Cl-Loss dynamics in the dissociative photoionization of CF3Cl with threshold photoelectron–photoion coincidence imaging
Literature Information
Xiangkun Wu, Guoqiang Tang, Hanhui Zhang, Xiaoguo Zhou, Shilin Liu, Fuyi Liu, Liusi Sheng, Bing Yan
The dissociative photoionization of CF3Cl was investigated in the photon energy range of 12.30–18.50 eV. The low-lying electronic states of CF3Cl+ cations were prepared by the method of threshold photoelectron–photoion coincidence (TPEPICO). The threshold photoelectron spectrum and the coincident time-of-flight mass spectra at the specific photon energies were recorded. Only a CF3+ fragment was observed at lower energy, while a CF2Cl+ fragment appeared for C2E and D2E states. As Cl-loss from the ground ionic state is statistical, the total kinetic energy release distribution (KERD) is represented as a Boltzmann profile, and a 0 K appearance energy of AP0 =12.79 ± 0.02 eV is derived from the statistical modelling of the breakdown diagram from 12.60 to 12.85 eV without taking into account the kinetic shift. For the A2A1 and B2A2 states of CF3Cl+ cations, the total KERDs are bimodal, where a parallel faster dissociation appears together with the statistical distribution. At higher energies like the C2E and D2E ionic states, a bimodal distribution similar to that of the A2A1 and B2A2 states is also observed for the KERD. With the aid of the calculated Cl-loss potential energy curves, the dissociative mechanisms of internal energy-selected CF3Cl+ cations are proposed.
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