Mapping of the full polarization switching pathways for HfO 2 and its implications

IF 9.1 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Proceedings of the National Academy of Sciences of the United States of America Pub Date : 2025-02-12 DOI:10.1073/pnas.2419685122
Qi Hu, Shuning Lv, Hsiaoyi Tsai, Yufeng Xue, Xixiang Jing, Fanrong Lin, Chuanjia Tong, Tengfei Cao, Gilberto Teobaldi, Li-Min Liu
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Abstract

The discovery of ferroelectric phases in HfO 2 offers insights into ferroelectricity. Its unique fluorite structure and complex polarization switching pathways exhibit distinct characteristics, challenging conventional analysis methods. Combining group theory and first-principles calculations, we identify numerous unconventional electric polarization switching pathways in HfO 2 with energy barriers of 0.32 to 0.57 eV as a function of the different shift in the suboxygen lattices. In total, we identify 47 switching pathways for the orthorhombic phase, corresponding to the left cosets of the F m 3 ¯ m group with P c a 2 1 group. Contrary to the conception that the tetracoordinated oxygen (O IV ) layers are inactive, our result demonstrates that both the tricoordinated oxygen (O III ) and O IV can be displaced, leading to polarization switching along any axial direction. The multiple switching pathways in HfO 2 result in both 180° polarization reversal and the formation of 90° domains observed experimentally. Calculations show that specific switching pathways depend on the orientation of the applied electric field relative to the HfO 2 growth surface. This allows HfO 2 to automatically adjust the in-plane polarization direction under an out-of-plane electric field, thereby maximizing the out-of-plane component and contributing to the wake-up process. These findings redefine the roles of O III and O IV layers, clarify unconventional switching pathways, and enhance our understanding of electric field response mechanisms, wake-up, and fatigue in ferroelectrics.
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HfO 2全极化开关路径的映射及其意义
铁电相的发现为研究铁电性提供了新的思路。其独特的萤石结构和复杂的极化开关路径表现出鲜明的特征,挑战了传统的分析方法。结合群论和第一线原理计算,我们在HfO 2中发现了许多非常规的电极化开关路径,其能量势垒在0.32至0.57 eV之间,是亚氧晶格不同位移的函数。总的来说,我们确定了47个正交相位的切换路径,对应于fm3¯m群与pca21群的左共集。与四配位氧(oiv)层不活跃的概念相反,我们的结果表明,三配位氧(oiii)和oiv层都可以移位,导致沿任何轴向的极化开关。实验观察到,HfO - 2中的多种开关途径导致了180°极化反转和90°畴的形成。计算表明,特定的开关路径取决于外加电场相对于HfO生长表面的取向。这使得HfO 2能够在面外电场下自动调整面内极化方向,从而最大化面外成分,有助于唤醒过程。这些发现重新定义了oiii和oiv层的作用,阐明了非常规的开关途径,并增强了我们对铁电体中电场响应机制、唤醒和疲劳的理解。
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来源期刊
CiteScore
19.00
自引率
0.90%
发文量
3575
审稿时长
2.5 months
期刊介绍: The Proceedings of the National Academy of Sciences (PNAS), a peer-reviewed journal of the National Academy of Sciences (NAS), serves as an authoritative source for high-impact, original research across the biological, physical, and social sciences. With a global scope, the journal welcomes submissions from researchers worldwide, making it an inclusive platform for advancing scientific knowledge.
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