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Donor–acceptor polymers containing thiazole-fused benzothiadiazole acceptor units for organic solar cells

Two p-type semiconducting donor–acceptor polymers were designed and synthesized for use in organic solar cells. The polymers combine a benzodithiophene (BDT) donor and a thiazole-fused benzothiadiazole (TzBT) acceptor. Two TzBT acceptor units are compared, one with an alkylthio group (P1) and the ot...

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Autores principales: Nakamura, Tomoya, Ishikura, Yasuhisa, Arakawa, Noriko, Hori, Megumi, Satou, Motoi, Endo, Masaru, Masui, Hisashi, Fuse, Shinichiro, Takahashi, Takashi, Murata, Yasujiro, Murdey, Richard, Wakamiya, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061114/
https://www.ncbi.nlm.nih.gov/pubmed/35519982
http://dx.doi.org/10.1039/c9ra00229d
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author Nakamura, Tomoya
Ishikura, Yasuhisa
Arakawa, Noriko
Hori, Megumi
Satou, Motoi
Endo, Masaru
Masui, Hisashi
Fuse, Shinichiro
Takahashi, Takashi
Murata, Yasujiro
Murdey, Richard
Wakamiya, Atsushi
author_facet Nakamura, Tomoya
Ishikura, Yasuhisa
Arakawa, Noriko
Hori, Megumi
Satou, Motoi
Endo, Masaru
Masui, Hisashi
Fuse, Shinichiro
Takahashi, Takashi
Murata, Yasujiro
Murdey, Richard
Wakamiya, Atsushi
author_sort Nakamura, Tomoya
collection PubMed
description Two p-type semiconducting donor–acceptor polymers were designed and synthesized for use in organic solar cells. The polymers combine a benzodithiophene (BDT) donor and a thiazole-fused benzothiadiazole (TzBT) acceptor. Two TzBT acceptor units are compared, one with an alkylthio group (P1) and the other with a more strongly electron-withdrawing alkylsulfonyl group (P2) at the fused thiazole ring. The strongly electron-accepting nature of the TzBT unit lowers the lowest unoccupied molecular orbital (LUMO) energy of P1 and P2 relative to that of the BT analog (PBDT-BT), without altering the energy of the highest occupied molecular orbital (HOMO). Despite the smaller optical band gaps, bulk heterojunction organic solar cells fabricated using these polymers in a PC(71)BM blend showed high open-circuit voltages. The power conversion efficiency (PCE) of the P1-based device reached 6.13%. Though efficiency of the P2-based device was lower, photoelectric conversion extended into the near-IR region up to 950 nm.
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spelling pubmed-90611142022-05-04 Donor–acceptor polymers containing thiazole-fused benzothiadiazole acceptor units for organic solar cells Nakamura, Tomoya Ishikura, Yasuhisa Arakawa, Noriko Hori, Megumi Satou, Motoi Endo, Masaru Masui, Hisashi Fuse, Shinichiro Takahashi, Takashi Murata, Yasujiro Murdey, Richard Wakamiya, Atsushi RSC Adv Chemistry Two p-type semiconducting donor–acceptor polymers were designed and synthesized for use in organic solar cells. The polymers combine a benzodithiophene (BDT) donor and a thiazole-fused benzothiadiazole (TzBT) acceptor. Two TzBT acceptor units are compared, one with an alkylthio group (P1) and the other with a more strongly electron-withdrawing alkylsulfonyl group (P2) at the fused thiazole ring. The strongly electron-accepting nature of the TzBT unit lowers the lowest unoccupied molecular orbital (LUMO) energy of P1 and P2 relative to that of the BT analog (PBDT-BT), without altering the energy of the highest occupied molecular orbital (HOMO). Despite the smaller optical band gaps, bulk heterojunction organic solar cells fabricated using these polymers in a PC(71)BM blend showed high open-circuit voltages. The power conversion efficiency (PCE) of the P1-based device reached 6.13%. Though efficiency of the P2-based device was lower, photoelectric conversion extended into the near-IR region up to 950 nm. The Royal Society of Chemistry 2019-03-01 /pmc/articles/PMC9061114/ /pubmed/35519982 http://dx.doi.org/10.1039/c9ra00229d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Nakamura, Tomoya
Ishikura, Yasuhisa
Arakawa, Noriko
Hori, Megumi
Satou, Motoi
Endo, Masaru
Masui, Hisashi
Fuse, Shinichiro
Takahashi, Takashi
Murata, Yasujiro
Murdey, Richard
Wakamiya, Atsushi
Donor–acceptor polymers containing thiazole-fused benzothiadiazole acceptor units for organic solar cells
title Donor–acceptor polymers containing thiazole-fused benzothiadiazole acceptor units for organic solar cells
title_full Donor–acceptor polymers containing thiazole-fused benzothiadiazole acceptor units for organic solar cells
title_fullStr Donor–acceptor polymers containing thiazole-fused benzothiadiazole acceptor units for organic solar cells
title_full_unstemmed Donor–acceptor polymers containing thiazole-fused benzothiadiazole acceptor units for organic solar cells
title_short Donor–acceptor polymers containing thiazole-fused benzothiadiazole acceptor units for organic solar cells
title_sort donor–acceptor polymers containing thiazole-fused benzothiadiazole acceptor units for organic solar cells
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061114/
https://www.ncbi.nlm.nih.gov/pubmed/35519982
http://dx.doi.org/10.1039/c9ra00229d
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