4.6 Article

Time-resolved photoelectron spectroscopy of the CH3I (BE)-E-1 6s [2] state

期刊

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 12, 期 48, 页码 15644-15652

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c004220j

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资金

  1. ANR COCOMOUV
  2. ANR HARMODYN
  3. L'Universite Paul Sabatier
  4. CNRS
  5. US Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences [DE-AC02-06CH11357]
  6. European Union [MOLCOTUV-041732]

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The predissociation dynamics of the vibrationless level of the 6s (B E-2) Rydberg state of CH3I was studied by femtosecond-resolved velocity map imaging of photoelectrons. By monitoring the decay of the CH3I+ produced by photoionizing the B state, the predissociation lifetime was measured to be 1310 +/- 70 fs. Photoelectron spectra were recorded as a function of the excitation scheme (one or two photons to the B state), and as a function of the ionizing wavelength. All of these photoelectron spectra show a simple time dependence that is consistent with the decay time of the CH3I+ ion signal. The photoelectron angular distributions for the ionization of the B state depend on the excitation scheme and the ionizing wavelength, and show a strong dependence on the vibrational modes excited in the resulting CH3I+. At long delays, the photoelectron spectra are characterized by photoionization of the I(P-2(1/2)) fragment formed by predissociation of the B state.

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