Ionic interactions and collision dynamics in cold traps: rotational quenching of OH−(1Σ+) by Rb(2S)
Department of Chemistry and CNISM, The University of Rome
“La Sapienza”, P.le A. Moro 5, 00185 Rome, Italy
Corresponding author: a firstname.lastname@example.org
Published online: 30 July 2008
A newly computed potential energy surface, which describes the forces at play between the OH anionic molecule (treated as a rigid rotor at its equilibrium geometry) and the Rb(2S) atomic gas was obtained from fully ab initio methods, yielding highly correlated electronic wavefunctions for the interacting partners. It is in turn employed to calculate their rotationally quenching collision cross sections at ultralow energies and for different initial rotational states of the molecular anion. The results suggest that these strongly interacting partners are among the most efficient systems in providing very large internal de-excitation rates whenever the collision regime of an ultracold trap can occur for the partners. The collision encounters at such vanishing values of translational energies are seen to be strongly controlled by the behaviour of the real part of the scattering length as a function of the initial rotational state: the latter indicates, in fact, the presence of several virtual states close to the dissociation threshold of the complex.
PACS: 34.10.+x – General theories and models of atomic and molecular collisions and interactions (including statistical theories, transition state, stochastic and trajectory models, etc.) / 34.50.Ez – Rotational and vibrational energy transfer
© EDP Sciences, Società Italiana di Fisica, Springer-Verlag, 2008