Alberto Anadón

Double-helix (DH) nanowires provide a platform to study the influence of geometric chirality on spin chirality. Their three-dimensional (3D) helical architecture and tunable inter-strand coupling enable control of spin chirality, including the stabilization of topological 3D magnetic states such as helical domains and domain walls, topological stray fields, and extended helical vortex/skyrmion tubes. So far, the study of these and other 3D nanostructures is usually confined to a limited number of magnetic microscopy experiments in large facilities. Here, we investigate the reversal mechanism of a single DH nanowire using dark-field magneto-optical Kerr effect (DF-MOKE) magnetometry under external 3D magnetic fields. By analyzing the angular dependence of the DF-MOKE signal, we fit the reversal process using established models for domain-wall nucleation and propagation, finding a characteristic behavior similar to that reported for cylindrical nanowires. Micromagnetic simulations indicate that the reversal process goes through nucleation of the helical vortex tube in a curling manner, while ptychographic x-ray magnetic circular dichroism data reveal that this helical vortex tube state forms through a mixed nucleation-propagation process. These observations provide a consistent microscopic picture of reversal mediated by a helical vortex tube extending along the nanowire. Our work provides a comprehensive characterization of magnetization reversal in DH nanowires and demonstrates that DF-MOKE magnetometry is effective for probing reversal mechanisms in single 3D nanostructures. This lab-based approach expands the range of accessible experiments beyond large-scale facilities, enabling extensive exploration of the rich spin states supported by 3D nano-geometries.

Magnetic imaging techniques are widespread critical tools used in fields such as magnetism, spintronics, or even superconductivity. Among them, one of the most versatile methods is the magneto-optical Kerr effect. However, as soon as light is blocked from interacting with the magnetic layer, such as in deeply buried layers, optical techniques become ineffective. In this work, we present a spin accumulation based magneto-optical Kerr effect microscopy technique that enables imaging of a magnetic thin-film covered by thick and opaque metallic layers. The technique is based on the generation and detection of transient spin accumulations that propagate through the thick metallic layer. These spin accumulation signals are directly triggered and detected optically on the same side, lifting any substrate transparency requirements. The spin accumulation signals detected on a Cu layer decay with a characteristic length of 60 nm, much longer than the 12 nm optical penetration depth, allowing for the detection of magnetic contrast with Cu capping layers up to hundreds of nm. This method should enable magnetic imaging in a wide range of experiments where the surface of interest is covered by electrodes.

Engineering and controlling heat and spin transport on the femtosecond timescale in spintronic devices opens up new ways to manipulate magnetization with unprecedented speed. Yet the underlying reversal mechanisms remain poorly understood due to the challenges of probing ultrafast, nonequilibrium spin dynamics. In this Letter, we demonstrate that typical magneto-optical experiments can be leveraged to access the time evolution of the spin accumulation generated within a magnetic multilayer following an ultrafast laser excitation. Furthermore, our analysis shows that the final magnetic state of the free layer in a spin valve is mainly dictated by the ultrafast dynamics of the reference-layer magnetization. Our results disentangle magnetization and spin transport dynamics within a multilayer stack and identify demagnetization and remagnetization-driven spin accumulation as the key mechanism for all-optical switching. These findings establish new design principles for ultrafast spintronic devices based on tailored spin current engineering.

We study laser-induced ultrafast magnetization reversal in a ferromagnetic spin valve by comparing the effects of direct laser excitation and ultrashort hot-electron pulses. A wedged Cu layer is deposited atop the spin valve to tune energy transmission to the magnetic stack for both optical and hot-electron excitation. We demonstrate single-shot magnetization reversal of the free layer using hot-electron pulses. Moreover, such reversal is achieved even with picosecond laser pulses. The influence of laser fluence, Cu thickness (t_{Cu}), and pulse duration is investigated in detail. Our results indicate that the key factor enabling magnetization reversal is full demagnetization of the free layer, driven by a rapid rise in its electronic temperature-achieved via either direct laser or hot-electron excitation. This work advances the understanding of ultrafast magnetization reversal via nonlocal heat and spin transport under strongly out-of-equilibrium conditions.

Electrical current pulses can be used to manipulate magnetization efficiently via spin–orbit torques. Pulse durations as short as a few picoseconds have been used to switch the magnetization of ferromagnetic films, reaching the terahertz regime. However, little is known about the reversal mechanisms and energy requirements in the ultrafast switching regime. In this work we quantify the energy cost for magnetization reversal over seven orders of magnitude in pulse duration, in both ferromagnetic and ferrimagnetic samples, bridging quasi-static spintronics and femtomagnetism. To this end, we develop a method to stretch picosecond pulses generated by a photoconductive switch by an order of magnitude. Thereby we can create current pulses from picoseconds to durations approaching the pulse width available with commercial instruments. We show that the energy cost for spin–orbit torque switching decreases by more than an order of magnitude in all samples when the pulse duration enters the picosecond range. We project an energy cost of 9 fJ for a 100 × 100 nm² ferrimagnetic device. Micromagnetic and macrospin simulations unveil a transition from a non-coherent to a coherent magnetization reversal with a strong modification of the magnetization dynamical trajectories as pulse duration is reduced. Our results show the potential for high-speed magnetic spin–orbit torque memories and highlight alternative magnetization reversal pathways at fast timescales.

Epitaxial graphene/ferromagnetic metal (Gr/FM) heterostructures deposited onto heavy metals have been proposed for the realization of spintronic devices because of their perpendicular magnetic anisotropy and sizable Dzyaloshinskii-Moriya interaction (DMI), allowing for both enhanced thermal stability and stabilization of chiral spin textures. However, establishing routes toward this goal requires the fundamental understanding of the microscopic origin of their unusual properties. Here, we elucidate the nature of the induced spin-orbit coupling (SOC) at Gr/Co interfaces on Ir. Through spin- and angle-resolved photoemission spectroscopy along with density functional theory, we show that the interaction of the heavy metals with the Gr layer via hybridization with the FM is the source of strong SOC in the Gr layer. Furthermore, our studies on ultrathin Co films underneath Gr reveal an energy splitting of ∼100 meV for in-plane and negligible for out-of-plane spin polarized Gr π-bands, consistent with a Rashba-SOC at the Gr/Co interface, which is either the fingerprint or the origin of the DMI. This mechanism vanishes at large Co thicknesses, where neither in-plane nor out-of-plane spin-orbit splitting is observed, indicating that Gr π-states are electronically decoupled from the heavy metal. The present findings are important for future applications of Gr-based heterostructures in spintronic devices.

The spin-to-charge current interconversion in bilayers composed of ferromagnetic and nonmagnetic layers with strong spin-orbit coupling has garnered considerable attention due to its exceptional potential in advancing spintronics devices for data storage and logic applications. Platinum (Pt) stands out as one of the most effective materials for generating spin current. While the spin conversion efficiency is isotropic in polycrystalline Pt samples, an ongoing debate persists regarding its dependence on the crystalline direction in single crystalline samples. In this study, we aim to comprehensively evaluate the in-plane anisotropy of spin-charge interconversion using an array of complementary spin Hall and inverse spin Hall techniques with both incoherent and coherent excitation. Specifically, we investigate the spin-to-charge interconversion in epitaxial, (111)-oriented, Co/Pt bilayers with low surface roughness, as resulted from x-ray experiments. By varying the thickness of the Pt layer, we gain insights into the spin-charge interconversion in epitaxial Pt and highlight the effects of the interfaces. Our results demonstrate an isotropic behavior within the limits of our detection uncertainty. This finding significantly enhances our understanding of spin conversion in one of the most relevant systems in spintronics, and it paves the way for future research in this field.

The spin-to-charge current interconversion in bilayers composed of ferromagnetic and nonmagnetic layers with strong spin-orbit coupling has garnered considerable attention due to its exceptional potential in advancing spintronics devices for data storage and logic applications. Platinum (Pt) stands out as one of the most effective materials for generating spin current. While the spin conversion efficiency is isotropic in polycrystalline Pt samples, an ongoing debate persists regarding its dependence on the crystalline direction in single crystalline samples. In this study, we aim to comprehensively evaluate the in-plane anisotropy of spin-charge interconversion using an array of complementary Spin Hall and inverse Spin Hall techniques with both incoherent and coherent excitation. Specifically, we investigate the spin-to-charge interconversion in epitaxial, (111)-oriented, Co/Pt bilayers with low surface roughness, as resulted from x-ray experiments. By varying the thickness of the Pt layer, we gain insights into the spin-charge interconversion in epitaxial Pt and highlight the effects of the interfaces. Our results demonstrate an isotropic behavior within the limits of our detection uncertainty. This finding significantly enhances our understanding of spin conversion in one of the most relevant systems in spintronics and paves the way for future research in this field.