Park Kunwoo, Kim Dongmin, Lee Kyoungjun, Lee Hyun-Jae, Kim Jihoon, Kang Sungsu, Lin Alex, Pattison Alexander J, Theis Wolfgang, Kim Chang Hoon, Choi Hyesung, Cho Jung Woo, Ercius Peter, Lee Jun Hee, Chae Seung Chul, Park Jungwon
Center for Nanoparticle Research, Institute for Basic Science (IBS), Seoul 08826, Republic of Korea.
School of Chemical and Biological Engineering, Institute of Chemical Process, Seoul National University, Seoul 08826, Republic of Korea.
ACS Nano. 2024 Sep 12. doi: 10.1021/acsnano.4c08721.
Ferroelectric HfO-based thin films have attracted much interest in the utilization of ferroelectricity at the nanoscale for next-generation electronic devices. However, the structural origin and stabilization mechanism of the ferroelectric phase are not understood because the film is typically nanocrystalline with active yet stochastic ferroelectric domains. Here, electron microscopy is used to map the in-plane domain network structures of epitaxially grown ferroelectric Y:HfO films in atomic resolution. The ferroelectricity is confirmed in free-standing Y:HfO films, allowing for investigating the structural origin for their ferroelectricity by 4D-STEM, high-resolution STEM, and iDPC-STEM. At the grain boundaries of <111>-oriented Pca2 orthorhombic grains, a high-symmetry mixed-(3, Pnm2) phase is induced, exhibiting enhanced polarization due to in-plane compressive strain. Nanoscale Pca2 orthorhombic grains and their grain boundaries with mixed-(3, Pnm2) phases of higher symmetry cooperatively determine the ferroelectricity of the Y:HfO film. It is also found that such ferroelectric domain networks emerge when the film thickness is beyond a finite value. Furthermore, in-plane mapping of oxygen positions overlaid on ferroelectric domains discloses that polarization is suppressed at vertical domain walls, while it is active when domains are aligned horizontally with subangstrom domain walls. In addition, randomly distributed 180° charged domain walls are confined by spacer layers.
铁电铪基薄膜在下一代电子器件的纳米级铁电应用中引起了广泛关注。然而,由于该薄膜通常是具有活跃但随机铁电畴的纳米晶体,铁电相的结构起源和稳定机制尚不清楚。在此,利用电子显微镜以原子分辨率绘制外延生长的铁电Y:HfO薄膜的面内畴网络结构。在独立的Y:HfO薄膜中证实了铁电性,从而可以通过4D-STEM、高分辨率STEM和iDPC-STEM研究其铁电性的结构起源。在<111>取向的Pca2正交晶系晶粒的晶界处,诱导出一种高对称混合-(3, Pnm2)相,由于面内压缩应变而表现出增强的极化。纳米级的Pca2正交晶系晶粒及其具有更高对称性的混合-(3, Pnm2)相的晶界共同决定了Y:HfO薄膜的铁电性。还发现当薄膜厚度超过一个有限值时会出现这种铁电畴网络。此外,覆盖在铁电畴上的氧位置的面内映射表明,极化在垂直畴壁处受到抑制,而当畴与亚埃级畴壁水平排列时极化是活跃的。此外,随机分布的180°带电畴壁被间隔层限制。