| Autor: |
Blanchet, Valerie, Raffael, Kevin, Turri, Giorgio, Chatel, Béatrice, Girard, Bertrand, Garcia, Ivan Anton, Wilkinson, Iain, Whitaker, Benjamin J |
| Rok vydání: |
2008 |
| Předmět: |
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| Zdroj: |
The Journal of Chemical Physics 128, 16 (2008) 164318 |
| Druh dokumentu: |
Working Paper |
| DOI: |
10.1063/1.2913167 |
| Popis: |
Pump-probe photoionization has been used to map the relaxation processes taking place from highly vibrationally excited levels of the S2 state of azulene, populated directly or via internal conversion from the S4 state. Photoelectron spectra obtained by 1+2[prime] two-color time-resolved photoelectron imaging are invariant (apart from in intensity) to the pump-probe time delay and to the pump wavelength. This reveals a photoionization process which is driven by an unstable electronic state (e.g., doubly excited state) lying below the ionization potential. This state is postulated to be populated by a probe transition from S2 and to rapidly relax via an Auger-like process onto highly vibrationally excited Rydberg states. This accounts for the time invariance of the photoelectron spectrum. The intensity of the photoelectron spectrum is proportional to the population in S2. An exponential energy gap law is used to describe the internal conversion rate from S2 to S0. The vibronic coupling strength is found to be larger than 60$\pm$5 $\mu$eV. |
| Databáze: |
arXiv |
| Externí odkaz: |
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