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...
Gespeichert in:
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: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 17944 |
---|---|
container_issue | 47 |
container_start_page | 17936 |
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_rsc_p</sourceid><recordid>TN_cdi_rsc_primary_d2tc03956g</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2747830107</sourcerecordid><originalsourceid>FETCH-LOGICAL-c281t-5810814eec34e7b73f404818b3dc4ff30ff61d14361aa22886c0f18e21e3bee93</originalsourceid><addsrcrecordid>eNpFkU1LAzEQhoMoWGov3oWAN2E1H_uRHqVqFQoerOclm52U1G2yJtnD_iN_pqktdS7vkPeZDMOL0DUl95Tw-UPLokpalJszNGGkIFlV8Pz81LPyEs1C2JJUgpainE_Qz0f0g4qDlx02VncDWAUBO417774HY51pkyWVgj46j3fOQDR7wuLopQ0m7J978Nr5nUzDWNoWt643doOV7GVjOhNHnGzcmi-Irh-9d91RIGtkgDQwyC47bVHOboeNjMnoXTfuwIcrdKFlF2B21Cn6fHleL16z1fvybfG4yhQTNGaFoOm2HEDxHKqm4jonuaCi4a3KteZE65K2NOcllZIxIUpFNBXAKPAGYM6n6Pbw79_9EGK9dYO3aWXNqrwSnFBSJeruQCnvQvCg696bnfRjTUm9D6N-YuvFXxjLBN8cYB_UifsPi_8CX9mMIQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2747830107</pqid></control><display><type>article</type><title>Structural influences of proquinoidal acceptor moieties on transistor performance and doping capability for diketopyrrolopyrrole-based dual-acceptor conjugated polymers</title><source>Royal Society Of Chemistry Journals 2008-</source><creator>Wu, Ying-Sheng ; Li, Jian-Sian ; Chang, Chih-Yuan ; He, Waner ; Michinobu, Tsuyoshi ; Lin, Yan-Cheng ; Chen, Wen-Chang ; Chueh, Chu-Chen</creator><creatorcontrib>Wu, Ying-Sheng ; Li, Jian-Sian ; Chang, Chih-Yuan ; He, Waner ; Michinobu, Tsuyoshi ; Lin, Yan-Cheng ; Chen, Wen-Chang ; Chueh, Chu-Chen</creatorcontrib><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.</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. C, Materials for optical and electronic devices, 2022-12, Vol.1 (47), p.17936-17944</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c281t-5810814eec34e7b73f404818b3dc4ff30ff61d14361aa22886c0f18e21e3bee93</citedby><cites>FETCH-LOGICAL-c281t-5810814eec34e7b73f404818b3dc4ff30ff61d14361aa22886c0f18e21e3bee93</cites><orcidid>0000-0001-6948-1189 ; 0000-0003-1203-4227 ; 0000-0002-2914-6762 ; 0000-0003-3170-7220</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Wu, Ying-Sheng</creatorcontrib><creatorcontrib>Li, Jian-Sian</creatorcontrib><creatorcontrib>Chang, Chih-Yuan</creatorcontrib><creatorcontrib>He, Waner</creatorcontrib><creatorcontrib>Michinobu, Tsuyoshi</creatorcontrib><creatorcontrib>Lin, Yan-Cheng</creatorcontrib><creatorcontrib>Chen, Wen-Chang</creatorcontrib><creatorcontrib>Chueh, Chu-Chen</creatorcontrib><title>Structural influences of proquinoidal acceptor moieties on transistor performance and doping capability for diketopyrrolopyrrole-based dual-acceptor conjugated polymers</title><title>Journal of materials chemistry. 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.
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><subject>Coplanarity</subject><subject>Doping</subject><subject>Free radicals</subject><subject>Polymers</subject><subject>Semiconductor devices</subject><subject>Transistors</subject><issn>2050-7526</issn><issn>2050-7534</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpFkU1LAzEQhoMoWGov3oWAN2E1H_uRHqVqFQoerOclm52U1G2yJtnD_iN_pqktdS7vkPeZDMOL0DUl95Tw-UPLokpalJszNGGkIFlV8Pz81LPyEs1C2JJUgpainE_Qz0f0g4qDlx02VncDWAUBO417774HY51pkyWVgj46j3fOQDR7wuLopQ0m7J978Nr5nUzDWNoWt643doOV7GVjOhNHnGzcmi-Irh-9d91RIGtkgDQwyC47bVHOboeNjMnoXTfuwIcrdKFlF2B21Cn6fHleL16z1fvybfG4yhQTNGaFoOm2HEDxHKqm4jonuaCi4a3KteZE65K2NOcllZIxIUpFNBXAKPAGYM6n6Pbw79_9EGK9dYO3aWXNqrwSnFBSJeruQCnvQvCg696bnfRjTUm9D6N-YuvFXxjLBN8cYB_UifsPi_8CX9mMIQ</recordid><startdate>20221208</startdate><enddate>20221208</enddate><creator>Wu, Ying-Sheng</creator><creator>Li, Jian-Sian</creator><creator>Chang, Chih-Yuan</creator><creator>He, Waner</creator><creator>Michinobu, Tsuyoshi</creator><creator>Lin, Yan-Cheng</creator><creator>Chen, Wen-Chang</creator><creator>Chueh, Chu-Chen</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><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></search><sort><creationdate>20221208</creationdate><title>Structural influences of proquinoidal acceptor moieties on transistor performance and doping capability for diketopyrrolopyrrole-based dual-acceptor conjugated polymers</title><author>Wu, Ying-Sheng ; Li, Jian-Sian ; Chang, Chih-Yuan ; He, Waner ; Michinobu, Tsuyoshi ; Lin, Yan-Cheng ; Chen, Wen-Chang ; Chueh, Chu-Chen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c281t-5810814eec34e7b73f404818b3dc4ff30ff61d14361aa22886c0f18e21e3bee93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Coplanarity</topic><topic>Doping</topic><topic>Free radicals</topic><topic>Polymers</topic><topic>Semiconductor devices</topic><topic>Transistors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Ying-Sheng</creatorcontrib><creatorcontrib>Li, Jian-Sian</creatorcontrib><creatorcontrib>Chang, Chih-Yuan</creatorcontrib><creatorcontrib>He, Waner</creatorcontrib><creatorcontrib>Michinobu, Tsuyoshi</creatorcontrib><creatorcontrib>Lin, Yan-Cheng</creatorcontrib><creatorcontrib>Chen, Wen-Chang</creatorcontrib><creatorcontrib>Chueh, Chu-Chen</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of materials chemistry. C, Materials for optical and electronic devices</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Ying-Sheng</au><au>Li, Jian-Sian</au><au>Chang, Chih-Yuan</au><au>He, Waner</au><au>Michinobu, Tsuyoshi</au><au>Lin, Yan-Cheng</au><au>Chen, Wen-Chang</au><au>Chueh, Chu-Chen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural influences of proquinoidal acceptor moieties on transistor performance and doping capability for diketopyrrolopyrrole-based dual-acceptor conjugated polymers</atitle><jtitle>Journal of materials chemistry. 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> |
fulltext | fulltext |
identifier | ISSN: 2050-7526 |
ispartof | Journal of materials chemistry. C, Materials for optical and electronic devices, 2022-12, Vol.1 (47), p.17936-17944 |
issn | 2050-7526 2050-7534 |
language | eng |
recordid | cdi_rsc_primary_d2tc03956g |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T18%3A36%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_rsc_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Structural%20influences%20of%20proquinoidal%20acceptor%20moieties%20on%20transistor%20performance%20and%20doping%20capability%20for%20diketopyrrolopyrrole-based%20dual-acceptor%20conjugated%20polymers&rft.jtitle=Journal%20of%20materials%20chemistry.%20C,%20Materials%20for%20optical%20and%20electronic%20devices&rft.au=Wu,%20Ying-Sheng&rft.date=2022-12-08&rft.volume=1&rft.issue=47&rft.spage=17936&rft.epage=17944&rft.pages=17936-17944&rft.issn=2050-7526&rft.eissn=2050-7534&rft_id=info:doi/10.1039/d2tc03956g&rft_dat=%3Cproquest_rsc_p%3E2747830107%3C/proquest_rsc_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2747830107&rft_id=info:pmid/&rfr_iscdi=true |