COMPUTER-SIMULATION OF THE OXYGEN MOBILITY IN CAMNO3-X

The perovskite-type metal oxide CaMnO3-x is known to accommodate subst antial amounts of oxygen vacancies. High-resolution electron microscop e investigations give evidence for ordering of the vacancies, i.e. wel l-defined structures in the compositional range of CaMnO2.5 < CaMnO3-x < CaMnO3. Within this range the metal cation positions do not change, i.e. perovskitic framework is conserved while a remarkably high oxyge n anion mobility is recorded. In addition, the electronic and magnetic structure, and thus the physical properties, depend directly on the o xygen stoichiometry. This contribution focusses on the oxygen mobility in different CaMnO3-x phases exhibiting oxygen vacancy ordered struct ures, i.e. CaMnO3.0, CaMnO2.80, CaMnO2.75, CaMnO2.66, CaMnO2.55 and Ca MnO2.50. In these compounds the formal oxidation state of manganese ch anges from Mn4+ (x=0) to Mn3+ (x=0.5). For the computer simulation of the defect structure and for the mobility of the oxygen anions within these defect structures we applied the method of interatomic potential s in a simple rigid-ion approximation. The parameters of interaction w ere calibrated on the basis of empirical data, i.e. equilibrium geomet ry and cohesive energies of the binary oxides CaO, MnO2 and Mn2O3 were taken into account for the present calculations. Stabilities, oxygen migration barriers and dielectric constants of selected representants of CaMnO3-x are presented.