Theoretical study of the influence of cation vacancies on catalytic properties of vanadium antimonate

S. MESSINA; A, JUAN; S. LARRONDO; BEARIZ IRIGOYEN; N. AMADEO

APPLIED SURFACE SCIENCE

ELSEVIER SCIENCE BV

Lugar: Amsterdam; Año: 2008 vol. 254 p. 5837 - 5843

0169-4332

We have theoretical studied the influence of antimony and vanadium cation vacancies in the electronic structure and reactivity of vanadium antimonate, using molecular orbital methods. from tha analysys of the electronic properties of the VSbO4 crystal structure, we can infer that both antimony and vanadium vacancies increase te oxidation  state of closer V cations. this would indicate that , in the rutile type VSbO4 phase the Sv and V cations defects stabilize the V in a higher oxidation state (V4+) . Calculations of the adsorption energy for different toluene adsorption geometries on the VSbO4 (110) surface have also been performed. The oxidation state of Sb, V and O atoms and the overlap population  of metal -oxygen bonds hae been evaluated . Our results indicate that the cation defects influence in the toluene adsorption reactions is slight. We have computed different alternatives for the reoxidation of the VSbO4 (110) surface active sites which were computed during the oxygenated products formation. these calculations indicate that the V cations in the higher oxidation state (V4+) are the species , which preferentially incorporate lattice oxygen to the reduced Sb cations. thus, the cation defects would stabilize the V4+ species in the VSbO4 stucture, determining to provide lattice oxygen as a reactant.