Manipulation of magnetisation with ultrashort laser pulses is promising for information storage device applications. The dynamics of the magnetisation response depends on the energy transfer from the photons to the spins during the initial laser excitation. A material of special interest for magnetic storage are FePt nanoparticles, for which switching of the magnetisation with optical angular momentum was demonstrated recently. The mechanism remained unclear. Here we investigate experimentally and theoretically the all-optical switching of FePt nanoparticles. We show that the magnetisation switching is a stochastic process. We develop a complete multiscale model which allows us to optimize the number of laser shots needed to switch the magnetisation of high anisotropy FePt nanoparticles in our experiments. We conclude that only angular momentum induced optically by the inverse Faraday effect will provide switching with one single femtosecond laser pulse.

Magnetization manipulation is essential for basic research and applications. A fundamental question is, how fast can the magnetization be reversed in nanoscale magnetic storage media. When subject to an ultrafast laser pulse, the speed of the magnetization dynamics depends on the nature of the energy transfer pathway. The order of the spin system can be effectively influenced through spin-flip processes mediated by hot electrons. It has been predicted that as electrons drive spins into the regime close to almost total demagnetization, characterized by a loss of ferromagnetic correlations near criticality, a second slower demagnetization process takes place after the initial fast drop of magnetization. By studying FePt, we unravel the fundamental role of the electronic structure. As the ferromagnet Fe becomes more noble in the FePt compound, the electronic structure is changed and the density of states around the Fermi level is reduced, thereby driving the spin correlations into the limit of critical fluctuations. We demonstrate the impact of the electrons and the ferromagnetic interactions, which allows a general insight into the mechanisms of spin dynamics when the ferromagnetic state is highly excited and identifies possible recording speed limits in heat-assisted magnetization reversal.

We derive the Landau-Lifshitz-Bloch (LLB) equation for a two-component magnetic system valid up to the Curie temperature. As an example, we consider disordered GdFeCo ferrimagnet where the ultrafast optically induced magnetization switching under the action of heat alone has been recently reported. The two-component LLB equation contains the longitudinal relaxation terms responding to the exchange fields from the proper and the neighboring sublattices. We show that the sign of the longitudinal relaxation rate at high temperatures can change depending on the dynamical magnetization value and a dynamical polarization of one material by another can occur. We discuss the differences between the LLB and the Baryakhtar equations, recently used to explain the ultrafast switching in ferrimagnets. The two-component LLB equation forms the basis for the large-scale micromagnetic modeling of nanostructures at high temperatures and ultrashort time scales. DOI: http://dx.doi.org/10.1103/PhysRevB.86.104414 ©2012 American Physical Society

A hierarchical multiscale approach to model the magnetization dynamics of ferromagnetic random alloys is presented. First-principles calculations of the Heisenberg exchange integrals are linked to atomistic spin models based upon the stochastic Landau-Lifshitz-Gilbert (LLG) equation to calculate temperature-dependent parameters (e.g., effective exchange interactions, damping parameters). These parameters are subsequently used in the Landau-Lifshitz-Bloch (LLB) model for multisublattice magnets to calculate numerically and analytically the ultrafast demagnetization times. The developed multiscale method is applied here to FeNi (permalloy) as well as to copper-doped FeNi alloys. We find that after an ultrafast heat pulse the Ni sublattice demagnetizes faster than the Fe sublattice for the here-studied FeNi-based alloys.

The detailed derivation of the quantum Landau-Lifshitz-Bloch (qLLB) equation for simple spin-flip scattering mechanisms based on spin-phonon and spin-electron interactions is presented and the approximations are discussed. The qLLB equation is written in a form suitable for comparison with its classical counterpart. The temperature dependence of the macroscopic relaxation rates is discussed for both mechanisms. It is demonstrated that the magnetization dynamics is slower in the quantum case than in the classical one.