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p-Type Conjugated Polymers Containing Electron-Deficient Pentacyclic Azepinedione

[Image: see text] Bisthienoazepinedione (BTA) has been reported for constructing high-performing p-type conjugated polymers in organic electronics, but the ring extended version of BTA is not well explored. In this work, we report a new synthesis of a key building block to the ring expanded electron...

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Autores principales: He, Qiao, Shaw, Jessica, Firdaus, Yuliar, Hu, Xiantao, Ding, Bowen, Marsh, Adam V., Dumon, Alexandre S., Han, Yang, Fei, Zhuping, Anthopoulos, Thomas D., McNeill, Christopher R., Heeney, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413964/
https://www.ncbi.nlm.nih.gov/pubmed/37576475
http://dx.doi.org/10.1021/acs.macromol.3c00843
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author He, Qiao
Shaw, Jessica
Firdaus, Yuliar
Hu, Xiantao
Ding, Bowen
Marsh, Adam V.
Dumon, Alexandre S.
Han, Yang
Fei, Zhuping
Anthopoulos, Thomas D.
McNeill, Christopher R.
Heeney, Martin
author_facet He, Qiao
Shaw, Jessica
Firdaus, Yuliar
Hu, Xiantao
Ding, Bowen
Marsh, Adam V.
Dumon, Alexandre S.
Han, Yang
Fei, Zhuping
Anthopoulos, Thomas D.
McNeill, Christopher R.
Heeney, Martin
author_sort He, Qiao
collection PubMed
description [Image: see text] Bisthienoazepinedione (BTA) has been reported for constructing high-performing p-type conjugated polymers in organic electronics, but the ring extended version of BTA is not well explored. In this work, we report a new synthesis of a key building block to the ring expanded electron-deficient pentacyclic azepinedione (BTTA). Three copolymers of BTAA with benzodithiophene substituted by different side chains are prepared. These polymers exhibit similar energy levels and optical absorption in solution and solid state, while significant differences are revealed in their film morphologies and behavior in transistor and photovoltaic devices. The best-performing polymers in transistor devices contained alkylthienyl side chains on the BDT unit (pBDT-BTTA-2 and pBDT-BTTA-3) and demonstrated maximum saturation hole mobilities of 0.027 and 0.017 cm(2) V(–1) s(–1). Blends of these polymers with PC(71)BM exhibited a best photovoltaic efficiency of 6.78% for pBDT-BTTA-3-based devices. Changing to a low band gap non-fullerene acceptor (BTP-eC9) resulted in improved efficiency of up to 13.5%. Our results are among the best device performances for BTA and BTTA-based p-type polymers and highlight the versatile applications of this electron-deficient BTTA unit.
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spelling pubmed-104139642023-08-11 p-Type Conjugated Polymers Containing Electron-Deficient Pentacyclic Azepinedione He, Qiao Shaw, Jessica Firdaus, Yuliar Hu, Xiantao Ding, Bowen Marsh, Adam V. Dumon, Alexandre S. Han, Yang Fei, Zhuping Anthopoulos, Thomas D. McNeill, Christopher R. Heeney, Martin Macromolecules [Image: see text] Bisthienoazepinedione (BTA) has been reported for constructing high-performing p-type conjugated polymers in organic electronics, but the ring extended version of BTA is not well explored. In this work, we report a new synthesis of a key building block to the ring expanded electron-deficient pentacyclic azepinedione (BTTA). Three copolymers of BTAA with benzodithiophene substituted by different side chains are prepared. These polymers exhibit similar energy levels and optical absorption in solution and solid state, while significant differences are revealed in their film morphologies and behavior in transistor and photovoltaic devices. The best-performing polymers in transistor devices contained alkylthienyl side chains on the BDT unit (pBDT-BTTA-2 and pBDT-BTTA-3) and demonstrated maximum saturation hole mobilities of 0.027 and 0.017 cm(2) V(–1) s(–1). Blends of these polymers with PC(71)BM exhibited a best photovoltaic efficiency of 6.78% for pBDT-BTTA-3-based devices. Changing to a low band gap non-fullerene acceptor (BTP-eC9) resulted in improved efficiency of up to 13.5%. Our results are among the best device performances for BTA and BTTA-based p-type polymers and highlight the versatile applications of this electron-deficient BTTA unit. American Chemical Society 2023-07-26 /pmc/articles/PMC10413964/ /pubmed/37576475 http://dx.doi.org/10.1021/acs.macromol.3c00843 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle He, Qiao
Shaw, Jessica
Firdaus, Yuliar
Hu, Xiantao
Ding, Bowen
Marsh, Adam V.
Dumon, Alexandre S.
Han, Yang
Fei, Zhuping
Anthopoulos, Thomas D.
McNeill, Christopher R.
Heeney, Martin
p-Type Conjugated Polymers Containing Electron-Deficient Pentacyclic Azepinedione
title p-Type Conjugated Polymers Containing Electron-Deficient Pentacyclic Azepinedione
title_full p-Type Conjugated Polymers Containing Electron-Deficient Pentacyclic Azepinedione
title_fullStr p-Type Conjugated Polymers Containing Electron-Deficient Pentacyclic Azepinedione
title_full_unstemmed p-Type Conjugated Polymers Containing Electron-Deficient Pentacyclic Azepinedione
title_short p-Type Conjugated Polymers Containing Electron-Deficient Pentacyclic Azepinedione
title_sort p-type conjugated polymers containing electron-deficient pentacyclic azepinedione
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413964/
https://www.ncbi.nlm.nih.gov/pubmed/37576475
http://dx.doi.org/10.1021/acs.macromol.3c00843
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