International Workshop on ''Atomic Physics''
mpipks

November 26 – 30, 2012


Molecular dynamics with ultrafast x-rays: Opportunities with
non-linear spectroscopy

Philippe Wernet
Helmholtz-Zentrum Berlin
Molecular structure and chemical bonding determine the dynamic pathways of molecules in their multidimensional landscapes and hence define the outcome of chemical reactions. Characterizing structure and bonding in short-lived reaction intermediates and transient states of molecules during chemical reactions is hence the key to understanding chemical selectivity. Free electron lasers offer a unique approach to the atomic-scale chemical dynamics as they allow for the first time for a complete mapping of the electronic structure of atoms and molecules during chemical reactions. Time-resolved femtosecond soft x-ray spectroscopy in particular promises to reveal chemical bonding both in real time of the reaction and from the atomís perspective in an element-selective way. Here we present our time-resolved soft x-ray view of molecular dissociation reactions both in the gas phase and in solution. Opportunities with non-linear two color x-ray methods and with stimulated x-ray emission and inelastic x-ray scettering in particular will be discussed.