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Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide
Doping of organic semiconductors is currently an intensely studied field, since it is a powerful tool to optimize the performance of various organic electronic devices, ranging from organic solar cells, to thermoelectric modules, and bio-medical sensors. Despite recent advances, there is still a nee...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333274/ https://www.ncbi.nlm.nih.gov/pubmed/30713690 http://dx.doi.org/10.1039/c8tc01593g |
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author | Hofmann, Anna I. Kroon, Renee Yu, Liyang Müller, Christian |
author_facet | Hofmann, Anna I. Kroon, Renee Yu, Liyang Müller, Christian |
author_sort | Hofmann, Anna I. |
collection | PubMed |
description | Doping of organic semiconductors is currently an intensely studied field, since it is a powerful tool to optimize the performance of various organic electronic devices, ranging from organic solar cells, to thermoelectric modules, and bio-medical sensors. Despite recent advances, there is still a need for the development of highly conducting polymer:dopant systems with excellent long term stability and a high resistance to elevated temperatures. In this work we study the doping of the polar polythiophene derivative p(g(4)2T-T) by various sulfonic acids and bistriflimide via different processing techniques. We demonstrate that simple co-processing of p(g(4)2T-T) with an acid dopant yields conductivities of up to 120 S cm(–1), which remain stable for more than six months under ambient conditions. Notably, a high conductivity is only achieved if the doping is carried out in air, which can be explained with a doping process that involves an acid mediated oxidation of the polymer through O(2). P(g(4)2T-T) doped with the non-toxic and inexpensive 1,3-propanedisulfonic acid was found to retain its electrical conductivity for at least 20 hours upon annealing at 120 °C, which allowed the bulk processing of the doped polymer into conducting, free-standing and flexible films and renders the di-acid a promising alternative to commonly used redox dopants. |
format | Online Article Text |
id | pubmed-6333274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-63332742019-02-01 Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide Hofmann, Anna I. Kroon, Renee Yu, Liyang Müller, Christian J Mater Chem C Mater Chemistry Doping of organic semiconductors is currently an intensely studied field, since it is a powerful tool to optimize the performance of various organic electronic devices, ranging from organic solar cells, to thermoelectric modules, and bio-medical sensors. Despite recent advances, there is still a need for the development of highly conducting polymer:dopant systems with excellent long term stability and a high resistance to elevated temperatures. In this work we study the doping of the polar polythiophene derivative p(g(4)2T-T) by various sulfonic acids and bistriflimide via different processing techniques. We demonstrate that simple co-processing of p(g(4)2T-T) with an acid dopant yields conductivities of up to 120 S cm(–1), which remain stable for more than six months under ambient conditions. Notably, a high conductivity is only achieved if the doping is carried out in air, which can be explained with a doping process that involves an acid mediated oxidation of the polymer through O(2). P(g(4)2T-T) doped with the non-toxic and inexpensive 1,3-propanedisulfonic acid was found to retain its electrical conductivity for at least 20 hours upon annealing at 120 °C, which allowed the bulk processing of the doped polymer into conducting, free-standing and flexible films and renders the di-acid a promising alternative to commonly used redox dopants. Royal Society of Chemistry 2018-07-14 2018-06-22 /pmc/articles/PMC6333274/ /pubmed/30713690 http://dx.doi.org/10.1039/c8tc01593g Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Hofmann, Anna I. Kroon, Renee Yu, Liyang Müller, Christian Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide |
title | Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide
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title_full | Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide
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title_fullStr | Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide
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title_full_unstemmed | Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide
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title_short | Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide
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title_sort | highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333274/ https://www.ncbi.nlm.nih.gov/pubmed/30713690 http://dx.doi.org/10.1039/c8tc01593g |
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