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dc.creatorGlab, W. L.en_US
dc.creatorPratt, S. T.en_US
dc.date.accessioned2006-06-15T19:11:24Z
dc.date.available2006-06-15T19:11:24Z
dc.date.issued1998en_US
dc.identifier1998-WG-15en_US
dc.identifier.urihttp://hdl.handle.net/1811/19162
dc.description$^{a}$ W.L. Glab was partially supported by the Robert A. Welch Foundation $^{b}$ S.T. Pratt was supported by the U.S. Department of Energy, Office of Energy Research, Office of Basic Energy Sciences, under Contract W-31-109-Eng-38en_US
dc.descriptionAuthor Institution: Department of Physics, Texas Tech University; Argonne National Laboratory, Argonneen_US
dc.description.abstractWe have studied the dynamics of vibrational autoionization of Rydberg states of water using energy-dispersive photoelectron spectroscopy. A high-resolution magnetic bottle photoelectron spectrometer was used to acquire rotationally resolved photoelectron spectra following vibrational autoionization of fully quantum-state selected Rydberg states with $n=6$ and $n\sim 9$. The Rydberg states were excited through a $(2+1^{\prime})$ REMPI process through selected rovibrational levels of the $\tilde{C}(1,0,0)$ state. The photoelectron spectra provide considerable dynamical information on the mechanisms of energy and angular momentum transfer between the Rydberg electron and the ion core, and also give information which will be valuable for firm identifications for the Rydberg state transitions. The spectra directly display the degree of 1-mixing between different partial waves.en_US
dc.format.extent118933 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleROTATIONALLY RESOLVED PHOTOELECTRON SPECTROSCOPY OF AUTOIONIZING STATES OF WATERen_US
dc.typearticleen_US


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