No abstract

Magnetic phenomena are ubiquitous in our surroundings and indispensable for modern science and technology, but it is notoriously difficult to change the magnetic order of a material in a rapid way. However, if a thin nickel film is subjected to ultrashort laser pulses, it can lose its magnetic order almost completely within merely femtosecond times [1]. This phenomenon, in the meantime also observed in many other materials [2-7], has connected magnetism with femtosecond optics in an efficient, ultrafast and complex way, offering opportunities for rapid information processing [8-12] or ultrafast spintronics at frequencies approaching those of light [8,9,13]. Consequently, the physics of ultrafast demagnetization is central to modern material research [1-7,14-28], but a crucial question has remained elusive: If a material loses its magnetization within only femtoseconds, where is the missing angular momentum in such short time? Here we use ultrafast electron diffraction to reveal in nickel an almost instantaneous, long-lasting, non-equilibrium population of anisotropic highfrequency phonons that appear as quickly as the magnetic order is lost. The anisotropy plane is perpendicular to the direction of the initial magnetization and the atomic oscillation

Ultrafast demagnetization of rare-earth metals is distinct from that of 3d ferromagnets, as rare-earth magnetism is dominated by localized 4f electrons that cannot be directly excited by an optical laser pulse. Their demagnetization must involve excitation of magnons, driven either through exchange coupling between the 5d6s-itinerant and 4f-localized electrons or by coupling of 4f spins to lattice excitations. Here, we disentangle the ultrafast dynamics of 5d6s and 4f magnetic moments in terbium metal by time-resolved photoemission spectroscopy. We show that the demagnetization time of the Tb 4f magnetic moments of 400 fs is set by 4f spin–lattice coupling. This is experimentally evidenced by a comparison to ferromagnetic gadolinium and supported by orbital-resolved spin dynamics simulations. Our findings establish coupling of the 4f spins to the lattice via the orbital momentum as an essential mechanism driving magnetization dynamics via ultrafast magnon generation in technically relevant materials with strong magnetic anisotropy.

Ultrafast spin dynamics in magnetic materials is generally associated with ultrafast heating of the electronic system by a near infrared femtosecond laser pulse, thus offering only an indirect and nonselective access to the spin order. Here we explore spin dynamics in ferromagnets by means of extremely intense THz pulses, as at these low frequencies the magnetic field provides a direct and selective route to coherently control the magnetization. We find that, at low fields, the observed off-resonantly excited spin precession is phase locked to the THz magnetic field. At extreme THz fields, the coherent spin dynamics become convoluted with an ultrafast incoherent magnetic quenching due to the absorbed energy. This demagnetization takes place upon a single shot exposure. The magnetic properties are found to be permanently modified above a THz pump fluence of ≈100 mJ/cm 2 . We conclude that magnetization switching cannot be reached. Our atomistic spin-dynamics simulations excellently explain the measured magnetization response. We find that demagnetization driven by THz laser-field coupling to electron charges occurs, suggesting nonconducting materials for achieving coherent THz-magnetization reversal.

Control of magnetic domain wall motion holds promise for efficient manipulation and transfer of magnetically stored information. Thermal magnon currents, generated by temperature gradients, can be used to move magnetic textures, from domain walls, to magnetic vortices and skyrmions. In the last years, theoretical studies have centered in ferro-and antiferromagnetic spin structures, where domain walls always move towards the hotter end of the thermal gradient. Here we perform numerical studies using atomistic spin dynamics simulations and complementary analytical calculations to derive an equation of motion for the domain wall velocity. We demonstrate that in ferrimagnets, domain wall motion under thermal magnon currents shows a much richer dynamics. Below the Walker breakdown, we find that the temperature gradient always pulls the domain wall towards the hot end by minimizating its free energy, in agreement with the observations for ferro-and antiferromagnets in the same regime. Above Walker breakdown, the ferrimagnetic domain wall can show the opposite, counterintuitive behavior of moving towards the cold end. We show that in this case, the motion to the hotter or the colder ends is driven by angular momentum transfer and therefore strongly related to the angular momentum compensation temperature, a unique property of ferrimagnets where the intrinsic angular momentum of the ferrimagnet is zero while the sublattice angular momentum remains finite. In particular, we find that below the compensation temperature the wall moves towards the cold end, whereas above it, towards the hot end. Moreover, we find that for ferrimagnets, there is a torque compensation temperature at which the domain wall dynamics shows similar characteristics to antiferromagnets, that is, quasi-inertia-free motion and the absence of Walker breakdown. This finding opens the door for fast control of magnetic domains as given by the antiferromagnetic character while conserving the advantage of ferromagnets in terms of measuring and control by conventional means such as magnetic fields. arXiv:1911.05393v1 [cond-mat.mtrl-sci]