Hydrogen bond dynamics in water studied by depolarized Rayleigh scattering

نویسندگان

  • O. Conde
  • J. Teixeira
چکیده

2014 We measured the depolarized Rayleigh light scattering by water from 80°C down to 17°C. The spectra obtained could be analysed into two lines, a broad and a sharp one. From the sharp line we deduced a relaxation time which can be interpreted as a reorientational time due to rotations. The broad line gives a relaxation time which is Arrhenius temperature dependent, with an activation energy E = 2.7 kcal/mole. This shorter time can be associated with the mean lifetime of H-bonds in water and E is the activation energy of the formation and breaking of H-bonds process. This interpretation can be supported by recent measurements on quasi-elastic neutron scattering and by taking into account the librational frequencies from Raman spectroscopy. J. Physique 44 (1983) 525-529 AVRIL 1983,

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تاریخ انتشار 2016