Yao Lide, Inkinen Sampo, Komsa Hannu-Pekka, van Dijken Sebastiaan
NanoSpin, Department of Applied Physics, Aalto University School of Science, P.O. Box 15100, Aalto, FI-00076, Finland.
Department of Applied Physics, Aalto University School of Science, P.O. Box 11100, Aalto, FI-00076, Finland.
Small. 2021 Mar;17(10):e2006273. doi: 10.1002/smll.202006273. Epub 2021 Feb 16.
Oxygen vacancy migration and ordering in perovskite oxides enable manipulation of material properties through changes in the cation oxidation state and the crystal lattice. In thin-films, oxygen vacancies conventionally order into equally spaced planes. Here, it is shown that the planar 2D symmetry is broken if a mechanical nanoprobe restricts the chemical lattice expansion that the vacancies generate. Using in situ scanning transmission electron microscopy, a transition from a perovskite structure to a 3D vacancy-ordered phase in an epitaxial La Sr MnO film during voltage pulsing under local mechanical straining is imaged. The never-before-seen ordering pattern consists of a complex network of distorted oxygen tetrahedra, pentahedra, and octahedra that, together, produce a corrugated atomic structure with lattice constants varying between 3.5 and 4.6 Å. The giant lattice distortions respond sensitively to strain variations, offering prospects for non-volatile nanoscale physical property control driven by voltage and gated by strain.
钙钛矿氧化物中的氧空位迁移和有序排列能够通过阳离子氧化态和晶格的变化来调控材料性能。在薄膜中,氧空位通常会排列成等间距的平面。在此,研究表明,如果机械纳米探针限制了空位所产生的化学晶格膨胀,二维平面对称性就会被打破。利用原位扫描透射电子显微镜,对在外加局部机械应变的电压脉冲作用下,外延LaSrMnO薄膜从钙钛矿结构向三维空位有序相的转变进行了成像。这种前所未见的有序排列模式由扭曲的氧四面体、氧五面体和氧八面体组成的复杂网络构成,它们共同形成了一种波纹状原子结构,其晶格常数在3.5至4.6 Å之间变化。巨大的晶格畸变对应变变化敏感响应,为通过电压驱动并受应变门控的非易失性纳米级物理性能控制提供了前景。