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首页> 外文期刊>Nature Communications >Coupling between intra- and intermolecular motions in liquid water revealed by two-dimensional terahertz-infrared-visible spectroscopy
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Coupling between intra- and intermolecular motions in liquid water revealed by two-dimensional terahertz-infrared-visible spectroscopy

机译:二维太赫兹-红外-可见光谱揭示的液态水中分子内和分子间运动的耦合

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The interaction between intramolecular and intermolecular degrees of freedom in liquid water underlies fundamental chemical and physical phenomena such as energy dissipation and proton transfer. Yet, it has been challenging to elucidate the coupling between these different types of modes. Here, we report on the direct observation and quantification of the coupling between intermolecular and intramolecular coordinates using two-dimensional, ultra-broadband, terahertz-infrared-visible (2D TIRV) spectroscopy and molecular dynamics calculations. Our study reveals strong coupling of the O-H stretch vibration, independent of the degree of delocalization of this high-frequency mode, to low-frequency intermolecular motions over a wide frequency range from 50 to 250?cm?1, corresponding to both the intermolecular hydrogen bond bending (≈?60?cm?1) and stretching (≈?180?cm?1) modes. Our results provide mechanistic insights into the coupling of the O-H stretch vibration to collective, delocalized intermolecular modes.
机译:液态水中分子内和分子间自由度之间的相互作用是基础化学和物理现象的基础,例如能量耗散和质子转移。然而,阐明这些不同类型的模式之间的耦合一直是具有挑战性的。在这里,我们报告使用二维,超宽带,太赫兹红外可见(2D TIRV)光谱学和分子动力学计算对分子间和分子内坐标之间的耦合进行直接观察和定量。我们的研究表明,OH拉伸振动与这种高频模式的离域程度无关,与50-250?cm?1的宽频率范围内的低频分子间运动之间存在强耦合,这两个分子间都存在氢键弯曲(≈?60?cm?1)和拉伸(≈?180?cm?1)模式。我们的结果为O-H拉伸振动与集体,离域分子间模式的耦合提供了机械学见解。

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