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Diketopyrrolopyrrole‐Based Conjugated Polymer Entailing Triethylene Glycols as Side Chains with High Thin‐Film Charge Mobility without Post‐Treatments
Side chain engineering of conjugated donor–acceptor polymers is a new way to manipulate their optoelectronic properties. Two new diketopyrrolopyrrole (DPP)‐terthiophene‐based conjugated polymers PDPP3T‐1 and PDPP3T‐2, with both hydrophilic triethylene glycol (TEG) and hydrophobic alkyl chains, are r...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566237/ https://www.ncbi.nlm.nih.gov/pubmed/28852623 http://dx.doi.org/10.1002/advs.201700048 |
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author | Yang, Si‐Fen Liu, Zi‐Tong Cai, Zheng‐Xu Dyson, Matthew J. Stingelin, Natalie Chen, Wei Ju, Hua‐Jun Zhang, Guan‐Xin Zhang, De‐Qing |
author_facet | Yang, Si‐Fen Liu, Zi‐Tong Cai, Zheng‐Xu Dyson, Matthew J. Stingelin, Natalie Chen, Wei Ju, Hua‐Jun Zhang, Guan‐Xin Zhang, De‐Qing |
author_sort | Yang, Si‐Fen |
collection | PubMed |
description | Side chain engineering of conjugated donor–acceptor polymers is a new way to manipulate their optoelectronic properties. Two new diketopyrrolopyrrole (DPP)‐terthiophene‐based conjugated polymers PDPP3T‐1 and PDPP3T‐2, with both hydrophilic triethylene glycol (TEG) and hydrophobic alkyl chains, are reported. It is demonstrated that the incorporation of TEG chains has a significant effect on the interchain packing and thin‐film morphology with noticeable effect on charge transport. Polymer chains of PDPP3T‐1 in which TEG chains are uniformly distributed can self‐assemble spontaneously into a more ordered thin film. As a result, the thin film of PDPP3T‐1 exhibits high saturated hole mobility up to 2.6 cm(2) V(−1) s(−1) without any post‐treatment. This is superior to those of PDPP3T with just alkyl chains and PDPP3T‐2. Moreover, the respective field effect transistors made of PDPP3T‐1 can be utilized for sensing ethanol vapor with high sensitivity (down to 100 ppb) and good selectivity. |
format | Online Article Text |
id | pubmed-5566237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55662372017-08-29 Diketopyrrolopyrrole‐Based Conjugated Polymer Entailing Triethylene Glycols as Side Chains with High Thin‐Film Charge Mobility without Post‐Treatments Yang, Si‐Fen Liu, Zi‐Tong Cai, Zheng‐Xu Dyson, Matthew J. Stingelin, Natalie Chen, Wei Ju, Hua‐Jun Zhang, Guan‐Xin Zhang, De‐Qing Adv Sci (Weinh) Full Papers Side chain engineering of conjugated donor–acceptor polymers is a new way to manipulate their optoelectronic properties. Two new diketopyrrolopyrrole (DPP)‐terthiophene‐based conjugated polymers PDPP3T‐1 and PDPP3T‐2, with both hydrophilic triethylene glycol (TEG) and hydrophobic alkyl chains, are reported. It is demonstrated that the incorporation of TEG chains has a significant effect on the interchain packing and thin‐film morphology with noticeable effect on charge transport. Polymer chains of PDPP3T‐1 in which TEG chains are uniformly distributed can self‐assemble spontaneously into a more ordered thin film. As a result, the thin film of PDPP3T‐1 exhibits high saturated hole mobility up to 2.6 cm(2) V(−1) s(−1) without any post‐treatment. This is superior to those of PDPP3T with just alkyl chains and PDPP3T‐2. Moreover, the respective field effect transistors made of PDPP3T‐1 can be utilized for sensing ethanol vapor with high sensitivity (down to 100 ppb) and good selectivity. John Wiley and Sons Inc. 2017-04-18 /pmc/articles/PMC5566237/ /pubmed/28852623 http://dx.doi.org/10.1002/advs.201700048 Text en © 2017 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the Creative Commons Attribution (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 Yang, Si‐Fen Liu, Zi‐Tong Cai, Zheng‐Xu Dyson, Matthew J. Stingelin, Natalie Chen, Wei Ju, Hua‐Jun Zhang, Guan‐Xin Zhang, De‐Qing Diketopyrrolopyrrole‐Based Conjugated Polymer Entailing Triethylene Glycols as Side Chains with High Thin‐Film Charge Mobility without Post‐Treatments |
title | Diketopyrrolopyrrole‐Based Conjugated Polymer Entailing Triethylene Glycols as Side Chains with High Thin‐Film Charge Mobility without Post‐Treatments |
title_full | Diketopyrrolopyrrole‐Based Conjugated Polymer Entailing Triethylene Glycols as Side Chains with High Thin‐Film Charge Mobility without Post‐Treatments |
title_fullStr | Diketopyrrolopyrrole‐Based Conjugated Polymer Entailing Triethylene Glycols as Side Chains with High Thin‐Film Charge Mobility without Post‐Treatments |
title_full_unstemmed | Diketopyrrolopyrrole‐Based Conjugated Polymer Entailing Triethylene Glycols as Side Chains with High Thin‐Film Charge Mobility without Post‐Treatments |
title_short | Diketopyrrolopyrrole‐Based Conjugated Polymer Entailing Triethylene Glycols as Side Chains with High Thin‐Film Charge Mobility without Post‐Treatments |
title_sort | diketopyrrolopyrrole‐based conjugated polymer entailing triethylene glycols as side chains with high thin‐film charge mobility without post‐treatments |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566237/ https://www.ncbi.nlm.nih.gov/pubmed/28852623 http://dx.doi.org/10.1002/advs.201700048 |
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