Reactive intercalation and oxidation at the buried graphene-germanium interface
Author(s) -
Philipp BraeuningerWeimer,
Oliver J. Burton,
Robert S. Weatherup,
Ruizhi Wang,
Pavel Dudin,
Barry Brennan,
Andrew J. Pollard,
Bernhard C. Bayer,
Vlad P. Veigang-Radulescu,
Jannik C. Meyer,
Billy J. Murdoch,
Peter J. Cumpson,
Stephan Hofmann
Publication year - 2019
Publication title -
apl materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.571
H-Index - 60
ISSN - 2166-532X
DOI - 10.1063/1.5098351
Subject(s) - graphene , materials science , raman spectroscopy , intercalation (chemistry) , passivation , oxide , monolayer , germanium , graphene oxide paper , secondary ion mass spectrometry , chemical vapor deposition , electrochemistry , inorganic chemistry , chemical engineering , analytical chemistry (journal) , layer (electronics) , nanotechnology , ion , electrode , optoelectronics , silicon , chemistry , organic chemistry , optics , physics , engineering , metallurgy
We explore a number of different electrochemical, wet chemical, and gas phase approaches to study intercalation and oxidation at the buried graphene-Ge interface. While the previous literature focused on the passivation of the Ge surface by chemical vapor deposited graphene, we show that particularly via electrochemical intercalation in a 0.25 N solution of anhydrous sodium acetate in glacial acetic acid, this passivation can be overcome to grow GeO2 under graphene. Angle resolved photoemission spectroscopy, Raman spectroscopy, He ion microscopy, and time-of-flight secondary ion mass spectrometry show that the monolayer graphene remains undamaged and its intrinsic strain is released by the interface oxidation. Graphene acts as a protection layer for the as-grown Ge oxide, and we discuss how these insights can be utilized for new processing approaches.
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