Fullerene Desymmetrization as a Means to Achieve Single-Enantiomer Electron Acceptors with Maximized Chiroptical Responsiveness

© 2020 The Authors. Advanced Materials published by Wiley-VCH GmbH.

Détails bibliographiques
Publié dans:Advanced materials (Deerfield Beach, Fla.). - 1998. - 33(2021), 1 vom: 26. Jan., Seite e2004115
Auteur principal: Shi, Wenda (Auteur)
Autres auteurs: Salerno, Francesco, Ward, Matthew D, Santana-Bonilla, Alejandro, Wade, Jessica, Hou, Xueyan, Liu, Tong, Dennis, T John S, Campbell, Alasdair J, Jelfs, Kim E, Fuchter, Matthew J
Format: Article en ligne
Langue:English
Publié: 2021
Accès à la collection:Advanced materials (Deerfield Beach, Fla.)
Sujets:Journal Article chiral materials chiroptical response circularly polarized light fullerenes organic field-effect transistors
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520 |a Solubilized fullerene derivatives have revolutionized the development of organic photovoltaic devices, acting as excellent electron acceptors. The addition of solubilizing addends to the fullerene cage results in a large number of isomers, which are generally employed as isomeric mixtures. Moreover, a significant number of these isomers are chiral, which further adds to the isomeric complexity. The opportunities presented by single-isomer, and particularly single-enantiomer, fullerenes in organic electronic materials and devices are poorly understood however. Here, ten pairs of enantiomers are separated from the 19 structural isomers of bis[60]phenyl-C61-butyric acid methyl ester, using them to elucidate important chiroptical relationships and demonstrating their application to a circularly polarized light (CPL)-detecting device. Larger chiroptical responses are found, occurring through the inherent chirality of the fullerene. When used in a single-enantiomer organic field-effect transistor, the potential to discriminate CPL with a fast light response time and with a very high photocurrent dissymmetry factor (gph  = 1.27 ± 0.06) is demonstrated. This study thus provides key strategies to design fullerenes with large chiroptical responses for use as chiral components of organic electronic devices. It is anticipated that this data will position chiral fullerenes as an exciting material class for the growing field of chiral electronic technologies 
650 4 |a Journal Article 
650 4 |a chiral materials 
650 4 |a chiroptical response 
650 4 |a circularly polarized light 
650 4 |a fullerenes 
650 4 |a organic field-effect transistors 
700 1 |a Salerno, Francesco  |e verfasserin  |4 aut 
700 1 |a Ward, Matthew D  |e verfasserin  |4 aut 
700 1 |a Santana-Bonilla, Alejandro  |e verfasserin  |4 aut 
700 1 |a Wade, Jessica  |e verfasserin  |4 aut 
700 1 |a Hou, Xueyan  |e verfasserin  |4 aut 
700 1 |a Liu, Tong  |e verfasserin  |4 aut 
700 1 |a Dennis, T John S  |e verfasserin  |4 aut 
700 1 |a Campbell, Alasdair J  |e verfasserin  |4 aut 
700 1 |a Jelfs, Kim E  |e verfasserin  |4 aut 
700 1 |a Fuchter, Matthew J  |e verfasserin  |4 aut 
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773 1 8 |g volume:33  |g year:2021  |g number:1  |g day:26  |g month:01  |g pages:e2004115 
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