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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7507313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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