材料科学
正交晶系
四方晶系
铁电性
单斜晶系
凝聚态物理
掺杂剂
结晶学
密度泛函理论
电介质
原子单位
晶体结构
兴奋剂
化学
计算化学
光电子学
量子力学
物理
作者
Yao Lulu,Sambit Das,Xin Liu,Kai Wu,Yonghong Cheng,Vikram Gavini,Bing Xiao
标识
DOI:10.1088/1361-6463/ac8f55
摘要
Abstract Combining the experimental characterization with the large-scale density functional theory calculations based on finite-element discretization (DFT-FE), we address the stabilization of polar orthorhombic phases (o-HfO 2 ) in Al:HfO 2 nanofilms by means of the atomic registry distortions and lattice deformation caused by Al substitutional defects (Al Hf ) and Schottky defects (2Al Hf + V O ) in tetragonal phases (t-HfO 2 ) or monoclinic phases (m-HfO 2 ). The phase transformation directly from the t-HfO 2 into polar o-HfO 2 are also elucidated within a heterogeneous distribution of Al dopants in both t-HfO 2 bulk crystal structure and Al:HfO 2 nanofilm. It is revealed using large-scale DFT calculations that the Al substitutional defects (Al Hf ) or the Schottky defect (2Al Hf + V O ) could induce the highly extended atomic registry distortions or lattice deformation in the t- and m-HfO 2 phases, but such effects are greatly diminished in ferroelectric orthorhombic phase. By purposely engineering the multiple Al Hf defects to form dopant-rich layers in paraelectric t-HfO 2 nanofilm or bulk crystal, the induced extended lattice distortions surrounding the defect sites exhibit the shearing-like atomic displacement vector field. The large-scale DFT calculations further predicted that the shearing-like microscopic lattice distortions could directly induce the phase transformation from the t-HfO 2 into polar orthorhombic phase in both Al:HfO 2 bulk crystal and nanofilms, leading to the large remanent polarization observed in Al:HfO 2 nanofilms with the presence of Al-rich layers. The current study demonstrates that the ferroelectricity of HfO 2 bulk crystal or thin film can be optimized and tuned by delicately engineering both the distribution and concentration of Al dopants in atomic layer deposition without applying the top capping electrode, providing the extra flexibility for designing the HfO 2 based electronic devices in the future.
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