Department of Chemistry and the Molecular Design Institute, New York University , 100 Washington Square East, New York, New York 10003-6688, United States.
ACS Nano. 2016 Jul 26;10(7):6424-8. doi: 10.1021/acsnano.6b03830. Epub 2016 Jun 23.
Thin film epitaxy typically invokes a superposition of a pair of rigid two-dimensional lattices with a well-defined orientation governed by some form of commensurism. A report by Meissner et al. in this issue of ACS Nano demonstrates that the organization of organic molecules on substrates may not be that simple, as static distortion waves involving miniscule shifts of atomic positions from substrate lattice points can lead to orientations of a molecular film that cannot be described by often used models. Herein, we provide some highlights of epitaxy, with a focus on configurations that reflect the delicate balance between intermolecular interactions within a molecular film and molecule-substrate interactions. Although geometric models for explaining and predicting epitaxial configurations can be used to guide synthesis of materials, their use must recognize energetic factors and the possibility of more complex, and possibly less predictable, interface structures.
薄膜外延通常涉及到一对具有明确定位的刚性二维晶格的叠加,这种定位由某种形式的共格决定。Meissner 等人在本期 ACS Nano 上的报告表明,有机分子在衬底上的组织可能并不那么简单,因为涉及原子位置从衬底晶格点微小移动的静态畸变波可能导致分子膜的取向不能用常用模型来描述。在此,我们提供了外延的一些要点,重点介绍了反映分子膜内分子间相互作用和分子-衬底相互作用之间微妙平衡的构型。虽然用于解释和预测外延构型的几何模型可用于指导材料的合成,但它们的使用必须认识到能量因素以及可能更复杂、可能更不可预测的界面结构的可能性。