Pressure-DrivenPolar Orthorhombic to Tetragonal PhaseTransition in Hafnia at Room Temperature

Oxides are legendary for their complex energy landscapes, sensitivity to external stimuli, and property control through chemical substitution. Of these, the binary oxide HfO₂ is one of the most fascinating because of the extraordinary number competing phases and opportunities to stabilize unique and useful properties. In this work, we combined synchrotron-based infrared absorbance and Raman scattering spectroscopies with diamond anvil cell techniques and first-principles calculations to explore the properties of polar orthorhombic hafnia (chemical formula HfO₂:<i>x</i>Y, where <i>x</i> = 12%) under pressure. Compression drives this system to the tetragonal form above 22 GPaquite different from the more conventional phase diagram derived from pressurization of monoclinic HfO₂ where the tetragonal phase resides at elevated temperatures. In addition to evidence for a complex energy landscape, we unveil a wide coexistence region, order-of-magnitude differences in phonon lifetimes, and an <i>A</i>_1<i>g</i> symmetry phonon in the tetragonal phase with a negative mode Grüneisen parameter that drives the system toward the cubic phase. Similar pressure pathways may connect other metastable phases in this family of materials.