2009-10-01
Ultrafast intermolecular energy transfer in heavy water
Publication
Publication
Phys. Chem. Chem. Phys. , Volume 11 p. 9033- 9038
We report on a study of the vibrational energy relaxation and resonant vibrational (Förster) 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 Förster 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 Förster radius of the OD vibration of HDO in H2O to be r0 = 2.3 ± 0.2 Å.
Additional Metadata | |
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doi.org/10.1039/b908975f | |
Phys. Chem. Chem. Phys. | |
Organisation | Ultrafast Spectroscopy |
Piatkowski, L., Eisenthal, K. B., & Bakker, H. (2009). Ultrafast intermolecular energy transfer in heavy water. Phys. Chem. Chem. Phys., 11, 9033–9038. doi:10.1039/b908975f |