The ultrafast dynamics and dissociative ionization of CS2 were studied using the pump-probe method with time-of-flight mass spectroscopy. The transient behavior of both parent ion (CS2+) and fragment ions (S+ and CS+) was observed. It was found that all the ionic signals decay exponentially with lifetimes that were different for delay times, t>0 and t<0, which can be attributed to the evolution of different Rydberg states pumped by 267-nm and 400-nm laser pulses. The lifetimes of two Rydberg states were obtained simultaneously from one fitting of the transients. The fragment ions were produced by the dissociation of CS2+, and it is suggested that the final ionic state is the C2Σg+ state of CS2+ based on the measured S+/CS+ branching ratio. The S+/CS+ ratio is dependent on the delay time of the two lasers, indicating that the dissociation process of CS2+ is related to the evolution of the intermediate Rydberg state.
ZHANG DongDong FAN Zhen SUN ErPing ZHANG JunFeng LIU Hang XU HaiFeng JIN MingXing DING DaJun
This paper reports that a one-colour fs pump-probe measurement has been carried out for studying photoionization/photodissociation of cyclohexanone (C6H10O) in intense laser field. Two of the fragments from cyclohexanone, C2H3+ and C3H3+ , are studied under 800 nm laser pump-probe and the results obtained show similar time evolutions. It proposes a feasible model for analysing the experimental observations of the one-colour fs pump-probe measurement. The results demonstrate that as an intermediate product, the excited molecular parent ions play a very important role in photionization/photodissociation processes in intense laser field.
