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.
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.
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 .
We have observed the sharply resonant enhancement of the cross section of the collision process $ns+ns\ensuremath{\rightarrow}np+(n\ensuremath{-}1)p$ between two Nans (16<n<27) atoms which occurs when the levels are shifted by an electric field so that the ns level lies midway between the two p states. The widths of the collisional resonances scale as ${n}^{\ensuremath{-}2}$ and the magnitudes of the cross sections as n4, with values of 0.5 GHz and 8\ifmmode\times\else\texttimes\fi{}108A˚2 for the 20s state. These results are in good agreement with calculations based on the long-range dipole-dipole interaction between the two atoms.
The large electric dipole moments associated with transitions between Rydberg states of atoms or molecules, make them ideal model systems with which to study Förster resonance energy transfer in collisions with other Rydberg atoms or molecules, or with polar ground-state molecules [1,2]. The sensitivity of high Rydberg states to electric fields allows these energy transfer processes to be tuned thorough resonance by exploiting the Stark effect. In this talk, I will describe recent experiments in which we have observed the resonant transfer of energy from the ground-state inversion sublevels in ammonia, to helium atoms in triplet Rydberg states with principal quantum numbers between 38 and 43. The experiments were performed at translational temperatures below 1 K in seeded, pulsed supersonic beams [3]. Electric fields up to ~10 V/cm were used to tune transitions between selected Rydberg states into resonance with the transitions between the inversion sublevels. Resonant energy transfer was identified by Rydberg-state-selective electric-field ionisation. The experimental data exhibit quantum-state-dependent resonance widths that range from 200 to 700 MHz and, in general, reduce as the value of the principal quantum number is increased. Comparison with the results of numerical calculations of the Rydberg energy-level structure and transition moments, shows a dependence of the measured widths on the electric dipole transition moments of the Rydberg-Rydberg transitions. These results are of particular interest, e.g., for applications in coherent control and quantum sensing [4-6], and in the study of low-temperature ion-molecule reactions performed within the orbit of a Rydberg electron [7]. [1] T. F. Gallagher, Phys. Rep. 210, 319 (1992) [2] F. B. Dunning, S. Buathong, Int. Rev. Phys. Chem. 37, 287 (2018) [3] K. Gawlas and S. D. Hogan, J. Phys. Chem. Lett. 11, 83 (2020) [4] M. Zeppenfeld, Euro. Phys. Lett. 118, 13002 (2017). [5] E. Kuznetsova, S. T. Rittenhouse, H. R. Sadeghpour, and S. F. Yelin, Phys. Rev. A 94, 032325 (2016). [6] E. Kuznetsova, S. T. Rittenhouse, H. R. Sadeghpour, and S. F. Yelin, Phys. Chem. Chem. Phys. 13, 17115 (2011). [7] K. Höveler, J. Deiglmayr, J. A. Agner, H. Schmutz and F. Merkt, Phys. Chem. Chem. Phys. 23, 2676 (2021).
We have observed resonant-energy-transfer collisions between K Rydberg atoms. We have tuned the ns1/2+(n-2)dj\ensuremath{\rightarrow}${\mathrm{np}}_{\mathrm{j}\ensuremath{'}}$+(n-1)${\mathrm{p}}_{\mathrm{j}\mathrm{\ensuremath{''}}}$ collisional process into resonance with a static electric field. The measured resonance field positions from n=24 to 29 agree well with the calculated positions. We show that the dipole-dipole selection rule, \ensuremath{\Delta}mj=0,\ifmmode\pm\else\textpm\fi{}1, is valid for these resonances but that \ensuremath{\Delta}J=0,\ifmmode\pm\else\textpm\fi{}1 is not, due to the presence of the electric field. In addition, the polarization of the lasers used to excite the Rydberg states can suppress many of the resonances.
Microwave-assisted resonant collisional energy transfer process $\mathrm{Na}(\mathrm{ns})+\mathrm{Na}(\mathrm{ns})+h\ensuremath{\nu}\ensuremath{\rightarrow}\mathrm{Na}(\mathrm{np})+\mathrm{Na}((n\ensuremath{-}1)p)$ is observed between two colliding Na(ns) atoms. The collisional resonance occurs when the microwave frequency $\ensuremath{\nu}$ equals the collisional energy defect $\frac{\ensuremath{\Delta}W}{h}$. The observed cross sections are very large (\ensuremath{\sim}108A˚2) and require very low microwave power, \ensuremath{\sim}10 W/cm2. These observations are in good agreement with an intuitive two-photon absorption model for these collisions.
The resonant transfer of energy from the inversion sublevels in NH 3 to He atoms in triplet Rydberg states with principal quantum number n = 38 has been controlled using electric fields below 15 V/cm in intrabeam collisions at translational temperatures of ∼1 K. The experiments were performed in pulsed supersonic beams of NH 3 seeded in He at a ratio of 1:19. The He atoms were prepared in the metastable 1s2s 3 S 1 level in a pulsed electric discharge in the trailing part of the beams. The velocity slip between the heavy NH 3 and the lighter metastable He was exploited to perform collision studies at center-of-mass collision speeds of ∼70 m/s. Resonant energy transfer in the atom–molecule collisions was identified by Rydberg-state-selective electric-field ionization. The experimental data have been compared to a theoretical model of the resonant dipole–dipole interactions between the collision partners based on the impact parameter method.