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Reconsideration of the relaxational and vibrational line shapes of liquid water based on ultrabroadband dielectric spectroscopy

机译:基于超高压介电光谱的液态水分重新介绍液态水

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摘要

The Debye relaxation function is widely used to describe the large dielectric dispersion of ambient water around 20 GHz. However, from a theoretical point of view, this function is supposed to give incorrect predictions at high frequencies owing to the inappropriate assumption that inertial effects and intermolecular interactions do not affect the relaxation dynamics. Our ultrabroadband spectroscopy investigation of liquid water ranging from 500 MHz to 400 THz did demonstrate that the Debye function is inaccurate far above the microwave region. As an alternative, we tried a stochastic frequency modulation (SFM) model assuming instantaneous modification of the line shapes by the correlation with the surrounding system. The SFM relaxation model reproduced the experimental dielectric spectra up to 400 THz, showing that the hydrogen-bond dynamics are associated with the inertial effect that causes the non-exponential relaxation behaviour in a very short time (typically 25 fs). Within the framework of this relaxation model, the hindered translation modes are able to be approximated as fast modulation (homogeneous) line shapes because the interaction time with frequency modulation is too short. Compared with them, the libation mode is found to have a relatively slow modulation (inhomogeneous) origin, where disturbance of water hydrogen bonds induced by the hindered translations leads to fluctuations in the libration frequency.
机译:德拜德弛豫功能广泛用于描述20GHz约20GHz的环境水的大介电分散。然而,从理论的角度来看,由于惯性效应和分子间相互作用不影响放松动态的不适当,这函数应该在高频下给出不正确的预测。我们的超型光谱调查从500 MHz到400泰铢的液体水分进行了表明,Debye功能远远超过微波区域。作为替代方案,我们尝试了一种随机调制(SFM)模型,假设通过与周围系统的相关性的线形状的瞬时修改。 SFM弛豫模型再现高达400至THz的实验介电光谱,表明氢键动力学与在非常短的时间(通常25 fs)中导致非指数松弛行为的惯性效果相关。在该放松模型的框架内,阻碍翻译模式能够近似为快速调制(均匀)线形状,因为频率调制的交互时间太短。与它们相比,发现了LIBOATION模式具有相对较慢的调制(不均匀)原点,其中受阻翻转诱导的水氢键的干扰导致自动频率的波动。

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    RIKEN Ctr Integrat Med Sci Tsurumi Ku Suehiro Cho Yokohama Kanagawa 2300045 Japan;

    Kyoto Univ Dept Phys Grad Sch Sci Sakyo Ku Kitashirakawa Oiwakecho Kyoto 6068502 Japan;

    Kyoto Univ Dept Phys Grad Sch Sci Sakyo Ku Kitashirakawa Oiwakecho Kyoto 6068502 Japan;

    Inst Mol Sci Dept Theoret &

    Computat Mol Sci Okazaki Aichi 4448585 Japan;

    Kyoto Univ Grad Sch Agr Sakyo Ku Kitashirakawa Oiwakecho Kyoto 6068502 Japan;

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  • 正文语种 eng
  • 中图分类 物理学;化学;
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