Graduate School of Natural Science and Technology, Kanazawa University, Kanazawa, Ishikawa, 920-1192, Japan.
School of Materials Science, Japan Advanced Institute of Science and Technology, Nomi, Ishikawa, 923-1292, Japan.
Sci Rep. 2017 Jun 22;7(1):4054. doi: 10.1038/s41598-017-04376-3.
The interfaces between solids and water films in air play fundamental roles in physicochemical phenomena, biological functions, and nano-fabrication. Though the properties of the interfaces have been considered to be irrelevant to the water film thickness, we found distinctive mechanical features of the interface between a cleaved muscovite mica surface and a thin water film grown in humid air, dissimilar to those in bulk water, using frequency-modulation atomic force microscopy. The thin water film grew with quasi-stabilized hydration networks of water molecules, tightly bound each other at the interface, to a thickness of ~2 nm at near-saturating humidity. Consequently, defective structures of the hydration networks persisted vertically through the hydration layers at the interface, and K ions on the cleaved surface remained without dissolution into the water film. The results provide atomistic insights into thin water films in regard to epitaxial-like growth from vapour and the motion of water molecules and ions therein.
固体与空气水膜之间的界面在物理化学现象、生物功能和纳米制造中起着至关重要的作用。尽管界面的性质被认为与水膜厚度无关,但我们使用调频原子力显微镜发现,在湿度空气中生长的薄水膜与劈开的白云母表面之间的界面具有独特的力学特征,与在体相水中的特征不同。薄水膜通过水分子的准稳定水合网络生长,在界面处彼此紧密结合,在接近饱和湿度时达到约 2nm 的厚度。因此,水合网络的缺陷结构在界面处的水合层中垂直延伸,而劈开表面上的 K 离子则不会溶解到水膜中。这些结果为从蒸汽中进行类似外延的薄水膜生长以及其中水分子和离子的运动提供了原子尺度的见解。