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An Organic Borate Salt with Superior p‐Doping Capability for Organic Semiconductors

Molecular doping allows enhancement and precise control of electrical properties of organic semiconductors, and is thus of central technological relevance for organic (opto‐) electronics. Beyond single‐component molecular electron acceptors and donors, organic salts have recently emerged as a promis...

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Autores principales: Wegner, Berthold, Lungwitz, Dominique, Mansour, Ahmed E., Tait, Claudia E., Tanaka, Naoki, Zhai, Tianshu, Duhm, Steffen, Forster, Michael, Behrends, Jan, Shoji, Yoshiaki, Opitz, Andreas, Scherf, Ullrich, List‐Kratochvil, Emil J. W., Fukushima, Takanori, Koch, Norbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507313/
https://www.ncbi.nlm.nih.gov/pubmed/32995128
http://dx.doi.org/10.1002/advs.202001322
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author Wegner, Berthold
Lungwitz, Dominique
Mansour, Ahmed E.
Tait, Claudia E.
Tanaka, Naoki
Zhai, Tianshu
Duhm, Steffen
Forster, Michael
Behrends, Jan
Shoji, Yoshiaki
Opitz, Andreas
Scherf, Ullrich
List‐Kratochvil, Emil J. W.
Fukushima, Takanori
Koch, Norbert
author_facet Wegner, Berthold
Lungwitz, Dominique
Mansour, Ahmed E.
Tait, Claudia E.
Tanaka, Naoki
Zhai, Tianshu
Duhm, Steffen
Forster, Michael
Behrends, Jan
Shoji, Yoshiaki
Opitz, Andreas
Scherf, Ullrich
List‐Kratochvil, Emil J. W.
Fukushima, Takanori
Koch, Norbert
author_sort Wegner, Berthold
collection PubMed
description Molecular doping allows enhancement and precise control of electrical properties of organic semiconductors, and is thus of central technological relevance for organic (opto‐) electronics. Beyond single‐component molecular electron acceptors and donors, organic salts have recently emerged as a promising class of dopants. However, the pertinent fundamental understanding of doping mechanisms and doping capabilities is limited. Here, the unique capabilities of the salt consisting of a borinium cation (Mes(2)B(+); Mes: mesitylene) and the tetrakis(penta‐fluorophenyl)borate anion [B(C(6)F(5))(4)](−) is demonstrated as p‐type dopant for polymer semiconductors. With a range of experimental methods, the doping mechanism is identified to comprise electron transfer from the polymer to Mes(2)B(+), and the positive charge on the polymer is stabilized by [B(C(6)F(5))(4)](−). Notably, the former salt cation leaves during processing and is not present in films. The anion [B(C(6)F(5))(4)](−) even enables the stabilization of polarons and bipolarons in poly(3‐hexylthiophene), not yet achieved with other molecular dopants. From doping studies with high ionization energy polymer semiconductors, the effective electron affinity of Mes(2)B(+)[B(C(6)F(5))(4)](−) is estimated to be an impressive 5.9 eV. This significantly extends the parameter space for doping of polymer semiconductors.
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spelling pubmed-75073132020-09-28 An Organic Borate Salt with Superior p‐Doping Capability for Organic Semiconductors Wegner, Berthold Lungwitz, Dominique Mansour, Ahmed E. Tait, Claudia E. Tanaka, Naoki Zhai, Tianshu Duhm, Steffen Forster, Michael Behrends, Jan Shoji, Yoshiaki Opitz, Andreas Scherf, Ullrich List‐Kratochvil, Emil J. W. Fukushima, Takanori Koch, Norbert Adv Sci (Weinh) Full Papers Molecular doping allows enhancement and precise control of electrical properties of organic semiconductors, and is thus of central technological relevance for organic (opto‐) electronics. Beyond single‐component molecular electron acceptors and donors, organic salts have recently emerged as a promising class of dopants. However, the pertinent fundamental understanding of doping mechanisms and doping capabilities is limited. Here, the unique capabilities of the salt consisting of a borinium cation (Mes(2)B(+); Mes: mesitylene) and the tetrakis(penta‐fluorophenyl)borate anion [B(C(6)F(5))(4)](−) is demonstrated as p‐type dopant for polymer semiconductors. With a range of experimental methods, the doping mechanism is identified to comprise electron transfer from the polymer to Mes(2)B(+), and the positive charge on the polymer is stabilized by [B(C(6)F(5))(4)](−). Notably, the former salt cation leaves during processing and is not present in films. The anion [B(C(6)F(5))(4)](−) even enables the stabilization of polarons and bipolarons in poly(3‐hexylthiophene), not yet achieved with other molecular dopants. From doping studies with high ionization energy polymer semiconductors, the effective electron affinity of Mes(2)B(+)[B(C(6)F(5))(4)](−) is estimated to be an impressive 5.9 eV. This significantly extends the parameter space for doping of polymer semiconductors. John Wiley and Sons Inc. 2020-07-06 /pmc/articles/PMC7507313/ /pubmed/32995128 http://dx.doi.org/10.1002/advs.202001322 Text en © 2020 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Wegner, Berthold
Lungwitz, Dominique
Mansour, Ahmed E.
Tait, Claudia E.
Tanaka, Naoki
Zhai, Tianshu
Duhm, Steffen
Forster, Michael
Behrends, Jan
Shoji, Yoshiaki
Opitz, Andreas
Scherf, Ullrich
List‐Kratochvil, Emil J. W.
Fukushima, Takanori
Koch, Norbert
An Organic Borate Salt with Superior p‐Doping Capability for Organic Semiconductors
title An Organic Borate Salt with Superior p‐Doping Capability for Organic Semiconductors
title_full An Organic Borate Salt with Superior p‐Doping Capability for Organic Semiconductors
title_fullStr An Organic Borate Salt with Superior p‐Doping Capability for Organic Semiconductors
title_full_unstemmed An Organic Borate Salt with Superior p‐Doping Capability for Organic Semiconductors
title_short An Organic Borate Salt with Superior p‐Doping Capability for Organic Semiconductors
title_sort organic borate salt with superior p‐doping capability for organic semiconductors
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507313/
https://www.ncbi.nlm.nih.gov/pubmed/32995128
http://dx.doi.org/10.1002/advs.202001322
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