在面向 (110) 的 PMN-PT 基质上生长的铁电性 SrMnO3 薄膜

Seong Min Park, Jaegyu Kim, G. Anoop, W. Seol, Su Yong Lee, Hyunjin Joh, Tae Yeon Kim, Jeonyong Choi, Seungbum Hong, Chan‐Ho Yang, Hyeon Jun Lee, J. Jo
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摘要

要探索氧化物包晶的独特物理性质,就必须在不同的单晶基底上生长它们。由于包晶 SrMnO3(SMO)具有新兴的室温多铁性,因此其薄膜生长一直是研究的重点。本文在压电(110)取向(1-x)Pb(Mg1/3Nb2/3)O3-xPbTiO3(PMN-PT)基底上生长了取向(110)的 SMO 外延薄膜。系统研究了厚度和氧退火对 SMO 薄膜晶体结构、化学计量学和铁电特性的影响。大块 SMO 和 PMN-PT 衬底之间的晶格失配产生的拉伸应变导致 c-晶格平行于衬底面内方向膨胀。薄膜的 a、b 和 c-晶格参数大于块体材料,导致单位晶胞体积膨胀。这种晶格膨胀可归因于高弹性应变导致的形成能降低所驱动的氧空位的产生。压电显微镜显示,SMO 薄膜包含具有应变介导的面内极化和空位介导的面外极化的畴。此外,PMN-PT 衬底的压电响应可有效调节 SMO 薄膜中的双轴拉伸应变,为控制 SMO 的晶体结构和铁电特性提供了一种潜在的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ferroelectric SrMnO3 Thin Film Grown on (110)‐Oriented PMN‐PT Substrate
Exploring the unique physical properties of oxide perovskites necessitates their growth on diverse single‐crystal substrates. The thin‐film growth of perovskite SrMnO3 (SMO) has been a particular focus of research due to its emerging room‐temperature multiferroicity. Herein, the epitaxial thin films of (110)‐oriented SMO are grown on the piezoelectric (110)‐oriented (1–x)Pb(Mg1/3Nb2/3)O3–xPbTiO3 (PMN‐PT) substrate. The effects of the thickness and oxygen annealing on the crystal structure, stoichiometry, and ferroelectric properties of the SMO thin film are systematically investigated. The tensile strain produced by the lattice mismatch between the bulk SMO and the PMN‐PT substrate causes an expansion of the c‐lattice parallel to the in‐plane direction of the substrate. The films show larger a‐, b‐, and c‐lattice parameters than the bulk material, resulting in volume expansion of the unit cell. This lattice expansion is attributed to the generation of oxygen vacancies driven by the reduced formation energy caused by the high elastic strain. Piezoelectric force microscopy reveals that the SMO film contains domains with strain‐mediated in‐plane and vacancy‐mediated out‐of‐plane polarization. Furthermore, the piezoelectric response of the PMN‐PT substrate effectively modulates the biaxial tensile strain in the SMO film, offering a potential strategy for controlling the crystal structure and ferroelectric properties of SMO.
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