Oxygen-promoted synthesis of armchair graphene nanoribbons on Cu(111)

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On-surface synthesis has received great attention as a method to create atomically-precise one-dimensional (1D) and two-dimensional (2D) polymers with intriguing properties. In particular, graphene nanoribbons (GNRs), a category of quasi-1D nanomaterials derived from graphene, have been widely studied due to their tunable electronic properties and potential applications in semiconductor devices, such as field-effect transistors and spintronics. A series of top-down approaches have been pursued to produce GNRs, but a lack of control over the ribbon width and edge structure has hindered their further development.

In 2010, Cai et al. firstly reported the fabrication of an atomically-precise armchair GNR (AGNR) on the Au(111) surface using a bottom-up approach. The basic mechanism involves thermally-activated dehalogenation, surface-assisted polymerization and finally cyclodehydrogenation.

In the following decade, this bottom-up approach has been extended to synthesize a wide variety of GNRs, including AGNRs with different widths, zigzag GNRs, GNR heterojunctions, chiral GNRs and chemically- doped GNRs. Based on the periodic similarity of their electronic structures, AGNRs can be classified into three families, 3p, 3p+1 and 3p+2 (representing the number of carbon atoms in the narrow direction).

So far, few studies have focused on GNR on Cu(111) due to the stronger surface interaction, despite the lower temperature for dehalogenation. It has been shown that chiral GNRs can be synthesized on Cu(111) using the same precursor which yields non-chiral 7-AGNR on Au(111) and that dehalogenation can be reversible on Au(111) but not Cu(111), which implies that the reaction pathway and products achieved could be controlled through the choice of substrate.

Oxygen-promoted synthesis of armchair graphene nanoribbons on Cu(111)
Scanning tunneling microscopy images of the synthesis of 3P sub-family armchair graphene nanoribbons through the lateral fusion of 3-AGNR on Cu(111). The introduction of O2 can reduce the temperature of the reaction by 180 K. Credit: Science China Press

A second approach to tailor the in surface-confined synthesis is to introduce different atomic species, which has been considered in only a few recent studies. Exposure to iodine creates a monolayer intercalated between the polymers and the Ag(111) surface that decouples their electronic interactions. In addition, hydrogen was shown to remove halogen by-products and to induce covalent coupling, and sulfur to switch the surface-confined Ullmann reaction on or off.

Prof. Lifeng Chi's research group in Soochow University recently investigated the effect of oxygen on the synthesis of 3-AGNRs by surface-confined Ullmann coupling and determined that it, instead, caused a 1D to 2D transformation of the organometallic (OM) structures.

Here, their objective was to investigate the synthesis of 3p-AGNRs on Cu(111), extending from the previous study on Au(111), and to examine the effect of oxygen on lateral fusion of 3-AGNRs, inspired by their potential to promote C-H activation.

Their investigation demonstrated the successful synthesis of 3p-AGNRs on Cu(111) via lateral fusion of poly(para-phenylene) (i.e. 3-AGNR). Introduction of co-adsorbed atomic oxygen substantially reduced the temperature required to induce the lateral fusion reaction. The identification of this catalytic effect could benefit on-surface synthesis that applies dehydrogenation reactions, not restricting to GNRs, and highlights the potential of additional atomic adsorbates to steer surface reactions.

More information: Penghui Ji et al, Oxygen-promoted synthesis of armchair graphene nanoribbons on Cu(111), Science China Chemistry (2021). DOI: 10.1007/s11426-021-9966-x

Citation: Oxygen-promoted synthesis of armchair graphene nanoribbons on Cu(111) (2021, April 2) retrieved 18 July 2024 from https://phys.org/news/2021-04-oxygen-promoted-synthesis-armchair-graphene-nanoribbons.html
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