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向热力学稳定性较低相的相变:苯并噻吩并苯并噻吩衍生物薄膜生长导致的交叉成核。

Phase Transition toward a Thermodynamically Less Stable Phase: Cross-Nucleation due to Thin Film Growth of a Benzothieno-benzothiophene Derivative.

作者信息

Hofer Sebastian, Hofer Andreas, Simbrunner Josef, Ramsey Michael, Sterrer Martin, Sanzone Alessandro, Beverina Luca, Geerts Yves, Resel Roland

机构信息

Institute of Solid State Physics, Graz University of Technology, 8010 Graz, Austria.

Division of Neuroradiology, Vascular and Interventional Radiology, Medical University Graz, 8010 Graz, Austria.

出版信息

J Phys Chem C Nanomater Interfaces. 2021 Dec 30;125(51):28039-28047. doi: 10.1021/acs.jpcc.1c06610. Epub 2021 Dec 20.

Abstract

The molecule 2-decyl-7-phenyl-[1]benzothieno[3,2-][1]benzothiophene is an organic semiconductor, with outstanding properties in terms of molecular packing and its use in organic electronics. The asymmetric shape of the molecule causes a double layer crystal structure at room temperature. In this work we report its thin film growth by physical vapor deposition starting from the monolayer regime up to thick films. The films are studied in terms of their morphology, crystallographic properties, and thermal stability by atomic force microscopy and X-ray diffraction methods. It is found that the bulk molecular packing of the bilayer is formed at the initial thin film growth stage. After a thickness of one double layer, a transition into a new polymorph is observed which is of metastable character. The new phase represents a single layer phase; the crystal structure could be solved by a combination of X-ray diffraction and molecular dynamics simulations. The observed thin film growth is outstanding in terms of surface crystallization: the formation of a metastable phase is not associated with the initial thin film growth, since the first growth stage represents rather the bulk crystal structure of this molecule. Its formation is associated with cross-nucleation of one polymorph by another, which explains why a metastable phase can be formed on top of a thermodynamically more stable phase.

摘要

分子2-癸基-7-苯基-[1]苯并噻吩并[3,2-][1]苯并噻吩是一种有机半导体,在分子堆积及其在有机电子学中的应用方面具有出色的性能。分子的不对称形状导致在室温下形成双层晶体结构。在这项工作中,我们报告了通过物理气相沉积从单层状态到厚膜的薄膜生长情况。通过原子力显微镜和X射线衍射方法研究了薄膜的形貌、晶体学性质和热稳定性。结果发现,双层的体相分子堆积在薄膜生长的初始阶段就已形成。在达到一个双层厚度后,观察到向一种具有亚稳特性的新多晶型物的转变。新相代表单层相;晶体结构可以通过X射线衍射和分子动力学模拟相结合的方法解析。观察到的薄膜生长在表面结晶方面非常突出:亚稳相的形成与薄膜生长的初始阶段无关,因为第一个生长阶段更代表该分子的体相晶体结构。它的形成与一种多晶型物由另一种多晶型物的交叉成核有关,这解释了为什么亚稳相可以在热力学上更稳定的相之上形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0612/8724801/555248ade303/jp1c06610_0001.jpg

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