My project is to study the dissociation of O2+ in a strong field produced by ultrashort intense laser pulses. I am interested in the a 4Πu → f 4Πg transition, which represents the excitation and dissociation of the O2+ molecule into O+ + O due to the absorption of one photon. Photons with energies of 3.2 eV and 4.8 eV generated by the second (390 nm) and third (263 nm) harmonics of a 790 nm laser pulse are used in this study. The harmonics are generated through passing the 790 nm laser pulse, created by a Ti:sapphire laser, through a series of optical crystals, waveplates and filters. My goal is to study the Cooper minima in O2+ dissociation, which describes local minima in the transitional probabilities shown in figure 1. I compared the locations of the Cooper minima found in my theoretical calculations with our experimental kinetic energy release (KER) spectra recorded this summer.

Figure 1: This graph represents the transition probabilities for different vibrational states of the O2+ molecule. The arrows represent Cooper minima within the spectra. |
I would like to say thank you to KSU Physics REU Program, Larry Weaver and Kristan Corwin for giving me the opportunity to participate in this program. I would also like to thank my mentor Itzik Ben-Itzhak, and grad students Mohammad Zohrabi, Utuq Ablikim, Nora G. Johnson and Ben Berry for helping guide me in my research as well as helping me understand any questions I came across. |