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arXiv:0808.1648 · Physical Review A

Radio-frequency-driven dipole-dipole interactions in spatially separated volumes

Atreju Tauschinsky, C. S. E. van Ditzhuijzen, Lambertus D. Noordam, H. B. van Linden van den Heuvell

Published Dec 5, 2008• 27 citations
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Abstract

Radio-frequency (rf) fields in the MHz range are used to induce resonant energy transfer between cold Rydberg atoms in spatially separated volumes. After laser preparation of the Rydberg atoms, dipole-dipole coupling excites the $49s$ atoms in one cylinder to the $49p$ state while the $41d$ atoms in the second cylinder are transferred down to the $42p$ state. The energy exchanged between the atoms in this process is $33\phantom{\rule{0.3em}{0ex}}\mathrm{GHz}$. An external rf field brings this energy transfer into resonance. The strength of the interaction has been investigated as a function of amplitude $(0--1\phantom{\rule{0.3em}{0ex}}\mathrm{V}∕\mathrm{cm})$ and frequency $(1--30\phantom{\rule{0.3em}{0ex}}\mathrm{MHz})$ of the rf field and as a function of a static-field offset. Multiphoton transitions up to fifth order as well as selection rules prohibiting the process at certain fields have been observed. The width of the resonances has been reduced compared to earlier results by switching off external magnetic fields of the magneto-optical trap, making sub-MHz spectroscopy possible. All features are well reproduced by theoretical calculations taking the strong ac Stark shift due to the rf field into account.

DOI
10.1103/physreva.78.063409

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This thesis reports the use of both dc and ac electric fi eld induced resonant \nenergy transfer, RET, between cold Rydberg atoms as a useful tool for enhancement \nof interatomic interactions. A general technique for laser frequency stabilization and \nits suitability for Rydberg atom excitation is also demonstrated. \nRET between cold Rydberg atoms was used to determine Rydberg atom energy \nlevels. The ⁸⁵Rb atoms are laser cooled and trapped in a magneto-optical trap. \nFor energy level determination experiment, atoms were optically excited to 32d₅/₂ \nRydberg states. The two-atom process 32d₅/₂ + 32d₅/₂ → 34p₃/₂+30g is resonant at \nan electric fi eld of approximately 0.3 V/cm through dipole dipole interaction. The \nexperimentally observed resonant fi eld, together with the Stark map calculation is \nused to make a determination of the ⁸⁵Rb ng-series quantum defect to be ⵒg(n = \n30) = 0.00405(6). \nThe ac Stark eff ect was also used to induce RET between cold Rydberg atoms. \nWhen a 28.5 GHz dressing field was set at speci fic fi eld strengths, the two-atom \ndipole-dipole process 43d₅/₂ + 43d₅/₂ → 45p₃/₂ + 41f was dramatically enhanced, \ndue to induced degeneracy of the initial and final states. This method for enhancing \ninteractions is complementary to dc electric- field-induced RET, but has more \n \nflexibility due to the possibility of varying the applied frequency. At a dressing field \nof 28.5 GHz all of the participating levels (43d₅/₂, 45p₃/₂ and 41f) show signi cant \nshifts and these give a complicated series of resonances. An oscillating electric \nfi eld at 1.356 GHz was also used to promote the above RET process where the \natoms are initially excited to the 43d₅/₂ Rydberg states. The ac fi eld strength was \nscanned to collect RET spectra. Di fferent resonances were observed for diff erent \nmagnetic sublevels involved in the process. Compared to the higher dressing field \nfrequency of 28.5 GHz, the choice of dressing frequency of 1.356 GHz, which is \nslightly blue detuned from the 41f - 41g transition, and structure of the spectra \nmay be understood, by analogy with the dc field case.

•May 19, 2010•1 citation
Radio-frequency (rf) fields in the MHz range are used to induce resonant energy transfer between cold Rydberg atoms in spatially separated volumes. After laser preparation of the Rydberg atoms, dipole-dipole coupling excites the 49s49s49s atoms in one cylinder to the 49p49p49p state while the 41d41d41d atoms in the second cylinder are transferred down to the 42p42p42p state. The energy exchanged between the atoms in this process is 33GHz33\phantom{\rule{0.3em}{0ex}}\mathrm{GHz}33GHz. An external rf field brings this energy transfer into resonance. The strength of the interaction has been investigated as a function of amplitude (0−−1V∕cm)(0--1\phantom{\rule{0.3em}{0ex}}\mathrm{V}∕\mathrm{cm})(0−−1V∕cm) and frequency (1−−30MHz)(1--30\phantom{\rule{0.3em}{0ex}}\mathrm{MHz})(1−−30MHz) of the rf field and as a function of a static-field offset. Multiphoton transitions up to fifth order as well as selection rules prohibiting the process at certain fields have been observed. The width of the resonances has been reduced compared to earlier results by switching off external magnetic fields of the magneto-optical trap, making sub-MHz spectroscopy possible. All features are well reproduced by theoretical calculations taking the strong ac Stark shift due to the rf field into account.
We have observed resonant energy transfer between cold Rydberg atoms in spatially separated cylinders. Resonant dipole-dipole coupling excites the 49s atoms in one cylinder to the 49p state while the 41d atoms in the second cylinder are transferred down to the 42p state. We have measured the production of the 49p state as a function of separation of the cylinders (0-80 microm) and the interaction time (0-25 micros). In addition, we measured the width of the electric field resonances. A full many-body quantum calculation reproduces the main features of the experiments.
A microwave dressing field was used to induce resonant energy transfer in translationally cold Rydberg atoms. The Rb Rydberg atoms were obtained by laser excitation of cold atoms in a magneto-optical trap. When the amplitude of a 1.356 GHz dressing field was scanned, the two-atom dipole-dipole process 43d5/2 + 43d5/2 → 45p3/2 + 41f5/2,7/2 was enhanced due to the induced degeneracy of the initial and final states. The resulting spectrum had a series of resonant field amplitudes corresponding to different magnetic sublevels possible for the states involved. The scanned field amplitude was calibrated using microwave spectroscopy of the 43d5/2− 41f transition under the influence of non-resonant dressing fields. The calibrated resonant field amplitudes agree well with ac Stark shift calculations performed using the Floquet approach. This method for enhancing interactions is complementary to dc electric field induced resonant energy transfer, but benefits from the ability to shift energy levels in either direction by choice in frequency.
We have observed St\"uckelberg oscillations in the dipole-dipole interaction between Rydberg atoms with an externally applied radio-frequency field. The oscillating rf field brings the interaction between cold Rydberg atoms in two separated volumes into resonance. We observe multiphoton transitions when varying the amplitude of the rf field and the static electric field offset. The angular momentum states we use show a quadratic Stark shift, which leads to a fundamentally different behavior than linearly shifting states. Both cases are studied theoretically using the Floquet approach and are compared. The amplitude of the sidebands, related to the interaction strength, is given by the Bessel function in the linearly shifting case and by the generalized Bessel function in the quadratically shifting case. The oscillatory behavior of both functions corresponds to St\"uckelberg oscillations, an interference effect described by the semiclassical Landau-Zener-St\"uckelberg model. The measurements prove coherent dipole-dipole interaction during at least $0.6\text{ }\ensuremath{\mu}\text{s}$.
The ac Stark effect was used to induce resonant energy transfer between translationally cold 85Rb Rydberg atoms. When a 28.5 GHz dressing field was set at specific field strengths, the two-atom dipole-dipole process 43d5/2+43d5/2-->45p3/2+41f was dramatically enhanced, due to induced degeneracy of the initial and final states. This method for enhancing interactions is complementary to dc electric-field-induced resonant energy transfer, but has more flexibility due to the possibility of varying the applied frequency.
Ultracold Rydberg atoms in a static electric field can exchange energy via the dipole-dipole interaction. The Stark effect shifts the energy levels of the atoms which tunes the energy exchange into resonance at specific values of the electric field (F\"orster resonances). We excite rubidium atoms to Rydberg states by focusing either a 480 nm beam from a tunable dye laser or a pair of diode lasers into a magneto-optical trap. The trap lies at the center of a configuration of electrodes. We scan the electric field by controlling the voltage on the electrodes while measuring the fraction of atoms that interact. Dipole-dipole interaction spectra are presented for initially excited rubidium ndndnd states for n=31n=31n=31 to 46 and for four different pairs of initially excited rubidium nsnsns states. We also present the dipole-dipole interaction spectra for individual rubidium 32ddd (j,mj)(j,\phantom{\rule{0.16em}{0ex}}{m}_{j})(j,mj​) fine structure levels that have been selectively excited. The data are compared to calculated spectra.
This thesis reports the use of both dc and ac electric fi eld induced resonant \nenergy transfer, RET, between cold Rydberg atoms as a useful tool for enhancement \nof interatomic interactions. A general technique for laser frequency stabilization and \nits suitability for Rydberg atom excitation is also demonstrated. \nRET between cold Rydberg atoms was used to determine Rydberg atom energy \nlevels. The ⁸⁵Rb atoms are laser cooled and trapped in a magneto-optical trap. \nFor energy level determination experiment, atoms were optically excited to 32d₅/₂ \nRydberg states. The two-atom process 32d₅/₂ + 32d₅/₂ → 34p₃/₂+30g is resonant at \nan electric fi eld of approximately 0.3 V/cm through dipole dipole interaction. The \nexperimentally observed resonant fi eld, together with the Stark map calculation is \nused to make a determination of the ⁸⁵Rb ng-series quantum defect to be ⵒg(n = \n30) = 0.00405(6). \nThe ac Stark eff ect was also used to induce RET between cold Rydberg atoms. \nWhen a 28.5 GHz dressing field was set at speci fic fi eld strengths, the two-atom \ndipole-dipole process 43d₅/₂ + 43d₅/₂ → 45p₃/₂ + 41f was dramatically enhanced, \ndue to induced degeneracy of the initial and final states. This method for enhancing \ninteractions is complementary to dc electric- field-induced RET, but has more \n \nflexibility due to the possibility of varying the applied frequency. At a dressing field \nof 28.5 GHz all of the participating levels (43d₅/₂, 45p₃/₂ and 41f) show signi cant \nshifts and these give a complicated series of resonances. An oscillating electric \nfi eld at 1.356 GHz was also used to promote the above RET process where the \natoms are initially excited to the 43d₅/₂ Rydberg states. The ac fi eld strength was \nscanned to collect RET spectra. Di fferent resonances were observed for diff erent \nmagnetic sublevels involved in the process. Compared to the higher dressing field \nfrequency of 28.5 GHz, the choice of dressing frequency of 1.356 GHz, which is \nslightly blue detuned from the 41f - 41g transition, and structure of the spectra \nmay be understood, by analogy with the dc field case.