RESUMEN
Optically induced intersite spin transfer (OISTR) promises manipulation of spin systems within the ultimate time limit of laser excitation. Following its prediction, signatures of ultrafast spin transfer between oppositely aligned spin sublattices have been observed in magnetic alloys and multilayers. However, it is known neither from theory nor from experiment whether the band structure immediately follows the ultrafast change in spin polarization or whether the exchange split bands remain rigid. We show that ultrafast spin transfer occurs even in ferromagnetic gadolinium metal. Charge transfer between localized surface and extended valence-band states leads to a decrease of the surface spin polarization. This synchronously alters the exchange splitting of the bulk valence bands during laser excitation. Moreover, the onset of demagnetization can be tuned by over 200 fs by changing the temperature-dependent spin mixing. Our results show a promising route to ultrafast control of the magnetization, widening the impact and applicability of OISTR.
RESUMEN
We studied the magnetization dynamics of gadolinium metal after femtosecond laser excitation recording the x-ray magnetic circular dichroism in reflection (XMCD-R) at the Gd M 5 absorption edge. Varying the photon energy of the pump pulse allows us to change the initial energy distribution of photoexcited carriers. The overall similar response for excitation with 0.95, 1.55 and 3.10 eV photons at comparable pump fluences indicates that ultrafast ballistic carrier transport leads to a homogeneous energy distribution on the femtosecond timescale in the probed sample volume. Differences are observed in the initial ultrafast demagnetization magnitude. They are attributed to an enhanced spin-flip probability at higher electron energies characterizing the non-thermal electron distribution.
