材料科学
矫顽力
铁电性
退火(玻璃)
电场
极化(电化学)
工程物理
光电子学
凝聚态物理
电介质
复合材料
工程类
化学
量子力学
物理
物理化学
作者
Jiachen Li,Weijin Pan,Zhengxu Zhu,Hansheng Zhu,Yuchen Wang,Shengchun Shen,Yuewei Yin,Xiaoguang Li
标识
DOI:10.1016/j.jmat.2025.101061
摘要
Hafnium oxide–based ferroelectric materials emerged as promising candidates for constructing next-generation high-density memory devices due to their silicon compatibility. However, the high coercive field ( E c , typically exceeding 1.0 MV/cm) puts forward challenges to high operating voltage and limited endurance performance. To overcome these limitations, a strategy is utilized by applying an in-situ direct current electric field during rapid thermal process (RTP). This approach enables simultaneous reduction of coercive field and enhancement of ferroelectric polarization in Hf 0.5 Zr 0.5 O 2 (HZO). Notably, a record-low E c (∼0.79 MV/cm) is achieved among atomic layer deposition-grown Zr-doped HfO 2 ferroelectric films , facilitating lower operation voltage, faster switching speed, and improved endurance characteristics. High-resolution transmission electron microscopy analysis reveals that the ferroelectric domains in samples through electric field assisted-RTP exhibit a relatively preferential out-of-plane orientation compared to normal RTP-treated samples, which is the underlying mechanism in reducing the coercive field and enhancing ferroelectric polarization. This study introduces a practical and effective method for optimizing the overall performance of HZO films, underscoring their potential for application in non-volatile memory technologies.
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