Wang Fengmei, Mathur Nitish, Janes Aurora N, Sheng Hongyuan, He Peng, Zheng Xueli, Yu Peng, DeRuiter Andrew J, Schmidt J R, He Jun, Jin Song
CAS Center for Excellence in Nanoscience, CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, National Center for Nanoscience and Technology, Beijing 100190, P. R. China.
Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, WI 53706, USA.
Sci Adv. 2021 Oct 22;7(43):eabj4086. doi: 10.1126/sciadv.abj4086.
Controlling the magnetic spin states of two-dimensional (2D) van der Waals (vdW) materials with strong electronic or magnetic correlation is important for spintronic applications but challenging. Crystal defects that are often present in 2D materials such as transition metal phosphorus trisulfides (MPS) could influence their physical properties. Here, we report the effect of sulfur vacancies on the magnetic exchange interactions and spin ordering of few-layered vdW magnetic NiCoPS nanosheets. Magnetic and structural characterization in corroboration with theoretical calculations reveal that sulfur vacancies effectively suppress the strong intralayer antiferromagnetic correlation, giving rise to a weak ferromagnetic ground state in NiCoPS nanosheets. Notably, the magnetic field required to tune this ferromagnetic state (<300 Oe) is much lower than the value needed to tune a typical vdW antiferromagnet (> several thousand oersted). These findings provide a previously unexplored route for controlling competing correlated states and magnetic ordering by defect engineering in vdW materials.
通过强电子或磁关联来控制二维(2D)范德华(vdW)材料的磁自旋态对于自旋电子学应用而言至关重要,但颇具挑战性。诸如过渡金属三硫化磷(MPS)等二维材料中常常存在的晶体缺陷可能会影响其物理性质。在此,我们报告了硫空位对少层vdW磁性NiCoPS纳米片的磁交换相互作用和自旋排序的影响。与理论计算相结合的磁性和结构表征表明,硫空位有效地抑制了强层内反铁磁关联,在NiCoPS纳米片中产生了弱铁磁基态。值得注意的是,调节这种铁磁态所需的磁场(<300奥斯特)远低于调节典型vdW反铁磁体所需的磁场值(>几千奥斯特)。这些发现为通过vdW材料中的缺陷工程来控制竞争的关联态和磁排序提供了一条此前未被探索的途径。