Using polycyclic aromatic hydrocarbons for graphene growth on Cu(111) under ultra-high vacuum

Author:

Klein Benedikt P.12ORCID,Stoodley Matthew A.12ORCID,Edmondson Matthew3ORCID,Rochford Luke A.1,Walker Marc4ORCID,Sattler Lars5,Weber Sebastian M.5,Hilt Gerhard5ORCID,Williams Leon B. S.167ORCID,Lee Tien-Lin1,Saywell Alex3ORCID,Maurer Reinhard J.2ORCID,Duncan David A.1ORCID

Affiliation:

1. Diamond Light Source, Harwell Science and Innovation Campus, Didcot OX11 0DE, United Kingdom

2. Department of Chemistry, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, United Kingdom

3. School of Physics and Astronomy, University of Nottingham, University Park, Nottingham NG7 2RD, United Kingdom

4. Department of Physics, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, United Kingdom

5. Institut für Chemie, Carl von Ossietzky Universität Oldenburg, Carl-von-Ossietzky-Straße 9-11, 26111 Oldenburg, Germany

6. School of Chemistry, University of Glasgow, University Avenue, Glasgow G12 8QQ, United Kingdom

7. School of Physics and Astronomy, University of Glasgow, University Avenue, Glasgow G12 8QQ, United Kingdom

Abstract

Ultra-high vacuum deposition of the polycyclic aromatic hydrocarbons azupyrene and pyrene onto a Cu(111) surface held at a temperature of 1000 K is herein shown to result in the formation of graphene. The presence of graphene was proven using scanning tunneling microscopy, x-ray photoelectron spectroscopy, angle-resolved photoemission spectroscopy, Raman spectroscopy, and low energy electron diffraction. The precursors, azupyrene and pyrene, are comparatively large aromatic molecules in contrast to more commonly employed precursors like methane or ethylene. While the formation of the hexagonal graphene lattice could naively be expected when pyrene is used as a precursor, the situation is more complex for azupyrene. In this case, the non-alternant topology of azupyrene with only 5- and 7-membered rings must be altered to form the observed hexagonal graphene lattice. Such a rearrangement, converting a non-alternant topology into an alternant one, is in line with previous reports describing similar topological alterations, including the isomerization of molecular azupyrene to pyrene. The thermal synthesis route to graphene, presented here, is achievable at comparatively low temperatures and under ultra-high vacuum conditions, which may enable further investigations of the growth process in a strictly controlled and clean environment that is not accessible with traditional precursors.

Funder

Deutsche Forschungsgemeinschaft

UK Research and Innovation

Diamond Light Source

Royal Society

University of Warwick

University of Warwick, Warwick Analytical Science Centre

Publisher

AIP Publishing

Subject

Physics and Astronomy (miscellaneous)

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