RESUMO
Laser-driven non-local electron dynamics in ultrathin magnetic samples on a sub-10 nm length scale is a key process in ultrafast magnetism. However, the experimental access has been challenging due to the nanoscopic and femtosecond nature of such transport processes. Here, we present a scattering-based experiment relying on a laser-induced electro- and magneto-optical grating in a Co/Pd ferromagnetic multilayer as a new technique to investigate non-local magnetization dynamics on nanometer length and femtosecond timescales. We induce a spatially modulated excitation pattern using tailored Al near-field masks with varying periodicities on a nanometer length scale and measure the first four diffraction orders in an x-ray scattering experiment with magnetic circular dichroism contrast at the free-electron laser facility FERMI, Trieste. The design of the periodic excitation mask leads to a strongly enhanced and characteristic transient scattering response allowing for sub-wavelength in-plane sensitivity for magnetic structures. In conjunction with scattering simulations, the experiment allows us to infer that a potential ultrafast lateral expansion of the initially excited regions of the magnetic film mediated by hot-electron transport and spin transport remains confined to below three nanometers.
RESUMO
We present an experimental setup of a laser-driven x-ray plasma source for femtosecond x-ray diffraction. Different normalization schemes accounting for x-ray source intensity fluctuations are discussed in detail. We apply these schemes to measure the temporal evolution of Bragg peak intensities of perovskite superlattices after ultrafast laser excitation.
Assuntos
Lasers , Gases em Plasma/química , Difração de Raios X/instrumentação , Compostos de Cálcio/química , Fenômenos Ópticos , Óxidos/química , Fatores de Tempo , Titânio/químicaRESUMO
We have obtained first solid evidence of strong charge separation that is caused by relaxing localized electrons in a polar medium: Space-charge gratings induced in highly-doped LiNbO(3):Fe crystals by interfering nanosecond light pulses at 532 nm show a highly peculiar long term behavior (buildup or/and decay) in the dark. It depends strongly on the applied electric field E(0) (ranging from -140 to +640 kV/cm) and occurs on a time scale of (1 - 100) s which is much larger than the relaxation time of photo-electrons and smaller than the dark dielectric relaxation time. All peculiarities observed are fully described by a charge-transport model that incorporates the energy relaxation of electrons within a band of localized Fe(2+) states and a long-living, field-gradient-independent "polar current" directed along the polar axis.