Stability of Single Metal Atoms on Defective and Doped Diamond Surfaces

Abstract

Polycrystalline boron-doped diamond (BDD) is widely used as a working electrode material in electrochemistry, and its properties, such as its stability, make it an appealing support material for nanostructures for electrocatalytic applications. Recent experiments have shown that electrodeposition can lead to the creation of stable small nanoclusters and even single metal adatoms on BDD surfaces. We investigate the adsorption energy and kinetic stability of single metal atoms adsorbed onto an atomistic model of BDD surfaces using density functional theory. The surface model is constructed using hybrid quantum/molecular mechanics embedding techniques and is based on an oxygen-terminated diamond (110) surface. We use the hybrid quantum mechanics/molecular mechanics method to assess the ability of different density-functional approximations to predict the adsorption structure, energy and the barrier for diffusion on pristine and defective surfaces. We find that surface defects (vacancies and surface dopants) strongly anchor metal adatoms on vacancy sites. We further investigate the thermal stability of metal adatoms, which reveals high barriers associated with lateral diffusion away from the vacancy site. The result provides an explanation for the high stability of experimentally imaged single metal adatoms on BDD and a starting point to investigate the early stages of nucleation during metal surface deposition.