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Artificial Constructionof the Layered Ruddlesden–PopperManganite La2Sr2Mn3O10 by Reflection High Energy Electron Diffraction Monitored PulsedLaser Deposition

机译:人工施工Ruddlesden-Popper的分层反射法高能电子衍射监测La2Sr2Mn3O10锰激光沉积

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摘要

Pulsed laser deposition has been used to artificially construct the n = 3 Ruddlesden–Popper structure La2Sr2Mn3O10 in epitaxial thin film form by sequentially layering La1–xSrxMnO3 and SrO unit cells aided by in situ reflection high energy electron diffraction monitoring. The interval deposition technique was used to promote two-dimensional SrO growth. X-ray diffraction and cross-sectional transmission electron microscopy indicated that the trilayer structure had been formed. A site ordering was found to differ from that expected thermodynamically, with the smaller Sr2+ predominantly on the R site due to kinetic trapping of the deposited cation sequence. A dependence of the out-of-plane lattice parameter on growth pressure was interpreted as changing the oxygen content of the films. Magnetic and transport measurements on fully oxygenated films indicated a frustrated magnetic ground state characterized as a spin glass-like magnetic phase with the glass temperature Tg ≈ 34 K. The magnetic frustration has a clear in-plane (ab) magnetic anisotropy, which is maintained up to temperatures of150 K. Density functional theory calculations suggest competing antiferromagneticand ferromagnetic long-range orders, which are proposed as the originof the low-temperature glassy state.
机译:通过在原位反射高能电子衍射监测的帮助下,依次层叠La1-xSrxMnO3和SrO晶胞,已采用脉冲激光沉积法以外延薄膜形式人工构建n = 3的Ruddlesden-Popper结构La2Sr2Mn3O10。间隔沉积技术用于促进二维SrO的生长。 X射线衍射和截面透射电子显微镜表明已形成三层结构。发现位点顺序不同于热力学预期的位点顺序,较小的Sr 2 + 主要是在R位点上,这是由于沉积阳离子序列的动力学捕获所致。平面外晶格参数对生长压力的依赖性被解释为改变膜的氧含量。在完全氧化的薄膜上进行的磁性和迁移测量表明,受挫的磁性基态为玻璃态温度Tg≈34 K的自旋玻璃状磁性相。磁性受挫态具有明显的面内(ab)磁各向异性,这种各向异性得以维持高达150K。密度泛函理论计算表明竞争性反铁磁和铁磁远程订单,它们被认为是起源的低温玻璃态。

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