We present a route to non-destructive functionalization of graphene via assembly of vertical all-carbon van der Waals heterostructures. To this end, we employ singlelayer graphene (SLG) sheets grown by low-pressure methane CVD on Cu foils and large-a
rea dielectric ~1 nm thick amino-terminated carbon nanomembranes (NH2-CNMs) generated by electron-beam-induced crosslinking of aromatic self-assembled monolayers. We encapsulate SLG sheets on oxidized silicon wafers with NH2-CNMs via mechanical stacking and characterize structural, chemical and electronic properties of the formed heterostructures by Raman spectroscopy and X-ray photoelectron spectroscopy as well as by electric and electromagnetic transport measurements. We show that functional amino groups are brought in close vicinity of the SLG sheets and that their transport characteristics are not impaired by this functionalization; moreover, we demonstrate a functional response of the heterostructure devices to the protonation of the amino groups in water. Due to its relative simplicity, the suggested approach opens broad avenues for implementations in graphene-based electronic devices where non-destructive chemical functionalization of graphene is required (e.g., for engineering electrical transducers for chemical and bio-sensing) or as complementary dielectric to graphene in hieratical heterostructures.
We demonstrate how self-assembled monolayers of aromatic molecules on copper substrates can be converted into high-quality single-layer graphene using low-energy electron irradiation and subsequent annealing. We characterize this two-dimensional soli
d state transformation on the atomic scale and study the physical and chemical properties of the formed graphene sheets by complementary microscopic and spectroscopic techniques and by electrical transport measurements. As substrates we successfully use Cu(111) single crystals and the technologically relevant polycrystalline copper foils.
