Uhlig Frank, Marsalek Ondrej, Jungwirth Pavel
Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Flemingovo nám. 2, CZ-16610 Prague 6, Czech Republic.
J Phys Chem Lett. 2013 Jan 17;4(2):338-43. doi: 10.1021/jz3020953. Epub 2013 Jan 8.
The hydrated electron is a crucial species in radiative processes, and it has been speculated that its behavior at the water surface could lead to specific interfacial chemical properties. Here, we address fundamental questions concerning the structure and energetics of an electron at the surface of water. We use the method of ab initio molecular dynamics, which was shown to provide a faithful description of solvated electrons in large water clusters and in bulk water. The present results clearly demonstrate that the surface electron is mostly buried in the interfacial water layer, with only about 10 % of its density protruding into the vapor phase. Consequently, it has a structure that is very similar to that of an electron solvated in the aqueous bulk. This points to a general feature of charges at the surface of water, namely, that they do not behave as half-dehydrated but rather as almost fully hydrated species.
水合电子是辐射过程中的关键物种,据推测其在水面的行为可能导致特定的界面化学性质。在此,我们探讨了关于电子在水面的结构和能量学的基本问题。我们使用从头算分子动力学方法,该方法已被证明能够准确描述大型水团簇和本体水中的溶剂化电子。目前的结果清楚地表明,表面电子大部分埋在界面水层中,只有约10%的密度突出到气相中。因此,它具有与本体水中溶剂化电子非常相似的结构。这指出了水表面电荷的一个普遍特征,即它们的行为不是半脱水的,而是几乎完全水合的物种。