Peter M. Oppeneer

Superdiffusive Spin Transport as a Mechanism of Ultrafast Demagnetization

We propose a semiclassical model for femtosecond laser-induced demagnetization due to spin-polarized excited electron diffusion in the superdiffusive regime. Our approach treats the finite elapsed time and transport in space between multiple electronic collisions exactly, as well as the presence of several metal films in the sample. Solving the derived transport equation numerically we show that this mechanism accounts for the experimentally observed demagnetization within 200 fs in Ni, without the need to invoke any angular momentum dissipation channel.

Ultrafast magnetization enhancement in metallic multilayers driven by superdiffusive spin current

Uncovering the physical mechanisms that govern ultrafast charge and spin dynamics is crucial for understanding correlated matter as well as the fundamental limits of ultrafast spin-based electronics. Spin dynamics in magnetic materials can be driven by ultrashort light pulses, resulting in a transient drop in magnetization within a few hundred femtoseconds. However, a full understanding of femtosecond spin dynamics remains elusive. Here we spatially separate the spin dynamics using Ni/Ru/Fe magnetic trilayers, where the Ni and Fe layers can be ferro- or antiferromagnetically coupled. By exciting the layers with a laser pulse and probing the magnetization response simultaneously but separately in Ni and Fe, we surprisingly find that optically induced demagnetization of the Ni layer transiently enhances the magnetization of the Fe layer when the two layer magnetizations are initially aligned parallel. Our observations are explained by a laser-generated superdiffusive spin current between the layers.

Terahertz spin current pulses controlled by magnetic heterostructures

1. Department of Physical Chemistry, Fritz Haber Institute, Berlin, Germany. 2. Department of Physics and Astronomy, Uppsala University, Uppsala, Sweden. 3. I. Physikalisches Institut, Georg-August-Universität Göttingen, Göttingen, Germany. 4. Helmholtz-Zentrum Berlin fϋr Materialien und Energie, Berlin, Germany. 5. Peter Grünberg Institute and Institute for Advanced Simulation, Forschungszentrum Jülich and JARA, Jülich, Germany.In spin-based electronics, information is encoded by the spin state of electron bunches. Processing this information requires the controlled transport of spin angular momentum through a solid, preferably at frequencies reaching the so far unexplored terahertz regime. Here, we demonstrate, by experiment and theory, that the temporal shape of femtosecond spin current bursts can be manipulated by using specifically designed magnetic heterostructures. A laser pulse is used to drive spins from a ferromagnetic iron thin film into a non-magnetic cap layer that has either low (ruthenium) or high (gold) electron mobility. The resulting transient spin current is detected by means of an ultrafast, contactless amperemeter based on the inverse spin Hall effect, which converts the spin flow into a terahertz electromagnetic pulse. We find that the ruthenium cap layer yields a considerably longer spin current pulse because electrons are injected into ruthenium d states, which have a much lower mobility than gold sp states. Thus, spin current pulses and the resulting terahertz transients can be shaped by tailoring magnetic heterostructures, which opens the door to engineering high-speed spintronic devices and, potentially, broadband terahertz emitters.

Ultrafast spin transport as key to femtosecond demagnetization

Irradiating a ferromagnet with a femtosecond laser pulse is known to induce an ultrafast demagnetization within a few hundred femtoseconds. Here we demonstrate that direct laser irradiation is in fact not essential for ultrafast demagnetization, and that electron cascades caused by hot electron currents accomplish it very efficiently. We optically excite a Au/Ni layered structure in which the 30 nm Au capping layer absorbs the incident laser pump pulse and subsequently use the X-ray magnetic circular dichroism technique to probe the femtosecond demagnetization of the adjacent 15 nm Ni layer. A demagnetization effect corresponding to the scenario in which the laser directly excites the Ni film is observed, but with a slight temporal delay. We explain this unexpected observation by means of the demagnetizing effect of a superdiffusive current of non-equilibrium, non-spin-polarized electrons generated in the Au layer.

Observation of topological nodal fermion semimetal phase in ZrSiS

The search for new topological phases of matter is a major new direction in condensed matter physics. Recent experimental realizations of Dirac and Weyl semimetal phases pave the way to look for other exotic phases of matter in real materials. In this paper, the authors present a systematic angle-resolved photoemission spectroscopy study of ZrSiS, a potential topological nodal semimetal candidate. Their systematic measurements establish the spinless nodal fermion semimetal phase in ZrSiS, which is supported by their first-principles calculations. This work puts forward the ZrSiS-type material family as a new platform to explore exotic states of quantum matter.

Direct observation of a ferri-to-ferromagnetic transition in a fluoride-bridged 3d–4f molecular cluster

We report on the synthesis, crystal structure and magnetic characterisation of the trinuclear, fluoride-bridged, molecular nanomagnet [Dy(hfac)3(H2O)–CrF2(py)4–Dy(hfac)3(NO3)] (1) (hfacH = 1,1,1,5,5,5-hexafluoroacetylacetone, py = pyridine) and a closely related dinuclear species [Dy(hfac)4–CrF2(py)4]·½CHCl3 (2). Element-specific magnetisation curves obtained on 1 by X-ray magnetic circular dichroism (XMCD) allow us to directly observe the field-induced transition from a ferrimagnetic to a ferromagnetic arrangement of the Dy and Cr magnetic moments. By fitting a spin-Hamiltonian model to the XMCD data we extract a weak antiferromagnetic exchange coupling of j = −0.18 cm−1 between the DyIII and CrIII ions. The value found from XMCD is consistent with SQUID magnetometry and inelastic neutron scattering measurements. Furthermore, alternating current susceptibility and muon-spin relaxation measurements reveal that 1 shows thermally activated relaxation of magnetisation with a small effective barrier for magnetisation reversal of Δeff = 3 cm−1. Density-functional theory calculations show that the Dy–Cr couplings originate from superexchange via the fluoride bridges.

Efficient metallic spintronic emitters of ultrabroadband terahertz radiation

Ultrashort pulses covering the 1–30 THz range are generated from a W/CoFeB/Pt trilayer and originate from photoinduced spin currents, the inverse spin Hall effect and a broadband Fabry–Perot resonance. The resultant peak fields are several 100 kV cm–1.

Sum rules for electron energy loss near edge spectra

We derive four sum-rule expressions for spectra measured in electron energy loss near edge structure experiments. These sum rules permit the determination of spin and orbital magnetic moments, spin-orbit interaction, and number of states, analogously to the sum rules of x-ray magnetic circular dichroism. The derivation of the sum rules is based on dynamical electron diffraction theory and the properties of the mixed dynamic form factor. The accuracy of the sum rules is tested by a complete evaluation of the thickness-dependent electron energy loss spectra for iron, cobalt, and nickel crystals. We find that the sum rules reproduce both spin and orbital moments with very good accuracy. Our results provide a foundation for the use of the energy loss magnetic chiral dichroism technique as a quantitative probe of element-specific magnetic properties.

Ab Initio investigation of the Elliott-Yafet electron-phonon mechanism in laser-induced ultrafast demagnetization.

The spin-flip (SF) Eliashberg function is calculated from first principles for ferromagnetic Ni to accurately establish the contribution of Elliott-Yafet electron-phonon SF scattering to Nis femtosecond laser-driven demagnetization. This is used to compute the SF probability and demagnetization rate for laser-created thermalized as well as nonequilibrium electron distributions. Increased SF probabilities are found for thermalized electrons, but the induced demagnetization rate is extremely small. A larger demagnetization rate is obtained for nonequilibrium electron distributions, but its contribution is too small to account for femtosecond demagnetization.

Ab-initio molecular dynamics in the full-potential LMTO method: Derivation of a practical force theorem

A major advance in electronic structure calculations was the combination of local-density techniques with molecular dynamics by Car and Parrinello seven years ago. Unfortunately, application of the Car-Parrinello scheme has been limited essentially to sp materials because only in the plane-wave pseudopotential method forces are trivial to calculate. We present a systematic approach to derive force theorems with desired characteristics within complicated basis sets, which are applicable to all elements of the periodic table equally well. Application to the LMTO basis set yields an accurate force theorem, quite distinct from the Hellman-Feynman form, which is exceptionally insensitive to errors in the trial density. The forces were implemented in a new full-potential LMTO method which is suited to arbitrary geometries. First results for ab-initio molecular dynamics and simulated annealing runs are shown for some random small molecules and small clusters of silver atoms.