Wang Lei, Feng Chun, Li Yukun, Meng Fei, Wang Shiru, Yao Mingke, Xu Xiulan, Yang Feng, Li Baohe, Yu Guanghua
State Key Laboratory of Heavy Oil Processing , China University of Petroleum-Beijing , Beijing 102249 , China.
Department of Physics, School of Sciences , Beijing Technology and Business University , Beijing 100048 , China.
ACS Appl Mater Interfaces. 2019 Sep 4;11(35):32475-32480. doi: 10.1021/acsami.9b09342. Epub 2019 Aug 20.
Tailoring magnetic anisotropy of ferromagnetic films is a critical issue in constructing energy-efficient and high-density magnetic memory devices. Presently, the effective tunability was focused on a single-ion-manipulated electronic structure evolution. Here, we reported a new strategy of dual-ion-tuned orbital structure and magnetic anisotropy of ferromagnetic films. N-doped Fe/MgO bilayer films were deposited on shape memory alloy substrates which can generate a significant lattice strain on the films. Before the N ions participate into the manipulation, the Fe/MgO film shows an in-plane magnetic anisotropy, which may be due to excessive Fe-O orbital hybridization. Interestingly, the N and O ions synergistically manipulate electronic coordination of the Fe layer, which can be further modified by the lattice strain through a charge transfer among N-Fe-O. Under such effect, the magnetic anisotropy of the film is switchable from in-plane to perpendicular magnetic anisotropy (PMA). The X-ray line dichroism (XLD) characterization reveals that the anisotropy regulation is related to Fe 3d orbital evolution: N-Fe orbital hybridization promotes the Fe d orbital occupation effectively, which is beneficial in increasing PMA by strengthening Fe-O orbital hybridization along the out-of-plane direction. However, the compressive strain induces a N-Fe-O charge transfer and reduces the Fe d electronic occupation, which weakens the PMA of films. These findings provide a new dimensionality for regulating orbital performance of ferromagnetic materials and developing strain-assisted memory devices.
调整铁磁薄膜的磁各向异性是构建节能型高密度磁存储器件的关键问题。目前,有效的可调性集中在单离子操纵的电子结构演化上。在此,我们报道了一种双离子调节铁磁薄膜轨道结构和磁各向异性的新策略。在形状记忆合金衬底上沉积了氮掺杂的铁/氧化镁双层薄膜,该衬底可在薄膜上产生显著的晶格应变。在氮离子参与调控之前,铁/氧化镁薄膜表现出面内磁各向异性,这可能是由于铁-氧轨道过度杂化所致。有趣的是,氮离子和氧离子协同操纵铁层的电子配位,通过氮-铁-氧之间的电荷转移,晶格应变可进一步对其进行修饰。在这种效应下,薄膜的磁各向异性可从面内切换为垂直磁各向异性(PMA)。X射线线二色性(XLD)表征表明,各向异性调控与铁3d轨道演化有关:氮-铁轨道杂化有效地促进了铁d轨道占据,这有利于通过增强面外方向的铁-氧轨道杂化来增加垂直磁各向异性。然而,压缩应变会引起氮-铁-氧电荷转移并减少铁d电子占据,从而削弱薄膜的垂直磁各向异性。这些发现为调控铁磁材料的轨道性能和开发应变辅助存储器件提供了新的维度。