RESUMO
Polycyclic aromatic hydrocarbons (PAHs) play an important role in interstellar chemistry and are subject to high energy photons that can induce excitation, ionization, and fragmentation. Previous studies have demonstrated electronic relaxation of parent PAH monocations over 10-100 femtoseconds as a result of beyond-Born-Oppenheimer coupling between the electronic and nuclear dynamics. Here, we investigate three PAH molecules: fluorene, phenanthrene, and pyrene, using ultrafast XUV and IR laser pulses. Simultaneous measurements of the ion yields, ion momenta, and electron momenta as a function of laser pulse delay allow a detailed insight into the various molecular processes. We report relaxation times for the electronically excited PAH*, PAH+* and PAH2+* states, and show the time-dependent conversion between fragmentation pathways. Additionally, using recoil-frame covariance analysis between ion images, we demonstrate that the dissociation of the PAH2+ ions favors reaction pathways involving two-body breakup and/or loss of neutral fragments totaling an even number of carbon atoms.
RESUMO
We demonstrate the generation of a broadband coherent continuum extreme-ultraviolet (XUV) radiation produced by the interaction of gases with a many-cycle infrared (IR) laser field, utilizing a compact collinear many cycle-polarization gating (CMC-PG) device. The spectral width of the XUV radiation can support isolated pulses of 200 asec duration. The CMC-PG device forms a high energy content ultra-short temporal gate in a many-cycle laser pulse, within which the XUV emission is taking place. The gate width has been measured and is in agreement with the theoretical calculations. The simplicity, the compactness, the long term stability, and the high IR energy output within the gate, make the CMC-PG device an ideal tool for generating energetic isolated attosecond pulses and measure the carrier-envelope phase of a high-power many-cycle laser field.
