Abstract
Field ionization of high Rydberg manifold states $(n=112\text{--}137)$ of rubidium-85 under a rotating electric field has been investigated experimentally and theoretically. Applying a rapidly reversed electric field with a small static perpendicular field to rotate the total electric field around zero, we have observed substantial increase of the fraction of the tunneling field-ionization process and a profound broadening of its ionization peak over a wide range of field strengths with increasing transverse electric field. The observed tunneling field-ionization fraction is almost independent of the slew rate of the applied electric field, and also on the principal quantum number $n$ over the range investigated. To compare with these experimental results, theoretical calculations have been performed with a successive two-step regime. As the first step we calculated the redistributions of magnetic quantum number ${m}_{\ensuremath{\ell}}$ and parabolic quantum number ${n}_{1}\ensuremath{-}{n}_{2}$ of the states under the rotating electric field. Then the following time evolution of the manifold states with $\ensuremath{\mid}{m}_{\ensuremath{\ell}}\ensuremath{\mid}\ensuremath{\leqslant}3$ was traced on the Stark map in a coherent as well as an incoherent model. The calculated results are generally in good agreement with the experimental ones. The increase of the tunneling field-ionization fraction under a rotating electric field plays an essential role in achieving the high efficiency in the recently proposed selective-field-ionization scheme for high Rydberg atoms.
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