Translational control of Rydberg atoms in electric fields

Yu Pu, Barry F. Dunning

Martin Zeppenfeld, Ferdinand Jarisch

F. Tudorica, Oleg Kritsun, H. Metcalf

A L Goodgame, T. P. Softley

A novel theoretical study of the control of translational motion of atomic and molecular Rydberg states in inhomogeneous static electric fields is presented. Simulations have been carried out demonstrating that, under realistic conditions, the deflection and focusing of Rydberg atoms and molecules should be achievable. Advantage is taken of the high susceptibility of the Rydberg states to external electric fields, allowing the use of much smaller fields than would be necessary for ground state neutrals. The simulations presented are for trajectories of Rydberg states with n = 18-20 in the fields of an electric dipole, quadrupole and hexapole. A deflection of 7 mm is predicted for n = 18 Rydberg states travelling parallel to the dipole after 100 µs time of flight. In the hexapole n = 20 Rydberg states are refocused to a spot size of the order of the laser beam waist (10 µm) after 20 µs. It is demonstrated that the hexapole can also act as a cylindrical lens if its axis is perpendicular to the Rydberg beam direction. Spontaneous emission and black-body decay rates are also calculated, and their variation with the applied field is investigated. The potential applications of this work might include the use of focusing and deflection for controlled low-energy collisions of Rydberg molecules with surfaces.

David A. Harmin

K. Gawlas, S. D. Hogan

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.