Nonreciprocal collective magnetostatic wave modes in geometrically asymmetric bilayer structure with nonmagnetic spacer.

Nonreciprocity, i.e. inequivalence in amplitudes and frequencies of spin waves propagating in opposite directions, is a key property underlying functionality in prospective magnonic devices. Here we demonstrate experimentally and theoretically a simple approach to induce frequency nonreciprocity in a magnetostatically coupled ferromagnetic bilayer structure with a nonmagnetic spacer by its geometrical asymmetry. Using Brillouin light scattering, we show the formation of two collective spin wave modes in Fe81Ga19/Cu/Fe81Ga19 structure with different thicknesses of ferromagnetic layers. Experimental reconstruction and theoretical modeling of the dispersions of acoustic and optical collective spin wave modes reveal that both possess nonreciprocity reaching several percent at the wavenumber of 22 × 104 rad cm-1. The analysis demonstrates that the shift of the amplitudes of counter-propagating coupled modes towards either of the layers is responsible for the nonreciprocity because of the pronounced dependence of spin wave frequency on the layers' thickness. The proposed approach enables the design of multilayered ferromagnetic structures with a given spin wave dispersion for magnonic logic gates.

Laser-induced THz magnetism of antiferromagnetic CoF2.

Excitation, detection, and control of coherent THz magnetic excitation in antiferromagnets are challenging problems that can be addressed using ever shorter laser pulses. We study experimentally excitation of magnetic dynamics at THz frequencies in an antiferromagnetic insulator CoF2by sub-10 fs laser pulses. Time-resolved pump-probe polarimetric measurements at different temperatures and probe polarizations reveal laser-induced transient circular birefringence oscillating at the frequency of 7.45 THz and present below the Néel temperature. The THz oscillations of circular birefringence are ascribed to oscillations of the magnetic moments of Co2+ions induced by the laser-driven coherentEgphonon mode via the THz analogue of the transverse piezomagnetic effect. It is also shown that the same pulse launches coherent oscillations of the magnetic linear birefringence at the frequency of 3.4 THz corresponding to the two-magnon mode. Analysis of the probe polarization dependence of the transient magnetic linear birefringence at the frequency of the two-magnon mode enables identifying its symmetry.

Effect of laser pulse propagation on ultrafast magnetization dynamics in a birefringent medium.

Light propagation effects can strongly influence the excitation and the detection of laser-induced magnetization dynamics. We investigated experimentally and analytically the effects of crystallographic linear birefringence on the excitation and detection of ultrafast magnetization dynamics in the rare-earth orthoferrites (Sm0.5Pr0.5)FeO3 and (Sm0.55Tb0.45)FeO3, which possess weak and strong linear birefringence, respectively. Our finding is that the effect of linear birefringence on the result of a magneto-optical pump-probe experiment strongly depends on the mechanism of excitation. When magnetization dynamics, probed by means of the Faraday effect, is excited via a rapid, heat-induced phase transition, the measured rotation of the probe pulse polarization is strongly suppressed due to the birefringence. This contrasts with the situation for magnetization dynamics induced by the ultrafast inverse Faraday effect, where the corresponding probe polarization rotation values were larger in the orthoferrite with strong linear birefringence. We show that this striking difference results from an interplay between the polarization transformations experienced by pump and probe pulses in the birefringent medium.

Extreme ultraviolet resonant inelastic X-ray scattering (RIXS) at a seeded free-electron laser.

In the past few years, we have been witnessing an increased interest for studying materials properties under non-equilibrium conditions. Several well established spectroscopies for experiments in the energy domain have been successfully adapted to the time domain with sub-picosecond time resolution. Here we show the realization of high resolution resonant inelastic X-ray scattering (RIXS) with a stable ultrashort X-ray source such as an externally seeded free electron laser (FEL). We have designed and constructed a RIXS experimental endstation that allowed us to successfully measure the d-d excitations in KCoF3 single crystals at the cobalt M2,3-edge at FERMI FEL (Elettra-Sincrotrone Trieste, Italy). The FEL-RIXS spectra show an excellent agreement with the ones obtained from the same samples at the MERIXS endstation of the MERLIN beamline at the Advanced Light Source storage ring (Berkeley, USA). We established experimental protocols for performing time resolved RIXS experiments at a FEL source to avoid X ray-induced sample damage, while retaining comparable acquisition time to the synchrotron based measurements. Finally, we measured and modelled the influence of the FEL mixed electromagnetic modes, also present in externally seeded FELs, and the beam transport with ~120 meV experimental resolution achieved in the presented RIXS setup.

Coherent control of the route of an ultrafast magnetic phase transition via low-amplitude spin precession.

Time-resolved magneto-optical imaging of laser-excited rare-earth orthoferrite (SmPr)FeO3 demonstrates that a single 60 fs circularly polarized laser pulse is capable of creating a magnetic domain on a picosecond time scale with a magnetization direction determined by the helicity of light. Depending on the light intensity and sample temperature, pulses of the same helicity can create domains with opposite magnetizations. We argue that this phenomenon relies on a twofold effect of light which (i) instantaneously excites coherent low-amplitude spin precession and (ii) triggers a spin reorientation phase transition. The former dynamically breaks the equivalence between two otherwise degenerate states with opposite magnetizations in the high-temperature phase and thus controls the route of the phase transition.

Ultrafast heating as a sufficient stimulus for magnetization reversal in a ferrimagnet.

The question of how, and how fast, magnetization can be reversed is a topic of great practical interest for the manipulation and storage of magnetic information. It is generally accepted that magnetization reversal should be driven by a stimulus represented by time-non-invariant vectors such as a magnetic field, spin-polarized electric current, or cross-product of two oscillating electric fields. However, until now it has been generally assumed that heating alone, not represented as a vector at all, cannot result in a deterministic reversal of magnetization, although it may assist this process. Here we show numerically and demonstrate experimentally a novel mechanism of deterministic magnetization reversal in a ferrimagnet driven by an ultrafast heating of the medium resulting from the absorption of a sub-picosecond laser pulse without the presence of a magnetic field.

Ultrafast path for optical magnetization reversal via a strongly nonequilibrium state.

Using time-resolved single-shot pump-probe microscopy we unveil the mechanism and the time scale of all-optical magnetization reversal by a single circularly polarized 100 fs laser pulse. We demonstrate that the reversal has a linear character, i.e., does not involve precession but occurs via a strongly nonequilibrium state. Calculations show that the reversal time which can be achieved via this mechanism is within 10 ps for a 30 nm domain. Using two single subpicosecond laser pulses we demonstrate that for a 5 microm domain the magnetic information can be recorded and readout within 30 ps, which is the fastest "write-read" event demonstrated for magnetic recording so far.

Impulsive generation of coherent magnons by linearly polarized light in the easy-plane antiferromagnet FeBO3.

Polarization-dependent excitation of coherent spin precession by 150 fs linearly polarized laser pulses is observed in the easy-plane antiferromagnet FeBO3. We show that the mechanism of excitation is impulsive stimulated Raman scattering. This process is shown to be determined not only by the magneto-optical constants of the material, but also by the properties of the spin precession itself. Though carrying no angular momentum, the linearly polarized laser pulses act on the spins as effective fields that can be considered as an ultrafast inverse Cotton-Mouton effect.

Magnetic-field-induced second-harmonic generation in semiconductor GaAs.

We show that application of a magnetic field induces optical second-harmonic generation (SHG) in GaAs. This phenomenon arises from field-induced symmetry breaking causing new optical nonlinearities. A series of narrow SHG lines is observed in the spectral range from 1.52 to 1.77 eV that we attribute to Landau-level quantization of the band energy spectrum. The rotational anisotropy of the SHG signal distinctly differs from that of the electric-dipole approximation. Model calculations reveal that nonlinear magneto-optical spatial dispersion that comes together with the electric-dipole term is the dominant mechanism for this nonlinearity.