Time-resolved X-ray Magnetic Circular Dichroism Research Articles

Microscopic evaluation of spin and orbital moment in ferromagnetic resonance

Time-resolved X-ray magnetic circular dichroism under the effects of ferromagnetic resonance (FMR), known as X-ray ferromagnetic resonance (XFMR) measurements, enables direct detection of precession dynamics of magnetic moment. Here we demonstrated XFMR measurements and Bayesian analyses as a quantitative probe for the precession of spin and orbital magnetic moments under the FMR effect. Magnetization precessions in two different Pt/Ni-Fe thin film samples were directly detected. Furthermore, the ratio of dynamical spin and orbital magnetic moments was evaluated quantitatively by Bayesian analyses for XFMR energy spectra around the Ni L2,3\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$L_{2,3}$$\\end{document} absorption edges. Our study paves the way for a microscopic investigation of the contribution of the orbital magnetic moment to magnetization dynamics.

Photocarrier transport of ferroelectric photovoltaic thin films detected by the magnetic dynamics of adjacent ferromagnetic layers

We have observed photocarrier transport behaviors in ${\mathrm{BiFeO}}_{3}/{\mathrm{La}}_{1\ensuremath{-}x}{\mathrm{Sr}}_{x}{\mathrm{MnO}}_{3}$ (BFO/LSMO) heterostructures by using time-resolved synchrotron x-ray magnetic circular dichroism in reflectivity. The magnetization of LSMO layers was used as a probe of photo-induced carrier dynamics in the photovoltaic BFO layers. During the photo-induced demagnetization process, the decay time of LSMO ($x$=0.2) magnetization strongly depends on the ferroelectric polarization direction of the BFO layer. The variation of decay time should be attributed to the different sign of accumulated photocarriers at the BFO/LSMO interface induced by the photovoltaic effect of the BFO layer. The photocarriers can reach the BFO/LSMO interface and influence the magnetization distribution in the LSMO layers within the timescale of $\ensuremath{\sim}100$ ps. Our results provide a novel strategy to investigate carrier dynamics and mechanisms of optical control of magnetization in thin film heterostructures.

X-ray magnetic circular dichroism spectroscopy at the Fe L edges with a picosecond laser-driven plasma source

Time-resolved x-ray magnetic circular dichroism (XMCD) enables a unique spectroscopic view on complex spin and charge dynamics in multi-elemental magnetic materials. So far, its application in the soft-x-ray range has been limited to synchrotron-radiation sources and free-electron lasers. By combining a laser-driven plasma source with a magnetic thin-film polarizer, we generate up to 30% circular polarization in the soft-x-ray regime, enabling the first XMCD spectroscopy at the Fe L edges in a laser laboratory, to our knowledge. Our approach can be readily adapted to other transition metal L and rare earth M absorption edges, and with a temporal resolution of <10ps, a wide range of ultrafast magnetization studies can be realized.

Laser induced ultrafast Gd 4f spin dynamics in Co100-xGdx alloys by means of time-resolved XMCD

We have studied the laser induced ultrafast quenching of Gd 4f magnetic order in ferrimagnetic Co100-xGdx alloys to highlight the role of the inter-atomic exchange coupling. We have taken advantage of the ultrashort soft X-ray pulses deliver by the femtoslicing beamline at the BESSY II synchrotron radiation source at the Helmholtz-Zentrum Berlin to perform element- and time-resolved X-ray Magnetic Circular Dichroism spectroscopy.Our results show that the laser induced quenching of Gd 4f magnetic order occurs on very different time-scales for the Co72Gd28, the Co77Gd23 and the Co79Gd21 alloys. Most of the magnetic moment losses occur within the first picosecond (ps) while the electron distribution is strongly out of equilibrium. After the equilibration of the electrons and lattice temperatures (t > 1 ps), the magnetic losses occur on slower rates that depend on the alloy composition: increasing the Co composition speeds up the demagnetization of Gd 4f sublattice. The strength of the inter-atomic exchange coupling which depends on composition, determines the efficiency of the angular momentum flow from the Gd 4f spin towards the lattice. Our results are in qualitative agreements with the predictions of the microscopic three temperatures model for ferrimagnetic alloys.

Experimental confirmation of the delayed Ni demagnetization in FeNi alloy

Element-selective techniques are central for the understanding of ultrafast spin dynamics in multi-element materials, such as magnetic alloys. Recently, however, it turned out that the commonly used technique of the transverse magneto-optical Kerr effect (T-MOKE) in the extreme ultraviolet range may have issues with unwanted crosstalk between different elemental signals and energy-dependent non-linear response. This problem can be sizeable, which puts recent observations of ultrafast spin transfer from Fe to Ni sites in FeNi alloys into question. In this study, we investigate the Fe-to-Ni spin transfer in a crosstalk-free time-resolved x-ray magnetic circular dichroism (XMCD) experiment with a reliable time reference. With XMCD near the absorption maxima, we find a very similar Fe and Ni dynamics as with T-MOKE from identical samples. Considering the potential non-linearities of the T-MOKE response, such a good agreement in our findings is remarkable. Our data provide the ongoing discussion about ultrafast spin-transfer mechanisms in FeNi systems with a broader experimental basis.

Photo-induced antiferromagnetic-ferromagnetic and spin-state transition in a double-perovskite cobalt oxide thin film

Investigation of ultrafast dynamic behaviors can provide novel insights about the coupling mechanisms among multiple degrees of freedom in condensed matters, such as lattice, magnetism and electronic structure. Here we investigate both the ferromagnetic (FM) and antiferromagnetic (AFM) dynamics of a strongly correlated oxide system, GdBaCo2O5.5 thin film by time-resolved x-ray magnetic circular dichroism in reflectivity (XMCDR) and resonant magnetic x-ray diffraction (RMXD). A photo-induced AFM-FM transition characterized by an increase of the transient XMCDR (sensitive to FM order) beyond the unpumped value and a decay of RMXD (sensitive to AFM order) was observed. The photon-energy dependence of the transient XMCDR and reflectivity could be interpreted as a concomitant photo-induced spin-state transition (SST). The AFM-FM transition and SST couple with each other in the time domain, resulting in unusual dynamic behaviors of the magnetism.

Correlation between Spin and Orbital Dynamics during Laser-Induced Femtosecond Demagnetization

Spin and orbital angular momenta are two intrinsic properties of an electron and are responsible for the physics of a solid. How the spin and orbital evolve with respect to each other on several hundred femtoseconds is largely unknown, but it is at the center of laser-induced ultrafast demagnetization. In this paper, we introduce a concept of the spin-orbital correlation diagram, where spin angular momentum is plotted against orbital angular momentum, much like the position-velocity phase diagram in classical mechanics. We use four sets of highly accurate time-resolved x-ray magnetic circular dichroism (TR-XMCD) data to construct four correlation diagrams for iron and cobalt. To our surprise, a pattern emerges. The trace on the correlation diagram for iron is an arc, and at the end of demagnetization, it has a pronounced cusp. The correlation diagram for cobalt is different and appears more linear, but with kinks. We carry out first-principles calculations with two different methods: time-dependent density functional theory (TDDFT) and time-dependent Liouville density functional theory (TDLDFT). These two methods agree that the experimental findings for both Fe and Co are not due t experimental errors. It is the spin-orbit coupling that correlates the spin dynamics to the orbital dynamics.Microscopically, Fe and Co have different orbital occupations, which leads to distinctive correlation diagrams. We believe that this correlation diagram presents a useful tool to better understand spin and orbital dynamics on an ultrafast time scale. A brief discussion on the magnetic anisotropy energy is also provided.

A local view of the laser induced magnetic domain dynamics in CoPd stripe domains at the picosecond time scale

The dynamics of the magnetic structure in a well ordered ferromagnetic CoPd stripe domain pattern has been investigated upon excitation by femtosecond infrared laser pulses. Time-resolved x-ray magnetic circular dichroism in photoemission electron microscopy (TR-XMCD-PEEM) is used to perform real space magnetic imaging with 100 ps time resolution in order to show local transformations of the domains structures. Using the time resolution of the synchrotron radiation facility of the Helmholtz-Zentrum Berlin, we are able to image the transient magnetic domains in a repetitive pump and probe experiment. In this work, we study the reversible and irreversible transformations of the excited magnetic stripe domains as function of the laser fluence. Our results can be explained by thermal contributions, reducing the XMCD amplitude in each stripe domain below a threshold fluence of 12 mJ cm−2. Above this threshold fluence, irreversible transformations of the magnetic domains are observed. Static XMCD-PEEM images reveal the new partially ordered stripe domain structures characterized by a new local magnetic domain distribution showing an organized pattern at the micrometer scale. This new arrangement is attributed to the recovery of the magnetic anisotropy during heat dissipation under an Oersted field.

Ultrafast demagnetization of Pt magnetic moment in L10-FePt probed by magnetic circular dichroism at a hard x-ray free electron laser

Unraveling the origin of ultrafast demagnetization in multisublattice ferromagnetic materials requires femtosecond x-ray techniques to trace the magnetic moment dynamics on individual elements, but this could not yet be achieved in the hard x-ray regime. We demonstrate here the first ultrafast demagnetization dynamics in the ferromagnetic heavy 5d-transition metal Pt using circularly-polarized hard x-rays at an x-ray free electron laser (XFEL). The decay time of laser-induced demagnetization of L10-FePt is determined to be using time-resolved x-ray magnetic circular dichroism at the Pt L3 edge, whereas magneto-optical Kerr measurements indicate the decay time for the total magnetization as . A transient magnetic state with a photo-modulated ratio of the 3d and 5d magnetic moments is demonstrated for pump–probe delays larger than 1 ps. We explain this distinct photo-modulated transient magnetic state by the induced-moment behavior of the Pt atom and the x-ray probing depth. Our findings pave the way for the future use of XFELs to disentangle atomic spin dynamics contributions.

Ultrafast demagnetization in buried Co80Dy20 as fingerprint of hot-electron transport

Abstract The generation of ultrashort hot-electron pulses in metallic heterostructures offers attractive perspectives for the ultrafast spin manipulation on the picosecond time scale. In such approach, the hot-electron pulses are produced by exciting a non-magnetic capping layer with femtosecond infrared laser pulses. These hot-electron pulses propagate towards a buried magnetic layer to trigger ultrafast demagnetization. Lately, it was shown that the demagnetization onset and characteristic demagnetization times are both affected by the transport regime (ballistic or diffusive) of the photo-excited hot-electrons. In this work, we show that the hot-electron pulses produced by photo-exciting a Al(3)/Ta(3)/Cu(60) capping layer undergo a temporal stretching and delays when they go across a [Co(0.1)/Ni(0.6)]x5 multilayer. These information were extracted from a study of hot-electron induced demagnetization in CoDy alloys by means of Time-Resolved X-Ray Magnetic Circular Dichroism.

Angular Momentum Flow During Ultrafast Demagnetization of a Ferrimagnet.

One of the key processes setting the speed of the ultrafast magnetization phenomena is the angular momentum transfer from and into the spin system. However, the way the angular momentum flows during ultrafast demagnetization and magnetization switching phenomena remains elusive so far. We report on time-resolved soft x-ray magnetic circular dichroism measurements of the ferrimagnetic GdFeCo alloy allowing us to record the dynamics of elemental spin and orbital moments at the Fe and Gd sites during femtosecond laser-induced demagnetization. We observe a complete transfer of spin and orbital angular momentum to the lattice during the first hundreds of femtoseconds of the demagnetization process.

Proposal of X-ray absorption spectroscopy and magnetic circular dichroism using broadband free-electron lasers.

X-ray free-electron lasers (XFELs) have been widely used for applications such as X-ray crystallography and magnetic spin probes because of their unprecedented performance. Recently, time-resolved X-ray magnetic circular dichroism (XMCD) with ultrafast XFEL pulses have made it possible to achieve an instantaneous view of atomic de-excitation. However, owing to the narrow bandwidth and coherence of XFELs, X-ray absorption spectroscopy (XAS) and XMCD are time- and effort-consuming for both machine scientists and users of XFELs. In this work, an efficient scheme using a broadband XFEL pulse and single-shot X-ray spectrometer is proposed, in which the XAS and XMCD measurements can be accomplished with the same machine conditions. An evolutionary multi-objective optimization algorithm is used to maximize the XFEL bandwidth offered by the Shanghai Soft X-ray FEL user facility without additional hardware. A numerical example using MnO is demonstrated, showing that, by using approximately 1000 consecutive XFEL shots with a central photon energy of 650 eV and full bandwidth of 4.4%, precise spectral measurements for XAS and XMCD can be achieved. Additional considerations related to single-shot XAS and XMCD are discussed.

Time and Spatially Resolved Hard X-Ray MCD Measurement on a Co/Pt Multilayer Dot Excited by Pulsed RF Field

Understanding of magnetization behavior in magnetic nanostructures is a key issue for future magnetic/spintronic devices. Time-resolved X-ray magnetic circular dichroism (XMCD) is a powerful measurement technique with potential of nanometer spatial resolution, picosecond time resolution, and element selectivity. We have carried out time and spatially resolved XMCD microscopy measurement on a Co/Pt multilayer dot by detecting XMCD at the Pt $L_{3}$ edge at BL39XU of SPring-8 using hard X-ray. Transient magnetic response of Co/Pt multilayer dots with diameter of $2.6~\mu \text{m}$ was investigated against pulsed RF field with frequency around 2.5 GHz and the maximum amplitude of about 400 Oe. By synchronizing excitation RF field pulse with X-ray pulses, the growth of magnetization precession of the induced Pt magnetic moment in the dot was clearly observed with sub-100 ps time resolution and submicrometer spatial resolution. The developed measurement setup can be applicable for a wide range of studies for time-resolved hard X-ray experiments.

Spin currents during ultrafast demagnetization of ferromagnetic bilayers

Ultrafast spin currents induced by femtosecond laser excitation of ferromagnetic metals have been found to contribute to sub-picosecond demagnetization, and to cause a transient enhancement of the magnetization of the bottom Fe layer in a Ni/Ru/Fe layered structure. We analyze the ultrafast magnetization dynamics in such layered structures by element- and femtosecond time-resolved x-ray magnetic circular dichroism, for different Ni and Fe layer thicknesses, Ru and Ta interlayers, and by varying the pump laser fluence. While we do not observe the transient enhancement of the magnetization in Ni/Ru/Fe discovered previously, we do find a reduced demagnetization of the Fe layer compared to a Ni/Ta/Fe layered structure. In the latter, the spin-scattering Ta layer suppresses spin currents from the Ni layer into Fe, consistent with previous results. Any spin current arriving in the lower Fe layer will counteract other, local demagnetization mechanisms such as phonon-mediated spin-flip scattering. We find by increasing the Ni and Fe layer thicknesses in Ni/Ru/Fe a decreasing effect of spin currents on the buried Fe layer, consistent with a mean free path of the laser-induced spin currents of just a few nm. Our results suggest that in order to utilize ultrafast spin currents in an efficient manner, the sample design has to be optimized with these considerations in mind, and further studies clarifying the role of interfaces in the employed layered structures are needed.

Capturing ultrafast magnetic dynamics by time-resolved soft x-ray magnetic circular dichroism

Experiments of time-resolved x-ray magnetic circular dichroism (Tr-XMCD) and resonant x-ray scattering at a beamline BL07LSU in SPring-8 with a time-resolution of under 50 ps are presented. A micro-channel plate is utilized for the Tr-XMCD measurements at nearly normal incidence in both the partial electron and total fluorescence yield (PEY and TFY) modes at the L2,3 absorption edges of the 3d transition-metals in the soft x-ray region. The ultrafast photo-induced demagnetization within 50 ps is observed on the dynamics of a magnetic material of FePt thin films, having a distinct threshold of the photon density. The spectrum in the PEY mode is less-distorted at both the L2,3 edges compared with that in the TFY mode and has the potential to apply the sum rule analysis for XMCD spectra in pump-probed experiments.

Direct Detection of Pure ac Spin Current by X-Ray Pump-Probe Measurements.

Despite recent progress in spin-current research, the detection of spin current has mostly remained indirect. By synchronizing a microwave waveform with synchrotron x-ray pulses, we use the ferromagnetic resonance of the Py (Ni_{81}Fe_{19}) layer in a Py/Cu/Cu_{75}Mn_{25}/Cu/Co multilayer to pump a pure ac spin current into the Cu_{75}Mn_{25} and Co layers, and then directly probe the spin current within the Cu_{75}Mn_{25} layer and the spin dynamics of the Co layer by x-ray magnetic circular dichroism. This element-resolved pump-probe measurement unambiguously identifies the ac spin current in the Cu_{75}Mn_{25} layer.

Femtosecond Magnetism When the Orbital Angular Momentum is Quenched

In femtosecond magnetism, a femtosecond laser pulse affects the spin moment only indirectly through the orbital angular momentum and the spin–orbit coupling. A long-standing puzzle is what happens if the orbital angular momentum itself is quenched. Here, we employ a four-level system to resolve this puzzle. The results show that the quenching of the orbital angular moment in the ground state has no direct relation to the spin moment change. By contrast, the orbital moment can be restored partially after the pulsed optical excitation and can affect the demagnetization. Importantly, this study confirms that the orbital moment indeed responds to the laser field faster than spin if the pulse duration is short, consistent with the recent time-resolved X-ray magnetic circular dichroism experiment. Therefore, our finding shines new light on femtosecond magnetism.

Ultrafast and Distinct Spin Dynamics in Magnetic Alloys

Controlling magnetic order on ultrashort timescales is crucial for engineering the next-generation magnetic devices that combine ultrafast data processing with ultrahigh-density data storage. An appealing scenario in this context is the use of femtosecond (fs) laser pulses as an ultrafast, external stimulus to fully set the orientation and the magnetization magnitude of a spin ensemble. Achieving such control on ultrashort timescales, e.g., comparable to the excitation event itself, remains however a challenge due to the lack of understanding the dynamical behavior of the key parameters governing magnetism: The elemental magnetic moments and the exchange interaction. Here, we investigate the fs laser-induced spin dynamics in a variety of multi-component alloys and reveal a dissimilar dynamics of the constituent magnetic moments on ultrashort timescales. Moreover, we show that such distinct dynamics is a general phenomenon that can be exploited to engineer new magnetic media with tailor-made, optimized dynamic properties. Using phenomenological considerations, atomistic modeling and time-resolved X-ray magnetic circular dichroism (XMCD), we demonstrate demagnetization of the constituent sub-lattices on significantly different timescales that depend on their magnetic moments and the sign of the exchange interaction. These results can be used as a “recipe” for manipulation and control of magnetization dynamics in a large class of magnetic materials.

Spin pumping in ferromagnet-topological insulator-ferromagnet heterostructures.

Topological insulators (TIs) are enticing prospects for the future of spintronics due to their large spin-orbit coupling and dissipationless, counter-propagating conduction channels in the surface state. However, a means to interact with and exploit the topological surface state remains elusive. Here, we report a study of spin pumping at the TI-ferromagnet interface, investigating spin transfer dynamics in a spin-valve like structure using element specific time-resolved x-ray magnetic circular dichroism, and ferromagnetic resonance. Gilbert damping increases approximately linearly with increasing TI thickness, indicating efficient behaviour as a spin sink. However, layer-resolved measurements suggest that a dynamic coupling is limited. These results shed new light on the spin dynamics of this novel material class, and suggest great potential for TIs in spintronic devices, through their novel magnetodynamics that persist even up to room temperature.

Ultrafast angular momentum transfer in multisublattice ferrimagnets

Femtosecond laser pulses can be used to induce ultrafast changes of the magnetization in magnetic materials. However, one of the unsolved questions is that of conservation of the total angular momentum during the ultrafast demagnetization. Here we report the ultrafast transfer of angular momentum during the first hundred femtoseconds in ferrimagnetic Co0.8Gd0.2 and Co0.74Tb0.26 films. Using time-resolved X-ray magnetic circular dichroism allowed for time-resolved determination of spin and orbital momenta for each element. We report an ultrafast quenching of the magnetocrystalline anisotropy and show that at early times the demagnetization in ferrimagnetic alloys is driven by the local transfer of angular momenta between the two exchange-coupled sublattices while the total angular momentum stays constant. In Co0.74Tb0.26 we have observed a transfer of the total angular momentum to an external bath, which is delayed by ~150 fs.