VIBRATIONAL RELAXATION IN THE $CO^{+}$ MOLECULAR ION
dc.creator | Bondybey, V. E. | en_US |
dc.creator | Miller, Terry A. | en_US |
dc.date.accessioned | 2006-06-15T14:05:04Z | |
dc.date.available | 2006-06-15T14:05:04Z | |
dc.date.issued | 1978 | en_US |
dc.identifier | 1978-RF-06 | en_US |
dc.identifier.uri | http://hdl.handle.net/1811/10523 | |
dc.description | Author Institution: Bell Telephone Laboratories | en_US |
dc.description.abstract | Ground state $X^{2} \Sigma^{+}\; CO^{+}$ molecular ions have been produced in a thermal He bath by Penning ionization of CO by He metastables. Specific rovibronic levels of the $A^{2} \Pi$ state of $CO^{+}$ have been excited by a tunable dye laser. Observation of the time-resolved laser-induced fluorescence allows the determination of the upper level lifetime as a function of He pressure. Radiative lifetimes and cross-sections for radiationless relaxation via He-$CO^{+}$ collisions are deduced for the v = 0-3 levels. The cross-sections are surprisingly large. Observations of laser-induced fluorescence from levels other than that initially excited indicates that relaxation between adjacent vibrational levels of the $A^{2}\Pi$ state is not direct. It is postulated that it may involve high vibrational levels of the ground $X^{2} \Sigma^{+}$ state. | en_US |
dc.format.extent | 96376 bytes | |
dc.format.mimetype | image/jpeg | |
dc.language.iso | English | en_US |
dc.publisher | Ohio State University | en_US |
dc.title | VIBRATIONAL RELAXATION IN THE $CO^{+}$ MOLECULAR ION | en_US |
dc.type | article | en_US |
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