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The nanoscale structure and macroscopic morphology of π-conjugated polymers are very important for their electronic application. While ordered single crystals of small molecules have been obtained via solution deposition, macroscopically aligned films of π-conjugated polymers deposited directly from solution have always required surface modification or complex pre-deposition processing of the solution. Here, ordered nanowires were obtained via shear-enhanced crystallization of π-conjugated polymers at the air–liquid–solid interface using simple deposition of the polymer solution onto an inclined substrate. The formation of macroscopically aligned nanowire arrays was found to be due to the synergy between intrinsic (π-conjugated backbone) and external (crystallization conditions) effects. The oriented nanowires showed remarkable improvement in the charge carrier mobility compared to spin-coated films as characterized in organic field-effect transistors (OFETs). Considering the simplicity and large-scale applicability, shear-enhanced crystallization of π-conjugated polymers provides a promising strategy to achieve high-performance polymer semiconductor films for electronics applications.
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What Is the Assembly Pathway of a Conjugated Polymer From Solution to Thin Films?
The hierarchical assembly of conjugated polymers has gained much attention due to its critical role in determining optical/electrical/mechanical properties. The hierarchical morphology encompasses molecular-scale intramolecular conformation (torsion angle, chain folds) and intermolecular ordering (π–π stacking), mesoscale domain size, orientation and connectivity, and macroscale alignment and (para)crystallinity. Such complex morphology in the solid state is fully determined by the polymer assembly pathway in the solution state, which, in turn, is sensitively modulated by molecular structure and processing conditions. However, molecular pictures of polymer assembly pathways remain elusive due to the lack of detailed structural characterizations in the solution state and the lack of understanding on how various factors impact the assembly pathways. In this mini-review, we present possible assembly pathways of conjugated polymers and their characteristics across length scales. Recent advances in understanding and controlling of assembly pathways are highlighted. We also discuss the current gap in our knowledge of assembly pathways, with future perspectives on research needed on this topic.
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- Award ID(s):
- 1847828
- PAR ID:
- 10212457
- Date Published:
- Journal Name:
- Frontiers in Chemistry
- Volume:
- 8
- ISSN:
- 2296-2646
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.3389/fchem.2020.583521
