Large-scale growth of high-quality hexagonal boron nitride has been a challenge in two-dimensional-material-based electronics. Herein, we present wafer-scale and wrinkle-free epitaxial growth of multilayer hexagonal boron nitride on a sapphire substrate by using high-temperature and low-pressure chemical vapor deposition. Microscopic and spectroscopic investigations and theoretical calculations reveal that synthesized hexagonal boron nitride has a single rotational orientation with AA' stacking order. A facile method for transferring hexagonal boron nitride onto other target substrates was developed, which provides the opportunity for using hexagonal boron nitride as a substrate in practical electronic circuits. A graphene field effect transistor fabricated on our hexagonal boron nitride sheets shows clear quantum oscillation and highly improved carrier mobility because the ultraflatness of the hexagonal boron nitride surface can reduce the substrate-induced degradation of the carrier mobility of two-dimensional materials.
The process of oxidation
of a copper surface coated by a layer
of graphene in water-saturated air at 50 °C was studied where
it was observed that oxidation started at the graphene edge and was
complete after 24 h. Isotope labeling of the oxygen gas and water
showed that the oxygen in the formed copper oxides originated from
water and not from the oxygen in air for both Cu and graphene-coated
Cu, and this has interesting potential implications for graphene as
a protective coating for Cu in dry air conditions. We propose a reaction
pathway where surface hydroxyl groups formed at graphene edges and
defects induce the oxidation of Cu. DFT simulation shows that the
binding energy between graphene and the oxidized Cu substrate is smaller
than that for the bare Cu substrate, which facilitates delamination
of the graphene. Using this process, dry transfer is demonstrated
using poly(bisphenol A carbonate) (PC) as the support layer. The high
quality of the transferred graphene is demonstrated from Raman maps,
XPS, STM, TEM, and sheet resistance measurements. The copper foil
substrate was reused without substantial weight loss to grow graphene
(up to 3 cycles) of equal quality to the first growth after each cycle.
It was found that dry transfer yielded graphene with less Cu impurities
as compared to methods using etching of the Cu substrate. Using PC
yielded graphene with less polymeric residue after transfer than the
use of poly(methyl methacrylate) (PMMA) as the supporting layer. Hence,
this dry and clean delamination technique for CVD graphene grown on
copper substrates is highly advantageous for the cost-effective large-scale
production of graphene, where the Cu substrate can be reused after
each growth.
There have been many investigations to reveal the nature of the hydrogen gas and ZnO nanopowder interaction at elevated temperatures, while at present no conclusive description of such an interaction has been confidently reported. In this work, we demonstrate that a hydroxyl group is formed during this interaction, depending on size and relative crystallinity of nanopowders. Our in situ Raman spectroscopy investigations show that the interaction directly affects the intensity of the Raman signal at 483 cm(-1), relative to the peak at 519 cm(-1). Ex situ x-ray diffraction (XRD) and infrared spectroscopy also show extra peaks at 44° and 1618 cm(-1), respectively, after hydrogenation. These peaks were all identified as surface hydroxyl groups, which can be related to the formation of water on the ZnO nanopowder surfaces.
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