Ionic conductivity enhancement in Ti-doped Sr11Mo4O23 defective double perovskites

FERNÁNDEZ-DÍAZ, M.T.; LÓPEZ, C.A.; ALONSO, J.A.; PEDREGOSA, J.C.

RSC Advances

Royal Society of Chemistry

Año: 2017 vol. 7 p. 16163 - 16172

A substantially higher ionic motion can be achieved by partially replacing Mo(vi) by Ti(iv) cations in the novel Sr11Mo4−xTixO23−δ (with x = 0.0, 0.5 and 1.0) electrolyte oxides, successfully enhancing the oxygen vacancy level. These phases can be rewritten as Sr1.75□0.25(Sr)(Mo,Ti)O5.75−δ highlighting the relationship with conventional double perovskites. This original structure presents a broken corner sharing connectivity of the octahedral framework, hence leading to a complex and highly defective network. These materials have been prepared in polycrystalline form by thermal treatment up to 1300 °C. The structures were refined from X-ray and neutron powder diffraction data collected at room temperature and at 500 and 800 °C for x = 1. At high temperature this perovskite shows a phase transition to cubic symmetry and also evidences a reversible process of removal/uptake of O-atoms as observed in the undoped phase. AC-conductivity measurements from impedance spectroscopy confirm that Ti-doping increases the ionic mobility by 70%, attaining ionic conductivity values as high as 3.2 × 10−3 and 1.8 × 10−2 S cm−1 at 650 and 800 °C, respectively.