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Register a new userInterlayer exchange coupling -- a general scheme turning chiral magnets into magnetic multilayers carrying atomic-scale skyrmions
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We report on a general principle using the interlayer exchange coupling to extend the regime of chiral magnetic films in which stable or metastable magnetic skyrmions can appear at zero magnetic field. We verify this concept on the basis of a first-principles model for a Mn monolayer on W(001) substrate, a prototype chiral magnet for which the atomic-scale magnetic texture is determined by the frustration of exchange interactions, impossible to unwind by laboratory magnetic fields. By means of textit{ab initio} calculations for the Mn/W$_m$/Co$_n$/Pt/W(001) multilayer system we show that for certain thicknesses $m$ of the W spacer and $n$ of the Co reference layer, the effective field of the reference layer fully substitutes the required magnetic field for skyrmion formation.
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Noncollinear spin textures in ferromagnetic ultrathin films are currently the subject of renewed interest since the discovery of the interfacial Dzyaloshinskii-Moriya interaction (DMI). This antisymmetric exchange interaction selects a given chirality for the spin textures and allows stabilising configurations with nontrivial topology. Moreover, it has many crucial consequences on the dynamical properties of these topological structures, including chiral domain walls (DWs) and magnetic skyrmions. In the recent years the study of noncollinear spin textures has been extended from single ultrathin layers to magnetic multilayers with broken inversion symmetry. This extension of the structures in the vertical dimension allows very efficient current-induced motion and room-temperature stability for both Neel DWs and skyrmions. Here we show how in such multilayered systems the interlayer interactions can actually lead to more complex, hybrid chiral magnetisation arrangements. The described thickness-dependent reorientation of DWs is experimentally confirmed by studying demagnetised multilayers through circular dichroism in x-ray resonant magnetic scattering. We also demonstrate a simple yet reliable method for determining the magnitude of the DMI from static domains measurements even in the presence of these hybrid chiral structures, by taking into account the actual profile of the DWs. The advent of these novel hybrid chiral textures has far-reaching implications on how to stabilise and manipulate DWs as well as skymionic structures in magnetic multilayers.
The exchange coupling underlies ferroic magnetic coupling and is thus the key element that governs statics and dynamics of magnetic systems. This fundamental interaction comes in two flavors - symmetric and antisymmetric coupling. While symmetric coupling leads to ferro- and antiferromagnetism, antisymmetric coupling has attracted significant interest owing to its major role in promoting topologically non-trivial spin textures that promise high-speed and energy-efficient devices. So far, the antisymmetric exchange coupling rather short-ranged and limited to a single magnetic layer has been demonstrated, while the symmetric coupling also leads to long-range interlayer exchange coupling. Here, we report the missing component of the long-range antisymmetric interlayer exchange coupling in perpendicularly magnetized synthetic antiferromagnets with parallel and antiparallel magnetization alignments. Asymmetric hysteresis loops under an in-plane field unambiguously reveal a unidirectional and chiral nature of this novel interaction, which cannot be accounted for by existing coupling mechanisms, resulting in canted magnetization alignments. This can be explained by spin-orbit coupling combined with reduced symmetry in multilayers. This new class of chiral interaction provides an additional degree of freedom for engineering magnetic structures and promises to enable a new class of three-dimensional topological structures.
For epitaxial trilayers of the magnetic rare-earth metals Gd and Tb, exchange coupled through a non-magnetic Y spacer layer, element-specific hysteresis loops were recorded by the x-ray magneto-optical Kerr effect at the rare-earth $M_5$ thresholds. This allowed us to quantitatively determine the strength of interlayer exchange coupling (IEC). In addition to the expected oscillatory behavior as a function of spacer-layer thickness $d_Y$, a temperature-induced sign reversal of IEC was observed for constant $d_Y$, arising from magnetization-dependent electron reflectivities at the magnetic interfaces.
In this work, we use the liquid ammonia method to successfully intercalate potassium atoms into ZrTe5 single crystal, and find a transition from semimetal to semiconductor at low temperature in the intercalated ZrTe5. The resistance anomalous peak is gradually suppressed and finally disappears with increasing potassium concentration. Whilst, the according sign reversal is always observed in the Hall resistance measurement. We tentatively attribute the semimetal-semiconductor transition to the lattice expansion induced by atomic intercalation and thereby a larger energy band gap.
Changing the interlayer exchange coupling between magnetic layers in-situ is a key issue of spintronics, as it allows for the optimization of properties that are desirable for applications, including magnetic sensing and memory. In this paper, we utilize the phase change material VO2 as a spacer layer to regulate the interlayer exchange coupling between ferromagnetic layers with perpendicular magnetic anisotropy. The successful growth of ultra-thin (several nanometres) VO2 films is realized by sputtering at room temperature, which further enables the fabrication of [Pt/Co]2/VO2/[Co/Pt]2 multilayers with distinct interfaces. Such a magnetic multilayer exhibits an evolution from antiferromagnetic coupling to ferromagnetic coupling as the VO2 undergoes a phase change. The underlying mechanism originates from the change in the electronic structure of the spacer layer from an insulating to a metallic state. As a demonstration of phase change spintronics, this work may reveal the great potential of material innovations for next-generation spintronics.
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