Search Results
Jitter-correction for IR/UV-XUV pump-probe experiments at the FLASH free-electron laser
2017-04-10, Savelyev, Evgeny, Boll, Rebecca, Bomme, Cédric, Schirmel, Nora, Redlin, Harald, Erk, Benjamin, Düsterer, Stefan, Müller, Erland, Höppner, Hauke, Toleikis, Sven, Müller, Jost, Kristin Czwalinna, Marie, Treusch, Rolf, Kierspel, Thomas, Mullins, Terence, Trippel, Sebastian, Wiese, Joss, Küpper, Jochen, Brauβe, Felix, Krecinic, Faruk, Rouzée, Arnaud, Rudawski, Piotr, Johnsson, Per, Amini, Kasra, Lauer, Alexandra, Burt, Michael, Brouard, Mark, Christensen, Lauge, Thøgersen, Jan, Stapelfeldt, Henrik, Berrah, Nora, Müller, Maria, Ulmer, Anatoli, Techert, Simone, Rudenko, Artem, Rolles, Daniel
In pump-probe experiments employing a free-electron laser (FEL) in combination with a synchronized optical femtosecond laser, the arrival-time jitter between the FEL pulse and the optical laser pulse often severely limits the temporal resolution that can be achieved. Here, we present a pump-probe experiment on the UV-induced dissociation of 2,6-difluoroiodobenzene (C6H3F2I) molecules performed at the FLASH FEL that takes advantage of recent upgrades of the FLASH timing and synchronization system to obtain high-quality data that are not limited by the FEL arrival-time jitter. We discuss in detail the necessary data analysis steps and describe the origin of the time-dependent effects in the yields and kinetic energies of the fragment ions that we observe in the experiment.
Self-compression of 120 fs pulses in a white-light filament
2010, Bethge, Jens, Steinmeyer, Günter, Stibenz, Gero, Staudt, Peter, Brée, Carsten, Demircan, Ayhan, Redlin, Harald, Düsterer, Stefan
Self-compression of pulses with >100 fs input pulse duration from a 10 Hz laser system is experimentally demonstrated, with a compression factor of 3.3 resulting in output pulse durations of 35 fs. This measurement substantially widens the range of applicability of this compression method, enabling self-compression of pulsed laser sources that neither exhibit extremely low pulse-to-pulse energy fluctuations nor a particularly clean beam profile. The experimental demonstration is numerically modeled, revealing the exact same mechanisms at work as at shorter input pulse duration. Additionally, the role of controlled beam clipping with an adjustable aperture is numerically substantiated
Photodissociation of aligned CH3I and C6H3F2I molecules probed with time-resolved Coulomb explosion imaging by site-selective extreme ultraviolet ionization
2018, Amini, Kasra, Savelyev, Evgeny, Brauße, Felix, Berrah, Nora, Bomme, Cédric, Brouard, Mark, Burt, Michael, Christensen, Lauge, Düsterer, Stefan, Erk, Benjamin, Höppner, Hauke, Kierspel, Thomas, Krecinic, Faruk, Lauer, Alexandra, Lee, Jason W. L., Müller, Maria, Müller, Erland, Mullins, Terence, Redlin, Harald, Schirmel, Nora, Thøgersen, Jan, Techert, Simone, Toleikis, Sven, Treusch, Rolf, Trippel, Sebastian, Ulmer, Anatoli, Vallance, Claire, Wiese, Joss, Johnsson, Per, Küpper, Jochen, Rudenko, Artem, Rouzée, Arnaud, Stapelfeldt, Henrik, Rolles, Daniel, Boll, Rebecca
We explore time-resolved Coulomb explosion induced by intense, extreme ultraviolet (XUV) femtosecond pulses from a free-electron laser as a method to image photo-induced molecular dynamics in two molecules, iodomethane and 2,6-difluoroiodobenzene. At an excitation wavelength of 267 nm, the dominant reaction pathway in both molecules is neutral dissociation via cleavage of the carbon-iodine bond. This allows investigating the influence of the molecular environment on the absorption of an intense, femtosecond XUV pulse and the subsequent Coulomb explosion process. We find that the XUV probe pulse induces local inner-shell ionization of atomic iodine in dissociating iodomethane, in contrast to non-selective ionization of all photofragments in difluoroiodobenzene. The results reveal evidence of electron transfer from methyl and phenyl moieties to a multiply charged iodine ion. In addition, indications for ultrafast charge rearrangement on the phenyl radical are found, suggesting that time-resolved Coulomb explosion imaging is sensitive to the localization of charge in extended molecules.