Abstract
The ultimate control of magnetic states of matter at femtosecond (or even faster) timescales defines one of the most pursued paradigm shifts for future information technology. In this context, ultrafast laser pulses developed into extremely valuable stimuli for the all-optical magnetisation reversal in ferrimagnetic and ferromagnetic alloys and multilayers, while this remains elusive in elementary ferromagnets. Here we demonstrate that a single laser pulse with sub-picosecond duration can lead to the reversal of the magnetisation of bulk nickel, in tandem with the expected demagnetisation. As revealed by realistic time-dependent electronic structure simulations, the central mechanism is ultrafast light-induced torques acting on the magnetisation, which are only effective if the laser pulse is circularly polarised on a plane that contains the initial orientation of the magnetisation. We map the laser pulse parameter space enabling the magnetisation switching and unveil rich intra-atomic orbital-dependent magnetisation dynamics featuring transient inter-orbital non-collinear states. Our findings open further perspectives for the efficient implementation of optically-based spintronic devices.
Colloidal Plasmonic Nanoparticles for Ultrafast Optical Switching and Laser Pulse Generation
