Supercritical Water is not Hydrogen Bonded

被引:34
|
作者
Schienbein, Philipp [1 ]
Marx, Dominik [1 ]
机构
[1] Ruhr Univ Bochum, Lehrstuhl Theoret Chem, D-44780 Bochum, Germany
关键词
ab initio calculations; hydrogen bonds; molecular dynamics; supercritical fluids; water; LIQUID WATER; DYNAMIC PROPERTIES; SPECTROSCOPY; DIFFRACTION; NETWORK; FLUIDS; COOPERATIVITY; SIMULATIONS; PRESSURES;
D O I
10.1002/anie.202009640
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:18578 / 18585
页数:8
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