Exploring the impact of the inverse Faraday effect on all-optical helicity-dependent magnetization switching

Abstract

All-optical helicity-dependent magnetization switching (AO-HDS) is the quickest data recording technique using only ultrashort laser pulses. FePt grains provide an ideal platform for examining the interaction of effects conducting magnetization switching. We identify the magnetic circular dichroism (MCD) and the inverse Faraday effect (IFE) as the primary switching forces. Ultrafast photon absorption rapidly elevates electron temperatures, quenching magnetization. The MCD's helicity-dependent absorption ensures distinct electron temperatures, holding a finite switching probability by generating different spin noise rates in each spin channel. The IFE induces a magnetic moment, enhancing this probability. We present ultrashort laser pulse (<200 fs) AO-HDS experiments in the near-infrared spectral range from 800 nm to 1500 nm, demonstrating a correlation between switching efficiency and absorbed energy density. Elevating electron temperatures to the Curie point enables the IFE to induce a magnetic moment for deterministic switching in the quenched magnetization state. Unlike in films or multilayers, where domain wall motion and domain growth govern the switching process, increasing the MCD in nanometer-sized grains does not enhance switching efficiency. Electrons around the Curie temperature typically reach increased switching rates for higher induced magnetization generated by the IFE. The MCD sets the necessary switching condition, separating electron temperatures. The IFE generates a magnetic moment, directing spins toward the desired orientation and improving switching efficiency. Every laser pulse initiates a new switching probability for each grain, increasing the role of direction indication by the IFE. Stronger absorption assures higher induced magnetization at low switching fluences.