Zhang Rui, Yan Ye, Zhang Qiang, Liang Qiuju, Zhang Jidong, Yu Xinhong, Liu Jiangang, Han Yanchun
State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022, China.
Department of Physics, Chemistry and Biology (IFM), Linköping University, Linköping 581 83, Sweden.
ACS Appl Mater Interfaces. 2021 May 12;13(18):21756-21764. doi: 10.1021/acsami.1c02984. Epub 2021 Apr 28.
In crystalline/crystalline polymer blend systems, complex competition and coupling of crystallization and morphology usually happen due to the different crystal nucleation and growth processes of polymers, making the morphology and crystallization behavior difficult to control. Herein, we probe the crystallization sequence during the film formation process (crystallize simultaneously, component A crystallizes prior to B or inverse) to illustrate the micro-morphology evolution process in poly(3-hexylthiophene) (P3HT) and poly[[,-bis(2-octyldodecyl)-napthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]- alt-5, 5'-(2,2'-bithiophene)] (N2200) blend using UV-vis absorption spectra and two-dimensional grazing incidence X-ray diffraction (2D GIXRD). When P3HT and N2200 crystallize simultaneously, a large-sized morphology structure is formed. When strengthening the solution aggregation of P3HT by increasing the solvent-polymer interaction, P3HT crystallizes prior to N2200. A P3HT-based micro-morphology structure is obtained. As the molecular weight of N2200 increases to a critical value (72.0 kDa), the crystallization of N2200 dominates the film formation process. A N2200-based micro-morphology is formed guided by N2200 domains. The results confirm that the crystallization sequence is one of the most important factors to determine the micro-morphology structure in all-crystalline polymer blends.
在结晶/结晶聚合物共混体系中,由于聚合物的晶体成核和生长过程不同,通常会发生结晶与形态的复杂竞争和耦合,使得形态和结晶行为难以控制。在此,我们探究了成膜过程中的结晶顺序(同时结晶、组分A先于B结晶或相反),以利用紫外可见吸收光谱和二维掠入射X射线衍射(2D GIXRD)来说明聚(3-己基噻吩)(P3HT)和聚[[,-双(2-辛基十二烷基)-萘-1,4,5,8-双(二甲酰亚胺)-2,6-二基]-alt-5,5'-(2,2'-联噻吩)](N2200)共混物中的微观形态演变过程。当P3HT和N2200同时结晶时,会形成大尺寸的形态结构。通过增加溶剂与聚合物的相互作用来增强P3HT的溶液聚集时,P3HT先于N2200结晶。得到了基于P3HT的微观形态结构。当N2200的分子量增加到临界值(72.0 kDa)时,N2200的结晶主导了成膜过程。在N2200域的引导下形成了基于N2200的微观形态。结果证实,结晶顺序是决定全结晶聚合物共混物微观形态结构的最重要因素之一。