ELECTRONIC SPECTROSCOPY OF COBALT-NEON
dc.creator | Cheng, T. C. | en_US |
dc.creator | Hasbrouck, S. | en_US |
dc.creator | Duncan, M. A. | en_US |
dc.date.accessioned | 2010-07-12T13:51:37Z | |
dc.date.available | 2010-07-12T13:51:37Z | |
dc.date.issued | 2010 | en_US |
dc.identifier | 2010-RG-07 | en_US |
dc.identifier.uri | http://hdl.handle.net/1811/46074 | |
dc.description | Author Institution: Department of Chemistry, University of Georgia, Athens, GA 30602-2556 | en_US |
dc.description.abstract | Co$^+$Ne was generated via laser vaporization in a pulsed supersonic expansion source, mass selected, and analyzed by visible photodissociation spectroscopy. An electronic band system was observed with an origin beginning at 13503 cm$^{-1}$. A progression of peaks beginning from the origin until the convergence limit can be seen, corresponding to the vibrational bands in the excited state of Co$^+$Ne. The excited state constants (we ??=124 cm$^{-1}$) were determined and the electronic cycle leads to a ground state binding energy (D$_0$ ? =948 cm$^{-1}$). The ground state binding energy can be compared to other rare gas binding energies, which is correlated to the polarizability of the rare gas. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Ohio State University | en_US |
dc.title | ELECTRONIC SPECTROSCOPY OF COBALT-NEON | en_US |
dc.type | Article | en_US |
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