ROTATIONALLY RESOLVED ELECTRONIC SPECTRA FOR URANIUM MONOXIDE
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Abstract
Previous attempts to observe the electronic band systems of uranium monoxide (UO) have been hindered by overlapping spectra which arise from the large number of polymeric oxides that coexist with vapor phase UO. We have overcome these problems by the use of sequential muliphoton ionization of a molecular beam of UO, followed by mass selected ion detection. Several vibronic bands of UO have now been observed by this technique. Spectra were recorded by tuning a pulsed dye laser through the single photon resonances, and ionizing the excited molecules with pulses from a XeCl laser. A time of flight mass spectrometer was used to ensure that only
Description
Author Institution: Department of Chemistry, Illinois Institute of Technology; Chemistry Division, Argonne National Laboratory