AVS 57th International Symposium & Exhibition | |
Graphene Focus Topic | Monday Sessions |
Session GR+NS-MoA |
Session: | Graphene: Chemical Reactions |
Presenter: | N.C. Bartelt, Sandia National Laboratories |
Authors: | E. Starodub, Sandia National Laboratories N.C. Bartelt, Sandia National Laboratories K.F. McCarty, Sandia National Laboratories |
Correspondent: | Click to Email |
We have used low-energy electron microscopy to investigate how graphene is removed from Ru(0001) and Ir(111) by reaction with oxygen. We find two mechanisms on Ru(0001). At short times, oxygen reacts with carbon monomers on the surrounding Ru surface, decreasing their concentration below the equilibrium value. This undersaturation causes a flux of carbon from graphene to the monomer gas. In this initial mechanism, graphene is etched at a rate that is given precisely by the same nonlinear dependence on carbon monomer concentration that governs growth. Thus, during both growth and etching, carbon attaches and detaches to graphene as clusters of several carbon atoms. At later times, etching accelerates. We present evidence that this process involves intercalated oxygen, which destabilizes graphene. On Ir, this mechanism creates observable holes. It also occurs most quickly near wrinkles in the graphene islands, depends on the orientation of the graphene with respect to the Ir substrate, and, in contrast to the first mechanism, can increase the density of carbon monomers. We also observe that both layers of bilayer graphene islands on Ir etch together, not sequentially. Work at Sandia was supported by the Office of Basic Energy Sciences, Division of Materials Sciences, U. S. Department of Energy under Contract No. DE-AC04-94AL85000.