Li Tianyu, Yang Yali, Deng Shiqing, Zhu Fangyuan, Zhang Tianfu, Chen Yu, Wang Huanhua, Long Feixiang, Li Xiaolong, Wang Jia-Ou, Zhu Tao, Tang Mingxue, He Jiangang, Diéguez Oswaldo, Guo Er-Jia, Chen Jun
University of Science and Technology Beijing, Department of Physical Chemistry, Beijing 100083, China.
University of Science and Technology Beijing, Beijing Advanced Innovation Center for Materials Genome Engineering, Beijing 100083, China.
Phys Rev Lett. 2025 Jan 10;134(1):016702. doi: 10.1103/PhysRevLett.134.016702.
Ferromagnetic insulators are receiving ever-increasing research activities driven not only by the unique advantage of low power loss during spin-wave-based information processing but also by the potential to construct next-generation spintronic devices. However, either the exceedingly rare candidates or the low Curie temperature far below room temperature greatly hinder their practical application. Here, through the modulation of a novel three-dimensional (3D) tensile strain, a room-temperature ferromagnetic insulating state with a Curie temperature as high as 594 K is achieved in self-assembled LaCoO_{3}:MgO nanocomposite thin films. Atomically resolved electron microscopy quantifications identify the 3D strain state of the thin film, where the +2.6% out-of-plane and +2.1% in-plane tensile strains are attributed to the interphase mismatch between the LaCoO_{3} and MgO building blocks and epitaxial constraint, respectively. Combined with the assessment of electronic states and theoretical analysis, we correlate the strain state with the resulting ferromagnetic insulating property and clarify the underlying mechanisms, by which the emergent strain states break the degeneracy of crystal-field splitting and tailor the on-site Coulomb interactions and spin configuration. These findings underscore the efficacy of a three-dimensional strain strategy in engineering the long-desired high-temperature ferromagnetic insulators via the manipulation of strong spin-lattice coupling, providing a promising approach for the exploitation of exotic functionalities in correlated oxides.
铁磁绝缘体正受到越来越多的研究关注,这不仅是因为基于自旋波的信息处理过程中具有低功耗的独特优势,还因为其在构建下一代自旋电子器件方面的潜力。然而,极为稀少的候选材料或远低于室温的居里温度极大地阻碍了它们的实际应用。在此,通过调制一种新型的三维(3D)拉伸应变,在自组装的LaCoO₃:MgO纳米复合薄膜中实现了居里温度高达594 K的室温铁磁绝缘态。原子分辨电子显微镜定量分析确定了薄膜的3D应变状态,其中面外+2.6%和面内+2.1%的拉伸应变分别归因于LaCoO₃和MgO结构单元之间的界面失配和外延约束。结合电子态评估和理论分析,我们将应变状态与由此产生的铁磁绝缘特性相关联,并阐明了其潜在机制,即出现的应变状态打破了晶体场分裂的简并性,并调整了在位库仑相互作用和自旋构型。这些发现强调了三维应变策略在通过操纵强自旋-晶格耦合来设计长期以来期望的高温铁磁绝缘体方面的有效性,为开发相关氧化物中的奇异功能提供了一种有前景的方法。