Ultrafast Relaxation Dynamics of Highly-excited States in N2 Molecules Excited by Femtosecond XUV Pulses

Abstract

We used velocity-map-imaging to measure electronic and nuclear dynamics in N2 molecules excited by a train of attosecond pulses. A time-to-space mapping of autoionization channel is demonstrated. It is found that the autoionization becomes energetically allowed when the two nuclei are still very close (~ 3 Å) and that it can be coherently manipulated by a strong femtosecond infrared pulse.