Faculty of Mathematics and Physics, Charles University, Prague, 121 16, Czech Republic.
Instytut Fizyki Doswiadczalnej, Universytet Wroclawski, Wroclaw, 50-001, Poland.
Sci Rep. 2017 Aug 4;7(1):7357. doi: 10.1038/s41598-017-07277-7.
Self-assembly of organic molecules is a mechanism crucial for design of molecular nanodevices. We demonstrate unprecedented control over the self-assembly, which could allow switching and patterning at scales accessible by lithography techniques. We use the scanning tunneling microscope (STM) to induce a reversible 2D-gas-solid phase transition of copper phthalocyanine molecules on technologically important silicon surface functionalized by a metal monolayer. By means of ab-initio calculations we show that the charge transfer in the system results in a dipole moment carried by the molecules. The dipole moment interacts with a non-uniform electric field of the STM tip and the interaction changes the local density of molecules. To model the transition, we perform kinetic Monte Carlo simulations which reveal that the ordered molecular structures can form even without any attractive intermolecular interaction.
有机分子的自组装是设计分子纳米器件的关键机制。我们证明了对自组装的前所未有的控制,这可能允许在光刻技术可达到的尺度上进行切换和图案化。我们使用扫描隧道显微镜(STM)在通过金属单层功能化的技术上重要的硅表面上诱导铜酞菁分子的可逆 2D-气体-固体相转变。通过从头算计算,我们表明该系统中的电荷转移导致分子携带偶极矩。偶极矩与 STM 尖端的非均匀电场相互作用,并且该相互作用改变了分子的局部密度。为了模拟转变,我们进行了动力学蒙特卡罗模拟,该模拟表明即使没有任何分子间吸引力,有序的分子结构也可以形成。