Orientational dynamics on glassformer 2 [Ca(NO3)2] · 3[KNO3]: A study by transient optical Kerr effect

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Abstract

The fast orientational dynamics of molten 2[Ca(NO3)2] · 3[KNO3] is investigated by time-resolved optical Kerr effect (OKE) with subpicosecond resolution in the temperature range 380-620 K. Apart from the instantaneous electronic response and a very fast decay, the OKE intensity profiles show clearly the presence of a nonexponential decay. The simplest function which fits the experimental data is a biexponential with time constants ranging from 120 to 15 and 10 to 3 ps, respectively. The results are discussed in terms of an integrated correlation time τc that does not show a diverging behavior approaching the glass transition. At high temperatures τc follows a typical Arrhenius law with activation energy of 1.5 kcal/M. Different possible interpretations of the observed behavior (α-β bifurcation, domain size effect) are discussed. The main conclusion is that rotational motions are decoupled from translational ones even for temperatures well above the liquid-glass transition. © 1993 American Institute of Physics.

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Ricci, M., Foggi, P., Righini, R., & Torre, R. (1993). Orientational dynamics on glassformer 2 [Ca(NO3)2] · 3[KNO3]: A study by transient optical Kerr effect. The Journal of Chemical Physics, 98(6), 4892–4896. https://doi.org/10.1063/1.464944

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