Velpula Gangamallaiah, Martin Cristina, Daelemans Brent, Hennrich Gunther, Van der Auweraer Mark, Mali Kunal S, De Feyter Steven
Division of Molecular Imaging and Photonics, Department of Chemistry, KU Leuven Celestijnenlaan 200F 3001 Leuven Belgium
Unidad NanoCRIB, Centro Regional de Investigaciones Biomédicas Albacete-02071 Spain.
Chem Sci. 2021 Sep 16;12(39):13167-13176. doi: 10.1039/d1sc02950a. eCollection 2021 Oct 13.
Self-assembled molecular networks (SAMNs) on surfaces evoke a lot of interest, both from a fundamental as well as application point of view. When formed at the liquid-solid interface, precise control over different polymorphs can be achieved by simply adjusting the concentration of molecular building blocks in solution. Significant influence of solute concentration on self-assembly behavior has been observed, whether the self-assembly behavior is controlled by either van der Waals forces or hydrogen bonding interactions. In both cases, high- and low-density supramolecular networks have been observed at high and low solute concentrations, respectively. In contrast to this "concentration-in-control" self-assembly concept here we report an atypical concentration dependent self-assembly behavior at a solution-solid interface. At the interface between heptanoic acid (HA) and highly oriented pyrolytic graphite (HOPG), we show, using scanning tunneling microscopy (STM), the formation of a low-density porous network at high solute concentrations, and a high-density compact network at low solute concentrations. This intriguing inverse concentration dependent self-assembly behavior has been attributed to the preaggregation of solute molecules in the heptanoic acid solution as revealed by UV-vis spectroscopy. The observed results have been correlated to the molecular density of self-assembled monolayers attained at the HA/HOPG interface.
表面上的自组装分子网络(SAMNs)从基础研究以及应用的角度都引起了广泛关注。当在液-固界面形成时,通过简单地调节溶液中分子构建单元的浓度,就可以实现对不同多晶型物的精确控制。无论是自组装行为由范德华力还是氢键相互作用控制,溶质浓度对自组装行为都有显著影响。在这两种情况下,分别在高溶质浓度和低溶质浓度下观察到了高密度和低密度的超分子网络。与这种“浓度控制”的自组装概念不同,在这里我们报道了一种在溶液-固体界面处非典型的浓度依赖性自组装行为。在庚酸(HA)与高度取向热解石墨(HOPG)的界面处,我们使用扫描隧道显微镜(STM)表明,在高溶质浓度下形成了低密度多孔网络,而在低溶质浓度下形成了高密度致密网络。这种有趣的浓度依赖性相反的自组装行为归因于紫外-可见光谱所揭示的溶质分子在庚酸溶液中的预聚集。观察结果与在HA/HOPG界面处获得的自组装单分子层的分子密度相关。