Understanding the transfer of spin angular momentum is essential in modern magnetism research. A model case is the generation of magnons in magnetic insulators by heating an adjacent metal film. Here, we reveal the initial steps of this spin Seebeck effect with <27 fs time resolution using terahertz spectroscopy on bilayers of ferrimagnetic yttrium iron garnet and platinum. Upon exciting the metal with an infrared laser pulse, a spin Seebeck current js arises on the same ~100 fs time scale on which the metal electrons thermalize. This observation highlights that efficient spin transfer critically relies on carrier multiplication and is driven by conduction electrons scattering off the metal–insulator interface. Analytical modeling shows that the electrons’ dynamics are almost instantaneously imprinted onto js because their spins have a correlation time of only ~4 fs and deflect the ferrimagnetic moments without inertia. Applications in material characterization, interface probing, spin-noise spectroscopy and terahertz spin pumping emerge.
The vision of using light to manipulate electronic and spin excitations in materials on their fundamental time and length scales requires new approaches in experiment and theory to observe and understand these excitations. The ultimate speed limit for all-optical manipulation requires control schemes for which the electronic or magnetic subsystems of the materials are coherently manipulated on the time scale of the laser excitation pulse. In our work, we provide experimental evidence of such a direct, ultrafast, and coherent spin transfer between two magnetic subsystems of an alloy of Fe and Ni. Our experimental findings are fully supported by time-dependent density functional theory simulations and, hence, suggest the possibility of coherently controlling spin dynamics on subfemtosecond time scales, i.e., the birth of the research area of attomagnetism.
The accurate calculation of laser energy absorption during femto-or picosecond laser pulse experiments is very important for the description of the formation of periodic surface structures. On a rough material surface, a crack or a step edge, ultrashort laser pulses can excite surface plasmon polaritons (SPP), i.e. surface plasmons coupled to a laser-electromagnetic wave. The interference of such plasmon wave and the incoming pulse leads to a periodic modulation of the deposited laser energy on the surface of the sample. In the present work, within the frames of a Two Temperature Model we propose the analytical form of the source term, which takes into account SPP excited at a step edge of a dielectric-metal interface upon irradiation of an ultrashort laser pulse at normal incidence. The influence of the laser pulse parameters on energy absorption is quantified for the example of gold. This result can be used for nanophotonic applications and for the theoretical investigation of the evolution of electronic and lattice temperatures and, therefore, of the formation of surfaces with predestined properties under controlled conditions. *
Electron-electron thermalization and electron-phonon relaxation processes in laser-excited solids are often assumed to occur on different timescales. This is true for the majority of the conduction band electrons in a metal. However, electron-phonon interactions can influence the thermalization process of the excited electrons. We study the interplay of the underlying scattering mechanisms for the case of a noble metal with help of a set of complete Boltzmann collision integrals. We trace the transient electron distribution in copper and its deviations from a Fermi-Dirac distribution due to the excitation with an ultrashort laser pulse. We investigate the different stages of electronic nonequilibrium after an excitation with an ultrashort laser-pulse of 800 nm wavelength and 10 fs pulse duration. Our calculations show a strong nonequilibrium during and directly after the end of the laser pulse. Subsequently, we find a fast thermalization of most electrons. Surprisingly, we observe a long-lasting nonequilibrium, which can be attributed to the electron-phonon scattering. This nonequilibrium establishes at energies around peaks in the density of states of the electrons and persists on the timescale of electron-phonon energy relaxation. It influences in turn the electron phonon coupling strength. * weber@physik.uni-kl.de 1 A. Vogel and V. Venugopalan, Chemical Reviews 103, 577
We investigate the dynamics of band occupation in gold after excitation with short laser pulses. Strong non‐equilibrium distributions can be created by intra‐ and inter‐band transitions driven by the absorption of photons with different wavelengths. First, we briefly discuss how photons can be used as a probe and how electrons with non‐Fermi distributions can be described. Then we focus on the relaxation stage where a temperature has been established but the occupation numbers in the different bands are not yet in equilibrium with this newly established elevated temperature. We describe the relaxation towards a system with a common chemical potential with rate equations that also include the energy transfer to the lattice or ions. Finally, we give an outlook on the optical response of the relaxing electron system to a probe pulse of radiation.
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