铁电性
材料科学
正交晶系
兴奋剂
凝聚态物理
外延
极化(电化学)
结晶度
薄膜
光电子学
纳米技术
作者
Yu Yun,Pratyush Buragohain,Ming Li,Zahra Ahmadi,Yizhi Zhang,Xin Li,Haohan Wang,Jing Li,Ping Lu,Lingling Tao,Jijie Huang,Jeffrey E Shield,Evgeny Y. Tsymbal,Alexei Gruverman,Xiaoshan Xu
出处
期刊:Nature Materials
[Springer Nature]
日期:2022-06-27
卷期号:21 (8): 903-909
被引量:1
标识
DOI:10.1038/s41563-022-01282-6
摘要
Ferroelectric HfO2-based materials hold great potential for the widespread integration of ferroelectricity into modern electronics due to their compatibility with existing Si technology. Earlier work indicated that a nanometre grain size was crucial for the stabilization of the ferroelectric phase. This constraint, associated with a high density of structural defects, obscures an insight into the intrinsic ferroelectricity of HfO2-based materials. Here we demonstrate that stable and enhanced polarization can be achieved in epitaxial HfO2 films with a high degree of structural order (crystallinity). An out-of-plane polarization value of 50 μC cm–2 has been observed at room temperature in Y-doped HfO2(111) epitaxial thin films, with an estimated full value of intrinsic polarization of 64 μC cm–2, which is in close agreement with density functional theory calculations. The crystal structure of films reveals the Pca21 orthorhombic phase with small rhombohedral distortion, underlining the role of the structural constraint in stabilizing the ferroelectric phase. Our results suggest that it could be possible to exploit the intrinsic ferroelectricity of HfO2-based materials, optimizing their performance in device applications.
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