Orientation-dependent binding energy of graphene on palladium
Branden Kappes (), Abbas Ebnonnasir (), Suneel Kodambaka (), Cristian Ciobanu (Colorado School of Mines)
Synthesis, Characterization, and Modeling of Low-Dimensional Nanomaterials
Tue 9:00 - 10:30
Salomon 202
Using density functional theory calculations, we show that the binding strength of a graphene monolayer on Pd(111) can vary between physisorption and chemisorption depending on its orientation. By studying the interfacial charge transfer, we have identified a specific four-atom carbon cluster that is responsible for the local bonding of graphene to Pd(111). The areal density of such clusters varies with the in-plane orientation of graphene, causing the binding energy to change accordingly. Similar investigations can also apply to other metal substrates and suggests that physical, chemical, and mechanical properties of graphene may be controlled by changing its orientation.