High-temperature heat capacity and thermal expansion ofSrTiO3andSrZrO3perovskites

Abstract
The heat capacity and thermal expansion of SrZrO3 and SrTiO3 have been determined by drop calorimetry and energy-dispersive x-ray diffraction from 300 up to 1800 K or more. For both compounds, thermal history has a slight influence on relative enthalpies in the range 900–1400 K but a satisfactory precision was obtained through systematic quenches from 1820 K before the calorimetric measurements. Strontium titanate is cubic at room temperature. Up to 1800 K, its heat capacity increases smoothly and its thermal-expansion coefficient remains almost independent of temperature with a value of 3.23(2) 105 K1. At room temperature, strontium zirconate is orthorhombic (space group Pbnm). The phase transitions from orthorhombic Pbnm to orthorhombic Cmcm at 995 K and then to tetragonal I4/mcm at 1105 K are revealed by symmetric, λ-type variations of the heat capacity. A more diffuse thermal effect characterizes the I4/mcm to cubic Pm3m transition at 1440 K, above which the cubic phase shows an apparently low heat capacity at the highest temperatures. With the resolution of the x-ray technique, only the transition from orthorhombic Pbnm to orthorhombic Cmcm at 970 K was detected with a small volume change of 0.14%. Thermal expansion below 970 K is constant at 2.98(2) 105 K1. At higher temperatures, the apparent thermal expansion decreases smoothly from 2.78(2) to 2.43(2) 105 K1 between 1000 and 1800 K. With recent data on CaTiO3, the effects of (Ca,Sr) and (Ti,Zr) substitutions on thermal expansion and on the energetics of the phase transitions are discussed. © 1996 The American Physical Society.

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