Illumination alters the structure of gels formed from the model optoelectronic material P3HT. (13th January 2017)

• Record Type: Journal Article
• Authors: Morgan, Brian; Dadmun, Mark D.
• Is Part Of: Polymer. Volume 108(2016)
• Page Start: 313
• Page End: 321
• Publication Date: 2017-01-13
• Subjects: Optically active conjugated polymers -- Polymer gels -- Neutron scattering; Polymers -- Periodicals; Polymerization -- Periodicals; Polymères -- Périodiques; Polymérisation -- Périodiques; 547.7
• DOI: 10.1016/j.polymer.2016.11.056
• Languages: English
• ISSNs: 0032-3861

Abstract

Abstract: Studying the gelation process of conjugated optoelectronic polymers has often been employed as a means of better understanding the final morphology and assembly in active layers of organic electronic devices due to the correlation between the experimentally observed sol-gel transition and many common solution based fabrication techniques. The nature of the percolated network structures formed through the molecular assembly that occurs during this gelation directly affects device performance in conjugated polymer based active layers. Thus, precise knowledge of the evolution of structures during gelation provides crucial information that is needed to rationally improve device performance by directing the assembly during processing. Additionally, observing the effects of environmental factors such as ambient light exposure upon the gelation process will direct efforts towards improving universally overlooked facets of the typical fabrication procedure. Thus, we have conducted a series of ultra small angle and small angle neutron scattering experiments to probe the temperature-driven gelation process of the conjugated photoactive polymer poly(3-hexylthiophene-2, 5-diyl) (P3HT) in both the presence and absence of white light. Analysis of the resultant scattering data shows that the gelation process consists of the creation and steady growth of cylindrical aggregates formed by the agglomeration of free chain P3HT. Furthermore, clear differences in the gel structure and assembly between illuminated and non-illuminated gels are observed across multiple length scales, pointing towards an optically-induced variation in the gelation process. Our results indicate that simple white light exposure sharply retards the growth of conjugated polymer microstructures, which clearly suggests that ignoring illumination conditions throughout organic electronic fabrication processes risks producing inconsistent and non-reproducible active layer architectures and ultimately endangers dependable device performance. Graphical abstract: Highlights: The impact of illumination on the gelation of a conjugated polymer is studied. The experiment is completed with and without in-situ white light illumination. SANS and USANS analysis quantifies structural evolution during gelation. Light exposure clearly effects structure and assembly over observed length scales. Aggregate formation is hindered by the presence of white light exposure.