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通过金属锰氧化物中的界面诱导极相来实现轨道占据的可逆调制。

Reversible modulation of orbital occupations via an interface-induced polar state in metallic manganites.

机构信息

Department of Physics and ‡Department of Applied Physics and Applied Mathematics, Columbia University , New York, New York 10027, United States.

出版信息

Nano Lett. 2014 Sep 10;14(9):4965-70. doi: 10.1021/nl501209p. Epub 2014 Aug 28.

Abstract

The breaking of orbital degeneracy on a transition metal cation and the resulting unequal electronic occupations of these orbitals provide a powerful lever over electron density and spin ordering in metal oxides. Here, we use ab initio calculations to show that reversibly modulating the orbital populations on Mn atoms can be achieved at ferroelectric/manganite interfaces by the presence of ferroelectric polarization on the nanoscale. The change in orbital occupation can be as large as 10%, greatly exceeding that of bulk manganites. This reversible orbital splitting is in large part controlled by the propagation of ferroelectric polar displacements into the interfacial region, a structural motif absent in the bulk and unique to the interface. We use epitaxial thin film growth and scanning transmission electron microscopy to verify this key interfacial polar distortion and discuss the potential of reversible control of orbital polarization via nanoscale ferroelectrics.

摘要

过渡金属阳离子的轨道简并的打破以及由此导致的这些轨道的电子占据的不平等,为控制金属氧化物中的电子密度和自旋有序性提供了一个有力的手段。在这里,我们使用从头算计算表明,通过纳米尺度上的铁电极化,在铁电/锰酸盐界面可以实现对 Mn 原子轨道占据数的可逆调节。轨道占据的变化可以高达 10%,远远超过体锰酸盐的变化。这种可逆的轨道分裂在很大程度上受到铁电极化位移在界面区域传播的控制,这种结构模式在体相中不存在,是界面所特有的。我们使用外延薄膜生长和扫描透射电子显微镜来验证这种关键的界面极变形,并讨论通过纳米尺度铁电体实现轨道极化的可逆控制的潜力。

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