Demagnetization Dynamics Research Articles

Itinerant and Localized Magnetization Dynamics in Antiferromagnetic Ho.

Using femtosecond time-resolved resonant magnetic x-ray diffraction at the Ho L_{3} absorption edge, we investigate the demagnetization dynamics in antiferromagnetically ordered metallic Ho after femtosecond optical excitation. Tuning the x-ray energy to the electric dipole (E1, 2p→5d) or quadrupole (E2, 2p→4f) transition allows us to selectively and independently study the spin dynamics of the itinerant 5d and localized 4f electronic subsystems via the suppression of the magnetic (2 1 3-τ) satellite peak. We find demagnetization time scales very similar to ferromagnetic 4f systems, suggesting that the loss of magnetic order occurs via a similar spin-flip process in both cases. The simultaneous demagnetization of both subsystems demonstrates strong intra-atomic 4f-5d exchange coupling. In addition, an ultrafast lattice contraction due to the release of magneto-striction leads to a transient shift of the magnetic satellite peak.

A Dual-Colour Architecture for Pump-Probe Spectroscopy of Ultrafast Magnetization Dynamics in the Sub-10-femtosecond Range

Current time-resolution-limited dynamic measurements clearly show the need for improved techniques to access processes on the sub-10-femtosecond timescale. To access this regime, we have designed and constructed a state-of-the-art time-resolved magneto-optic Kerr effect apparatus, based on a new dual-color scheme, for the measurement of ultrafast demagnetization and precessional dynamics in magnetic materials. This system can operate well below the current temporal ranges reported in the literature, which typically lie in the region of around 50 fs and above. We have used a dual-colour scheme, based on ultra broadband hollow-core fibre and chirped mirror pulse compression techniques, to obtain unprecedented sub-8-fs pump and probe pulse durations at the sample plane. To demonstrate the capabilities of this system for ultrafast demagnetization and precessional dynamics studies, we have performed measurements in a ferrimagnetic GdFeCo thin film. Our study has shown that the magnetization shows a sudden drop within the first picosecond after the pump pulse, a fast recovery (remagnetization) within a few picoseconds, followed by a clear oscillation or precession during a slower magnetization recovery. Moreover, we have experimentally confirmed for the first time that a sub-10-fs pulse is able to efficiently excite a magnetic system such as GdFeCo.

Demagnetization dynamics of C-doped FePt film

Magneto-optical information storage has been a hot research subject for several years. FePt exhibits abundant physical properties and has received much attention as a candidate material. Its alloy film with perpendicular anisotropy and small grain size has important applications in magnetic recordings due to the large intrinsic magnetic anisotropy which ensures long-time thermal stability of nanometer sized bits. However, the large coercive field of FePt is a significant factor that hinders its application. As is well known, the magnetic anisotropy in FePt alloy can be precisely modulated by carbon-doping, and as a result, the coercive field of FePt film can be modified effectively with the carbon dopant. On the other hand, the microscopic mechanism of magnetic storage relies on the motion of spin system. Ultrashort femtosecond laser has been demonstrated to be a very effective tool to investigate the dynamical coupling among different degrees of freedom, such as electron, spin and lattice in a ferromagnetic film. The research on spin dynamics has become a new frontier of condensed matter physics, which is crucial for ultrafast magnetic recording materials. In this work, by using the time-resolved magneto-optical Kerr effect spectroscopy, we study the ultrafast spin dynamics of two FePt alloy films with different carbon dopants under the applied magnetic field along the film surface. The FePt alloy films with different carbon dopants are fabricated on silicon substrates by the sputtering method. The main experimental findings in this work are as follows. (i) The transient Kerr signal is linearly proportional to the magnetization with the magnetic field up to 0.8 T, while the transient reflectivity of the film is independent of the applied magnetic field. (ii) For FePt alloy films with different coercive fields, it is found that the demagnetization time of the film with smaller coercive field is significantly faster than that of the larger counterpart: the former shows 0.8 ps demagnetization time, and the latter has a magnitude of 1.2 ps. The demagnetization times for both soft and hard magnetic films are independent of the applied magnetic field. (iii) With ultrafast laser pulse radiation, we observe the propagation of acoustic phonon with a resonance frequency of ～ 49 GHz, and the frequency of the acoustic phonon is independent of the applied magnetic field. From the above, the spin dynamics of the samples shows strong correlation with carbon-doping. Our experimental findings are desired for basic research as well as for the design and development of novel magneto-optical devices.

Simultaneous measurements of terahertz emission and magneto-optical Kerr effect for resolving ultrafast laser-induced demagnetization dynamics

Simultaneous detection of THz emission and transient magneto-optical response is employed to study ultrafast laser-induced magnetization dynamics in multisublattice magnets NdFeCo and GdFeCo amorphous alloys with in-plane magnetic anisotropy. A satisfactory quantitative agreement between the dynamics revealed with the help of these two techniques is obtained for GdFeCo. For NdFeCo the THz emission reveals faster dynamics than the magneto-optical response. This indicates that in addition to spin dynamics of Fe ultrafast laser excitation triggers faster magnetization dynamics of Nd.

Nonlocal ultrafast demagnetization dynamics of Co/Pt multilayers by optical field enhancement

The influence on ultrafast demagnetization dynamics of metallic nano-structured gratings deposited on thin films of magnetic Co/Pt multilayers is investigated by the time-resolved optical Kerr effect. Depending on the polarization of the pump pulse, a pronounced enhancement of the demagnetization amplitude is found. Calculation of the inhomogeneous optical field distribution due to plasmon interaction and time-dependent solutions of the coupled electron, lattice, and spin temperatures in two dimensions show good agreement with the experimental data, as well as giving evidence of non-local demagnetization dynamics due to electron diffusion.

Transient band structures in the ultrafast demagnetization of ferromagnetic gadolinium and terbium

We compare the laser-driven demagnetization dynamics of the rare earths gadolinium and terbium by mapping their transient valance band structures with time- and angle-resolved photoelectron spectroscopy. In both metals, the minority and majority spin valence bands evolve independently with different time constants after optical excitation. The ultrafast shift of the partially unoccupied minority spin bulk band to higher binding energy and of the majority spin surface state to lower binding energy suggests spin transport between surface and bulk. The slower response of the fully occupied majority spin band follows the lattice temperature and is attributed to Elliott-Yafet type spin-flip scattering. Terbium shows a stronger and faster decay of the exchange splitting, pointing to ultrafast magnon emission via $4f$ spin-to-lattice coupling.

Imaging Ultrafast Demagnetization Dynamics after a Spatially Localized Optical Excitation

Ultrashort, coherent x-ray pulses of a free-electron laser are used to holographically image the magnetization dynamics within a magnetic domain pattern after creation of a localized excitation via an optical standing wave. We observe a spatially confined reduction of the magnetization within a couple of hundred femtoseconds followed by its slower recovery. Additionally, the experimental results show evidence of a spatial evolution of magnetization, which we attribute to ultrafast transport of nonequilibrium spin-polarized electrons for early times and to a fluence-dependent remagnetization rate for later times.

Transverse Demagnetization Dynamics of a Unitary Fermi Gas

Understanding the quantum dynamics of strongly interacting fermions is a problem relevant to diverse forms of matter, including high-temperature superconductors, neutron stars, and quark-gluon plasma. An appealing benchmark is offered by cold atomic gases in the unitary limit of strong interactions. Here, we study the dynamics of a transversely magnetized unitary Fermi gas in an inhomogeneous magnetic field. We observe the demagnetization of the gas, caused by diffusive spin transport. At low temperatures, the diffusion constant saturates to the conjectured quantum-mechanical lower bound ≃ ħ/m, where m is the particle mass. The development of pair correlations, indicating the transformation of the initially noninteracting gas toward a unitary spin mixture, is observed by measuring Tan's contact parameter.

Investigating the role of superdiffusive currents in laser induced demagnetization of ferromagnets with nanoscale magnetic domains.

Understanding the loss of magnetic order and the microscopic mechanisms involved in laser induced magnetization dynamics is one of the most challenging topics in today's magnetism research. While scattering between spins, phonons, magnons and electrons have been proposed as sources for dissipation of spin angular momentum, ultrafast spin dependent transport of hot electrons has been pointed out as a potential candidate to explain ultrafast demagnetization without resorting to any spin dissipation channel. Here we use time resolved magneto-optical Kerr measurements to extract the influence of spin dependent transport on the demagnetization dynamics taking place in magnetic samples with alternating domains with opposite magnetization directions. We unambiguously show that whatever the sample magnetic configuration, the demagnetization takes place during the same time, demonstrating that hot electrons spin dependent transfer between neighboring domains does not alter the ultrafast magnetization dynamics in our systems with perpendicular anisotropy and 140 nm domain sizes.

Phototunable magnetism in copper octacyanomolybdate.

We introduce copper molybdenum cyanides of general formula Cu2[Mo(CN)8]·nH2O, which can serve as optofunctional magnetic devices. Their ground states generally stay paramagnetic down to temperatures of the K order but exhibit a spontaneous magnetization upon photoirradiation usually below a few tens of K. To interest us still further, such a ferromagnetic stateinduced by blue-laser irradiation is demagnetized step by step through further application of red or near-infrared laser pulses. We solve this intriguing photomagnetism. The ground-state properties are fully revealed by means of a group-theoretical technique. Taking account of experimental observations, we simulate applying pump laser pulses to a likely ground state and successfully reproduce both the magnetization and demagnetization dynamics. We monitor the photorelaxation process through angle-resolved photoemission spectroscopy. Electrons are fully itinerant in any of the photoinduced steady states, forming a striking contrast to the initial equilibrium state of atomic aspect. The fully demagnetized final steady state looks completely different from the initial paramagnetism but bears good analogy to one of the possible ground states available with the Coulomb repulsion on Cu sites suppressed.

Feedback Effect during Ultrafast Demagnetization Dynamics in Ferromagnets

Motivated by the recent controversy about the importance of spin-flip scattering for ultrafast demagnetization in ferromagnets, we study the spin-dependent electron dynamics based on a dynamical Elliott-Yafet mechanism. The key improvement to earlier approaches is the use of a modified Stoner model with a dynamic exchange splitting between majority and minority bands. In the framework of our microscopic model, we find a novel feedback effect between the time-dependent exchange splitting and the spin-flip scattering. This feedback effect allows us to reproduce important properties of the demagnetization dynamics quantitatively. Our results demonstrate that in general Elliott-Yafet spin-flip scattering needs to be taken into account to obtain a microscopic picture of demagnetization dynamics.

Modeling of the Laser-Heating Induced Ultrafast Demagnetization Dynamics in Ferrimagnetic Thin Films

Ultrafast demagnetization excited by laser pulses introduces the technological possibility for controlling the magnetic properties of materials on sub-picosecond regime. In this paper, the demagnetization dynamics of amorphous ferrimagnetic TbFeCo alloy is modeled by using the stochastic Landau-Lifshitz-Gilbert equation on an atomistic level. The transition metal (Fe, Co) and rare earth (Tb) atoms are constructed by two different sub-lattice systems. Laser-heating induced demagnetization processes are clearly demonstrated by a series of snapshots. Our simulations show that full demagnetization on the sub-picosecond time scale requires a temperature over the Curie point, and the demagnetization time increases with the Tb content.

Role of critical spin fluctuations in ultrafast demagnetization of transition-metal rare-earth alloys

Ultrafast magnetization dynamics induced by femtosecond laser pulses have been measured in ferrimagnetic Co0.8Gd0.2, Co.74Tb.26 and Co.86Tb.14 alloys. Using element sensitivity of X-ray magnetic circular dichroism at the Co L3, Tb M5 and Gd M5 edges we evidence that the demagnetization dynamics is element dependent. We show that a thermalization time as fast as 280 fs is observed for the rare-earth in the alloy, when the laser excited state temperature is below the compensation temperature. It is limited to 500 fs when the laser excited state temperature is below the Curie temperature (Tc). We propose critical spin fluctuations in the vicinity of TC as the mechanism which reduces the demagnetization rates of the 4f electrons in transition-metal rare-earth alloys whereas at any different temperature the limited demagnetization rates could be avoided.

Role of the inter-sublattice exchange coupling in short-laser-pulse-induced demagnetization dynamics of GdCo and GdCoFe alloys

ThedynamicsofthedemagnetizationinducedbyanultrashortlaserpulseinGdCoandGdCoFealloysisshown tobesubstantiallydifferentfromtheexpected trend.Wefindthattheintersublatticeexchange interactionbetween Gd and Co(Fe) is used as an additional route of heat transfer during the demagnetization process and leads to a temporary cooling of the Co(Fe) spin subsystem. The observed results are described by a four-temperature model (4T model) in which electrons, lattice, and 4f and 3d spins represent four reservoirs of heat energy. In this model, the coupling between the electron and spin reservoirs is responsible for an ultrafast demagnetization, while the intersublattice exchange coupling gives rise to an immediate remagnetization and serves as a thermal link between the Co(Fe) and Gd spins.

Ultrafast Demagnetization Measurements Using Extreme Ultraviolet Light: Comparison of Electronic and Magnetic Contributions

Ultrashort pulses of extreme ultraviolet light from high-harmonic generation are a new tool for probing coupled charge, spin, and phonon dynamics with element specificity, attosecond pump-probe synchronization, and time resolution of a few femtoseconds in a tabletop apparatus. In this paper, we address an important question in magneto-optics that has implications for understanding magnetism on the fastest time scales: Is the signal from the transverse magneto-optical Kerr effect at the M2,3 edges of a magnetic material purely magnetic or is it perturbed by nonmagnetic artifacts? Our measurements demonstrate conclusively that transverse magneto-optical Kerr measurements at the M2,3 edges sensitively probe the magnetic state, with almost negligible contributions from the transient variation of the refractive index by the nonequilibrium hot-electron distribution. In addition, we compare pump-probe demagnetization dynamics measured by both high harmonics and conventional visible-wavelength magneto-optics and find that the measured demagnetization times are in agreement.Received 26 October 2011DOI:https://doi.org/10.1103/PhysRevX.2.011005This article is available under the terms of the Creative Commons Attribution 3.0 License. Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI.Published by the American Physical Society

Ultrafast demagnetization dynamics of thin Fe/W(110) films: Comparison of time- and spin-resolved photoemission with time-resolved magneto-optic experiments

We report the results of time- and spin-resolved photoemission (TR-SPES) and time-resolved magneto-optical Kerr effect experiments on iron thin films. In particular, the extracted demagnetization times for both techniques are compared. It is shown that while for the Kerr measurements the demagnetization times are always limited by our time resolution ($250\ifmmode\pm\else\textpm\fi{}30$ fs), for the TR-SPES measurements this situation occurs only for relative quenching below $30%$. Above this value, the measured TR-SPES demagnetization time exceeds 500 fs. Different demagnetization probes can hence track different demagnetization times.

Time-resolved demagnetization ofCo2MnSi observed using x-ray magnetic circular dichroism and an ultrafast streak camera

The demagnetization dynamics of the Heusler alloyCo2MnSi was studied using picosecond time-resolved x-ray magnetic circular dichroism. The sample wasexcited using femtosecond laser pulses. In contrast to the sub-picosecond demagnetizationof the metal ferromagnet Ni, substantially slower demagnetization with a time constant of3.5 ± 0.5 ps was measured. This could be explained by a spin-dependentband gap inhibiting the spin-flip scattering of hot electrons inCo2MnSi, which is predicted to be half-metallic. A universal demagnetization time constant wasmeasured across a range of pump power levels.

Demagnetization on the fs time-scale by the Elliott-Yafet mechanism

An ultrashort laser pulse can change the magnetization of ferromagnetic metals such as Ni in less than a picosecond. Thereby, angular momentum is transferred from the spin system to the lattice. One possible candidate for this transfer is the Elliott-Yafet mechanism of spin-orbit mediated spin-flip scattering of electrons at phonons. Former ab-initio calculations have shown that for Ni and Co the Elliott-Yafet spin-mixing parameter which describes the degree of mixing of the two spin states for the electronic eigenstates – averaged over all states involved in the demagnetization process – is large enough to explain the experimentally observed demagnetization rates. In the present paper we calculate in addition the spin-mixing for the individual electronic states as function of their wavevector. Furthermore, the theory is extended to the case of Gd for which experiments have revealed a slower demagnetization dynamics than for Ni.

Ultrafast Demagnetization Dynamics at theMEdges of Magnetic Elements Observed Using a Tabletop High-Harmonic Soft X-Ray Source

We use few-femtosecond soft x-ray pulses from high-harmonic generation to extract element-specific demagnetization dynamics and hysteresis loops of a compound material for the first time. Using a geometry where high-harmonic beams are reflected from a magnetized Permalloy grating, large changes in the reflected intensity of up to 6% at the M absorption edges of Fe and Ni are observed when the magnetization is reversed. A short pump pulse is used to destroy the magnetic alignment, which allows us to measure the fastest, elementally specific demagnetization dynamics, with 55 fs time resolution. The use of high harmonics for probing magnetic materials promises to combine nanometer spatial resolution, elemental specificity, and femtosecond-to-attosecond time resolution, making it possible to address important fundamental questions in magnetism.

Ultrafast demagnetization of ferromagnetic transition metals: The role of the Coulomb interaction

The Elliott-Yafet mechanism is arguably the most promising candidate to explain the ultrafast demagnetization dynamics in ferromagnetic transition metals on timescales on the order of 100 femtoseconds. So far, only electron-phonon scattering has been analyzed as the scattering process needed to account for the demagnetization due to the Elliott-Yafet mechanism. We show for the first time that the electron-electron scattering contribution to the Elliott-Yafet mechanism has the potential to explain time-resolved magneto-optical Kerr effect measurements on thin magnetic cobalt and nickel films, without reference to a phononic "spin bath."