4.6 Article

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

期刊

APPLIED PHYSICS LETTERS
卷 121, 期 19, 页码 -

出版社

AIP Publishing
DOI: 10.1063/5.0122914

关键词

-

资金

  1. DFG under the Walter Benjamin Fellowship Programme [KL 3430/1-1]
  2. Analytical Science CDT at the University of Warwick
  3. UKRI Future Leaders Fellowship [MR/S016023/1]
  4. Royal Society University Research Fellowship
  5. Ben Breeze of the Spectroscopy Research Technology Platform, University of Warwick
  6. EPSRC [EP/V007688/1]

向作者/读者索取更多资源

This study demonstrates the formation of graphene through ultra-high vacuum deposition of polycyclic aromatic hydrocarbons azupyrene and pyrene on a Cu(111) surface at a temperature of 1000 K. Various characterization techniques, such as scanning tunneling microscopy, x-ray photoelectron spectroscopy, angle-resolved photoemission spectroscopy, Raman spectroscopy, and low energy electron diffraction, confirm the presence of graphene. The formation of the hexagonal graphene lattice differs for pyrene and azupyrene, with the latter requiring a rearrangement of its non-alternant topology. The thermal synthesis route to graphene in this study is performed at relatively low temperatures and under ultra-high vacuum conditions, enabling controlled investigations in a clean environment inaccessible with traditional precursors.
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. (C) 2022 Author(s).

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据