Magnetic van der Waals materials have mainly been investigated in their bulk form or as few-layer flakes. Because of the challenges in producing atomically thin films, only a few have been isolated as monolayers, which typically exhibit long-range magnetic order below 150 K. In this Letter, we use molecular beam epitaxy to synthesize Co-doped Fe_{5}GeTe_{2}, achieving precise control over both thickness and composition. We demonstrate ferromagnetism well above room temperature in multilayer samples and present clear evidence of ferromagnetic ordering in monolayers up to ∼200  K. The changes in Curie temperature and magnetic anisotropy as a function of composition exhibit similar trends in both monolayers and thicker films, indicating that the magnetic properties are primarily governed by intralayer magnetic interactions. Through element-specific x-ray magnetic circular dichroism and density-functional theory, we identify the substitution site of Co dopants and reveal the mechanism behind the Curie temperature enhancement induced by Co doping. Our findings suggest that, despite their weak magnetic moment, Co dopants strengthen the magnetic moments on neighboring Fe atoms and enhance the intralayer ferromagnetic exchange interactions.

We theoretically study the effect of in- and out-of-plane Dzyaloshinskii-Moriya interaction (DMI) on the magnetic ground states of two-dimensional (2D) Fe_3GeXTe (X=Te, Se, S) monolayers, where X=Se, S correspond to antisymmetric Janus structures with nonvanishing in-plane DMI. We perform atomistic spin simulations with the extended Heisenberg Hamiltonian parametrized by first principles calculations. While we find that the base DMI in all systems is too weak to stabilize noncollinear states, we show how the frustrated out-of-plane DMI tends to favor atomic-scale 3q magnetic textures at the edge of the Brillouin zone. Owing to the ability to tune the DMI in 2D magnets via applied strain or electric field, we study the evolution of the systems' ground state with increasing DMI amplitude. We find that nonplanar 3q states are favored under scaling factors as low as 3, while larger DMI tends to stabilize states reminiscent of nanoskyrmion lattices at the atomic-scale.

Spintronic terahertz (THz) emitters have established themselves as among the most practical broadband THz sources available, yet their performance remains fundamentally limited by the spin Hall conductivity of the nonmagnetic conversion layer - a quantity that is fixed once the material is chosen. Here, we demonstrate that in PtTe_2, a type-II Dirac semimetal within the transition metal dichalcogenide family, this limitation can be circumvented by exploiting the dramatic thickness-driven electronic phase evolution of the material itself. Using molecular beam epitaxy to grow PtTe_2 films with single-monolayer precision from 1 to 20 ML, we show that the spintronic THz emission tracks the underlying electronic phase diagram directly: it is absent in the single-layer semiconducting phase, turns on sharply at the semimetal transition near 2 ML, and reaches a peak amplitude six times that of an equivalent Pt reference at 10 ML, before declining at larger thicknesses due to THz reabsorption in the increasingly metallic film. This non-monotonic behavior is inconsistent with a bulk inverse spin Hall mechanism and instead reflects a multi-channel spin-to-charge conversion process in which spin-momentum-locked topological surface states and a thickness-dependent interfacial Rashba splitting both contribute and strengthen as the type-II Dirac band structure develops. First-principles calculations of the interfacial spin accumulation reproduce the experimental trend quantitatively, confirming this physical picture. These findings introduce thickness engineering of van der Waals semimetals as a new and accessible route to optimizing spintronic THz emitters and spin-orbit torques in magnetic memories (SOT-MRAMs), with direct implications for the broader class of dimensionally tunable topological materials.

Two-dimensional transition metal dichalcogenide (TMD) interfaces offer a versatile platform for studying quantum phenomena and developing device functionalities. When distinct TMD monolayers are stacked vertically or laterally stitched, their interfaces can exhibit unique electronic band alignments, giving rise to long-lived interlayer excitons, charge transfer effects, and moiré superlattices with correlated states. Here, we demonstrate that the interface between a large variety of two different epitaxially grown TMD monolayers controls the intensity and sign of the Rashba spin splitting, which is probed using THz spintronic emission. Optimized TMD heterobilayers, such as HfSe2/PtSe2, show enhanced THz emission that surpasses the spin-to-charge conversion efficiency of bulk TMDs, confirming the presence of Rashba states with large spin splitting at the interface. By combining spin- and angle-resolved photoemission spectroscopy with density functional theory, we reveal that the electronic hybridization between the two different TMD monolayers gives rise to extended in-gap states with strong Rashba spin-orbit coupling. The choice of TMD layers enables to engineer the sign and strength of spin-to-charge conversion in van der Waals heterobilayers, enabling to build efficient and tunable THz spintronic emitters.

Magnetic van der Waals materials have mainly been investigated in their bulk form or as few-layers flakes. Due to the challenges in producing atomically thin films, only a few have been isolated as monolayers, which typically exhibit long-range magnetic order below 150 K. In this work, we use molecular beam epitaxy to synthesize Co-doped Fe5GeTe2, achieving precise control over both thickness and composition. We demonstrate ferromagnetism well above room temperature in multilayer samples and present clear evidence of ferromagnetic ordering in monolayers up to ∼200 K. The changes in Curie temperature and magnetic anisotropy with composition exhibit similar trends in both monolayers and thicker films, indicating that the magnetic properties are primarily governed by intralayer magnetic interactions. Through element-specific X-ray magnetic circular dichroism and density functional theory, we identify the substitution site of Co dopants and reveal the mechanism behind the Curie temperature enhancement induced by Co doping. Our findings suggest that, despite their weak magnetic moment, Co dopants strengthen the magnetic moments on neighboring Fe atoms and enhance the intralayer ferromagnetic exchange interactions.

In ultrathin ferromagnetic films sandwiched between two distinct heavy metal layers or between a heavy metal and an oxide layer, the Dzyaloshinskii-Moriya interaction (DMI) is of interfacial origin. Its chirality and strength are determined by the properties of the adjacent heavy metals and the degree of oxidation at the interfaces. Here, we demonstrate that the DMI chirality can change solely with variations in the thickness of the ferromagnetic layer - an effect that has not been experimentally studied in details or explained until now. Our experimental observation in the trilayer system Ta/FeCoB/TaOx is supported by ab initio calculations: they reveal that variations in orbital filling and inter-atomic distances at the interface, driven by the structural relaxations in the ultrathin regime, lead to an inversion of DMI chirality. We hence propose a new degree of freedom to tune DMI chirality and the associated chiral spin textures by tailoring crystal structure e.g. using strain or surface acoustic waves.

Recent studies using Terahertz Time-Domain Spectroscopy (THz-TDS) with spintronic emitters as a source have revealed distinct signatures of the Rashba effect. This effect, which arises from the breaking of inversion symmetry in low-dimensional materials, has been recently investigated in CoFeB/PtSe_2/MoSe_2/LiNbO_3-based heterostructures [S. Massabeau et al., APL Mater. 13, 041102, 2025 ]. The observed phenomena are at the source of the generated THz far-field emission, typically through mechanisms such as spin-to-charge conversion triggered by the absorption of ultrafast optical pulses. In this work, we employ first-principles simulations to quantify the Rashba effect at PtSe_2/MoSe_2/LiNbO_3 interfaces, expanding the traditional understanding of spin transport by incorporating the orbital degree of freedom. Moreover, we quantify the degree of control on the THz emission depending on the polarization direction of LiNbO_3. In order to achieve this, we analyze the accumulation of both spin and orbital components using linear response theory, revealing distinct behaviors. These findings are crucial for a deeper understanding of the physical processes governing angular momentum-to-charge conversion and THz emission. Moreover, they may provide broader insights into various experimental outcomes, including those related to spin-orbit torque.

In the framework of the Keldysh formalism and the tight-binding model, we investigate spin-orbit phenomena such as the anomalous and spin Hall effects, tunneling anisotropic magnetoresistance, and Rashba-induced spin-orbit torque in single-barrier tunnel junctions. We focus on two configurations: one with a ferromagnetic metal [normal metal (NM)/insulator (I)/ferromagnetic metal (FM)] and the other with a ferromagnetic insulator [NM/ferromagnetic insulator (FI)/NM], both incorporating an asymmetric interfacial Rashba spin-orbit coupling. Using analytical methods and numerical simulations, we derive expressions for these spin-orbit phenomena. We find that while the anomalous Hall effect and spin-orbit torque behave similarly in both configurations, tunneling anisotropic magnetoresistance and the angular dependence of spin Hall effect are significantly enhanced by nearly an order of magnitude when a FI is used. This enhancement remains even for modest exchange splittings, suggesting that FIs such as Eu chalcogenides and spinel oxides are promising for high-efficiency spintronic applications. Additionally, we observe a sign reversal of these effects in NM/I/FM junctions as the system shifts from half-metallic to low-band-filling regimes, while no such reversal occurs in NM/FI/NM due to the spin-filtering effect of the barrier.

The diversity of 2D materials and their van der Waals (vdW) stacking presents fertile ground for engineering novel multifunctional materials and quantum states of matter. This permits unique opportunities to tailor the electronic properties of vdW heterostructures by the insertion of only a single 2D material layer. However, such vdW materials engineering at the atomic scale has yet to be investigated for spin-charge interconversion phenomena. Here, we report on the control of these effects at the monolayer level, where a drastic increase in intensity and change in sign of THz spintronic emission are demonstrated by inserting a single layer of MoSe2 between PtSe2 and graphene in a fully epitaxial, large area stacked structure. By using a combination of spin and angle resolved photoemission and density functional theory to reveal the electronic and spin structures, we illustrate two different mechanisms relying on charge transfer and electronic hybridization for the formation of Rashba states, which are responsible for spin-charge conversion and hence the THz spintronic emission. These findings open new pathways to design, at the atomic scale, efficient THz spintronic emitters made of 2D materials and other spintronic devices based on spin-charge interconversion phenomena.

Perpendicular magnetic anisotropy (PMA) and Dzyaloshinskii-Moriya interactions are key interactions in modern spintronics. These interactions are thought to be dominated by the oxidation of the Co|Al interface in the archetypal Platinum-Cobalt-Aluminum oxide system. Here, we observe a double sign change in the anisotropy and about threefold variation in interfacial chiral interaction, influenced not only by the oxidation, but also by the metallic Al thickness. Contrary to previous assumptions about negligible spin-orbit effects at light metal interfaces, we not only observe strong PMA with fully oxidized Al, decreasing and turning negative (in-plane) with less oxygen at the Co|Al interface, we also observe that the magnetic anisotropy reverts to positive (out-of-plane) values at fully metallic Co|Al interface. These findings suggest modification in Co d band via Co|Al orbital hybridization, an effect supported by X-ray absorption spectroscopy and ab initio theory calculations, highlighting the key impact of strain on interfacial mechanisms at fully metallic Co|Al interface.

The Edelstein effect is a promising mechanism for generating spin and orbital polarization from charge currents in systems without inversion symmetry. In ferroelectric materials, such as germanium telluride (GeTe), the combination of bulk Rashba splitting and voltage-controlled ferroelectric polarization provides a pathway for electrical control of the sign of the charge-spin conversion. In this work, we investigate current-induced spin and orbital magnetization in bulk GeTe using Wannier-based tight-binding models derived from ab initio calculations and semiclassical Boltzmann theory. Employing the modern theory of orbital magnetization, we demonstrate that the orbital Edelstein effect entirely dominates its spin counterpart. This difference is visualized through the spin and orbital textures at the Fermi surfaces, where the orbital moment surpasses the spin moment by one order of magnitude. Moreover, the orbital Edelstein effect remains largely unaffected in the absence of spin-orbit coupling, highlighting its distinct physical origin compared to the spin Edelstein effect.

We report a very large spin-orbit torque (SOT) capability of chromium-based transition metal dichalcogenides (TMD) in their Janus forms CrXTe, with X=S,Se. The structural inversion symmetry breaking, inherent to Janus structures is responsible for a large SOT response generated by giant Rashba splitting, equivalent to that obtained by applying a transverse electric field of $\sim 100 \,\text{V} \,\text{nm}^{-1}$ in non-Janus CrTe\textsubscript{2}, completely out of experimental reach. By performing transport simulations on custom-made Wannier tight-binding models, Janus systems are found to exhibit a SOT performance comparable to the most efficient two-dimensional materials, while allowing for field-free perpendicular magnetization switching owing to their reduced in-plane symmetry. Altogether, our findings evidence that magnetic Janus TMDs stand as suitable candidates for ultimate SOT-MRAM devices.

The magnetic proximity effect can induce a spin dependent exchange shift in the band structure of graphene. This produces a magnetization and a spin polarization of the electron/hole carriers in this material, paving the way for its use as an active component in spintronics devices. The electrostatic control of this spin polarization in graphene has however never been demonstrated so far. We show that interfacing graphene with the van der Waals antiferromagnet CrSBr results in an unconventional manifestation of the quantum Hall effect, which can be attributed to the presence of counterflowing spin-polarized edge channels originating from the spin-dependent exchange shift in graphene. We extract an exchange shift ranging from 27 to 32 meV, and show that it also produces an electrostatically tunable spin polarization of the electron/hole carriers in graphene ranging from -50% to +69% in the absence of a magnetic field. This proof of principle provides a starting point for the use of graphene as an electrostatically tunable source of spin current and could allow this system to generate a large magnetoresistance in gate tunable spin valve devices.

2D materials, such as transition metal dichalcogenides, are ideal platforms for spin‐to‐charge conversion (SCC) as they possess strong spin–orbit coupling (SOC), reduced dimensionality and crystal symmetries as well as tuneable band structure, compared to metallic structures. Moreover, SCC can be tuned with the number of layers, electric field, or strain. Here, SCC in epitaxially grown 2D PtSe 2 by THz spintronic emission is studied since its 1T crystal symmetry and strong SOC favor SCC. High quality of as‐grown PtSe 2 layers is demonstrated, followed by in situ ferromagnet deposition by sputtering that leaves the PtSe 2 unaffected, resulting in well‐defined clean interfaces as evidenced with extensive characterization. Through this atomic growth control and using THz spintronic emission, the unique thickness‐dependent electronic structure of PtSe 2 allows the control of SCC. Indeed, the transition from the inverse Rashba–Edelstein effect (IREE) in 1–3 monolayers (ML) to the inverse spin Hall effect (ISHE) in multilayers (>3 ML) of PtSe 2 enabling the extraction of the perpendicular spin diffusion length and relative strength of IREE and ISHE is demonstrated. This band structure flexibility makes PtSe 2 an ideal candidate to explore the underlying mechanisms and engineering of the SCC as well as for the development of tuneable THz spintronic emitters.

Integrating tunneling magnetoresistance (TMR) effect in memristors is a long-term aspiration because it allows to realize multifunctional devices, such as multi-state memory and tunable plasticity for synaptic function. However, the reported TMR in different multiferroic tunnel junctions is limited to 100%. This work demonstrates a giant TMR of -266% in La0.6Sr0.4MnO3(LSMO)/poly(vinylidene fluoride)(PVDF)/Co memristor with thin organic barrier. Different from the ferroelectricity-based memristors, this work discovers that the voltage-driven florine (F) motion in the junction generates a huge reversible resistivity change up to 106% with nanosecond (ns) timescale. Removing F from PVDF layer suppresses the dipole field in the tunneling barrier, thereby significantly enhances the TMR. Furthermore, the TMR can be tuned by different polarizing voltage due to the strong modification of spin-polarization at the LSMO/PVDF interface upon F doping. Combining of high TMR in the organic memristor paves the way to develop high-performance multifunctional devices for storage and neuromorphic applications.

Recent experiments by S. Krishnia et al. [Nano Lett. 2023, 23, 6785] reported an unprecedentedly large enhancement of torques upon inserting thin Al layer in Co/Pt heterostructure that suggested the presence of a Rashba-like interaction at the metallic Co/Al interface. Based on first-principles calculations, we reveal the emergence of a large helical orbital texture in reciprocal space at the interfacial Co layer, whose origin is attributed to the orbital Rashba effect due to the formation of the surface states at the Co/Al interface and where spin-orbit coupling is found to produce smaller contributions with a higher-order winding of the orbital moments. Our results unveil that the orbital texture gives rise to a nonequilibrium orbital accumulation producing large current-induced torques, thus providing an essential theoretical background for the experimental data and advancing the use of orbital transport phenomena in all-metallic magnetic systems with light elements.

Germanium telluride (GeTe), identified as a ferroelectric Rashba semiconductor, is a promising candidate for future electronic devices in computing and memory applications. However, its ferroelectric switching on a microscopic scale remains to be understood. Here, we propose that the migration of a domain wall can be the mechanism that mediates ferroelectric switching. By employing ab initio methods, such a mechanism is characterized by an energy barrier of 66.8 meV/nm(2), in a suitable range for retention and switchability. In accompanying the domain wall migration, the net Rashba effect is tunable, as it is a result of competition between layers with opposite electric polarization. These results shed light on the ferroelectric switching mechanism in GeTe, paving the way for the design of potential GeTe-based devices.

Magneto-ionics, an emerging approach to manipulate magnetism that relies on voltage-driven ion motion, holds the promise to boost energy efficiency in information technologies such as spintronic devices or future non-von Neumann computing architectures. For this purpose, stability, reversibility, endurance, and ion motion rates need to be synergistically optimized. Among various ions, nitrogen has demonstrated superior magneto-ionic performance compared to classical species such as oxygen or lithium. Here, we show that ternary Co1-xFexN compound exhibits an unprecedented nitrogen magneto-ionic response. Partial substitution of Co by Fe in binary CoN is shown to be favorable in terms of generated magnetization, cyclability and ion motion rates. Specifically, the Co0.35Fe0.65N films exhibit an induced saturation magnetization of 1,500 emu/cm3, a magneto-ionic rate of 35.5 emu/(cm3·s) and endurance exceeding 103 cycles. These values significantly surpass those of other existing nitride and oxide systems. This improvement can be attributed to the larger saturation magnetization of Co0.35Fe0.65 compared to individual Co and Fe, the nature and size of structural defects in as-grown films of different composition, and the dissimilar formation energies of Fe and Co with N in the various developed crystallographic structures.

Terahertz (THz) Spintronic emitters based on ferromagnetic/metal junctions have become an important technology for the THz range, offering powerful and ultra-large spectral bandwidths. These developments have driven recent investigations of two-dimensional (2D) materials for new THz spintronic concepts. 2D materials, such as transition metal dichalcogenides (TMDs), are ideal platforms for SCC as they possess strong spin-orbit coupling (SOC) and reduced crystal symmetries. Moreover, SCC and the resulting THz emission can be tuned with the number of layers, electric field or strain. Here, epitaxially grown 1T-PtSe$_2$ and sputtered Ferromagnet (FM) heterostructures are presented as a novel THz emitter where the 1T crystal symmetry and strong SOC favor SCC. High quality of as-grown PtSe$_2$ layers is demonstrated and further FM deposition leaves the PtSe$_2$ unaffected, as evidenced with extensive characterization. Through this atomic growth control, the unique thickness dependent electronic structure of PtSe$_2$ allows the control of the THz emission by SCC. Indeed, we demonstrate the transition from the inverse Rashba-Edelstein effect in one monolayer to the inverse spin Hall effect in multilayers. This band structure flexibility makes PtSe$_2$ an ideal candidate as a THz spintronic 2D material and to explore the underlying mechanisms and engineering of the SCC for THz emission.

2D materials, such as transition metal dichalcogenides, are ideal platforms for spin-to-charge conversion (SCC) as they possess strong spin-orbit coupling (SOC), reduced dimensionality and crystal symmetries as well as tuneable band structure, compared to metallic structures. Moreover, SCC can be tuned with the number of layers, electric field, or strain. Here, SCC in epitaxially grown 2D PtSe2 by THz spintronic emission is studied since its 1T crystal symmetry and strong SOC favor SCC. High quality of as-grown PtSe2 layers is demonstrated, followed by in situ ferromagnet deposition by sputtering that leaves the PtSe2 unaffected, resulting in well-defined clean interfaces as evidenced with extensive characterization. Through this atomic growth control and using THz spintronic emission, the unique thickness-dependent electronic structure of PtSe2 allows the control of SCC. Indeed, the transition from the inverse Rashba-Edelstein effect (IREE) in 1-3 monolayers (ML) to the inverse spin Hall effect (ISHE) in multilayers (>3 ML) of PtSe2 enabling the extraction of the perpendicular spin diffusion length and relative strength of IREE and ISHE is demonstrated. This band structure flexibility makes PtSe2 an ideal candidate to explore the underlying mechanisms and engineering of the SCC as well as for the development of tuneable THz spintronic emitters.