Polarisation-dependent single-pulse ultrafast optical switching of an elementary ferromagnet

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.

29 pages, 6 figures

References in corpus (6)

• Super-Diffusive Spin-Transport as a Mechanism of Ultrafast Demagnetization
• All-optical control of ferromagnetic thin films and nanostructures
• Perspective: Ultrafast magnetism and THz spintronics
• Laser-induced torques in metallic ferromagnets
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Cited by in corpus (3)

• All-optical non-linear chiral ultrafast magnetization dynamics driven by circularly polarized magnetic fields
• Ultrafast chiral precession of spin and orbital angular momentum induced by circularly polarized laser pulse
• Adiabatic spin dynamics and effective exchange interactions from constrained tight-binding electronic structure theory: Beyond the Heisenberg regime