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Multichannel decay dynamics of Rydberg atoms and molecules

J. B. M. Warntjes

Published Jan 1, 2001• 0 citations
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Bulletin of the American Physical Society•Mar 3, 2014•0 citations
A generalized class of ultralong-range Rydberg molecules is predicted which consist of a multichannel Rydberg atom whose outermost electron creates a chemical bond with a distant ground state atom. Such multichannel Rydberg molecules exhibit favorable properties for laser excitation, because states exist where the quantum defect varies strongly with the principal quantum number. The resulting occurrence of near degeneracies with states of high orbital angular momentum promotes the admixture of low l into the high l deeply bound trilobite molecule states, thereby circumventing the usual difficulty posed by electric dipole selection rules. Such states also can exhibit multiscale binding possibilities that could present novel options for quantum manipulation.
A generalized class of ultralong-range Rydberg molecules is predicted which consist of a multichannel Rydberg atom whose outermost electron creates a chemical bond with a distant ground state atom. Such multichannel Rydberg molecules exhibit favorable properties for laser excitation, because states exist where the quantum defect varies strongly with the principal quantum number. The resulting occurrence of near degeneracies with states of high orbital angular momentum promotes the admixture of low l into the high l deeply bound "trilobite" molecule states, thereby circumventing the usual difficulty posed by electric dipole selection rules. Such states also can exhibit multiscale binding possibilities that could present novel options for quantum manipulation.
Excited states of atoms and molecules exhibit a rich array of diverse phenomena. This dissertation examines two exotic states of atoms at such excited levels: Rydberg molecules and atomic negative ions. Rydberg molecules are formed by a Rydberg atom and one or more ground state atoms, and can be highly polar due to their unusual electronic wave functions and enormous bond lengths. This dissertation expands the theory of these molecules by studying the formation and structure of polyatomic molecules, multichannel Rydberg molecules formed from divalent atoms, and spin effects and relativistic interactions. It also details intermolecular forces between Rydberg molecules, their manipulation via external fields, and their dependence on the intricacies of electron-atom scattering. This electron-atom interaction is also the main component of the latter portion of this thesis, which studies doubly excited states of alkali negative ions in very polarizable and nearly degenerate atomic states. Photodetachment of these states reveals electron correlation and long-range forces stemming from their high excitation.