Trade-off between processability and device performance in donor-acceptor semiconductors revealed using discrete siloxane side chains

Bart W.L. van den Bersselaar, Elisabeth H.W. Cattenstart, Kavinraaj Ella Elangovan, Chen Yen-Chi, Bas F.M. de Waal, Joost van der Tol, Ying Diao, E.W. Meijer, Ghislaine Vantomme (Corresponding author)

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Abstract

Donor-acceptor polymeric semiconductors are crucial for state-of-the-art applications, such as electronic skin mimics. The processability, and thus solubility, of these polymers in benign solvents is critical and can be improved through side chain engineering. Nevertheless, the impact of novel side chains on backbone orientation and emerging device properties often remains to be elucidated. Here, we investigate the influence of elongated linear and branched discrete oligodimethylsiloxane (oDMS) side chains on solubility and device performance. Thereto, diketopyrrolopyrrole-thienothiophene polymers are equipped with various oDMS pendants (PDPPTT-Sin) and subsequently phase separated into lamellar domains. The introduction of a branching point in the siloxane significantly enhanced the solubility of the polymer, as a result of increased backbone distortion. Simultaneously, the charge carrier mobility of the polymers decreased by an order of magnitude upon functionalization with long and/or branched siloxanes. This work unveils the intricate balance between processability and device performance in organic semiconductors, which is key for the development of next-generation electronic devices.

Original languageEnglish
Pages (from-to)6637-6644
Number of pages8
JournalJournal of Materials Chemistry C
Volume12
Issue number18
Early online date24 Apr 2024
DOIs
Publication statusPublished - 14 May 2024

Funding

This work was financially supported by the European Research Council (SYNMAT project ID 788618) and the Dutch Ministry of Education, Culture and Science (Gravity program 024.001.035). The authors gratefully acknowledge Dr. S. C. J. Meskers, Dr. M. H. C. van Son and Dr. N. Daub for fruitful discussions and help with the SWV measurements. The authors thank R. Wink for help with the mechanical characterization of the polymers. K. E. E. acknowledges the Fredrick Seitz Materials Research Laboratory Central Facilities, University of Illinois which were used in part of this work. This research used resources of the National Synchrotron Light Source II, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Brookhaven National Laboratory under Contract No. DE-SC0012704. Part of this work was supported by the US National Science Foundation, under award number 18-47828 (Y. D., Y.-C. C.) and the National Aeronautics and Space Administration (NASA) under grant number 80NSSC 21K0070 (Y. D., K. E. E.).

FundersFunder number
Brookhaven National LaboratoryDE-SC0012704
National Science Foundation18-47828
H2020 European Research Council788618
Ministerie van Onderwijs, Cultuur en Wetenschap024.001.035

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