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Effect of Alkyl Chain Branching Point on 3D Crystallinity in High N‐Type Mobility Indolonaphthyridine Polymers
Authors:Kealan J. Fallon  Annikki Santala  Nilushi Wijeyasinghe  Eric F. Manley  Niall Goodeal  Anastasia Leventis  David M. E. Freeman  Mohammed Al‐Hashimi  Lin X. Chen  Tobin J. Marks  Thomas D. Anthopoulos  Hugo Bronstein
Affiliation:1. Department of Chemistry, University College London, London, UK;2. Centre for Plastic Electronics, Imperial College London, London, UK;3. Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, IL, USA;4. Department of Chemistry, Materials Research Center and Argonne‐Northwestern Solar Energy Research Center, Northwestern University, Evanston, IL, USA;5. Department of Chemistry, Texas A&M University at Qatar, Doha, Qatar
Abstract:Herein, this study investigates the impact of branching‐point‐extended alkyl chains on the charge transport properties of three ultrahigh n‐type mobility conjugated polymers. Using grazing incidence wide‐angle X‐ray scattering, analysis of the crystallinity of the series shows that while π–π interactions are increased for all three polymers as expected, the impact of the side‐chain engineering on polymer backbone crystallinity is unique to each polymer and correlates to the observed changes in charge transport. With the three polymers exhibiting n‐type mobilities between 0.63 and 1.04 cm2 V?1 s?1, these results ratify that the indolonaphthyridine building block has an unprecedented intrinsic ability to furnish high‐performance n‐type organic semiconductors.
Keywords:conjugated polymers  electron transport  indolonapthryidine  Organic Field‐Effect Transistors (OFETs)  polymer crystallinity
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