The metal-insulator transition (MIT) of V6O11 is studied by means of electronic structure calculations using the augmented spherical wave method. The calculations are based on density functional theory and the local density approximation. Changes of the electronic structure at the MIT are discussed in relation to the structural transformations occurring simultaneously. The analysis is based on a unified point of view of the crystal structures of V6O11, VO2, and V2O3. This allows to group the electronic bands into states behaving similarly to the dioxide or the sesquioxide. While the sesquioxide-like V 3dyz states show rather weak changes on entering the low-temperature structure, some of the dioxide-like V 3dx2-y2 states display splittings and shifts similar to those known from VO2. The MIT of V6O11 arises as a combination of changes appearing in both of these compounds. Our results shed new light onto the role of particular electronic states for the MIT of V2O3.
ASJC Scopus subject areas
- General Physics and Astronomy