We have recently shown that by using a scaling approach for randomly distributed topological defects in graphene, reliable estimates for transmission properties of macroscopic samples can be calculated based even on single-defect calculations [A. Uppstu et al., Phys. Rev. B 85, 041401 (2012)]. We now extend this approach of energy-dependent scattering cross sections to the case of adsorbates on graphene by studying hydrogen and carbon adatoms as well as epoxide and hydroxyl groups. We show that a qualitative understanding of resonant scattering can be gained through density functional theory results for a single-defect system, providing a transmission "fingerprint" characterizing each adsorbate type. This information can be used to reliably predict the elastic mean free path for moderate defect densities directly using ab-initio methods. We present tight-binding parameters for carbon and epoxide adsorbates, obtained to match the density-functional theory based scattering cross sections.
@article{arxiv.1211.7170,
title = {Ab-initio transport fingerprints for resonant scattering in graphene},
author = {Karri Saloriutta and Andreas Uppstu and Ari Harju and Martti J. Puska},
journal= {arXiv preprint arXiv:1211.7170},
year = {2012}
}