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Physical Review Letters

Transform-limited collisions of K Rydberg atoms

D. S. Thomson, Michael J. Renn, Thomas F. Gallagher

Published Dec 24, 1990• 15 citations
Publisher

Abstract

By reducing the collision velocity of Rydberg atoms in resonant energy-transfer collisions, we have observed collisional resonances as narrow as 1 MHz, or collision times as long as 1.0 \ensuremath{\mu}s. Restricting the collision to a time less than the natural collision time results in transform broadening of the resonances, allowing us to know when an individual collision begins and ends. The latter point is verified by observing the dependence of the collision line shape on the phase of an oscillating field of frequency equal to the width of the collisional resonance.

DOI
10.1103/physrevlett.65.3273

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A large enhancement in the resonant collisional energy-transfer process $\mathrm{Na}(\mathrm{ns})+\mathrm{Na}(\mathrm{ns})\ensuremath{\rightarrow}\mathrm{Na}[(n\ensuremath{-}1)p]+\mathrm{Na}(\mathrm{nl})$ or $\mathrm{Na}(\mathrm{ns})+\mathrm{Na}(\mathrm{ns})\ensuremath{\rightarrow}\mathrm{Na}(\mathrm{np})+\mathrm{Na}[(n\ensuremath{-}1)l]$ is observed when the initial $\mathrm{ns}$ state lies midway between $(n\ensuremath{-}1)p$ and an $\mathrm{nl}$ state or between $\mathrm{np}$ and an $(n\ensuremath{-}1)l$ state. This resonance condition, achieved by the electric field tuning of the levels, leads to large cross sections \ensuremath{\sim} ${10}^{9}$ ${\mathrm{\AA{}}}^{2}$ and narrow linewidths \ensuremath{\sim} 1 GHz. These cross sections and linewidths are comparable to the previously observed resonant process $\mathrm{Na}(\mathrm{ns})+\mathrm{Na}(\mathrm{ns})\ensuremath{\rightarrow}\mathrm{Na}[(n\ensuremath{-}1)p]+\mathrm{Na}(\mathrm{np})$. We have also observed a similar collisional energy transfer starting from a completely different initial state, i.e., $\mathrm{Na}(15d)+\mathrm{Na}(15d)\ensuremath{\rightarrow}\mathrm{Na}(16f)+\mathrm{Na}(15p)$. In this case the enhancement in the cross section (\ensuremath{\sim} ${10}^{8}$ ${\mathrm{\AA{}}}^{2}$) is observed at a relatively low electric field \ensuremath{\sim} 17 V/cm.

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By reducing the collision velocity of Rydberg atoms in resonant energy-transfer collisions, we have observed collisional resonances as narrow as 1 MHz, or collision times as long as 1.0 \ensuremath{\mu}s. Restricting the collision to a time less than the natural collision time results in transform broadening of the resonances, allowing us to know when an individual collision begins and ends. The latter point is verified by observing the dependence of the collision line shape on the phase of an oscillating field of frequency equal to the width of the collisional resonance.
Resonant collisional energy transfer between atoms with small relative velocity is shown to have such long collision times, \ensuremath{\sim}0.17 \ensuremath{\mu}s, or equivalently such narrow linewidths, 6 MHz, that it may be used to make spectroscopic measurements. Specifically, we report the use of the sharply resonant collisional energy transfer ns+(n-2)d\ensuremath{\rightarrow}np +(n-1)p, between velocity-selected K atoms to determine an improved value, 1.711?5(5), and the K np-state quantum defect.
Resonant collisional energy transfer can be studied in uprecedented detail using Rydberg atoms. Using the dependence of the energy level spacing on principal quantum number it is possible to examine resonant energy transfer in collisions with molecules. Finer control of the level spacing is possible by varying the level spacings with an electric field. Using this approach it is possible to observe sharply resonant collisions between Rydberg atoms. They are resonant dipole-dipole collisions which have cross sections orders of magnitude larger than the geometric cross sections of the colliding Rydberg atoms. These collisions are interesting in themselves; for example, they exhibit intracollisional interference, and it is possible to know when individual collisions begin and end. Perhaps the most interesting aspect of these collisions is that, because of the large dipole moments of the Rydberg atoms, they are easily controlled by microwave and radio frequency fields.
We have observed radiatively assisted collisions between velocity-selected K Rydberg atoms in radio-frequency (rf) fields. The low relative velocity of the atoms leads to long collision times, or equivalently, narrow, 1-MHz, collisional resonances. We have carried out systematic measurements with rf fields in the strong-field regime, and have shown that the cross sections agree quantitatively with the predictions of the strong-field theory. We have also shown experimentally and theoretically that the sum over m of the cross sections for m photon-assisted cross sections is larger than the resonant-collision cross section in the absence of a rf field.
Resonant energy transfer collisions, those in which one atom or molecule transfers only internal energy, as oppposed to translational energy, to its collision partner require a precise match of the energy intervals in the two collision partners. Because of this energy specificity, resonant collisional energy transfer plays an important role in many laser applications, the He–Ne and CO 2 lasers being perhaps the best known examples. It is interesting to imagine an experiment in which we can tune the energy of the excited state of atom B through the energy of the excited state of atom A, as shown in Fig. 14.1. At resonance we would expect the cross section for collisionally transferring the energy from an excited A atom to a ground state B atom to increase sharply as shown in Fig. 14.1. In general, atomic and molecular energy levels are fixed, and the situation of Fig. 14.1 is impossible to realize. Nonetheless systematic studies of resonant energy transfer have been carried out by altering the collision partner, showing the importance of resonance in collisional energy transfer. The use of atomic Rydberg states, which have series of closely spaced levels, presents a natural opportunity for the study of resonant collisional energy transfer. One of the earliest experiments was the observation of resonant rotational to electronic energy transfer from NH 3 to Xe Rydberg atoms by Smith et al .
A large enhancement in the resonant collisional energy-transfer process $\mathrm{Na}(\mathrm{ns})+\mathrm{Na}(\mathrm{ns})\ensuremath{\rightarrow}\mathrm{Na}[(n\ensuremath{-}1)p]+\mathrm{Na}(\mathrm{nl})$ or $\mathrm{Na}(\mathrm{ns})+\mathrm{Na}(\mathrm{ns})\ensuremath{\rightarrow}\mathrm{Na}(\mathrm{np})+\mathrm{Na}[(n\ensuremath{-}1)l]$ is observed when the initial ns\mathrm{ns}ns state lies midway between $(n\ensuremath{-}1)p$ and an nl\mathrm{nl}nl state or between np\mathrm{np}np and an $(n\ensuremath{-}1)l$ state. This resonance condition, achieved by the electric field tuning of the levels, leads to large cross sections \ensuremath{\sim} 109{10}^{9}109 A˚2{\mathrm{\AA{}}}^{2}A˚2 and narrow linewidths \ensuremath{\sim} 1 GHz. These cross sections and linewidths are comparable to the previously observed resonant process $\mathrm{Na}(\mathrm{ns})+\mathrm{Na}(\mathrm{ns})\ensuremath{\rightarrow}\mathrm{Na}[(n\ensuremath{-}1)p]+\mathrm{Na}(\mathrm{np})$. We have also observed a similar collisional energy transfer starting from a completely different initial state, i.e., $\mathrm{Na}(15d)+\mathrm{Na}(15d)\ensuremath{\rightarrow}\mathrm{Na}(16f)+\mathrm{Na}(15p)$. In this case the enhancement in the cross section (\ensuremath{\sim} 108{10}^{8}108 A˚2{\mathrm{\AA{}}}^{2}A˚2) is observed at a relatively low electric field \ensuremath{\sim} 17 V/cm.