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The Role of the Side Chain on the Performance of N-type Conjugated Polymers in Aqueous Electrolytes
[Image: see text] We report a design strategy that allows the preparation of solution processable n-type materials from low boiling point solvents for organic electrochemical transistors (OECTs). The polymer backbone is based on NDI-T2 copolymers where a branched alkyl side chain is gradually exchan...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5953566/ https://www.ncbi.nlm.nih.gov/pubmed/29780208 http://dx.doi.org/10.1021/acs.chemmater.8b00321 |
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author | Giovannitti, Alexander Maria, Iuliana P. Hanifi, David Donahue, Mary J. Bryant, Daniel Barth, Katrina J. Makdah, Beatrice E. Savva, Achilleas Moia, Davide Zetek, Matyáš Barnes, Piers R.F. Reid, Obadiah G. Inal, Sahika Rumbles, Garry Malliaras, George G. Nelson, Jenny Rivnay, Jonathan McCulloch, Iain |
author_facet | Giovannitti, Alexander Maria, Iuliana P. Hanifi, David Donahue, Mary J. Bryant, Daniel Barth, Katrina J. Makdah, Beatrice E. Savva, Achilleas Moia, Davide Zetek, Matyáš Barnes, Piers R.F. Reid, Obadiah G. Inal, Sahika Rumbles, Garry Malliaras, George G. Nelson, Jenny Rivnay, Jonathan McCulloch, Iain |
author_sort | Giovannitti, Alexander |
collection | PubMed |
description | [Image: see text] We report a design strategy that allows the preparation of solution processable n-type materials from low boiling point solvents for organic electrochemical transistors (OECTs). The polymer backbone is based on NDI-T2 copolymers where a branched alkyl side chain is gradually exchanged for a linear ethylene glycol-based side chain. A series of random copolymers was prepared with glycol side chain percentages of 0, 10, 25, 50, 75, 90, and 100 with respect to the alkyl side chains. These were characterized to study the influence of the polar side chains on interaction with aqueous electrolytes, their electrochemical redox reactions, and performance in OECTs when operated in aqueous electrolytes. We observed that glycol side chain percentages of >50% are required to achieve volumetric charging, while lower glycol chain percentages show a mixed operation with high required voltages to allow for bulk charging of the organic semiconductor. A strong dependence of the electron mobility on the fraction of glycol chains was found for copolymers based on NDI-T2, with a significant drop as alkyl side chains are replaced by glycol side chains. |
format | Online Article Text |
id | pubmed-5953566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American
Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-59535662018-05-16 The Role of the Side Chain on the Performance of N-type Conjugated Polymers in Aqueous Electrolytes Giovannitti, Alexander Maria, Iuliana P. Hanifi, David Donahue, Mary J. Bryant, Daniel Barth, Katrina J. Makdah, Beatrice E. Savva, Achilleas Moia, Davide Zetek, Matyáš Barnes, Piers R.F. Reid, Obadiah G. Inal, Sahika Rumbles, Garry Malliaras, George G. Nelson, Jenny Rivnay, Jonathan McCulloch, Iain Chem Mater [Image: see text] We report a design strategy that allows the preparation of solution processable n-type materials from low boiling point solvents for organic electrochemical transistors (OECTs). The polymer backbone is based on NDI-T2 copolymers where a branched alkyl side chain is gradually exchanged for a linear ethylene glycol-based side chain. A series of random copolymers was prepared with glycol side chain percentages of 0, 10, 25, 50, 75, 90, and 100 with respect to the alkyl side chains. These were characterized to study the influence of the polar side chains on interaction with aqueous electrolytes, their electrochemical redox reactions, and performance in OECTs when operated in aqueous electrolytes. We observed that glycol side chain percentages of >50% are required to achieve volumetric charging, while lower glycol chain percentages show a mixed operation with high required voltages to allow for bulk charging of the organic semiconductor. A strong dependence of the electron mobility on the fraction of glycol chains was found for copolymers based on NDI-T2, with a significant drop as alkyl side chains are replaced by glycol side chains. American Chemical Society 2018-04-24 2018-05-08 /pmc/articles/PMC5953566/ /pubmed/29780208 http://dx.doi.org/10.1021/acs.chemmater.8b00321 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Giovannitti, Alexander Maria, Iuliana P. Hanifi, David Donahue, Mary J. Bryant, Daniel Barth, Katrina J. Makdah, Beatrice E. Savva, Achilleas Moia, Davide Zetek, Matyáš Barnes, Piers R.F. Reid, Obadiah G. Inal, Sahika Rumbles, Garry Malliaras, George G. Nelson, Jenny Rivnay, Jonathan McCulloch, Iain The Role of the Side Chain on the Performance of N-type Conjugated Polymers in Aqueous Electrolytes |
title | The Role of the Side Chain on the Performance of N-type
Conjugated Polymers in Aqueous Electrolytes |
title_full | The Role of the Side Chain on the Performance of N-type
Conjugated Polymers in Aqueous Electrolytes |
title_fullStr | The Role of the Side Chain on the Performance of N-type
Conjugated Polymers in Aqueous Electrolytes |
title_full_unstemmed | The Role of the Side Chain on the Performance of N-type
Conjugated Polymers in Aqueous Electrolytes |
title_short | The Role of the Side Chain on the Performance of N-type
Conjugated Polymers in Aqueous Electrolytes |
title_sort | role of the side chain on the performance of n-type
conjugated polymers in aqueous electrolytes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5953566/ https://www.ncbi.nlm.nih.gov/pubmed/29780208 http://dx.doi.org/10.1021/acs.chemmater.8b00321 |
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