Ionic conductivity in the hafnia-R 2O 3 systems

Abstract

The ionic conductivity of the hafnia-scandia, hafnia-yttria and hafnia-rare earth solid solutions with high dopant concentrations of 8, 10 and 14 m/o was measured in air at 600–1050°C. Impedance spectroscopy was used to obtain lattice conductivity. A majority of the investigated samples exhibited linear Arrhenius plots of the lattice conductivity as a function of temperature. For all investigated dopant concentrations the ionic conductivity was shown to decrease as the dopant radius increased. The activation enthalpy for conduction was found to increase with dopant ionic radius. The fact that the highest ionic conductivity among 14 m/o doped systems was obtained with HfO 2−Sc 2O 3 suggested that the radius ratio approach should be used to predi ct the electrical conductivity behavior of HfO 2−R 2O 3 systems. A qualitative model based on the Kilner's lattice parameter ma p does not seem to apply to these systems. For the three systems HfO 2−Yb 2O 3, HfO 2−Y 2O 3 and H fO 3−Sm 2O 3 a conductivity maximum was observed near the dopant concentration of 10 m/o. Deep vacancy trapping is responsible for the decrease in the ionic conductivity at high dopant concentrations. Formation of microdomains of an ordered phase cannot explain obtained results. A comparison between the ionic conductivities of doped HfO 2 and ZrO 2 systems indicated that the ionic conductivities of HfO 2-systems are 1.5–2.2 times lower than the ionic conductivities of ZrO 2 systems.