ROTATIONAL EXCITATION OF $N_{2}^{+}$ AND VIBRATIONAL STATE RESOLVED ION MOLECULE REACTIONS

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1981

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Ohio State University

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The N2+ first negative system (B2Σu+X2Σg+) has been recorded by laser induced fluorescences of N2+ ions confined in an rf trap. The ions were produced by electron impact and had an initial rotational distribution close to the room temperature distribution of the target N2 gas. By admitting Ar gas at pressures 10 to 100 times in excess of the N2 pressure, variable numbers of N2+Ar collisions were allowed to occur before the N2+ distribution was interrogated by the laser. Since the N2+ was translationally energetic, being driven by the trap fields, a rapid and extensive T to R energy transfer was observed. In this way, high rotational states of N2+ were populated and the radiative lifetimes of these states were measured. Cross sections for the reaction of specific vibrational states of N2+ with Ar and H2(D2) have been measured.

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