اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدUltrafast reduction in exchange interaction by a laser pulse: Alternative path to femtomagnetism
41
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
Since the beginning of femtomagnetism, it has been hotly debated how an ultrafast laser pulse can demagnetize a sample and switch its spins within a few hundred femtoseconds, but no consensus has been reached. In this paper, we propose that an ultrafast reduction in the exchange interaction by a femtosecond laser pulse is mainly responsible for demagnetization and spin switching. The key physics is that the dipole selection rule demands two distinctive electron configurations for the ground and excited states and consequently changes the exchange interaction. Although the exchange interaction change is almost instantaneous, its effect on the spin is delayed by the finite spin wave propagation. Consistent with the experimental observation, the delay becomes longer with a stronger exchange interaction pulse. In spin-frustrated systems, the effect of the exchange interaction change is even more dramatic, where the spin can be directly switched from one direction to the other. Therefore, our theory has the potential to explain the essence of major observations in rare-earth transition metal compounds for the last seven years. Our findings are likely to motivate further research in the quest of the origin of femtomagnetism.
قيم البحث
اقرأ أيضاً
An ultrafast spin current can be induced by femtosecond laser excitation in a ferromagnetic (FM) thin film in contact with a nonmagnetic (NM) metal. The propagation of an ultrafast spin current into NM metal has recently been found in experiments to
generate transient spin accumulation. Unlike spin accumulation in equilibrium NM metals that occurs due to spin transport at the Fermi energy, transient spin accumulation involves highly nonequilibrium hot electrons well above the Fermi level. To date, the diffusion and dissipation of this transient spin accumulation has not been well studied. Using the superdiffusive spin transport model, we demonstrate how spin accumulation is generated in NM metals after laser excitation in an FM|NM bilayer. The spin accumulation shows an exponential decay from the FM|NM interface, with the decay length increasing to the maximum value and then decreasing until saturation. By analyzing the ultrafast dynamics of laser-excited hot electrons, the effective mean free path, which can be characterized by the averaged product of the group velocity and lifetime of hot electrons, is found to play a key role. The interface reflectivity has little influence on the spin accumulation in NM metals. Our calculated results are in qualitative agreement with recent experiments.
In recent years, the optical control of exchange interactions has emerged as an exciting new direction in the study of the ultrafast optical control of magnetic order. Here we review recent theoretical works on antiferromagnetic systems, devoted to i
) simulating the ultrafast control of exchange interactions, ii) modeling the strongly nonequilibrium response of the magnetic order and iii) the relation with relevant experimental works developed in parallel. In addition to the excitation of spin precession, we discuss examples of rapid cooling and the control of ultrafast coherent longitudinal spin dynamics in response to femtosecond optically induced perturbations of exchange interactions. These elucidate the potential for exploiting the control of exchange interactions to find new scenarios for both faster and more energy-efficient manipulation of magnetism.
Relaxation dynamics of embedded metal nanoparticles after ultrafast laser pulse excitation is driven by thermal phenomena of different origins the accurate description of which is crucial for interpreting experimental results: hot electron gas genera
tion, electron-phonon coupling, heat transfer to the particle environment and heat propagation in the latter. Regardingthis last mechanism, it is well known that heat transport in nanoscale structures and/or at ultrashort timescales may deviate from the predictions of the Fourier law. In these cases heat transport may rather be described by the Boltzmann transport equation. We present a numerical model allowing us to determine the electron and lattice temperature dynamics in a spherical gold nanoparticle core under subpicosecond pulsed excitation, as well as that of the surrounding shell dielectric medium. For this, we have used the electron-phonon coupling equation in the particle with a source term linked with the laser pulse absorption, and the ballistic-diffusive equations for heat conduction in the host medium. Either thermalizing or adiabatic boundary conditions have been considered at the shell external surface. Our results show that the heat transfer rate from the particle to the matrix can be significantly smaller than the prediction of Fouriers law. Consequently, the particle temperature rise is larger and its cooling dynamics might be slower than that obtained by using Fouriers law. This difference is attributed to the nonlocal and nonequilibrium heat conduction in the vicinity of the core nanoparticle. These results are expected to be of great importance for analyzing pump-probe experiments performed on single nanoparticles or nanocomposite media.
Multiferroics, where two or more ferroic order parameters coexist, is one of the hottest fields in condensed matter physics and materials science[1-9]. However, the coexistence of magnetism and conventional ferroelectricity is physically unfavoured[1
0]. Recently several remedies have been proposed, e.g., improper ferroelectricity induced by specific magnetic[6] or charge orders[2]. Guiding by these theories, currently most research is focused on frustrated magnets, which usually have complicated magnetic structure and low magnetic ordering temperature, consequently far from the practical application. Simple collinear magnets, which can have high magnetic transition temperature, have never been considered seriously as the candidates for multiferroics. Here, we argue that actually simple interatomic magnetic exchange interaction already contains a driving force for ferroelectricity, thus providing a new microscopic mechanism for the coexistence and strong coupling between ferroelectricity and magnetism. We demonstrate this mechanism by showing that even the simplest antiferromagnetic (AFM) insulator MnO, can display a magnetically induced ferroelectricity under a biaxial strain.
The fragmentation of a liquid metal droplet induced by a nanosecond laser pulse has been studied well. However, the fragmentation mechanism may be different, when a subpicosecond laser pulse is applied. To discover the details of the fragmentation pr
ocess, we perform a hydrodynamic simulation of a liquid tin droplet irradiated by a femtosecond laser pulse. We have found that the pressure pulse induced by an instantaneous temperature growth in the skin layer propagates from the one side of the surface of a spherical droplet and focuses in its center; at the release a big cavity is formed at the center of a droplet; the pressure wave release at the backside surface may cause the spallation.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
