A design of resonant inelastic X-ray scattering (RIXS) spectrometer for spatial- and time-resolved spectroscopy.

The optical design of a Hettrick-Underwood-style soft X-ray spectrometer with Wolter type 1 mirrors is presented. The spectrometer with a nominal length of 3.1 m can achieve a high resolving power (resolving power higher than 10000) in the soft X-ray regime when a small source beam (<3 µm in the grating dispersion direction) and small pixel detector (5 µm effective pixel size) are used. Adding Wolter mirrors to the spectrometer before its dispersive elements can realize the spatial imaging capability, which finds applications in the spectroscopic studies of spatially dependent electronic structures in tandem catalysts, heterostructures, etc. In the pump-probe experiments where the pump beam perturbs the materials followed by the time-delayed probe beam to reveal the transient evolution of electronic structures, the imaging capability of the Wolter mirrors can offer the pixel-equivalent femtosecond time delay between the pump and probe beams when their wavefronts are not collinear. In combination with some special sample handing systems, such as liquid jets and droplets, the imaging capability can also be used to study the time-dependent electronic structure of chemical transformation spanning multiple time domains from microseconds to nanoseconds. The proposed Wolter mirrors can also be adopted to the existing soft X-ray spectrometers that use the Hettrick-Underwood optical scheme, expanding their capabilities in materials research

Electronic structure of multiferroic BiFeO3 by resonant soft x-ray emission spectroscopy

[[abstract]]The electronic structure of multiferroic BiFeO3 has been studied using soft x-ray emission spectroscopy. The fluorescence spectra exhibit that the valence band is mainly composed of O 2p state hybridized with Fe 3d state. The band gap corresponding to the energy separation between the top of the O 2p valence band and the bottom of the Fe 3d conduction band is 1.3 eV. The soft x-ray Raman scattering reflects the features due to the charge-transfer transition from O 2p valence band to Fe 3d conduction band. These findings are similar to the result of electronic structure calculation by density-functional theory within the local spin-density approximation that included the effect of Coulomb repulsion between localized d states.[[booktype]]紙本[[booktype]]電子

High-efficiency in situ resonant inelastic x-ray scattering (iRIXS) endstation at the Advanced Light Source

An endstation with two high-efficiency soft x-ray spectrographs was developed at Beamline 8.0.1 of the Advanced Light Source, Lawrence Berkeley National Laboratory. The endstation is capable of performing soft x-ray absorption spectroscopy, emission spectroscopy, and, in particular, resonant inelastic soft x-ray scattering (RIXS). Two slit-less variable line-spacing grating spectrographsare installed at different detection geometries. The endstation covers the photon energy range from 80 to 1500 eV. For studying transition-metal oxides, the large detection energy window allows a simultaneous collection of x-ray emission spectra with energies ranging from the O K-edge to the Ni L-edge without moving any mechanical components. The record-high efficiency enables the recording of comprehensive two-dimensional RIXS maps with good statistics within a short acquisition time. By virtue of the large energy window and high throughput of the spectrographs, partial fluorescence yield and inverse partial fluorescence yield signals could be obtained for all transition metal L-edges including Mn. Moreover, the different geometries of these two spectrographs (parallel and perpendicular to the horizontal polarization of the beamline) provide contrasts in RIXS features with two different momentum transfers

The High-Spin and Low-Spin States of Co(III) Ion in Co3O4 Studied by X-ray Absorption Spectroscopy

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The High-Spin and Low-Spin States of Co(III) Ion in Co3O4 Studied by X-ray Absorption Spectroscopy

QC 20230522</p

Mg deposition observed by in situ electrochemical Mg K-edge X-ray absorption spectroscopy

The electrochemical deposition of magnesium from [Mg2(μ-Cl)3·6(OC4H8)]+ has been monitored in situ with X-ray absorption spectroscopy. The viability of the cell design was confirmed by a reversible shift in the X-ray absorption near-edge spectroscopy (XANES) of the Mg K-edge. In situ electrochemical XANES revealed the presence of an interfacial Mg intermediate below the equilibrium Mg/Mg2+ potential. A new method has been established to directly observe the complex electrochemical reduction process from Mg electrolytes. Keywords: In situ electrochemical/XAS, Magnesium batteries, Interface analysis, Electrodepositio