ExxonMobil Research and Engineering, 22777 Springwoods Village Parkway, Spring, Texas 77389, USA.
J Chem Phys. 2017 May 7;146(17):174104. doi: 10.1063/1.4982229.
It has been extensively demonstrated through first principles quantum mechanics calculations that water exhibits strong hydrogen bond cooperativity. Equations of state developed from statistical mechanics typically assume pairwise additivity, meaning they cannot account for these 3-body and higher cooperative effects. In this paper, we extend a second order thermodynamic perturbation theory to correct for hydrogen bond cooperativity in 4 site water. We demonstrate that the theory predicts hydrogen bonding structure consistent spectroscopy, neutron diffraction, and molecular simulation data. Finally, we implement the approach into a general equation of state for water.
通过第一性原理量子力学计算,已经广泛证明水表现出很强的氢键协同作用。从统计力学发展而来的状态方程通常假设两两加性,这意味着它们无法解释这些三体和更高阶的协同效应。在本文中,我们将二阶热力学微扰理论扩展到 4 位点水中以修正氢键协同作用。我们证明该理论可以预测氢键结构,与光谱、中子衍射和分子模拟数据一致。最后,我们将该方法应用于水的通用状态方程中。