铁电性
材料科学
缩放比例
锆
铪
极化(电化学)
氧化物
纳米技术
光电子学
电介质
物理化学
几何学
数学
化学
冶金
作者
Hyangsook Lee,Duk‐Hyun Choe,Sanghyun Jo,Jung-Hwa Kim,Hyun Hwi Lee,Hyun‐Joon Shin,Yeehyun Park,Seunghun Kang,Yeonchoo Cho,Seontae Park,Taehwan Moon,Deokjoon Eom,Mirine Leem,Yunseok Kim,Jinseong Heo,Eunha Lee,Hyoungsub Kim
标识
DOI:10.1021/acsami.1c08718
摘要
HfO 2 -based ferroelectrics are highly expected to lead the new paradigm of nanoelectronic devices owing to their unexpected ability to enhance ferroelectricity in the ultimate thickness scaling limit (≤2 nm). However, an understanding of its physical origin remains uncertain because its direct microstructural and chemical characterization in such a thickness regime is extremely challenging. Herein, we solve the mystery for the continuous retention of high ferroelectricity in an ultrathin hafnium zirconium oxide (HZO) film (∼2 nm) by unveiling the evolution of microstructures and crystallographic orientations using a combination of state-of-the-art structural analysis techniques beyond analytical limits and theoretical approaches. We demonstrate that the enhancement of ferroelectricity in ultrathin HZO films originates from textured grains with a preferred orientation along an unusual out-of-plane direction of (112). In principle, (112)-oriented grains can exhibit 62% greater net polarization than the randomly oriented grains observed in thicker samples (>4 nm). Our first-principles calculations prove that the hydroxyl adsorption during the deposition process can significantly reduce the surface energy of (112)-oriented films, thereby stabilizing the high-index facet of (112). This work provides new insights into the ultimate scaling of HfO 2 -based ferroelectrics, which may facilitate the design of future extremely small-scale logic and memory devices.
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