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Supercritical Water is not Hydrogen Bonded
Author(s) -
Schienbein Philipp,
Marx Dominik
Publication year - 2020
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202009640
Subject(s) - supercritical fluid , hydrogen bond , intermolecular force , van der waals force , chemical physics , molecular dynamics , ab initio , isotropy , materials science , chemistry , thermodynamics , computational chemistry , molecule , organic chemistry , physics , quantum mechanics
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.