Structural phase transition, equation of state and phase diagram of functional rare earth sesquioxide ceramics (Eu1−xLax)2O3
Autor: | S. Kalavathi, N. V. Chandra Shekar, K.A. Irshad, Velaga Srihari |
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Rok vydání: | 2020 |
Předmět: |
Materials science
Chemical physics lcsh:Medicine 02 engineering and technology Crystal structure 010402 general chemistry 01 natural sciences Article Sesquioxide Phase (matter) Structure of solids and liquids lcsh:Science Phase diagram Bulk modulus Multidisciplinary Rietveld refinement lcsh:R Hexagonal phase 021001 nanoscience & nanotechnology 0104 chemical sciences Crystallography Phase transitions and critical phenomena Thermodynamics lcsh:Q 0210 nano-technology Monoclinic crystal system |
Zdroj: | Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020) Scientific Reports |
ISSN: | 2045-2322 |
Popis: | The intriguing functional nature of ceramics containing rare earth sesquioxide (RES) is associated with the type of polymorphic structure they crystallize into. They prefer to be in the cubic, monoclinic or hexagonal structure in the increasing order of cation size, RRE. Since the functional properties of these ceramics varies with RRE, temperature and pressure, a systematic investigation delineating the cation size effect is indispensable. In the present work we report the structural stability and compressibility behaviour of the RES ceramics, (Eu1−xLax)2O3, of RESs with dissimilar structure and significant difference in cationic radii. The selected compositions of (Eu1−xLax)2O3 have been studied using the in-situ high pressure synchrotron X-ray diffraction and the structural parameters obtained through Rietveld refinement. The cubic structure, which is stable for 0.95 Å $$\le$$≤ RRE$$<0.98 Å at ambient temperature and pressure (ATP), prefers a cubic to hexagonal transition at high pressures. The biphasic region of cubic and monoclinic structure, which is stable for 0.98 Å $$\le$$≤ RRE$$<1.025 Å at ATP, prefers a cubic/monoclinic to hexagonal transition at high pressures. Further, in the biphasic region of monoclinic and hexagonal structure, observed for 1.025 Å $$\le$$≤RRE$$<1.055 Å, the monoclinic phase is found to be progressing towards the hexagonal phase with increasing pressure. The pure hexagonal phase obtained for 1.055 Å $$\le$$≤ RRE$$\le$$≤ 1.10 Å is found to be structurally stable at high pressures. The bulk moduli are obtained from the Birch–Murnaghan equation of state fit to the compressibility data and its dependance on the cation size is discussed. The microstrain induced by the difference in cation size causes an internal pressure in the crystal structure leading to a reduction in the bulk modulus of $$\textit{x}=0.2$$x=0.2 and 0.6. A pressure–concentration (P–x) phase diagram upto a pressure of 25 GPa is constructed for (Eu1−xLax)2O3. This would provide an insight to the fundamental and technological aspects of these materials and the RESs in general. |
Databáze: | OpenAIRE |
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