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An optical-optical double resonance experiment in LiH molecules: lifetime measurements in the C state

An optical-optical double resonance sub-Doppler experiment is used to measure short nonradiative lifetimes in the C (1)Sigma(+) state of LiH. These lifetimes are expected to result from the strong electronic interaction between the C (1)Sigma(+) state and the continuum of the A (1)Sigma(+) state and...

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Published in:The Journal of chemical physics 2004-10, Vol.121 (15), p.7237-7242
Main Authors: Bouloufa, N, Cabaret, L, Luc, P, Vetter, R, Luh, W T
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Language:English
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container_title The Journal of chemical physics
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creator Bouloufa, N
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description An optical-optical double resonance sub-Doppler experiment is used to measure short nonradiative lifetimes in the C (1)Sigma(+) state of LiH. These lifetimes are expected to result from the strong electronic interaction between the C (1)Sigma(+) state and the continuum of the A (1)Sigma(+) state and to vary with the vibrational quantum number, from nanoseconds to milliseconds. The experimental setup combines a molecular beam of LiH, a first cw laser beam locked to a given A-X absorption line, and a second cw laser beam scanned over C-A absorption profiles. Analysis of these absorption profiles in terms of Voigt profiles shows that their Lorentzian components significantly vary with the vibrational quantum numbers of the C state. Nonradiative decay rates deduced this way are systematically larger than the calculated ones but their variations are similar. Coherent saturation effects cannot be invoked to explain this discrepancy.
doi_str_mv 10.1063/1.1786919
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title An optical-optical double resonance experiment in LiH molecules: lifetime measurements in the C state
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