Volume 204, 2017

A new on-surface synthetic pathway to 5-armchair graphene nanoribbons on Cu(111) surfaces

Abstract

We report a new pathway to fabricate armchair graphene nanoribbons with five carbon atoms in the cross section (5-AGNRs) on Cu(111) surfaces. Instead of using haloaromatics as precursors, the 5-AGNRs are synthesized via a surface assisted decarboxylation reaction of perylene-3,4,9,10-tetracarboxylic dianhydride (PTCDA). The on-surface decarboxylation of PTCDA can produce extended copper–perylene chains on Cu(111) that are able to transform into graphene nanoribbons after annealing at higher temperatures (ca. 630 K). Due to the low yield (ca. 20%) of GNRs upon copper extrusion, various gases are introduced to assist the transformation of the copper–perylene chains into the GNRs. Typical reducing gases (H2 and CO) and oxidizing gas (O2) are evaluated for their performance in breaking aryl–Cu bonds. This method enriches on-surface protocols for the synthesis of AGNRs using non-halogen containing precursors.

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
11 Apr 2017
Accepted
10 May 2017
First published
22 May 2017

Faraday Discuss., 2017,204, 297-305

A new on-surface synthetic pathway to 5-armchair graphene nanoribbons on Cu(111) surfaces

K. Sun, P. Ji, H. Zhang, K. Niu, L. Li, A. Chen, Q. Li, K. Müllen and L. Chi, Faraday Discuss., 2017, 204, 297 DOI: 10.1039/C7FD00129K

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