Bishop Camille, Chen Zhenxuan, Toney Michael F, Bock Harald, Yu Lian, Ediger M D
Department of Chemistry, University of Wisconsin-Madison, 1101 University Ave, Madison, Wisconsin 53706, United States.
School of Pharmacy, University of Wisconsin-Madison, 777 Highland Ave, Madison, Wisconsin 53705, United States.
J Phys Chem B. 2021 Mar 18;125(10):2761-2770. doi: 10.1021/acs.jpcb.0c11564. Epub 2021 Mar 8.
We investigate vapor-deposited glasses of a phenanthroperylene ester, known to form an equilibrium hexagonal columnar phase, and show that liquid crystal-like order can be manipulated by the choice of deposition rate and substrate temperature during deposition. We find that rate-temperature superposition (RTS)-the equivalence of lowering the deposition rate and increasing the substrate temperature-can be used to predict and control the molecular orientation in vapor-deposited glasses over a wide range of substrate temperatures (0.75-1.0 ). This work extends RTS to a new structural motif, hexagonal columnar liquid crystal order, which is being explored for organic electronic applications. By several metrics, including the apparent average face-to-face nearest-neighbor distance, physical vapor deposition (PVD) glasses of the phenanthroperylene ester are as ordered as the glass prepared by cooling the equilibrium liquid crystal. By other measures, the PVD glasses are less ordered than the cooled liquid crystal. We explain the difference in the maximum attainable order with the existence of a gradient in molecular mobility at the free surface of a liquid crystal and its impact upon different mechanisms of structural rearrangement. This free surface equilibration mechanism explains the success of the RTS principle and provides guidance regarding the types of order most readily enhanced by vapor deposition. This work extends the applicability of RTS to include molecular systems with a diverse range of higher-order liquid-crystalline morphologies that could be useful for new organic electronic applications.
我们研究了一种菲并苝酯的气相沉积玻璃,已知其能形成平衡六方柱状相,并表明在沉积过程中,液晶状的有序性可通过沉积速率和衬底温度的选择来操控。我们发现速率 - 温度叠加(RTS)——降低沉积速率与提高衬底温度的等效性——可用于在很宽的衬底温度范围(0.75 - 1.0)内预测和控制气相沉积玻璃中的分子取向。这项工作将RTS扩展到一种新的结构基序,即六方柱状液晶序,该序正被用于有机电子应用的探索。通过包括表观平均面对面最近邻距离在内的多种指标衡量,菲并苝酯的物理气相沉积(PVD)玻璃与通过冷却平衡液晶制备的玻璃一样有序。但通过其他测量方法,PVD玻璃的有序性低于冷却后的液晶。我们通过液晶自由表面处分子迁移率存在梯度及其对不同结构重排机制的影响来解释最大可达到的有序性差异。这种自由表面平衡机制解释了RTS原理的成功之处,并为气相沉积最易增强的有序类型提供了指导。这项工作扩展了RTS的适用性,使其涵盖了具有多种高阶液晶形态的分子体系,这些体系可能对新型有机电子应用有用。