4.7 Article

Ultrafast photo-excitation dynamics in isolated, neutral water clusters

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JOURNAL OF CHEMICAL PHYSICS
卷 134, 期 9, 页码 -

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AMER INST PHYSICS
DOI: 10.1063/1.3556820

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  1. Deutsche Forschungsgemeinschaft (DFG) [SFB 450, TP A2]
  2. Alexander von Humboldt Foundation

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Using the efficient nonlinear conversion scheme which was recently developed in our group [M. Beutler, M. Ghotbi, F. Noack, and I. V. Hertel, Opt. Lett. 134, 1491 (2010); M. Ghotbi, M. Beutler, and F. Noack, ibid 35, 3492 (2010)] to provide intense sub-50 fs vacuum ultraviolet laser pulses we have performed the first real time study of ultrafast, photo-induced dynamics in the electronically excited (A) over tilde -state of water clusters (H2O)(n) and (D2O)(n), n = 2-10. Three relevant time scales, 1.8-2.5, 10-30, and 50-150 fs, can be distinguished which-guided by the available theoretical results-are attributed to H (D)-ejection, OH (OD) dissociation, and a nonadiabatic transition through a conical intersection, respectively. While a direct quantitative comparison is only very preliminary, the present results provide a crucial test for future modeling of excited state dynamics in water clusters, and should help to unravel some of the many still unresolved puzzles about water. (c) 2011 American Institute of Physics. [doi:10.1063/1.3556820]

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