Shi Guosheng, Shen Yue, Liu Jian, Wang Chunlei, Wang Ying, Song Bo, Hu Jun, Fang Haiping
Division of Interfacial Water and Key Laboratory of Interfacial Physics and Technology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China.
1] Division of Interfacial Water and Key Laboratory of Interfacial Physics and Technology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China [2] Salt Lake Resources and Chemistry Laboratory, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China.
Sci Rep. 2014 Oct 28;4:6793. doi: 10.1038/srep06793.
We directly observed molecular-thick aqueous salt-solution pancakes on a hydrophobic graphite surface under ambient conditions employing atomic force microscopy. This observation indicates the unexpected molecular-scale hydrophilicity of the salt solution on graphite surfaces, which is different from the macroscopic wetting property of a droplet standing on the graphite surface. Interestingly, the pancakes spontaneously displayed strong positively charged behavior. Theoretical studies showed that the formation of such positively charged pancakes is attributed to cation-π interactions between Na(+) ions in the aqueous solution and aromatic rings on the graphite surface, promoting the adsorption of water molecules together with cations onto the graphite surface; i.e., Na(+) ions as a medium adsorbed to the graphite surface through cation-π interactions on one side while at the same time bonding to water molecules through hydration interaction on the other side at a molecular scale. These findings suggest that actual interactions regarding carbon-based graphitic surfaces including those of graphene, carbon nanotubes, and biochar may be significantly different from existing theory and they provide new insight into the control of surface wettability, interactions and related physical, chemical and biological processes.
在环境条件下,我们使用原子力显微镜直接观察到了疏水性石墨表面上分子厚度的盐水溶液薄饼。这一观察结果表明,盐溶液在石墨表面具有出人意料的分子尺度亲水性,这与静置在石墨表面的液滴的宏观润湿性不同。有趣的是,这些薄饼自发地表现出强烈的带正电行为。理论研究表明,这种带正电薄饼的形成归因于水溶液中的Na(+)离子与石墨表面的芳环之间的阳离子-π相互作用,促进了水分子与阳离子一起吸附到石墨表面;也就是说,Na(+)离子作为一种介质,一方面通过阳离子-π相互作用吸附到石墨表面,另一方面在分子尺度上通过水合作用与水分子结合。这些发现表明,包括石墨烯、碳纳米管和生物炭在内的基于碳的石墨表面的实际相互作用可能与现有理论有显著不同,它们为控制表面润湿性、相互作用以及相关的物理、化学和生物过程提供了新的见解。