Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Hofmann, Anna I., Kroon, Renee, Yu, Liyang, Müller, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
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
_version_ 1783387534466744320
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
title_full Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide
title_fullStr Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide
title_full_unstemmed Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide
title_short Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide
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
work_keys_str_mv AT hofmannannai highlystabledopingofapolarpolythiophenethroughcoprocessingwithsulfonicacidsandbistriflimide
AT kroonrenee highlystabledopingofapolarpolythiophenethroughcoprocessingwithsulfonicacidsandbistriflimide
AT yuliyang highlystabledopingofapolarpolythiophenethroughcoprocessingwithsulfonicacidsandbistriflimide
AT mullerchristian highlystabledopingofapolarpolythiophenethroughcoprocessingwithsulfonicacidsandbistriflimide