No Arabic abstract
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 large curvature effects on micromagnetic energy of a thin ferromagnetic film with nonlocal dipolar energy are considered. We predict that the dipolar interaction and surface curvature can produce perpendicular anisotropy which can be controlled by engineering a special type of periodic surface shape structure. Similar effects can be achieved by a significant surface roughness in the film. We show that in general the anisotropy can point in an arbitrary direction depending on the surface curvature. We provide simple examples of these periodic surface structures to demonstrate how to engineer particular anisotropies in the film.
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.
The laser-induced precession of magnetization in (Ga,Mn)As samples with different magnetic anisotropy was studied by the time-resolved magneto-optical method. We observed that the dependence of the precession amplitude on the external magnetic field depends strongly on the magnetic anisotropy of (Ga,Mn)As and we explain this phenomenon in terms of competing cubic and uniaxial anisotropies. We also show that the corresponding anisotropy fields can be deduced from the magnetic field dependence of the precession frequency.
We report on the photo-induced precession of the ferromagnetically coupled Mn spins in (Ga,Mn)As, which is observed even with no external magnetic field applied. We concentrate on various experimental aspects of the time-resolved magneto-optical Kerr effect (TR-MOKE) technique that can be used to clarify the origin of the detected signals. We show that the measured data typically consist of several different contributions, among which only the oscillatory signal is directly connected with the ferromagnetic order in the sample.
We present a method to map the saturation magnetization of soft ultrathin films with perpendicular anisotropy, and we illustrate it to assess the compositional dependence of the magnetization of CoFeB(1 nm)/MgO films. The method relies on the measurement of the dipolar repulsion of parallel domain walls that define a linear domain. The film magnetization is linked to the field compressibility of the domain. The method also yields the minimal distance between two walls before their merging, which sets a practical limit to the storage density in spintronic devices using domain walls as storage entities.