Schienbein Philipp, Marx Dominik
Lehrstuhl für Theoretische Chemie, Ruhr-Universität Bochum, 44780, Bochum, Germany.
Angew Chem Int Ed Engl. 2020 Oct 12;59(42):18578-18585. doi: 10.1002/anie.202009640. Epub 2020 Sep 4.
Thinking about water is inextricably linked to hydrogen bonds, which are highly directional in character and determine the unique structure of water, in particular its tetrahedral H-bond network. Here, we assess if this common connotation also holds for supercritical water. We employ extensive ab initio molecular dynamics simulations to systematically monitor the evolution of the H-bond network mode of water from room temperature, where it is the hallmark of its fluctuating three-dimensional network structure, to supercritical conditions. Our simulations reveal that the oscillation period required for H-bond vibrations to occur exceeds the lifetime of H-bonds in supercritical water by far. Instead, the corresponding low-frequency intermolecular vibrations of water pairs as seen in supercritical water are found to be well represented by isotropic van-der-Waals interactions only. Based on these findings, we conclude that water in its supercritical phase is not a H-bonded fluid.
对水的思考与氢键紧密相连,氢键具有高度的方向性,决定了水的独特结构,尤其是其四面体氢键网络。在此,我们评估这种常见的内涵对于超临界水是否也成立。我们采用广泛的从头算分子动力学模拟,系统地监测水的氢键网络模式从室温(此时它是其波动的三维网络结构的标志)到超临界条件的演变。我们的模拟表明,氢键振动发生所需的振荡周期远远超过超临界水中氢键的寿命。相反,在超临界水中观察到的水对相应的低频分子间振动仅由各向同性的范德华相互作用很好地描述。基于这些发现,我们得出结论,处于超临界相的水不是氢键流体。