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Regioisomer effects of [70]fullerene mono-adduct acceptors in bulk heterojunction polymer solar cells

Despite numerous organic semiconductors being developed during the past decade, C(70) derivatives are predominantly used as electron acceptors in efficient polymer solar cells (PSCs). However, as-prepared C(70) mono-adducts intrinsically comprise regioisomers that would mask individual device perfor...

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Autores principales: Umeyama, Tomokazu, Miyata, Tetsushi, Jakowetz, Andreas C., Shibata, Sho, Kurotobi, Kei, Higashino, Tomohiro, Koganezawa, Tomoyuki, Tsujimoto, Masahiko, Gélinas, Simon, Matsuda, Wakana, Seki, Shu, Friend, Richard H., Imahori, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308288/
https://www.ncbi.nlm.nih.gov/pubmed/28451164
http://dx.doi.org/10.1039/c6sc02950g
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author Umeyama, Tomokazu
Miyata, Tetsushi
Jakowetz, Andreas C.
Shibata, Sho
Kurotobi, Kei
Higashino, Tomohiro
Koganezawa, Tomoyuki
Tsujimoto, Masahiko
Gélinas, Simon
Matsuda, Wakana
Seki, Shu
Friend, Richard H.
Imahori, Hiroshi
author_facet Umeyama, Tomokazu
Miyata, Tetsushi
Jakowetz, Andreas C.
Shibata, Sho
Kurotobi, Kei
Higashino, Tomohiro
Koganezawa, Tomoyuki
Tsujimoto, Masahiko
Gélinas, Simon
Matsuda, Wakana
Seki, Shu
Friend, Richard H.
Imahori, Hiroshi
author_sort Umeyama, Tomokazu
collection PubMed
description Despite numerous organic semiconductors being developed during the past decade, C(70) derivatives are predominantly used as electron acceptors in efficient polymer solar cells (PSCs). However, as-prepared C(70) mono-adducts intrinsically comprise regioisomers that would mask individual device performances depending on the substituent position on C(70). Herein, we separate the regioisomers of C(70) mono-adducts for PSC applications for the first time. Systematic investigations of the substituent position effect using a novel symmetric C(70) mono-adduct ([70]NCMA) and a prevalent, high-performance one ([70]PCBM) reveals that we can control the structures of the blend films with conjugated polymers and thereby improve the PSC performances by regioisomer separation. Our approach demonstrates the significance of exploring the best-matching regioisomer of C(70) mono-adducts with high-performance conjugated polymers, which would achieve a remarkable progress in PSC devices.
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spelling pubmed-53082882017-04-27 Regioisomer effects of [70]fullerene mono-adduct acceptors in bulk heterojunction polymer solar cells Umeyama, Tomokazu Miyata, Tetsushi Jakowetz, Andreas C. Shibata, Sho Kurotobi, Kei Higashino, Tomohiro Koganezawa, Tomoyuki Tsujimoto, Masahiko Gélinas, Simon Matsuda, Wakana Seki, Shu Friend, Richard H. Imahori, Hiroshi Chem Sci Chemistry Despite numerous organic semiconductors being developed during the past decade, C(70) derivatives are predominantly used as electron acceptors in efficient polymer solar cells (PSCs). However, as-prepared C(70) mono-adducts intrinsically comprise regioisomers that would mask individual device performances depending on the substituent position on C(70). Herein, we separate the regioisomers of C(70) mono-adducts for PSC applications for the first time. Systematic investigations of the substituent position effect using a novel symmetric C(70) mono-adduct ([70]NCMA) and a prevalent, high-performance one ([70]PCBM) reveals that we can control the structures of the blend films with conjugated polymers and thereby improve the PSC performances by regioisomer separation. Our approach demonstrates the significance of exploring the best-matching regioisomer of C(70) mono-adducts with high-performance conjugated polymers, which would achieve a remarkable progress in PSC devices. Royal Society of Chemistry 2017-01-01 2016-08-19 /pmc/articles/PMC5308288/ /pubmed/28451164 http://dx.doi.org/10.1039/c6sc02950g Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Umeyama, Tomokazu
Miyata, Tetsushi
Jakowetz, Andreas C.
Shibata, Sho
Kurotobi, Kei
Higashino, Tomohiro
Koganezawa, Tomoyuki
Tsujimoto, Masahiko
Gélinas, Simon
Matsuda, Wakana
Seki, Shu
Friend, Richard H.
Imahori, Hiroshi
Regioisomer effects of [70]fullerene mono-adduct acceptors in bulk heterojunction polymer solar cells
title Regioisomer effects of [70]fullerene mono-adduct acceptors in bulk heterojunction polymer solar cells
title_full Regioisomer effects of [70]fullerene mono-adduct acceptors in bulk heterojunction polymer solar cells
title_fullStr Regioisomer effects of [70]fullerene mono-adduct acceptors in bulk heterojunction polymer solar cells
title_full_unstemmed Regioisomer effects of [70]fullerene mono-adduct acceptors in bulk heterojunction polymer solar cells
title_short Regioisomer effects of [70]fullerene mono-adduct acceptors in bulk heterojunction polymer solar cells
title_sort regioisomer effects of [70]fullerene mono-adduct acceptors in bulk heterojunction polymer solar cells
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308288/
https://www.ncbi.nlm.nih.gov/pubmed/28451164
http://dx.doi.org/10.1039/c6sc02950g
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