4.6 Article

Ultrafast intermolecular energy transfer in heavy water

期刊

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 11, 期 40, 页码 9033-9038

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/b908975f

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资金

  1. European Union-Marie Curie [MEST-CT-2005-021000]
  2. Dutch organization for Scientific Research (NWO)
  3. NSF, Office of Basic Energy Sciences DOE [W911NF-07-1-0116]

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We report on a study of the vibrational energy relaxation and resonant vibrational (Forster) energy transfer of the OD vibrations of D2O and mixtures of D2O and H2O using femtosecond mid-infrared spectroscopy. We observe the lifetime of the OD vibrations of bulk D2O to be 400 +/- 30 fs. The rate of the Forster energy transfer is measured via the dynamics of the anisotropy of the OD vibrational excitation. For a solution of 0.5% D2O in H2O, resonant energy transfer is negligible, and the anisotropy shows a single exponential decay with a time constant of 2.6 +/- 0.1 ps, representing the time scale of the molecular reorientation. With increasing concentration, the anisotropy decay becomes faster and non-exponential, showing the increased contribution of resonant energy transfer between the OD vibrations. We determine the Forster radius of the OD vibration of HDO in H2O to be r(0) = 2.3 +/- 0.2 angstrom.

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