Molecular reorientation in hydrogen-bonding liquids: through algebraic relaxation toward exponential decay
arXiv:cond-mat/0604114 · doi:10.1063/1.2191058
Abstract
We present a model for the description of orientational relaxation in hydrogen-bonding liquids. The model contains two relaxation parameters which regulate the intensity and efficiency of dissipation, as well as the memory function which is responsible for the short-time relaxation effects. It is shown that the librational portion of the orientational relaxation is described by an algebraic contribution, on top of which more rapid and non-monotonous decays caused by the memory effects are superimposed. The long-time behavior of the orientational relaxation is exponential, although non-diffusional. It is governed by the rotational energy relaxation. We apply the model to interpret recent molecular dynamic simulations and polarization pump-probe experiments on in liquid [C. J. Fecko et al, J. Chem. Phys. 122, 054506 (2005)].
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