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Register a new userSpin-orbit torque-driven skyrmion dynamics revealed by time-resolved X-ray microscopy
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Magnetic skyrmions are topologically-protected spin textures with attractive properties suitable for high-density and low-power spintronic device applications. Much effort has been dedicated to understanding the dynamical behaviours of the magnetic skyrmions. However, experimental observation of the ultrafast dynamics of this chiral magnetic texture in real space, which is the hallmark of its quasiparticle nature, has so far remained elusive. Here, we report nanosecond-dynamics of a 100 nm-size magnetic skyrmion during a current pulse application, using a time-resolved pump-probe soft X-ray imaging technique. We demonstrate that distinct dynamic excitation states of magnetic skyrmions, triggered by current-induced spin-orbit torques, can be reliably tuned by changing the magnitude of spin-orbit torques. Our findings show that the dynamics of magnetic skyrmions can be controlled by the spin-orbit torque on the nanosecond time scale, which points to exciting opportunities for ultrafast and novel skyrmionic applications in the future.
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Current-induced spin-orbit torques (SOTs) represent one of the most effective ways to manipulate the magnetization in spintronic devices. The orthogonal torque-magnetization geometry, the strong damping, and the large domain wall velocities inherent to materials with strong spin-orbit coupling make SOTs especially appealing for fast switching applications in nonvolatile memory and logic units. So far, however, the timescale and evolution of the magnetization during the switching process have remained undetected. Here, we report the direct observation of SOT-driven magnetization dynamics in Pt/Co/AlO$_x$ dots during current pulse injection. Time-resolved x-ray images with 25 nm spatial and 100 ps temporal resolution reveal that switching is achieved within the duration of a sub-ns current pulse by the fast nucleation of an inverted domain at the edge of the dot and propagation of a tilted domain wall across the dot. The nucleation point is deterministic and alternates between the four dot quadrants depending on the sign of the magnetization, current, and external field. Our measurements reveal how the magnetic symmetry is broken by the concerted action of both damping-like and field-like SOT and show that reproducible switching events can be obtained for over $10^{12}$ reversal cycles.
We report the observation of a spin-orbit torque (SOT) originating from the surface Rashba-Edelstein effect. We found that the SOT in a prototypical spin-orbitronic system, a Pt/Co bilayer, can be manipulated by molecular self-assembly on the Pt surface. This evidences that the Rashba spin-orbit coupling at the Pt surface generates a sizable SOT, which has been hidden by the strong bulk and interface spin-orbit coupling. We show that the molecular tuning of the surface Rashba-Edelstein SOT is consistent with density functional theory calculations. These results illustrate the crucial role of the surface spin-orbit coupling in the SOT generation, which alters the landscape of metallic spin-orbitronic devices.
Efficient manipulation of magnetization at ultrashort time scales is of particular interest for future technology. Here, we numerically investigate the influence of the so-called field-derivative torque, which was derived earlier based on relativistic Dirac theory [Mondal et al., Phys. Rev. B 94, 144419 (2016)], on the spin dynamics triggered by ultrashort laser pulses. We find that only considering the THz Zeeman field can underestimate the spin excitation in antiferromagnetic oxide systems as, e.g., NiO and CoO. However, accounting for both, the THz Zeeman torque and the field-derivative torque, the amplitude of the spin excitation increases significantly. Studying the damping dependence of field-derivative torque we observe larger effects for materials having larger damping constants.
Magnetic skyrmion is a promising building block for developing information storage and computing devices. It can be stabilized in a ferromagnetic thin film with the Dzyaloshinskii-Moriya interaction (DMI). The moving ferromagnetic skyrmion may show the skyrmion Hall effect, that is, the skyrmion shows a transverse shift when it is driven by a spin current. Here, we numerically and theoretically study the current-driven dynamics of a ferromagnetic nanoscale skyrmion in the presence of the anisotropic DMI, where the skyrmion has an elliptical shape. The skyrmion Hall effect of the elliptical skyrmion is investigated. It is found that the skyrmion Hall angle can be controlled by tuning the profile of elliptical skyrmion. Our results reveal the relation between the skyrmion shape and the skyrmion Hall effect, which could be useful for building skyrmion-based spintronic devices with preferred skyrmion Hall angle. Also, our results provide a method for the minimization of skyrmion Hall angle for applications based on in-line motion of skyrmions.
Spintronic devices based on magnetic skyrmions are a promising candidate for next-generation memory applications due to their nanometre-size, topologically-protected stability and efficient current-driven dynamics. Since the recent discovery of room-temperature magnetic skyrmions, there have been reports of current-driven skyrmion displacement on magnetic tracks and demonstrations of current pulse-driven skyrmion generation. However, the controlled annihilation of a single skyrmion at room temperature has remained elusive. Here we demonstrate the deterministic writing and deleting of single isolated skyrmions at room temperature in ferrimagnetic GdFeCo films with a device-compatible stripline geometry. The process is driven by the application of current pulses, which induce spin-orbit torques, and is directly observed using a time resolved nanoscale X-ray imaging technique. We provide a current-pulse profile for the efficient and deterministic writing and deleting process. Using micromagnetic simulations, we also reveal the microscopic mechanism of the topological fluctuations that occur during this process.
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