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Physical Review A

Comment on “Measurement of the lifetimes of S and D states below n=31 using cold Rydberg gas”

Duncan Tate

Published Jun 29, 2007• 8 citations
Publisher

Abstract

A recent paper by [Nascimento et al., Phys. Rev. A 74, 054501 (2006)], and a previous paper from the same group [de Oliveira et al., Phys. Rev. A 65 031401(R) (2002)], report measurements of Rydberg lifetimes in rubidium in the range $27\ensuremath{\le}n\ensuremath{\le}44$. In this Comment, we point out one apparent flaw of experimental technique in these papers that may lead to systematic errors in the results. We also clarify a point of theoretical interpretation used in these papers which suggests that the agreement between experiment and theory may not be as good as it seems.

DOI
10.1103/physreva.75.066502

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Reply to “Comment on ‘Measurement of the lifetimes of S and D states below n=31 using cold Rydberg gas”’

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A recent paper by [Nascimento et al., Phys. Rev. A 74, 054501 (2006)], and a previous paper from the same group [de Oliveira et al., Phys. Rev. A 65 031401(R) (2002)], report measurements of Rydberg lifetimes in rubidium in the range 27\ensuremath≤n\ensuremath≤4427\ensuremath{\le}n\ensuremath{\le}4427\ensuremath≤n\ensuremath≤44. In this Comment, we point out one apparent flaw of experimental technique in these papers that may lead to systematic errors in the results. We also clarify a point of theoretical interpretation used in these papers which suggests that the agreement between experiment and theory may not be as good as it seems.
In this paper we have extended our previous work [de Oliveira et al., Phys. Rev. A 65, 031401 (2002)] by measuring the SSS and DDD Rydberg lifetimes for 85Rb^{85}\mathrm{Rb}85Rb for principal quantum number between n=26n=26n=26 and 31 using a sample of cold Rydberg atoms. This range is limited by the amplitude of the electric field that we can generate in our present setup.
In response to the preceding Comment, we present important experimental information on our SSS, PPP, and DDD Rydberg lifetime measurements for 85Rb^{85}\mathrm{Rb}85Rb using a sample of cold Rydberg atoms. We analyze and discuss the implications of blackbody radiation transfer on our results. We also discuss the limitation of the theory compared with our results.
We have measured the radiative lifetimes of ns, np and nd Rydberg states of rubidium in the range 28 < n < 45. To enable long-lived states to be measured, our experiment uses slow-moving Rb atoms in a magneto-optical trap (MOT). Two experimental techniques have been adopted to reduce random and systematic errors. First, a narrow-bandwidth pulsed laser is used to excite the target Rydberg state, resulting in minimal shot-to-shot variation in the initial state population. Second, we monitor the target state population as a function of time delay from the laser pulse using a short-duration, millimetre-wave pulse that is resonant with a one- or two-photon transition. We then selectively field ionize the monitor state, and detect the resulting electrons with a micro-channel plate. This signal is an accurate mirror of the target state population, and is uncontaminated by contributions from other states which are populated by black body radiation. Our results are generally consistent with other recent experimental results obtained using a less sensitive method, and are also in excellent agreement with theory.
There has been increasing interest in the energy spectrum of highly excited Rydberg states. The energy spectra of the sss, ppp, and ddd highly excited Rydberg states of a rubidium atom have been measured by different groups. However, there is a discrepancy between the reported data concerning the energy levels of highly excited sss and ddd states of Rb. We address this issue by performing accurate calculations of Rb(ns,np,ndns,np,ndns,np,nd) energy levels using the parametric one-electron valence potential [Marinescu, Sadeghpour, and Dalgarno, Phys. Rev. A 49, 982 (1994)] with spin-orbit coupling. We compare results with reference data from the National Institute of Standards and Technology and from available experiments. This enables us to recommend energy levels of highly excited Rydberg states of Rb that can be used as reference values.
The dipole blockade of Rydberg excitations is a hallmark of the strong interactions between atoms in these high-lying quantum states [M. Saffman, T. G. Walker, and K. Mølmer, Rev. Mod. Phys. 82, 2313 (2010); D. Comparat and P. Pillet, J. Opt. Soc. Am. B 27, A208 (2010)]. One of the consequences of the dipole blockade is the suppression of fluctuations in the counting statistics of Rydberg excitations, of which some evidence has been found in previous experiments. Here we present experimental results on the dynamics and the counting statistics of Rydberg excitations of ultracold rubidium atoms both on and off resonance, which exhibit sub- and super-Poissonian counting statistics, respectively. We compare our results with numerical simulations using a novel theoretical model based on Dicke states of Rydberg atoms including dipole-dipole interactions, finding good agreement between experiment and theory.
We report a precise determination of the lifetime of the (4p)2P3/2(4p){\phantom{\rule{0.16em}{0ex}}}^{2}{P}_{3/2}(4p)2P3/2​ state of 40Ca+^{40}\mathrm{Ca}^{+}40Ca+, ${\ensuremath{\tau}}_{{P}_{3/2}}=6.639(42)\phantom{\rule{0.16em}{0ex}}\mathrm{ns}$, using a combination of measurements of the induced light shift and scattering rate on a single trapped ion. Good agreement with the result of a recent high-level theoretical calculation, 6.69(6) ns [M. S. Safronova et al., Phys. Rev. A 83, 012503 (2011)], but a 6-$\ensuremath{\sigma}$ discrepancy with the most precise previous experimental value, 6.924(19) ns [J. Jin et al., Phys. Rev. Lett. 70, 3213 (1993)], is found. To corroborate the consistency and accuracy of the new measurements, relativistically corrected ratios of reduced-dipole-matrix elements are used to directly compare our result with a recent result for the P1/2{P}_{1/2}P1/2​ state, yielding a good agreement. The application of the present method to precise determinations of radiative quantities of molecular systems is discussed.