Dresden 2011 – wissenschaftliches Programm
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MO: Fachverband Molekülphysik
MO 23: Electronic Spectroscopy II
MO 23.2: Vortrag
Donnerstag, 17. März 2011, 15:00–15:15, MER 02
Probing dissociative molecular dications by mapping of vibrational wavefunctions — •Ralph Püttner1, Tiberiu Arion2, Marko Förstel2,3, Toralf Lischke2, Melanie Mucke2, Vladmir Sekushin1, Günter Kaindl1, Alexander Bradshaw2,4, and Uwe Hergenhahn2 — 1Institut für Experimentalphysik, Freie Universität Berlin, Germany — 2Max-Planck-Institut für Plasmaphysik c/o Helmholtz-Zentrum Berlin, Germany — 3Max-Planck-Institut für Kernphysik, Heidelberg, Germany — 4Fritz-Haber-Institut der Max-Planck-Gesellschaft, Berlin, Germany
We present high-resolution photoelectron-Auger electron coincidence spectra of CH4. Since the vibrational structure in the C 1s photoelectron spectrum is resolved, Auger spectra corresponding to the vibrational levels v=0 and 1 can be extracted. These spectra display pronounced differences due to the fact that the energy spectrum of a transition to a dissociative state reflects the squares of the vibrational wavefunction, Ψvib(Q), in the core-ionized state. By implementing this in a simultaneous fit of both spectra we have separated the Auger transitions to all 7 states of dicationic CH42+ present in this energy region. We were able to derive the energy values and slopes of the potential energy curves of the dicationic states and have found good agreement with other experimental and theoretical results.