Structural influences of proquinoidal acceptor moieties on transistor performance and doping capability for diketopyrrolopyrrole-based dual-acceptor conjugated polymers

In this study, we design and synthesize three DPP-based dual-acceptor conjugated polymers comprising different proquinoidal heterocyclic acceptors, including benzobisthiadizole ( SS ), triazolobenzothiadiazole ( NS ), and benzobistriazole ( NN ), and investigate their structure-property relationship...

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Veröffentlicht in:Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2022-12, Vol.1 (47), p.17936-17944
Hauptverfasser: Wu, Ying-Sheng, Li, Jian-Sian, Chang, Chih-Yuan, He, Waner, Michinobu, Tsuyoshi, Lin, Yan-Cheng, Chen, Wen-Chang, Chueh, Chu-Chen
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container_issue 47
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container_title Journal of materials chemistry. C, Materials for optical and electronic devices
container_volume 1
creator Wu, Ying-Sheng
Li, Jian-Sian
Chang, Chih-Yuan
He, Waner
Michinobu, Tsuyoshi
Lin, Yan-Cheng
Chen, Wen-Chang
Chueh, Chu-Chen
description In this study, we design and synthesize three DPP-based dual-acceptor conjugated polymers comprising different proquinoidal heterocyclic acceptors, including benzobisthiadizole ( SS ), triazolobenzothiadiazole ( NS ), and benzobistriazole ( NN ), and investigate their structure-property relationship using a transistor and their conductive states by doping. Owing to the high-spin and proquinoidal characteristics of the NN/NS/SS units, all the prepared polymers possess free radicals. However, a subtle difference in the proquinoidal characteristics among these acceptor units results in varied backbone rigidity and coplanarity of the derived polymers. DPP-NS and DPP-NN are shown to possess better solid-state stacking and crystallinity than DPP-SS , conferred by the alkyl side chains on the triazole unit. Hence, DPP-NS and DPP-NN can deliver enhanced mobilities of 3.0 × 10 −2 and 5.3 × 10 −2 cm 2 V −1 s −1 , respectively, after appropriate thermal annealing whereas the stiff DPP-SS only shows a minor improvement. Furthermore, the intrinsic intense radical characteristic of the NN unit is shown to facilitate the receivability of dopants. At a low doping concentration, DPP-NN delivers the highest conductivity of 23.8 S cm −1 among these polymers. Besides, owing to the higher degree of flexibility in chain packing and associated chain aggregation, DPP-NN displays a superior capability to resist the structural deconstruction in the doping state at a high concentration compared to DPP-NS and DPP-SS . Concisely, our results unravel the non-trivial influence of a proquinoidal acceptor moiety on transistor performance and doping capability of the derived polymers. Three DPP-based dual-acceptor conjugated polymers comprising different proquinoidal heterocyclic acceptors are synthesized and their structure-property relationship using a transistor and their conductive states by doping are investigated.
doi_str_mv 10.1039/d2tc03956g
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Owing to the high-spin and proquinoidal characteristics of the NN/NS/SS units, all the prepared polymers possess free radicals. However, a subtle difference in the proquinoidal characteristics among these acceptor units results in varied backbone rigidity and coplanarity of the derived polymers. DPP-NS and DPP-NN are shown to possess better solid-state stacking and crystallinity than DPP-SS , conferred by the alkyl side chains on the triazole unit. Hence, DPP-NS and DPP-NN can deliver enhanced mobilities of 3.0 × 10 −2 and 5.3 × 10 −2 cm 2 V −1 s −1 , respectively, after appropriate thermal annealing whereas the stiff DPP-SS only shows a minor improvement. Furthermore, the intrinsic intense radical characteristic of the NN unit is shown to facilitate the receivability of dopants. At a low doping concentration, DPP-NN delivers the highest conductivity of 23.8 S cm −1 among these polymers. Besides, owing to the higher degree of flexibility in chain packing and associated chain aggregation, DPP-NN displays a superior capability to resist the structural deconstruction in the doping state at a high concentration compared to DPP-NS and DPP-SS . Concisely, our results unravel the non-trivial influence of a proquinoidal acceptor moiety on transistor performance and doping capability of the derived polymers. Three DPP-based dual-acceptor conjugated polymers comprising different proquinoidal heterocyclic acceptors are synthesized and their structure-property relationship using a transistor and their conductive states by doping are investigated.</description><identifier>ISSN: 2050-7526</identifier><identifier>EISSN: 2050-7534</identifier><identifier>DOI: 10.1039/d2tc03956g</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Coplanarity ; Doping ; Free radicals ; Polymers ; Semiconductor devices ; Transistors</subject><ispartof>Journal of materials chemistry. 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C, Materials for optical and electronic devices</title><description>In this study, we design and synthesize three DPP-based dual-acceptor conjugated polymers comprising different proquinoidal heterocyclic acceptors, including benzobisthiadizole ( SS ), triazolobenzothiadiazole ( NS ), and benzobistriazole ( NN ), and investigate their structure-property relationship using a transistor and their conductive states by doping. Owing to the high-spin and proquinoidal characteristics of the NN/NS/SS units, all the prepared polymers possess free radicals. However, a subtle difference in the proquinoidal characteristics among these acceptor units results in varied backbone rigidity and coplanarity of the derived polymers. DPP-NS and DPP-NN are shown to possess better solid-state stacking and crystallinity than DPP-SS , conferred by the alkyl side chains on the triazole unit. Hence, DPP-NS and DPP-NN can deliver enhanced mobilities of 3.0 × 10 −2 and 5.3 × 10 −2 cm 2 V −1 s −1 , respectively, after appropriate thermal annealing whereas the stiff DPP-SS only shows a minor improvement. Furthermore, the intrinsic intense radical characteristic of the NN unit is shown to facilitate the receivability of dopants. At a low doping concentration, DPP-NN delivers the highest conductivity of 23.8 S cm −1 among these polymers. Besides, owing to the higher degree of flexibility in chain packing and associated chain aggregation, DPP-NN displays a superior capability to resist the structural deconstruction in the doping state at a high concentration compared to DPP-NS and DPP-SS . Concisely, our results unravel the non-trivial influence of a proquinoidal acceptor moiety on transistor performance and doping capability of the derived polymers. 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C, Materials for optical and electronic devices</jtitle><date>2022-12-08</date><risdate>2022</risdate><volume>1</volume><issue>47</issue><spage>17936</spage><epage>17944</epage><pages>17936-17944</pages><issn>2050-7526</issn><eissn>2050-7534</eissn><abstract>In this study, we design and synthesize three DPP-based dual-acceptor conjugated polymers comprising different proquinoidal heterocyclic acceptors, including benzobisthiadizole ( SS ), triazolobenzothiadiazole ( NS ), and benzobistriazole ( NN ), and investigate their structure-property relationship using a transistor and their conductive states by doping. Owing to the high-spin and proquinoidal characteristics of the NN/NS/SS units, all the prepared polymers possess free radicals. However, a subtle difference in the proquinoidal characteristics among these acceptor units results in varied backbone rigidity and coplanarity of the derived polymers. DPP-NS and DPP-NN are shown to possess better solid-state stacking and crystallinity than DPP-SS , conferred by the alkyl side chains on the triazole unit. Hence, DPP-NS and DPP-NN can deliver enhanced mobilities of 3.0 × 10 −2 and 5.3 × 10 −2 cm 2 V −1 s −1 , respectively, after appropriate thermal annealing whereas the stiff DPP-SS only shows a minor improvement. Furthermore, the intrinsic intense radical characteristic of the NN unit is shown to facilitate the receivability of dopants. At a low doping concentration, DPP-NN delivers the highest conductivity of 23.8 S cm −1 among these polymers. Besides, owing to the higher degree of flexibility in chain packing and associated chain aggregation, DPP-NN displays a superior capability to resist the structural deconstruction in the doping state at a high concentration compared to DPP-NS and DPP-SS . Concisely, our results unravel the non-trivial influence of a proquinoidal acceptor moiety on transistor performance and doping capability of the derived polymers. Three DPP-based dual-acceptor conjugated polymers comprising different proquinoidal heterocyclic acceptors are synthesized and their structure-property relationship using a transistor and their conductive states by doping are investigated.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2tc03956g</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-6948-1189</orcidid><orcidid>https://orcid.org/0000-0003-1203-4227</orcidid><orcidid>https://orcid.org/0000-0002-2914-6762</orcidid><orcidid>https://orcid.org/0000-0003-3170-7220</orcidid></addata></record>
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source Royal Society Of Chemistry Journals 2008-
subjects Coplanarity
Doping
Free radicals
Polymers
Semiconductor devices
Transistors
title Structural influences of proquinoidal acceptor moieties on transistor performance and doping capability for diketopyrrolopyrrole-based dual-acceptor conjugated polymers
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