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Register a new userOptical excitation of single- and multi-mode magnetization precession in Galfenol nanolayers
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We demonstrate a variety of precessional responses of the magnetization to ultrafast optical excitation in nanolayers of Galfenol (Fe,Ga), which is a ferromagnetic material with large saturation magnetization and enhanced magnetostriction. The particular properties of Galfenol, including cubic magnetic anisotropy and weak damping, allow us to detect up to 6 magnon modes in a 120-nm layer, and a single mode with effective damping ${alpha}_{eff}$ = 0.005 and frequency up to 100 GHz in a 4-nm layer. This is the highest frequency observed to date in time-resolved experiments with metallic ferromagnets. We predict that detection of magnetization precession approaching THz frequencies should be possible with Galfenol nanolayers.
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Laser induced ultrafast demagnetization in ferromagnetic metals was discovered almost 20 years ago, but currently there is still lack of consensus on the microscopic mechanism responsible for the corresponding transfer of angular momentum and energy between electron, lattice and spin subsystems. A distinct, but intrinsically correlated phenomenon occurring on a longer timescale is the magnetization precession after the ultrafast demagnetization process, if a magnetic field is applied to tilt the magnetization vector away from its easy direction, which can be attributed to the change of anisotropy after laser heating. In an in-plane magnetized Pt/Co/Pt thin film with perpendicular interface anisotropy, we found excellent agreement between theoretical prediction with plausible parameters and experimental data measured using time resolved magneto-optical Kerr effect. This agreement confirms that the time evolution of the anisotropy field, which is driven by the interaction between electrons and phonons, determines the magnetization precession completely. A detailed analysis shows that, even though the whole sample is magnetized in-plane, the dynamic interface anisotropy field dictates the initial phase of the magnetization precession, highlighting the significance of the interface anisotropy field in laser induced magnetization precession.
The rate and pathways of relaxation of a magnetic medium to its equilibrium following excitation with intense and short laser pulses are the key ingredients of ultrafast optical control of spins. Here we study experimentally the evolution of the magnetization and magnetic anisotropy of thin films of a ferromagnetic metal galfenol (Fe$_{0.81}$Ga$_{0.19}$) resulting from excitation with a femtosecond laser pulse. From the temporal evolution of the hysteresis loops we deduce that the magnetization $M_S$ and magnetic anisotropy parameters $K$ recover within a nanosecond, and the ratio between $K$ and $M_S$ satisfies the thermal equilibriums power law in the whole time range spanning from a few picoseconds to 3 nanoseconds. We further use the experimentally obtained relaxation times of $M_S$ and $K$ to analyze the laser-induced precession and demonstrate how they contribute to its frequency evolution at the nanosecond timescale.
We use femtosecond optical pulses to induce, control and monitor magnetization precession in ferromagnetic Ga0.965Mn0.035As. At temperatures below ~40 K we observe coherent oscillations of the local Mn spins, triggered by an ultrafast photoinduced reorientation of the in-plane easy axis. The amplitude saturation of the oscillations above a certain pump intensity indicates that the easy axis remains unchanged above ~TC/2. We find that the observed magnetization precession damping (Gilbert damping) is strongly dependent on pump laser intensity, but largely independent on ambient temperature. We provide a physical interpretation of the observed light-induced collective Mn-spin relaxation and precession.
Gate-induced superconductivity at the surface of nanolayers of semiconducting transition metal dichalcogenides (TMDs) has attracted a lot of attention in recent years, thanks to the sizeable transition temperature, robustness against in-plane magnetic fields beyond the Pauli limit, and hints to a non-conventional nature of the pairing. A key information necessary to unveil its microscopic origin is the geometry of the Fermi surface hosting the Cooper pairs as a function of field-effect doping, which is dictated by the filling of the inequivalent valleys at the K/K$^{prime}$ and Q/Q$^{prime}$ points of the Brillouin Zone. Here, we achieve this by combining Density Functional Theory calculations of the bandstructure with transport measurements on ion-gated 2H-MoS$_{2}$ nanolayers. We show that, when the number of layers and the amount of strain are set to their experimental values, the Fermi level crosses the bottom of the high-energy valleys at Q/Q$^{prime}$ at doping levels where characteristic kinks in the transconductance are experimentally detected. We also develop a simple 2D model which is able to quantitatively describe the broadening of the kinks observed upon increasing temperature. We demonstrate that this combined approach can be employed to map the dependence of the Fermi surface of TMD nanolayers on field-effect doping, detect Lifshitz transitions, and provide a method to determine the amount of strain and spin-orbit splitting between sub-bands from electric transport measurements in real devices.
Single-molecule magnets facilitate the study of quantum tunneling of magnetization at the mesoscopic level. The spin-parity effect is among the fundamental predictions that have yet to be clearly observed. It is predicted that quantum tunneling is suppressed at zero transverse field if the total spin of the magnetic system is half-integer (Kramers degeneracy) but is allowed in integer spin systems. The Landau-Zener method is used to measure the tunnel splitting as a function of transverse field. Spin-parity dependent tunneling is established by comparing the transverse field dependence of the tunnel splitting of integer and half-integer spin systems.
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