Shape-Resonance-Enhanced Nuclear-Motion Effects in Molecular Photoionization

Abstract
Shape resonances in molecular photoionization are shown to induce strong coupling between vibrational and electronic motion over a spectral range several times broader than the resonances half-width. This coupling is manifested by large deviations from Franck-Condon intensity distributions and strong dependence of photoelectron angular distributions on the vibrational state of the residual ion. These effects are illustrated for the 3σg photoionization channel of N2.

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