Chiral Materials: Fullerene Desymmetrization as a Means to Achieve Single‐Enantiomer Electron Acceptors with Maximized Chiroptical Responsiveness (Adv. Mater. 1/2021)
Source abstract
Abstract
Solubilized fullerene derivatives have revolutionized the development of organic photovoltaic devices, but the isomeric complexity that arises from addition of the solubilizing group is often ignored. In article number 2004115, Matthew J. Fuchter and co-workers separate 10 pairs of enantiomers from the 19 structural isomers of a common fullerene acceptor. They demonstrate the potential to discriminate circularly polarized light with a fast light-response time and with a very high photocurrent dissymmetry factor, enabled by a chiral fullerene.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Fullerene Chemistry and Applications
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Affiliations
Department of Chemistry and Molecular Sciences Research Hub Imperial College London White City Campus, 82 Wood Lane London W12 0BZ UK
Center for Processable Electronics Imperial College London South Kensington Campus London SW7 2AZ UK
Department of Physics Imperial College London South Kensington Campus London SW7 2AZ UK
School of Physics and Astronomy and Materials Research Institute Queen Mary University of London Mile End Road London E1 4NS UK
References
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