材料科学
铁电性
偶极子
多铁性
电介质
凝聚态物理
三元运算
极地的
钙钛矿(结构)
异质结
极化(电化学)
纳米技术
化学物理
光电子学
结晶学
化学
物理
物理化学
计算机科学
有机化学
程序设计语言
天文
作者
Jun Han Lee,Nguyen Xuan Duong,Min‐Hyoung Jung,Hyun‐Jae Lee,Ahyoung Kim,Youngki Yeo,Junhyung Kim,Gye‐Hyeon Kim,Byeong‐Gwan Cho,Jaegyu Kim,Furqanul Hassan Naqvi,Jong‐Seong Bae,Jeehoon Kim,Chang Won Ahn,Young‐Min Kim,Tae Kwon Song,Jae‐Hyeon Ko,T. Y. Koo,Changhee Sohn,Kibog Park
标识
DOI:10.1002/adma.202205825
摘要
Abstract Interaction between dipoles often emerges intriguing physical phenomena, such as exchange bias in the magnetic heterostructures and magnetoelectric effect in multiferroics, which lead to advances in multifunctional heterostructures. However, the defect‐dipole tends to be considered the undesired to deteriorate the electronic functionality. Here, deterministic switching between the ferroelectric and the pinched states by exploiting a new substrate of cubic perovskite, BaZrO3 is reported, which boosts the square‐tensile‐strain to BaTiO3 and promotes four‐variants in‐plane spontaneous polarization with oxygen vacancy creation. First‐principles calculations propose a complex of an oxygen vacancy and two Ti3+ ions coins a charge‐neutral defect‐dipole. Cooperative control of the defect‐dipole and the spontaneous polarization reveals ternary in‐plane polar states characterized by biased/pinched hysteresis loops. Furthermore, it is experimentally demonstrated that three electrically controlled polar‐ordering states lead to switchable and nonvolatile dielectric states for application of nondestructive electro‐dielectric memory. This discovery opens a new route to develop functional materials via manipulating defect‐dipoles and offers a novel platform to advance heteroepitaxy beyond the prevalent perovskite substrates.
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