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Critical Role of Side-Chain Attachment Density on the Order and Device Performance of Polythiophenes

Published

Author(s)

Regis J. Kline, Dean DeLongchamp, Daniel A. Fischer, Eric K. Lin, Lee J. Richter, Michael L. Chabinyc, Martin Heeney, Iain McCulloch

Abstract

High performance, solution processable semiconductors are critical to the realization of low cost, large area electronics. We show that a signature molecular packing motif - side-chain interdigitation - correlates to high performance for a large and important class of organic semiconductors. The side chains of recently developed high performance copolymers of poly(alkylthiophenes) can and do interdigitate substantially, whereas they do not in the most common form of the extensively studied, lower performance poly(alkythiophenes). Sidechain interdigitation provides a mechanism for three-dimensional ordering; without it, poly(alkylthiophenes) are limited to small domains and poor performance. We propose the synthetic design rule that three-dimensional ordering is promoted by side-chain attachment densities sufficiently low to permit interdigitation.
Citation
Macromolecules

Keywords

charge carrier mobility, conjugated polymer, P3HT, pBTTT, polymer morphology, side chains, thin-film transistor

Citation

Kline, R. , DeLongchamp, D. , Fischer, D. , Lin, E. , Richter, L. , Chabinyc, M. , Heeney, M. and McCulloch, I. (2007), Critical Role of Side-Chain Attachment Density on the Order and Device Performance of Polythiophenes, Macromolecules, [online], https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=852680 (Accessed January 27, 2022)
Created October 29, 2007, Updated October 12, 2021