铁电性
材料科学
凝聚态物理
微晶
极化(电化学)
各向异性
极地的
超晶格
格子(音乐)
拓扑(电路)
领域(数学分析)
光电子学
陶瓷
拓扑缺陷
纳米技术
铁电陶瓷
纳米尺度
边界(拓扑)
磁畴壁(磁性)
领域工程
作者
Xiali Liang,Jiyang Xie,Wanbiao Hu
标识
DOI:10.1002/adma.202514332
摘要
ABSTRACT The discovery of complex polar topologies in nanoscale ferroelectric superlattices has greatly enriched the ferroelectric topological domains. These domains, although different and intricate in their formats, origin, and strengths, generally arise from the intricate interplay between collective polarization behaviors and certain mechanical boundary conditions, for example, interfacial strains within ferroelectric superlattices. As most extensive prototype materials afford multiple functions, ceramics and/or polycrystalline films, hardly present polar topologies, and even become unreachable when the significantly enhanced polarizations are achieved simultaneously. Herein, we demonstrate the formation of a new ferroelectric topological domain, a polarization‐asymmetric flux‐non‐closure domain (much close to vortex pattern), in polycrystalline BiFeO 3 . This asymmetric ferroelectric topology, subjected to a driving force associated with local lattice defects, induces an antiphase boundary that relaxes the anisotropic lattice strains and structural distortion, resulting in greatly increased B‐site Fe displacements and FeO 6 rotation angles. The formation of abundant asymmetric flux‐non‐closure domains also creates large net polarizations that are responsible for the significantly enhanced ferroelectric polarizations, up to 165.6 µC cm −2 . Our findings provide a broader platform for modulating ferroelectric flux‐non‐closure patterns in extensive polycrystalline materials through facile lattice defect engineering to achieve optimized ferroelectric properties and new topological states.
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