First-principles Structural and Electronic Characterization of Ordered SiO2 Nanowires

Abstract

Density functional theory and molecular dynamics simulations have been used to optimize the structure of nanowires of SiO2. The starting structures were based on b-cristobalite, orthotridymite, b-tridymite, and rutile crystals. The analysis of the electronic structure has been validated by many-body perturbation calculations using the G0W0 and GW + Bethe-Salpeter equation approximations, in order to account for quasi-particle and excitonic effects. The calculations indicate that many of these nanowires have semiconducting character, while the corresponding bulk solids are insulators. In the case of thick rutile-like nanowires we found the gap congested with surface states. Electronic charge is transferred from silicon atoms to oxygen atoms, and the bonding in the nanowires is partly ionic and partly covalent. The magnitude of the band gap can be engineered by changing the structure and the thickness of the nanowires.