The femtosecond time-resolved ionization spectrum of the B-state of Na, has been studied theoretically, taking two nuclear degrees of freedom into account (bending mode and pseudorotation ). Special emphasis is put on a comparison between different approaches to the pseudorotational dynamics of Na,(
Femtosecond two-photon ionization spectroscopy of the B state of Na3 clusters
โ Scribed by T. Baumert; R. Thalweiser; G. Gerber
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 581 KB
- Volume
- 209
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
We report time-resolved experiments studying the dynamics of the Nas B-X system. Femtosecond pump-probe techniques combined with ion time-of-flight (TOF) and zero kinetic energy (ZEKE) photoelectron spectroscopy allow us to observe the three-dimensional wavepacket motion in the excited NaJ B state and in the Na3 X state. The ground state wavepacket is induced by stimulated emission pumping during the pump pulse. The X-state dynamics is dominated by the three vibrational modes of the Na,. Furthermore we observed pseudorotational wavepacket motion in the B state. We do not observe a fragmentation of the B state within a time interval of 10 ps.
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Vibrationally resolved electronic spectra of small heteroclusters B.S, of benzene (B) and sulfur hexafluoride (S) have been obtained by resonant two-photon ionization spectroscopy. Some spectroscopic details of the BISl and B,S2 complexes were studied in the spectral regions near the So-&, 08 and 6:
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