Protonation-induced charge transfer and polaron formation in organic semiconductors doped by Lewis acids
Affiliation
Wyant College of Optical Sciences, University of ArizonaIssue Date
2022
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Royal Society of ChemistryCitation
Bauch, F., Dong, C.-D., & Schumacher, S. (2022). Protonation-induced charge transfer and polaron formation in organic semiconductors doped by Lewis acids. RSC Advances, 12(22), 13999–14006.Journal
RSC AdvancesRights
Copyright © 2022 Heart Rhythm Society. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Lewis-acid doping of organic semiconductors (OSCs) opens up new ways of p-type doping and has recently become of significant interest. As for the mechanistic understanding, it was recently proposed that upon protonation of the OSC backbone, electron transfer occurs between the protonated polymer chain and a neutral chain nearby, inducing a positive charge carrier in the latter [B. Yurash, D. X. Cao, V. Brus et al., Nat. Mater., 2019, 18, 1327-1334]. To further clarify the underlying microscopic processes on a molecular level, in the present work, we theoretically analyze the influence of protons on the electronic properties of the widely used PCPDT-BT copolymer as a typical example. While we find that single protonation leads to formation of a localized polaron, double protonation leads to the release of a more delocalized polaron via an intrachain electron transfer. We also demonstrate the possibility of an interchain electron transfer. The vertical excitation spectra simulated for an ensemble of protonated polymers with different amounts of protons enable a detailed interpretation of the experimental observations and contribute to a molecular-level interpretation of the Lewis-acid doping process. © 2022 The Royal Society of ChemistryNote
Open access journalISSN
2046-2069Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1039/d2ra02032g
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Except where otherwise noted, this item's license is described as Copyright © 2022 Heart Rhythm Society. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).