Department of Chemistry, University of California, Berkeley, California 94720, United States.
Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
J Am Chem Soc. 2022 Jun 29;144(25):11178-11188. doi: 10.1021/jacs.2c01827. Epub 2022 Jun 13.
Experiments and computer simulations have established that liquid water's surfaces can deviate in important ways from familiar bulk behavior. Even in the simplest case of an air-water interface, distinctive layering, orientational biases, and hydrogen bond arrangements have been reported, but an overarching picture of their origins and relationships has been incomplete. Here we show that a broad set of such observations can be understood through an analogy with the basal face of crystalline ice. Using simulations, we demonstrate a number of structural similarities between water and ice surfaces, suggesting the presence of domains at the air-water interface with ice-like features that persist over 2-3 molecular diameters. Most prominent is a shared characteristic layering of molecular density and orientation perpendicular to the interface. Lateral correlations of hydrogen bond network geometry point to structural similarities in the parallel direction as well. Our results bolster and significantly extend previous conceptions of ice-like structure at the liquid's boundary and suggest that the much-discussed quasi-liquid layer on ice evolves subtly above the melting point into a quasi-ice layer at the surface of liquid water.
实验和计算机模拟已经证实,液态水的表面在重要方面可以偏离人们熟悉的体相行为。即使在最简单的气-液界面的情况下,也已经报道了独特的分层、取向偏差和氢键排列,但它们的起源和关系的全貌仍然不完整。在这里,我们通过与冰晶基面的类比表明,广泛的此类观察结果可以得到理解。我们使用模拟演示了水和冰表面之间的许多结构相似性,表明在气-液界面存在具有冰状特征的域,这些特征在 2-3 个分子直径范围内持续存在。最突出的是分子密度和垂直于界面的方向的共享特征分层。氢键网络几何形状的横向相关性表明平行方向也存在结构相似性。我们的结果支持并显著扩展了先前关于液体边界处冰状结构的概念,并表明在冰上讨论已久的准液体层在熔点以上微妙地演变成液态水表面的准冰层。