Search Results (17)

The performance of synchrotron beamlines critically depends on the optimal coupling between the undulator and the monochromator. This work presents the implementation and quantitative characterization of a synchronized scanning system for the elliptically polarizing undulator (EPU) and the variable-line-spacing plane-grating monochromator at the BL07U beamline of the Shanghai Synchrotron Radiation Facility (SSRF). The system ensures that the monochromator’s narrow bandwidth dynamically tracks the brilliant central cone of the undulator radiation. A linear correlation between the monochromator energy and the undulator gap, justified theoretically for small scan ranges and reinforced by a robust real-time calibration procedure, forms the control basis. The automation is built upon a standard software stack comprising EPICS for device control, the Bluesky Suite for experimental orchestration, and Phoebus for the human–machine interface. Through comparative X-ray absorption spectroscopy (XAS) measurements at the Fe L_2,3-edges, the synchronized mode is shown to enhance beam brilliance by 37% and stabilize the incident flux, reducing its variation from 4.2% to 1.8%. This directly results in absorption spectra with superior lineshape fidelity, a 40% reduction in noise, and the elimination of pre- and post-edge artifacts, unequivocally isolating the synchronization effect. This advancement provides a stable, high-brilliance photon source essential for high-quality XAS and X-ray magnetic circular/linear dichroism (XMCD/XMLD) studies. Full article

Magnetron sputtering offers a scalable route to magnetic topological insulators (MTIs) based on Cr-doped Sb₂Te₃. We combine a range of X-ray diffraction (XRD), reciprocal-space mapping (RSM), scanning transmission electron microscopy (STEM), scanning TEM-energy-dispersive X-ray spectroscopy (STEM-EDS), and X-ray absorption spectroscopy, and X-ray magnetic circular dichroism (XAS/XMCD) techniques to study the structure and magnetism of Cr-doped Sb₂Te₃ films. Symmetric $\theta$-2$\theta$ XRD and RSM establish a solubility window. Layered tetradymite order persists up to ∼10 at.-% Cr, while higher doping yields CrTe/Cr₂Te₃ secondary phases. STEM reveals nanocrystalline layered stacking at low Cr and loss of long-range layering at higher Cr concentrations, consistent with XRD/RSM. Magnetometry on a 6% film shows soft ferromagnetism at 5 K. XAS and XMCD at the Cr $L_{2,3}$ edges exhibits a depth dependence: total electron yield (TE; surface sensitive) shows both nominal Cr²⁺ and Cr³⁺, whereas fluorescence yield (FY; bulk sensitive) shows a much higher Cr²⁺ weight. Sum rules applied to TEY give $m_L=(0.20\pm 0.04)$${\mu }_{\mathrm{B}}$/Cr, and $m_S=(1.6\pm 0.2)$${\mu }_{\mathrm{B}}$/Cr, whereby we note that the applied maximum field (3 T) likely underestimates $m_S$. These results define a practical growth window and outline key parameters for MTI films. Full article

A single-molecule magnet (SMM) is a molecule that functions as a magnet. SMMs can be explored not only for emerging technology but also the fundamental science of their quantum nature, nanometer sizes, and their ease of engineering. This review encompasses the state-of-the-art experiments and theories developed so far for SMMs. We briefly explore their experimental synthesis and characterization. In the experimental synthesis, we cover ‘Click Chemistry’ and supramolecular chemistry. The main experimental characterizations comprise superconducting quantum interference devices, electron paramagnetic resonance, neutron scattering, and X-ray magnetic circular dichroism. The theoretical and computational works based on the density functional theory, the post-Hartree–Fock methods, and the theory of open quantum systems are discussed. Moreover, we exemplify the numerous promising research areas for SMMs by discussing quantum technologies. We envision a brilliant future for the fundamental research and emerging applications of SMMs. Full article

The multi-sublattice ferrimagnet Co₂FeO₂BO₃, a prominent example of lanthanide-free magnets, was the subject of element-selective studies using X-ray magnetic circular dichroism (XMCD) observations at the L- and K- X-ray absorption edges. Research findings indicate that the distinct magnetic characteristics of Co₂FeO₂BO₃, namely its remarkable high coercivity (which surpasses 7 Tesla at low temperatures), originate from an atypical arrangement of magnetic ions in the crystal structure (sp.gr. Pbam). The antiferromagnetic nature of the Co²⁺-O-Fe³⁺ exchange interaction was confirmed by identifying the spin and orbital contributions to the total magnetization from Co (m_L = 0.27 ± 0.1 μ_B/ion and m^eff_S = 0.53 ± 0.1 μ_B/ion) and Fe (m_L = 0.05 ± 0.1 μ_B/ion and m^eff_S = 0.80 ± 0.1 μ_B/ion) ions through element-selective XMCD analysis. Additionally, the research explicitly revealed that the strong magnetic anisotropy is a result of the significant unquenched orbital magnetic moment of Co, a feature that is also present in the related compound Co₃O₂BO₃. A complex magnetic structure in Co₂FeO₂BO₃, with infinite Co²⁺O₆ layers in the bc-plane and strong antiferromagnetic coupling through Fe³⁺ ions, is suggested by element-selective hysteresis data, which revealed that Co²⁺ ions contribute both antiferromagnetic and ferromagnetic components to the total magnetization. The findings underline the suitability of Co₂FeO₂BO₃ for applications in extreme environments, such as low temperatures and high magnetic fields, where its unique magnetic topology and anisotropy can be harnessed for advanced technologies, including materials for space exploration and quantum devices. This XMCD study opens the door to the production of novel high-coercivity, lanthanide-free magnetic materials by showing that targeted substitution at specific crystallographic sites can significantly enhance the magnetic properties of such materials. Full article

We report the research results of polynuclear complexes consisting of 3d-4f mixed-metal cores that are maintained by acetate ligands and multidentate Schiff base ligands with structurally exposed thioether groups. The presence of the latter at the periphery of these neutral compounds enables their anchoring onto substrate surfaces. Specifically, we investigated the electronic and magnetic properties as well as the structural arrangement in {Mn^II₃Mn^IVLn^III₃} with Ln = Dy, Yb coordination complexes using various complementary methods. We studied the electronic and atomic structure of the target compounds using the XAS and XES techniques. The molecular structures of the compounds were determined using density functional theory, and the magnetic data were obtained as a function of the magnetic field. Using the XMCD method, we followed the changes in the electronic and magnetic properties of adsorbed magnetic compounds induced by the reaction of ligands through interaction with the substrate. The complexes show antiferromagnetic exchange interactions between Mn and Ln ions. The spectroscopic analyses confirmed the structural and electronic integrity of complexes in organic solution. This study provides important input for a full understanding of the dependence of the magnetic properties and the molecule–substrate interaction of single adsorbed molecules on the type of ligands. It highlights the importance of chemical synthesis for controlling and tailoring the magnetic properties of metalorganic molecules for their use as optimized building blocks of future molecular spin electronics. Full article

In this paper, we determine the magnetic moment induced in graphene when grown on a cobalt film using polarised neutron reflectivity (PNR). A magnetic signal in the graphene was detected by X-ray magnetic circular dichroism (XMCD) spectra at the C K-edge. From the XMCD sum rules an estimated magnetic moment of 0.3 $\mu$_B/C atom, while a more accurate estimation of 0.49 $\mu$_B/C atom was obtained by carrying out a PNR measurement at 300 K. The results indicate that the higher magnetic moment in Co is counterbalanced by the larger lattice mismatch between the Co-C (1.6%) and the slightly longer bond length, inducing a magnetic moment in graphene that is similar to that reported in Ni/graphene heterostructures. Full article

In this work, we report a systematic study of the influence of film thickness on the structural and magnetic properties of epitaxial thin films of Pr_2−δNi_1−xMn_1+xO_6−y (PNMO) double perovskite grown on top of two different (001)-SrTiO₃ and (001)-LaAlO₃ substrates by RF magnetron sputtering. A strong dependence of the structural and magnetic properties on the film thickness is found. The ferromagnetic transition temperature (T_C) and saturation magnetization (Ms) are found to decrease when reducing the film thickness. In our case, the thinnest films show a loss of ferromagnetism at the film-substrate interface. In addition, the electronic structure of some characteristic PNMO samples is deeply analyzed using X-ray absorption spectroscopy (XAS) and X-ray magnetic circular dichroism (XMCD) measurements and compared with theoretical simulations. Our results show that the oxidation states of Ni and Mn ions are stabilized as Ni²⁺ and Mn⁴⁺, thus the ferromagnetism is mainly due to Ni²⁺-O-Mn⁴⁺ superexchange interactions, even in samples with poor ferromagnetic properties. XMCD results also make evident large variations on the spin and orbital contributions to the magnetic moment as the film’s thickness decreases. Full article

Single layer low-dimensional materials are presently of emerging interest, including in the context of magnetism. In the present report, on-surface supramolecular architecturing was further developed and employed to create surface supported two-dimensional binary spin arrays on atomically clean non-magnetic Au(111). By chemical programming of the modules, different checkerboards were produced combining phthalocyanines containing metals of different oxidation and spin states, diamagnetic zinc, and a metal-free ‘spacer’. In an in-depth, spectro-microscopy and theoretical account, we correlate the structure and the magnetic properties of these tunable systems and discuss the emergence of 2D Kondo magnetism from the spin-bearing components and via the physico-chemical bonding to the underlying substrate. The contributions of the individual elements, as well as the role of the electronic surface state in the bottom substrate, are discussed, also looking towards further in-depth investigations. Full article

X-ray absorption fine structure (XAFS) is a powerful technique used to analyze a local electronic structure, local atomic structure, and structural dynamics. In this review, I present examples of XAFS that apply to the local structure and dynamics of functional materials: (1) structure phase transition in perovskite PbTiO₃ and magnetic FeRhPd alloys; (2) nano-scaled fluctuations related to their magnetic properties in Ni–Mn alloys and Fe/Cr thin films; and (3) the Debye–Waller factors related to the chemical reactivity for catalysis in polyanions and ligand exchange reaction. This study shows that the local structure and dynamics are related to the characteristic function of the materials. Full article

Heusler alloys are a material class exhibiting various magnetic properties, including antiferromagnetism. A typical application of antiferromagnets is exchange bias that is a shift of the magnetization curve observed in a layered structure consisting of antiferromagnetic and ferromagnetic films. In this study, a layered sample consisting of a Heusler alloy, Mn${}_2$VAl and a ferromagnet, Fe, is selected as a material system exhibiting exchange bias. Although the fully ordered Mn${}_2$VAl is known as a ferrimagnet, with an optimum fabrication condition for the Mn${}_2$VAl layer, the Mn${}_2$VAl/Fe layered structure exhibits exchange bias. The appearance of the antiferromagnetic property in the Mn${}_2$VAl is remarkable; however, the details have been unclear. To clarify the microscopic aspects on the crystal structures and magnetic moments around the Mn${}_2$VAl/Fe interface, cross-sectional scanning transmission electron microscope (STEM) observation, and synchrotron soft X-ray magnetic circular dichroism (XMCD) measurements were employed. The high-angle annular dark-field STEM images demonstrated clusters of Mn${}_2$VAl with the L2${}_1$ phase distributed only around the interface to the Fe layer in the sample showing the exchange bias. Furthermore, antiferromagnetic coupling between the Mn- and Fe-moments were observed in element-specific hysteresis loops measured using the XMCD. The locally ordered L2${}_1$ phase and antiferromagnetic Mn-moments in the Mn${}_2$VAl were suggested as important factors for the exchange bias. Full article

The chemical and magnetic states of Fe/Fe₂O₃ thin films prepared by e-beam evaporation were investigated by using element-specific techniques, X-ray absorption spectroscopy (XAS) and X-ray magnetic circular dichroism (XMCD). It was clearly shown that the Fe layers are oxidized to form an antiferromagnetic (AFM) FeO_x<1, while the bottom oxide remained a weak ferromagnet (wFM) (α+γ)-type Fe₂O₃. Dependences of the peak intensities and lineshapes on the Fe thickness and measurement geometry further demonstrate that FeO_x<1 layers reside mostly at the interface realizing an FM (Fe)/AFM (FeO_x)/wFM (Fe₂O₃), whilst the spin directions lie in the sample plane for all the samples. The self-stabilized intermediate oxide can act as a physical barrier for spins to be injected into the wFM oxide, implying a substantial influence on tailoring the spin tunneling efficiency for spintronics application. Full article

Using a time-resolved detection scheme in scanning transmission X-ray microscopy (STXM), we measured element resolved ferromagnetic resonance (FMR) at microwave frequencies up to 10 GHz and a spatial resolution down to 20 nm at two different synchrotrons. We present different methods to separate the contribution of the background from the dynamic magnetic contrast based on the X-ray magnetic circular dichroism (XMCD) effect. The relative phase between the GHz microwave excitation and the X-ray pulses generated by the synchrotron, as well as the opening angle of the precession at FMR can be quantified. A detailed analysis for homogeneous and inhomogeneous magnetic excitations demonstrates that the dynamic contrast indeed behaves as the usual XMCD effect. The dynamic magnetic contrast in time-resolved STXM has the potential be a powerful tool to study the linear and nonlinear, magnetic excitations in magnetic micro- and nano-structures with unique spatial-temporal resolution in combination with element selectivity. Full article

Nowadays, a deep knowledge of procedures of synthesis of nanostructured materials plays an important role in achieving nano-materials with accurate and wanted properties and performances. Carbon-based nanostructured materials continue to attract a huge amount of research efforts, because of their wide-ranging properties. Using X-ray absorption (XAS) and X-ray magnetic circular dichroism (XMCD) spectroscopy in the soft X-ray regime, by the synchrotron radiation, we studied the L3,2 absorption edges of iron (Fe) nanoparticles, when they are embedded in oriented Multi Wall Carbon Nanotube (MWCNTs) layers grown by thermal Chemical Vapor Deposition (CVD) technique catalyzed by this transition metal. This could allow us to understand the valence state and role of catalysts and thus their electronic and magnetic structures. It is important to note that the control of the size of these tethered nanoparticles is of primary importance for the purpose of tailoring the physical and chemical properties of these hierarchical materials. The MWCNTs samples used in XAS and XMCD measurements were synthesized by the CVD technique. The actual measurements were carried out by the group NEXT of the INFN- LNF with the logistic experimental support of the INFM-CNR and the Synchrotron Elettra Trieste. Full article

The magnetic anisotropy and exchange coupling between spins localized at the positions of 3d transition metal atoms forming two-dimensional metal–organic coordination networks (MOCNs) grown on a Au(111) metal surface are studied. In particular, we consider MOCNs made of Ni or Mn metal centers linked by 7,7,8,8-tetracyanoquinodimethane (TCNQ) organic ligands, which form rectangular networks with 1:1 stoichiometry. Based on the analysis of X-ray magnetic circular dichroism (XMCD) data taken at T = 2.5 K, we find that Ni atoms in the Ni–TCNQ MOCNs are coupled ferromagnetically and do not show any significant magnetic anisotropy, while Mn atoms in the Mn–TCNQ MOCNs are coupled antiferromagnetically and do show a weak magnetic anisotropy with in-plane magnetization. We explain these observations using both a model Hamiltonian based on mean-field Weiss theory and density functional theory calculations that include spin–orbit coupling. Our main conclusion is that the antiferromagnetic coupling between Mn spins and the in-plane magnetization of the Mn spins can be explained by neglecting effects due to the presence of the Au(111) surface, while for Ni–TCNQ the metal surface plays a role in determining the absence of magnetic anisotropy in the system. Full article

Subsequent to the similar [Mn^III₆Cr^III]³⁺ single-molecule magnets (SMM), the recently studied [Fe^III₆Cr^III]³⁺ structural type adsorbed thin films prepared on Si and gold-coated glass substrates have been experimentally studied by means of spin-polarized electron spectroscopy (SPES) and X-ray magnetic circular dichroism (XMCD) at the Fe L_3,2 edge using circularly-polarized synchrotron radiation. The results are cross-compared to the corresponding data obtained from the recently published measurements with Mn-based SMM [1], also in terms of the local spin and orbital magnetic moments obtained. Furthermore, [Fe^III₆Cr^III]³⁺ single crystals have been experimentally studied by means of magnetometry and X-ray diffraction. Full article