Time-resolved imaging of bound and dissociating nuclear wave packets in strong-field ionized iodomethane. Issue 26 (28th January 2019)

• Record Type: Journal Article
• Authors: Malakar, Y.; Pearson, W. L.; Zohrabi, M.; Kaderiya, B.; P., Kanaka Raju; Ziaee, F.; Xue, S.; Le, A. T.; Ben-Itzhak, I.; Rolles, D.; Rudenko, A.
• Is Part Of: Physical chemistry chemical physics. Volume 21:Issue 26(2019)
• Page Start: 14090
• Page End: 14102
• Publication Date: 2019-01-28
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c8cp07032f
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : We report the results of a time-resolved coincident ion momentum imaging experiment probing nuclear wave packet dynamics in the strong-field ionization and dissociation of iodomethane (CH3 I). Abstract : We report the results of a time-resolved coincident ion momentum imaging experiment probing nuclear wave packet dynamics in the strong-field ionization and dissociation of iodomethane (CH3 I), a prototypical polyatomic system for photochemistry and ultrafast laser science. By measuring yields, kinetic energies, and angular distributions of CH3 + + I + and CH3 + + I ++ ion pairs as a function of the delay between two 25 fs, 790 nm pump and probe pulses, we map both, bound and dissociating nuclear wave packets in intermediate cationic states, thereby tracking different ionization and dissociation pathways. In both channels, we find oscillatory features with a 130 fs periodicity resulting from vibrational motion (C–I symmetric stretch mode) in the first electronically excited state of CH3 I + . This vibrational wave packet dephases within 1 ps, in good agreement with a simple wave packet propagation model. Our results indicate that the first excited cationic state plays a key role in the dissociative ionization of CH3 I and that it represents an important intermediate in the sequential double and multiple ionization at moderate intensities.