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Anion Doping of Ferromagnetic Thin Films of La0.74Sr0.26MnO3−δ via Topochemical Fluorination

机译:拓扑化学氟化法对La0.74Sr0.26MnO3-δ铁磁薄膜的阴离子掺杂

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摘要

Chemical doping via insertion of ions into the lattice of a host material is a key strategy to flexibly manipulate functionalities of materials. In this work, we present a novel case study on the topotactic insertion of fluoride ions into oxygen-deficient ferromagnetic thin films of La0.74Sr0.26MnO3−δ (LSMO) epitaxially grown onto single-crystal SrTiO3 (STO) substrates. The effect of fluorination on the film structure, composition, and magnetic properties is compared with the case of oxygen-deficient and fully-oxidized LSMO films. Although incorporation of F anions does not significantly alter the volume of the LSMO unit cell, a strong impact on the magnetic characteristics, including a remarkable suppression of Curie temperature and saturation magnetization accompanied by an increase in magnetic coercivity, was found. The change in magnetic properties can be ascribed to the disruption of the ferromagnetic exchange interactions along Mn-anion-Mn chains driven by F doping into the LSMO lattice. Our results indicate that F doping is a powerful means to effectively modify the magnetic functional properties of perovskite manganites.
机译:通过将离子插入主体材料的晶格中进行化学掺杂是灵活控制材料功能的关键策略。在这项工作中,我们提出了一个新的案例研究,即将氟化物离子外延生长到单晶SrTiO3(STO)衬底上的La0.74Sr0.26MnO3-δ(LSMO)的缺氧铁磁薄膜中。将氟化对膜结构,组成和磁性的影响与缺氧和完全氧化的LSMO膜的情况进行了比较。尽管掺入F -阴离子不会显着改变LSMO晶胞的体积,但对磁特性的影响很大,包括显着抑制居里温度和饱和磁化强度,并伴随着矫顽磁力的增加, 被找到。磁性能的变化可归因于由掺入LSMO晶格的F -驱动的沿着Mn-阴离子-Mn链的铁磁交换相互作用的破坏。我们的结果表明,F -掺杂是有效改变钙钛矿锰矿磁性功能的有力手段。

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