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首页> 外文期刊>ACS Omega >Giant Magnetoelectric Coupling in Multiferroic PbTi1–xVxO3 from Density Functional Calculations
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Giant Magnetoelectric Coupling in Multiferroic PbTi1–xVxO3 from Density Functional Calculations

机译:基于密度泛函计算的多铁性PbTi1–xVxO3中的巨磁电耦合

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Giant magnetoelectric coupling is a very rare phenomenon that has gained much attention in the past few decades due to fundamental interest as well as practical applications. Here, we have successfully achieved giant magnetoelectric coupling in PbTi1–xVxO3 (x = 0–1) using a series of generalized gradient-corrected GGA (generalized gradient approximation), including on-site Coulomb repulsion (U)-corrected spin-polarized calculations based on accurate density functional theory. Our total energy calculations show that PbTi1–xVxO3 stabilizes in C-type antiferromagnetic ground state for x > 0.123. With the substitution of V into PbTiO3, the tetragonal distortion is highly enhanced accompanied by a linear increase in polarization. In addition, our band structure analysis shows that for lower x values, the tendency to form two-dimensional magnetism of PbTi1–xVxO3 decreases. The orbital magnetic polarization was calculated with self-consistent field method by including orbital polarization correction in the calculation as well as from the computed X-ray magnetic dichroism spectra. A nonmagnetic metallic ground state is observed for the paraelectric phase for V concentration (x) = 1 competing with a volume change of 10% showing a large magnetovolume effect. Our orbital-projected density of states as well as orbital ordering analysis suggest that the orbital ordering plays a major role in the magnetic-to-nonmagnetic transition when going from ferroelectric to paraelectric phase. The calculated magnetic anisotropic energy shows that the direction [110] is the easy axis of magnetization for x = 1 composition. The partial polarization analysis shows that the Ti/V–O hybridization majorly contributes to the total electrical polarization. The present study adds a new series of compounds to the magnetoelectric family with rarely existing giant coupling between electric- and magnetic-order parameters. These results show that such kind of materials can be used for novel practical applications where one can change the magnetic properties drastically (magnetic to nonmagnetic, as shown here) with external electric field and vice versa.
机译:巨磁电耦合是一种非常罕见的现象,由于基本兴趣和实际应用,在过去的几十年中,它已经引起了广泛的关注。在这里,我们使用一系列广义梯度校正的GGA(广义梯度逼近)成功地实现了PbTi1–xVxO3(x = 0–1)中的巨大磁电耦合,包括现场库仑斥力(U)校正的自旋极化计算基于精确的密度泛函理论。我们的总能量计算表明,对于x> 0.123,PbTi1-xVxO3稳定在C型反铁磁基态。通过将V替换为PbTiO3,可以大大增强四边形畸变,并伴随线性增加的极化。此外,我们的能带结构分析表明,对于较低的x值,PbTi1-xVxO3形成二维磁性的趋势会降低。通过在计算中包括轨道极化校正以及根据计算出的X射线磁二色性光谱,使用自洽场方法来计算轨道磁极化。 V浓度(x)= 1的顺电相观察到非磁性金属基态,体积变化为10%,显示出较大的磁烟流效应。我们的轨道投影状态密度以及轨道有序分析表明,当从铁电相转变为顺电相时,轨道有序在磁-非磁转变中起主要作用。计算出的磁各向异性能表明,方向[110]是x = 1成分的易磁化轴。部分极化分析表明,Ti / V-O杂化主要有助于总电极化。本研究为磁电族增加了一系列新化合物,在电和磁序参数之间很少存在巨大的耦合。这些结果表明,这种材料可用于新颖的实际应用中,其中可以随着外部电场而急剧地改变磁性能(如此处所示,从磁性变为非磁性),反之亦然。

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