Abstract

The observation of ultrafast manipulation and coherent control of spins in magnetic materials at room temperature [1-2] has prompted the intense experimental and theoretical efforts to understand the underlying microscopic mechanisms and relevant interactions (exchange, spin-lattice, electron-phonon, coulomb etc.) driving such magnetic phenomena at sub-picosecond timescales. Stoichiometric B2 ordered epitaxial (001) FeRh undergoes a first order magnetic phase transition from antiferromagnetic (AFM) to ferromagnetic (FM) at ≈ 380K. In the AFM phase of FeRh, only Fe has net magnetic moment, whereas in the FM phase both Fe and Rh carry net moments. The phase transition is also accompanied by a ≈ 1% isotropic lattice expansion in the bulk BCC structure, and changes in electronic structure, see [3-5] and refs. therein.Since magnetic and structural dynamics occur at different timescales, it makes FeRh an ideal candidate for disentangling relevant interaction mechanisms at different timescales. The phase transition has been extensively studied theoretically and experimentally[6-8], in thermal equilibrium and in the time domain, but a precise understanding of the roles of the electronic, phononic and spin sub-systems remains elusive. We have studied the laser-driven AFM to FM phase transition in FeRh with small angle X-ray scattering (tr-SAXS) and X-ray absorption spectroscopy (tr-XAS) around the Fe L3 edge. The experiments were performed at the SCS Instrument of the European XFEL. We also performed the time-dependent density functional theory(TD-DFT) calculations to simulate the XAS spectra at different time delays. In this contribution, we will discuss the changes of the electronic structure of FeRh on the femto- and picosecond timescales, derived from the XAS and scattering measurements at the Fe L3 absorption edge performed at European XFEL, and compare them with the theoretical simulations (see the figure) , in order to show the relation between them and the first order AFM-FM phase transition in FeRh.

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