Tuning Orientational Order of Highly Aggregating P(NDI2OD-T<sub>2</sub>) by Solvent Vapor Annealing and Blade Coating

Daniel Trefz(University of Stuttgart), Yannic M. Gross(University of Stuttgart), Carsten Dingler(University of Stuttgart), Roman Tkachov(University of Stuttgart), Amer Hamidi‐Sakr(Centre National de la Recherche Scientifique), Anton Kiriy(Leibniz Institute of Polymer Research), Christopher R. McNeill(Monash University), Martin Brinkmann(Centre National de la Recherche Scientifique), Sabine Ludwigs(University of Stuttgart)
Macromolecules
December 17, 2018
Cited by 68Open Access
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Abstract

Its inherent strong tendency to aggregate in solution is used in the following study to prepare highly anisotropic films of the n-type copolymer poly{[N,N′-bis(2-octyldodecyl)naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,5′-(2,2′-bithiophene)} (P(NDI2OD-T2)). Solvent vapor annealing (SVA) allows to tune the size of oriented domains in spherulite-like superstructures with alignment up to several hundreds of micrometers. Blade coating (BC), on the other hand, yields square centimeter large perfectly oriented films with dichroic ratios of 18 and charge transport anisotropies up to 14. On the nanometer scale highly oriented fibers of form I are visible in the oriented areas with the fiber long axis parallel to the chain direction. We give experimental evidence that structure formation does involve liquid crystal (LC) mesophases at high solution concentrations which are frozen upon solvent removal. Temperature post-treatment of the oriented films gives, on the other hand, evidence for a classical semicrystalline nature of this polymer with spherulites consisting of crystalline and amorphous domains. These findings point to a different growth behavior than previously discussed for the well-studied p-type polymer poly(3-hexylthiophene) and suggests that the definition and distinction between liquid-crystalline and semicrystalline nature might need to be reassessed.


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