Element-resolved x-ray ferrimagnetic and ferromagnetic resonance spectroscopy

We report on the measurement of element-specific magnetic resonance spectra at gigahertz frequencies using x-ray magnetic circular dichroism (XMCD). We investigate the ferrimagnetic precession of Gd and Fe ions in Gd-substituted Yttrium Iron Garnet, showing that the resonant field and linewidth of Gd precisely coincide with Fe up to the nonlinear regime of parametric excitations. The opposite sign of the Gd x-ray magnetic resonance signal with respect to Fe is consistent with dynamic antiferromagnetic alignment of the two ionic species. Further, we investigate a bilayer metal film, Ni$_{80}$Fe$_{20}$(5 nm)/Ni(50 nm), where the coupled resonance modes of Ni and Ni$_{80}$Fe$_{20}$ are separately resolved, revealing shifts in the resonance fields of individual layers but no mutual driving effects. Energy-dependent dynamic XMCD measurements are introduced, combining x-ray absorption and magnetic resonance spectroscopies.Comment: 16 pages, 8 figure

A detailed investigation of the onion structure of exchanged coupled magnetic Fe3-dO4@CoFe2O4@Fe3-dO4 nanoparticles

Nanoparticles that combine several magnetic phases offer wide perspectives for cutting edge applications because of the high modularity of their magnetic properties. Besides the addition of the magnetic characteristics intrinsic to each phase, the interface that results from core-shell and, further, from onion structures leads to synergistic properties such as magnetic exchange coupling. Such a phenomenon is of high interest to overcome the superparamagnetic limit of iron oxide nanoparticles which hampers potential applications such as data storage or sensors. In this manuscript, we report on the design of nanoparticles with an onion-like structure which has been scarcely reported yet. These nanoparticles consist of a Fe3-dO4 core covered by a first shell of CoFe2O4 and a second shell of Fe3-dO4, e.g., a Fe3-dO4@CoFe2O4@Fe3-dO4 onion-like structure. They were synthesized through a multistep seed-mediated growth approach which consists consists in performing three successive thermal decomposition of metal complexes in a high-boiling-point solvent (about 300 °C). Although TEM micrographs clearly show the growth of each shell from the iron oxide core, core sizes and shell thicknesses markedly differ from what is suggested by the size increasing. We investigated very precisely the structure of nanoparticles in performing high resolution (scanning) TEM imaging and geometrical phase analysis (GPA). The chemical composition and spatial distribution of atoms were studied by electron energy loss spectroscopy (EELS) mapping and spectroscopy. The chemical environment and oxidation state of cations were investigated by 57Fe Mössbauer spectrometry, soft X-ray absorption spectroscopy (XAS) and X-ray magnetic circular dichroism (XMCD). The combination of these techniques allowed us to estimate the increase of Fe2+ content in the iron oxide core of the core@shell structure and the increase of the cobalt ferrite shell thickness in the core@shell@shell one, whereas the iron oxide shell appears to be much thinner than expected. Thus, the modification of the chemical composition as well as the size of the Fe3-dO4 core and the thickness of the cobalt ferrite shell have a high impact on the magnetic properties. Furthermore, the growth of the iron oxide shell also markedly modifies the magnetic properties of the core-shell nanoparticles, thus demonstrating the high potential of onion-like nanoparticles to accurately tune the magnetic properties of nanoparticles according to the desired applications. © 2021 American Chemical Society

X-ray ferromagnetic resonance spectroscopy

We present a method to measure continuous-wave ferromagnetic resonance (FMR) spectra based on the core-level absorption of circularly polarized x rays. The technique is demonstrated by using a monochromatic x-ray beam incident on an yttrium-iron-garnet sample excited by a microwave field at 2.47 GHz. FMR spectra are obtained by monitoring the x-ray absorption intensity at the photon energy corresponding to the maximum of the magnetic circular dichroism effect at the iron L2,3 edges as a function of applied magnetic field. The x-ray FMR signal is shown to be energy dependent, which makes the technique element sensitive and opens up new possibilities to perform element-resolved FMR in magnetic alloys and multilayers. © 2005 American Institute of Physics

Double-resonant x-ray and microwave absorption: Atomic spectroscopy of precessional orbital and spin dynamics

We show that double-resonance spectra recorded during the simultaneous absorption of x-ray and microwave (MW) photons are a fingerprint of the perturbed electronic configuration of atomic species driven to ferromagnetic resonance. X-ray absorption measurements performed as a function of x-ray energy and polarization over the Fe L2,3 edges of single-crystal yttrium-iron garnet reveal MW-induced multiplet features related to angular momentum transfer from the MW field to localized Fe 3d magnetic sublevels. O K-edge absorption spectra demonstrate the formation of dynamic 2p-orbital magnetization components at O sites coupled to the Fe magnetic moments at tetrahedral and octahedral sites. These results are compared with double-resonance x-ray absorption spectra of Permalloy, showing that the MW transition probability is distributed according to the hybridization character of the 3d states and proportional to the unperturbed unoccupied magnetic density of states of metals and insulators