铁电性
材料科学
四方晶系
凝聚态物理
哈夫尼亚
外延
密度泛函理论
纳米技术
结晶学
光电子学
计算化学
化学
复合材料
晶体结构
物理
电介质
图层(电子)
陶瓷
立方氧化锆
作者
Aldo Raeliarijaona,Ronald C. Cohen
标识
DOI:10.48550/arxiv.2108.09884
摘要
Ferroelectric hafnia is being explored for next generation electronics due to its robust ferroelectricity in nanoscale samples and its compatibility with silicon. However, its ferroelectricity is not understood. Other ferroelectrics usually lose their ferroelectricity for nanoscopic samples and thin films, and the hafnia ground state is non-polar baddeleyite. Here we study hafnia with density functional theory (DFT) under epitaxial strain, and find that strain not only stabilizes the ferroelectric phases, but also leads to unstable modes and a downhill path in energy from the high temperature tetragonal structure. We find that for tensile epitaxial strains corresponding to a square substrate of lattice constant $a_{epi} \geqslant 5.38$ \AA~the ferroelectric \oI is most stable, even more stable than baddeleyite. Furthermore, we find that under tensile epitaxial strain $\eta$ the tetragonal phase will distort to one of the two ferroelectric phases: for $\eta > 1.5$\%, the $\Gamma^{-}_{5}$ mode is unstable and leads to \oII , and at $\eta > 3.75$\% coupling between this mode and the zone boundary M1 mode leads to \oI.
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