@article{PontiusKachelSchuesslerLangeheineetal.2011,
  author    = {Pontius, N. and Kachel, T. and Sch{\"u}ssler-Langeheine, C. and Schlotter, W. F. and Beye, Martin and Sorgenfrei, Florian and Chang, C. F. and F{\"o}hlisch, Alexander and Wurth, W. and Metcalf, P. and Leonov, I. and Yaresko, A. and Stojanovic, N. and Berglund, Martin and Guerassimova, N. and Duesterer, S. and Redlin, H. and Duerr, H. A.},
  title     = {Time-resolved resonant soft x-ray diffraction with free-electron lasers femtosecond dynamics across the Verwey transition in magnetite},
  series = {Applied physics letters},
  volume    = {98},
  journal   = {Applied physics letters},
  number    = {18},
  publisher = {American Institute of Physics},
  address   = {Melville},
  issn      = {0003-6951},
  doi       = {10.1063/1.3584855},
  pages     = {3},
  year      = {2011},
  abstract  = {Resonant soft x-ray diffraction (RSXD) with femtosecond (fs) time resolution is a powerful tool for disentangling the interplay between different degrees of freedom in strongly correlated electron materials. It allows addressing the coupling of particular degrees of freedom upon an external selective perturbation, e. g., by an optical or infrared laser pulse. Here, we report a time-resolved RSXD experiment from the prototypical correlated electron material magnetite using soft x-ray pulses from the free-electron laser FLASH in Hamburg. We observe ultrafast melting of the charge-orbital order leading to the formation of a transient phase, which has not been observed in equilibrium.},
  language  = {en}
}
@article{SunHenniesPietzschetal.2011,
  author    = {Sun, Y. -P. and Hennies, Franz and Pietzsch, Annette and Kennedy, B. and Schmitt, Thorsten and Strocov, Vladimir N. and Andersson, Joakim and Berglund, Martin and Rubensson, Jan-Erik and Aidas, K. and Gel'mukhanov, F. and Odelius, Michael and F{\"o}hlisch, Alexander},
  title     = {Intramolecular soft modes and intermolecular interactions in liquid acetone},
  series = {Physical review : B, Condensed matter and materials physics},
  volume    = {84},
  journal   = {Physical review : B, Condensed matter and materials physics},
  number    = {13},
  publisher = {American Physical Society},
  address   = {College Park},
  issn      = {1098-0121},
  doi       = {10.1103/PhysRevB.84.132202},
  pages     = {4},
  year      = {2011},
  abstract  = {Resonant inelastic x-ray scattering spectra excited at the O1s(-1)pi* resonance of liquid acetone are presented. Scattering to the electronic ground state shows a resolved vibrational progression where the dominant contribution is due to the C-O stretching mode, thus demonstrating a unique sensitivity of the method to the local potential energy surface in complex molecular systems. For scattering to electronically excited states, soft vibrational modes and, to a smaller extent, intermolecular interactions give a broadening, which blurs the vibrational fine structure. It is predicted that environmental broadening is dominant in aqueous acetone.},
  language  = {en}
}
@article{HenniesPietzschBerglundetal.2010,
  author    = {Hennies, Franz and Pietzsch, Annette and Berglund, Martin and F{\"o}hlisch, Alexander and Schmitt, Thorsten and Strocov, Vladimir and Karlsson, Hans O. and Andersson, Joakim and Rubensson, Jan-Erik},
  title     = {Resonant inelastic scattering spectra of free molecules with vibrational resolution},
  issn      = {0031-9007},
  doi       = {10.1103/Physrevlett.104.193002},
  year      = {2010},
  abstract  = {Inelastic x-ray scattering spectra excited at the 1s(-1) pi* resonance of gas phase O-2 have been recorded with an overall energy resolution that allows for well-resolved vibrational progressions. The nuclear wave packet dynamics in the intermediate state is reflected in vibrational excitations of the electronic ground state, and by fine-tuning the excitation energy the dissociation dynamics in the predissociative B' (3) Pi(g) final state is controlled.},
  language  = {en}
}