ABSTRACT
The development of two-dimensional (2D) magnetism is driven not only by the interest of low-dimensional physics but also by potential applications in high-density miniaturized spintronic devices. However, 2D materials possessing a ferromagnetic order with a relatively high Curie temperature (Tc) are rare. In this paper, the evidence of ferromagnetism in monolayer FeCl2 on Au(111) surfaces, as well as the interlayer antiferromagnetic coupling of bilayer FeCl2, is characterized by using spin-polarized scanning tunneling microscopy. A Curie temperature (Tc) of â¼147 K is revealed for monolayer FeCl2, based on our static magneto-optical Kerr effect measurements. Furthermore, temperature-dependent magnetization dynamics is investigated by the time-resolved magneto-optical Kerr effect. A transition from one- to two-step demagnetization occurs as the lattice temperature approaches Tc, which supports the Elliott-Yafet spin relaxation mechanism. The findings contribute to a deeper understanding of the underlying mechanisms governing ultrafast magnetization in 2D ferromagnetic materials.
ABSTRACT
The fundamental mechanisms of ultrafast demagnetization and magnetization recovery processes in ferromagnetic materials remain incompletely understood. The investigation of different dynamic features which depend on various physical quantities requires a more systematic approach. Here, the femtosecond laser-induced demagnetization and recovery dynamics in L10-Fe0.5Pt0.5 alloy film are studied by utilizing time-resolved magneto-optical Kerr measurements, focusing on their dependences of excitation fluence and ambient temperature over broad ranges. Ultrafast demagnetization dominated by Elliott-Yafet spin-flip scattering, and two-step magnetization recovery processes are found to be involved in all observations. The fast recovery time corresponding to spin-lattice relaxation is much shorter than that of many ferromagnets and increase with excitation fluence. These can be ascribed to the strong spin-orbit coupling (SOC) demonstrated in FePt and the reduction of transient magnetic anisotropy, respectively. Surprisingly, the demagnetization time exhibits no discernible correlation with ambient temperature. Two competitive factors are proposed to account for this phenomenon. On the other hand, the spin-lattice relaxation accelerates as temperature decreases due to enhanced SOC at lower ambient temperature. A semiquantitative analysis is given to get a visualized understanding. These results offer a comprehensive understanding of the dynamic characteristics of ultrafast demagnetization and recovery processes in iron-based materials with strong SOC, highlighting the potential for regulating the magnetization recovery process through temperature and laser fluence adjustments.
ABSTRACT
Superdiffusive spin transport has been proposed as a new mechanism of ultrafast demagnetization in layered magnetic nanostructures and demonstrated experimentally. However, it is unknown if it is possible for phonon transport to occur and manipulate ultrafast demagnetization. Here, we explore the ultrafast dynamics of demagnetization of an antiferromagnet/ferromagnet bilayer nanostructure, of a FeMn/MnGa bilayer film prepared by molecular beam epitaxy. Ultrafast dynamics of a two-step demagnetization were observed through the time-resolved magneto-optical Kerr effect. The first-step fast component of the two-step demagnetization occurred within ~200 fs, while the second-step slow component emerged in a few tens of picoseconds. For a single MnGa film, only the ultrafast dynamics of the first-step fast demagnetization were observed, revealing that the second-step slow demagnetization originates from interlayer phonon transport. A four-temperature model considering phonon transport was developed and used to effectively reproduce the observed ultrafast dynamics of two-step demagnetization. Our results reveal the effect of phonon transport on demagnetization for the first time and open up a new route to manipulate ultrafast demagnetization in layered magnetic structures.