4.6 Article

The intermolecular stretching vibration mode in water isotopes investigated with broadband terahertz time-domain spectroscopy

Journal

CHEMICAL PHYSICS LETTERS
Volume 473, Issue 4-6, Pages 279-283

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.cplett.2009.03.075

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Funding

  1. Grant-in-Aid for the Global COE Program 'The Next Generation of Physics, Spun from Universality and Emergence
  2. Creative Scientific Research program [18GS0208]
  3. Scientific Research on Innovative Areas 'Optical science of dynamically correlated electrons (DYCE)' [20104007]
  4. Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan

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We determined the complex dielectric constants of the liquid water isotopes, H2O, D2O, and H-2 O-18 at 296 K from 0.2 to 7 THz by terahertz time-domain attenuated total reflection spectroscopy. We extracted the dispersion of the complex susceptibility of the intermolecular stretching vibration mode around 5 THz. The isotope effect on the vibration mode is clarified in its amplitude, frequency, and damping constant. Anticorrelation of the oscillator strength of the intermolecular stretching vibration mode between infrared activity and Raman activity indicates that H2O has the strongest structural disorder among water isotopes. (c) 2009 Elsevier B.V. All rights reserved.

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