13 research outputs found
Europium cyclooctatetraene nanowire carpets: A low-dimensional, organometallic, and ferromagnetic insulator
We investigate the magnetic and electronic properties of europium cyclooctatetraene (EuCot) nanowires by means of low-temperature X-ray magnetic circular dichroism (XMCD) and scanning tunneling microscopy (STM) and spectroscopy (STS). The EuCot nanowires are prepared in situ on a graphene surface. STS measurements identify EuCot as an insulator with a minority band gap of 2.3 eV. By means of Eu M5,4 edge XMCD, orbital and spin magnetic moments of (â0.1 ± 0.3)ÎŒB and (+7.0 ± 0.6)ÎŒB, respectively, were determined. Field-dependent measurements of the XMCD signal at the Eu M5 edge show hysteresis for grazing X-ray incidence at 5 K, thus confirming EuCot as a ferromagnetic material. Our density functional theory calculations reproduce the experimentally observed minority band gap. Modeling the experimental results theoretically, we find that the effective interatomic exchange interaction between Eu atoms is on the order of millielectronvolts, that magnetocrystalline anisotropy energy is roughly half as big, and that dipolar energy is approximately ten times lower
Interface-related magnetic and vibrational properties in Fe/MgO heterostructures from nuclear resonant spectroscopy and first-principles calculations
We combine â”â·Fe Mössbauer spectroscopy and â”â·Fe nuclear resonant inelastic x-ray scattering (NRIXS) on nanoscale polycrystalline [bccââ”â·Fe/MgO] multilayers with various Fe-layer thicknesses and layer-resolved density-functional-theory (DFT)-based first-principles calculations of a (001)-oriented [Fe(8 ML)/MgO(8 ML)](001) heterostructure (where ML denotes monolayer) to unravel the interface-related atomic vibrational properties of a multilayer system. Being consistent in theory and experiment, we observe enhanced hyperfine magnetic fields B_(hf) in the multilayers as compared to B_(hf) in bulk bcc Fe; this effect is associated with the Fe/MgO interface layers. NRIXS and DFT both reveal a strong reduction of the longitudinal acoustic phonon peak in combination with an enhancement of the low-energy vibrational density of states (VDOS) suggesting that the presence of interfaces and the associated increase in the layer-resolved magnetic moments results in drastic changes in the Fe-partial VDOS. From the experimental and calculated VDOS, vibrational thermodynamic properties have been determined as a function of Fe thickness and were found to be in excellent agreement
Electron population dynamics in resonant non-linear x-ray absorption in nickel at a free-electron laser
Free-electron lasers provide bright, ultrashort, and monochromatic x-ray pulses, enabling novel spectroscopic measurements not only with femtosecond temporal resolution: The high fluence of their x-ray pulses can also easily enter the regime of the non-linear x-rayâmatter interaction. Entering this regime necessitates a rigorous analysis and reliable prediction of the relevant non-linear processes for future experiment designs. Here, we show non-linear changes in the L3-edge absorption of metallic nickel thin films, measured with fluences up to 60âJ/cm2. We present a simple but predictive rate model that quantitatively describes spectral changes based on the evolution of electronic populations within the pulse duration. Despite its simplicity, the model reaches good agreement with experimental results over more than three orders of magnitude in fluence, while providing a straightforward understanding of the interplay of physical processes driving the non-linear changes. Our findings provide important insights for the design and evaluation of future high-fluence free-electron laser experiments and contribute to the understanding of non-linear electron dynamics in x-ray absorption processes in solids at the femtosecond timescale
Photon shot-noise limited transient absorption soft X-ray spectroscopy at the European XFEL
Femtosecond transient soft X-ray Absorption Spectroscopy (XAS) is a very
promising technique that can be employed at X-ray Free Electron Lasers (FELs)
to investigate out-of-equilibrium dynamics for material and energy research.
Here we present a dedicated setup for soft X-rays available at the Spectroscopy
& Coherent Scattering (SCS) instrument at the European X-ray Free Electron
Laser (EuXFEL). It consists of a beam-splitting off-axis zone plate (BOZ) used
in transmission to create three copies of the incoming beam, which are used to
measure the transmitted intensity through the excited and unexcited sample, as
well as to monitor the incoming intensity. Since these three intensity signals
are detected shot-by-shot and simultaneously, this setup allows normalized
shot-by-shot analysis of the transmission. For photon detection, the DSSC
imaging detector, which is capable of recording up to 800 images at 4.5 MHz
frame rate during the FEL burst, is employed and allows approaching the photon
shot-noise limit. We review the setup and its capabilities, as well as the
online and offline analysis tools provided to users.Comment: 11 figure
Femtosecond time resolved soft X ray spectroscopy for an element specific analysis of complex materials
Sandwich-molecular wires: Combining cyclooctatetraene with rare- and alkaline-earth metals on Gr/Ir(111)
Uniaxially Aligned 1D Sandwich-Molecular Wires: Electronic Structure and Magnetism
Sandwich-molecular wires consisting of europium and cyclooctatetraene (Cot) were grown in situ on the moirĂ© of graphene with Ir(110). The moirĂ© templates a uniaxial alignment of monolayer EuCot nanowire carpets and multilayer films with the EuCot wire axis along the [001] direction of the Ir substrate. Using angle-resolved photoemission spectroscopy, we investigate the band structure of the wire carpet films. While Ï-derived bands were not observed experimentally, we find a flat band 1.85 eV below the Fermi energy. Using density-functional theory and X-ray photoelectron spectroscopy and replacing europium through barium in the sandwich-molecular wires, it is concluded that the flat band is derived from Eu 4f states weakly mixed with Eu 5d states and slightly overlapping with Cot Ï states. X-ray magnetic circular dichroism is employed to characterize the magnetic properties of the EuCot wire carpet films at low temperatures. Clear evidence for an easy-axis magnetization along the wires is found
Europium Cyclooctatetraene Nanowire Carpets: A Low-Dimensional, Organometallic, and Ferromagnetic Insulator
We investigate the magnetic and electronic properties of europium cyclooctatetraene (EuCot) nanowires by means of low-temperature X-ray magnetic circular dichroism (XMCD) and scanning tunneling microscopy (STM) and spectroscopy (STS). The EuCot nanowires are prepared in situ on a graphene surface. STS measurements identify EuCot as an insulator with a minority band gap of 2.3 eV. By means of Eu M-5,M-4 edge XMCD, orbital and spin magnetic moments of (-0.1 +/- 0.3)mu(B) and (+7.0 +/- 0.6)mu(B), respectively, were determined. Field-dependent measurements of the XMCD signal at the Eu M-5 edge show hysteresis for grazing X-ray incidence at 5 K, thus confirming EuCot as a ferromagnetic material. Our density functional theory calculations reproduce the experimentally observed minority band gap. Modeling the experimental results theoretically, we find that the effective interatomic exchange interaction between Eu atoms is on the order of millielectronvolts, that magnetocrystalline anisotropy energy is roughly half as big, and that dipolar energy is approximately ten times lower
A full gap above the Fermi level: the charge density wave of monolayer VS2
In the standard model of charge density wave (CDW) transitions, the displacement along a single phonon mode lowers the total electronic energy by creating a gap at the Fermi level, making the CDW a metal-insulator transition. Here, using scanning tunneling microscopy and spectroscopy and ab initio calculations, we show that VS2 realizes a CDW which stands out of this standard model. There is a full CDW gap residing in the unoccupied states of monolayer VS2. At the Fermi level, the CDW induces a topological metal-metal (Lifshitz) transition. Non-linear coupling of transverse and longitudinal phonons is essential for the formation of the CDW and the full gap above the Fermi level. Additionally, x-ray magnetic circular dichroism reveals the absence of net magnetization in this phase, pointing to coexisting charge and spin density waves in the ground state. A charge density wave (CDW) normally creates a gap at the Fermi level, inducing a metal-insulator transition. Here, the authors report that a CDW gap resides in the unoccupied states but induces a topological metal-metal transition at the Fermi level in monolayer VS2