Department of Chemistry, Sookmyung Women's University , Seoul 140-742, Korea.
Department of Chemistry, Hanyang University , Seoul, 133-791, Korea.
ACS Appl Mater Interfaces. 2016 Jul 13;8(27):17489-98. doi: 10.1021/acsami.6b01856. Epub 2016 Jun 28.
Investigation of molecular interactions in polymeric films is crucial for understanding and engineering multiscale physical phenomena correlated to device function and performance, but this often involves a compromise between theoretical and experimental data, because of poor film uniformity. Here, we report the intramolecular and intermolecular interactions inside the ultrathin and conformal hybrid organic-inorganic alucone films grown by molecular layer deposition, based on sequential and self-limiting surface reactions. Varying the carbon chain length of organic precursors, which affects their molecular flexibility, caused intramolecular interactions such as double reactions by bending of the molecular backbone, resulting in formation of hole vacancies in the films. Furthermore, intermolecular interactions in alucone polymeric films are dependent on the thermal kinetics of molecules, leading to binding failures and cross-linking at low and high growth temperatures, respectively. We illustrate these key interactions and identify molecular geometries and potential energies by density functional theory calculations.
研究聚合薄膜中的分子相互作用对于理解和设计与器件功能和性能相关的多尺度物理现象至关重要,但由于薄膜均匀性差,这通常需要在理论和实验数据之间做出妥协。在这里,我们报告了通过分子层沉积在超薄和保形杂化有机-无机 alucone 薄膜中生长的分子内和分子间相互作用,这是基于顺序和自限制的表面反应。改变有机前体的碳链长度会影响其分子的柔韧性,导致分子主链的弯曲等分子内反应,从而在薄膜中形成空穴空位。此外,alucone 聚合物薄膜中的分子间相互作用取决于分子的热动力学,导致在低温和高温生长时分别出现结合失败和交联。我们通过密度泛函理论计算说明了这些关键相互作用,并确定了分子几何形状和势能。