Computational predictions of electronic properties of graphene with defects, adsorbed transition metal-oxides and water using density functional theory

摘要

The interfacial interactions between transition metal oxides (vanadium oxide VO2, vanadium pentoxide V2O5, cobalt oxide CoO and Co3O4, manganese oxide MnO2) and water adsorbates on graphene supports as solvated interfaces and influence of defects in graphene are studied using periodic density functional theory (DFT) calculations in view of their significance for applied electrochemistry. DFT complemented and synergized our experimental work. The optimized metal oxide adatom-graphene geometries identified the preferred adatom sites, whereas metal oxide-graphene strengths are correlated with the adatom distance from the graphene plane, the Metal-C overlap populations, and the adsorption energies. The presence of finite electronic density of states (DOS) near Fermi level and charge transfers between the adatom top layer and graphene supports reflect primarily covalent bonding nature. The presence of small orbital overlap integral of bonds between the s and p (and d) orbitals of the nearest carbon (graphene), carbon oxide (graphene oxide) and metal oxide atoms reveal localized orbital re-hybridization resulting in changes in DOS yielding high electrochemical activity. Moreover, for increased adatom coverage the extent of charge transfer reverses resulting in limited electroactivity. In fact, DFT calculations are corroborated with experimental findings, where graphene-based supports decorated with optimal mass loaded nanostructured Co3O4 and MnO2 (as well as V2O5) were capable of delivering maximum specific energy storage capacity (Cs) 550 F.g(-1) (Gupta et al. J. Mater. Res. 32, 301 (2017)) in contrast to higher or lower loading. The presence of defects in graphene materials results in new electronic states to endow unique functionalities that is not otherwise possible in the bulk and with adsorbed water molecules besides optimum C/O ratio in graphene oxide nanosheets that show redshift thus a decreasing bandgap and finite charge transfer from graphene to water molecules. The case examples studied in this work represent a first glimpse of what may become routine and integral step in materials design and discovery for alternative energy and sustainable environmental technologies.