Issue 31, 2020

Azobenzene-functionalized graphene nanoribbons: bottom-up synthesis, photoisomerization behaviour and self-assembled structures

Abstract

Azobenzene-functionalized graphene nanoribbons (GNRs) were synthesized through acid promoted alkyne benzannulation. The resulting GNRs showed high dispersibility in common organic solvents (up to 100 mg mL−1 in chlorobenzene) and underwent fast photoisomerization. A photostationary state was established in solution upon 365 nm light irradiation for 20 s and subsequently the initial state could be easily restored upon 500 nm light irradiation for 40 s. Photo-responsive GNR thin films were also prepared by spin coating. Moreover, the azobenzene-functionalized GNRs could self-assemble into nanowires with lengths ranging from several to tens of micrometers. This study opens an avenue for the functionalization of GNRs with stimuli-responsive functional groups, which holds great promise for applications in optoelectronic devices.

Graphical abstract: Azobenzene-functionalized graphene nanoribbons: bottom-up synthesis, photoisomerization behaviour and self-assembled structures

Supplementary files

Article information

Article type
Paper
Submitted
30 3月 2020
Accepted
27 4月 2020
First published
27 4月 2020

J. Mater. Chem. C, 2020,8, 10837-10843

Azobenzene-functionalized graphene nanoribbons: bottom-up synthesis, photoisomerization behaviour and self-assembled structures

Z. Shangguan, C. Yu, C. Li, X. Huang, Y. Mai and T. Li, J. Mater. Chem. C, 2020, 8, 10837 DOI: 10.1039/D0TC01609H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements