By introducing the IR-UV pump-probe technique to detect molecular quantum beats, this phenomenon is utilized as a Doppler-free time domain spectroscopy for the electronic ground state. The technique is demonstrated with Stark quantum beats of vibrationally excited So levels to determine the electric
Direct pump/probe spectroscopy of the near-IR band of the solvated electron in alcohols
β Scribed by Peter K. Walhout; Joseph C. Alfano; Yoshifumi Kimura; Carlos Silva; Philip J. Reid; Paul F. Barbara
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 474 KB
- Volume
- 232
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
We report femtosecond direct pump/probe data on the s-state to p-state transition of the solvated electron in alcohols. The data reveal a p-state lifetime of ~0.5 ps and a large spectral component due to displacement along the ground-state solvent coordinate involving slow diffusive solvent motions and subsequent relaxation. The large displacement is surprising considering the short excited-state lifetime and the long relaxation times of these modes. This effect is apparently the result of a previously unknown p-state to s-state nonadiabatic rearrangement of the solvent coordinate of solvated electrons in alcohols.
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We report on the first achievement of tunable two-band ``one-micron'' CW oscillation in the ^2^F~5/2~ β ^2^F~7/2~ channel of Yb^3+^ activator ions in Sc~2~O~3~ ceramics with CW laser-diode pumping, as well as on results of precise measurement of the refractive index and its dispersion in spectral ra