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Time-Resolved Coincidence Imaging Spectroscopy of Molecular Photodissociation

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Abstract

Femtosecond time resolved photoelectron-photoion Coincidence Imaging Spectroscopy was used to study the non-adiabatic photodissociation dynamics of the NO dimer at 209 nm. Correlated photoelectron-photofragment energy and angular distributions reveal new details of the dissociation dynamics.

© 2005 Optical Society of America

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