Quantum-mechanical simulation ofMgAl2O4under high pressure

Abstract

The equations of state and phase diagrams of the cubic spinel and two high-pressure polymorphs of ${\mathrm{MgAl}}_{2}{\mathrm{O}}_{4}$ have been investigated up to 65 GPa using density functional theory, the space-filling polyhedral partition of the unit cell, and the static approximation. Energy-volume curves have been obtained for the spinel phase, the recently observed calcium ferrite-type and calcium titanite-type phases, and the $\mathrm{MgO}+\ensuremath{\alpha}\ensuremath{-}{\mathrm{Al}}_{2}{\mathrm{O}}_{3}$ mixture. Zero-pressure unit lengths and compressibilities are well described by the theoretical model, that predicts static bulk moduli about 215 GPa for all the high-pressure forms. Computed equations of state are also in good agreement with the most recent experimental data for all compounds and polymorphs considered. We do not find a continuous pressure-induced phase sequence but the static simulations predict that the oxide mixture, the ferrite phase, and the titanite phase become more stable than the spinel form at 15, 35, and 62 GPa, respectively. A microscopic analysis in terms of polyhedral and bond compressibilities leads to identify the ionic displacements accompanying the phase transformations and to an appealing interpretation of the spinel response to compression.