair agreement is found in most cases.

DOI
10.1364/josab.4.000413

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One- and two-photon transitions between neighboring Rydberg states of rubidium with principal quantum numbers ranging from n = 50 to n = 63 have been studied. From these transition frequencies, corresponding to wavelengths in the centimeter domain, new values for quantum defects and fine- and hyperfine-structure splittings were obtained. The hyperfine structure of the 2S1/2 states was resolved up to n = 59. The data are compared with optically determined spectroscopic parameters, and fair agreement is found in most cases.
We report the measurement of transition frequencies of Rb85 atoms in a room-temperature vapor cell to nP1/2 (n=34–53) and nP3/2 (n=34–87) Rydberg levels by observing single-photon Rydberg excitation spectroscopy. Based on the spectroscopic data, we determine quantum defects that are in good agreement with previous measurements of low-lying Rydberg states. Furthermore, the residuals between observed and calculated values of fine-splitting intervals in our experiments are found to be less than 10 MHz.
Millimeter resonances corresponding to single- and double-photon transitions have been observed between Rydberg levels of sodium with principal quantum number nnn ranging from 23 to 41. The levels are prepared by laser excitation; transitions are induced by microwaves produced by a backwave oscillator working around 300 GHz; detection is performed through the selective field-ionization technique. Experimental values for quantum defects, fine-structure intervals, and polarizabilities are reported.
Abstract We present experiments on two‐photon excitation of 87Rb atoms to Rydberg states. For this purpose, two continuous‐wave (cw)‐laser systems for both 780 nm and 480 nm have been set up. These systems are optimized to a small linewidth (well below 1 MHz) to get both an efficient excitation process and good spectroscopic resolution. To test the performance of our laser system, we investigated the Stark splitting of Rydberg states. We were able to see for both of the n = 41D finestructure states the electrical field dependent |mj| splitting. To show the ability of spatially selective excitation to Rydberg states, we excited rubidium atoms in an electrical field gradient and investigated both linewidths and lineshifts. Furthermore we were able to excite the atoms selectively from the two hyperfine ground states to Rydberg states. Finally, we investigated the Autler‐Townes splitting of the 5S1/2(F = 2)→5P3/2(F = 3) transition coupled to the light field via a Rydberg state to determine the Rabi frequency of this excitation step.
We report the measurement of the absolute transition frequencies of 87Rb^{87}\mathrm{Rb}87Rb atoms to the nP1/2n{P}_{1/2}nP1/2​ (n=34−−52n=34--52n=34−−52) and nP3/2n{P}_{3/2}nP3/2​ (n=34−−90n=34--90n=34−−90) Rydberg states by performing single-photon Rydberg excitation spectroscopy in a vapor cell. Rydberg transitions were detected by monitoring the transmission of a 780-nm probe beam. Based on the spectroscopic data, we determined the fine-splitting intervals and oscillator-strength ratios of the nPnPnP doublets and also extracted the quantum defects and ionization frequency. These results extend the spectroscopic information of the nPnPnP Rydberg series, providing basic knowledge for further applications to Rydberg atoms.
The multiphoton excitation of rubidium has been investigated over the 4600-6500-\AA{} wavelength region with a tunable dye-laser source having a linewidth better than 0.1 \AA{} and a space-charge ionization detector sensitive to a few ions per second. Multiphoton transitions have been observed to occur both through intermediate atomic states and through intermediate continuum states of the rubidium molecule. In the former case two-photon transitions have been observed from the 52S5^{2}S52S ground state of atomic rubidium to higher-lying n2Dn^{2}Dn2D levels for values of nnn ranging from 9 to 34 and to n2Sn^{2}Sn2S levels for values of nnn from 11 through 20. The fine-structure intervals of the n2Dn^{2}Dn2D levels for n=9toc13n=9 \mathrm{to}c 13n=9toc13 were measured together with the line-strength ratios and were found to be in good agreement with the predictions of a simple theoretical model. At the shorter wavelengths hybrid two-photon resonances were observed to be excited through resonant intermediate continuum states of Rb2{\mathrm{Rb}}_{2}Rb2​. As a result the dispersion curve for two-photon absorption in rubidium showed what appears to be resonant intermediate $p\ensuremath{\pi}(^{3}\ensuremath{\Sigma}_{u1})$ and 0g+{0}_{g}^{+}0g+​ terms dissociating to give a 5P325{P}_{\frac{3}{2}}5P23​​ atom and resulting in the strong development of features corresponding to the $5^{2}P_{\frac{3}{2}}\ensuremath{\rightarrow}n^{2}D_{\frac{3}{2},\frac{5}{2}}$ part of the diffuse series, for $n\ensuremath{\le}50$ in absorption and the $5^{2}P_{\frac{3}{2}}\ensuremath{\rightarrow}n^{2}S_{\frac{1}{2}}$ part of the sharp series. Components to 322D32^{2}D322D and 302S30^{2}S302S were recorded to a precision of 0.3 ${\mathrm{cm}}^{\ensuremath{-}1}$ and quantum defects for these previously unobserved terms were derived. The corresponding hybrid two-photon resonances involving intermediate states dissociating to give a 52P125^{2}P_{\frac{1}{2}}52P21​​ atom were not observed in the wavelength interval available in this experiment.