Abstract
Fluorescence quantum yields of the cis-1,2-difluoroethylene cation in the lowest vibrational levels of the Ã2A1 electronic state have been determined. The principle of the measurements is based on the detection of coincidences between energy-analysed photoelectrons and undispersed photons using He(Iα) as a photoionisation source. The cis-1,2-difluoroethylene cation in the Ã2A1 state is one of the few polyatomic cations for which the radiative decay as well as fragment ions are detected. The radiative, non-radiative and fragmentation rate constants could be evaluated from all the available data. These show that for the lowest levels of the Ã2A1 state the non-radiative pathway competing with the radiative relaxation is internal conversion (and/or isomerisation) as the fragmentation rate (loss of HF) is much slower.

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