Chromium/Vanadium Mixed Oxide Films on Pt(111): Revealing Oxide Alloying Mechanisms in Two Dimensions.

The mixing characteristics of oxide materials largely depend on the dimensionality of the system, and many oxide-alloy structures in three dimensions (3D) do not have a 2D analog. To unravel fundamental alloying mechanisms in 2D, V/Cr mixing into oxide thin films is investigated on Pt(111) by scanning tunneling microscopy and density functional theory. The experiments reveal flat, double-stack islands made of a compact bottom and a honeycomb top layer with a 4.

Atomic Scale Insights into Reversible Oxygen Storage in Vanadium Oxide Thin Films.

Monolayer vanadium oxide films grown on Pt(111) can be reversibly switched between an oxygen-poor and an oxygen-rich composition, equivalent to VO and VO, respectively. While the overall oxygen storage capacity of the film is quantified by X-ray photoelectron spectroscopy, the atomic binding sites of the extra O species are determined by low-temperature scanning tunneling microscopy and electron diffraction. In the O-poor phase, the oxide takes the form of a honeycomb lattice that gets partially covered with vanadyl (V=O) groups at higher O exposure.

Electron stimulated desorption of vanadyl-groups from vanadium oxide thin films on Ru(0001) probed with STM.

Low-temperature scanning tunnelling microscopy (STM) is employed to study electron-stimulated desorption of vanadyl groups from an ultrathin vanadium oxide film. The vanadia patches are prepared by reactive vapour deposition of V onto a Ru(0001) surface and comprise a highly ordered network of six and twelve membered V-O rings, some of them terminated by upright V[double bond, length as m-dash]O groups. The vanadyl units can be desorbed via electron injection from the STM tip in a reliable fashion.