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This study measures the x-ray-absorption spectra of a series of nanodiamond thin films with grain diameters ranging from 3.5 nm to $5\ensuremath{\mu}\mathrm{m}$ at the C $K$-edge using the sample drain current mode at room temperature. Resonance peaks resembling the C $1s$ core exciton are observed. The exciton state and conduction band edge are found to shift to higher energies with the decrease of the grain size indicative of the presence of the quantum confinement effect.

We addressed the so-far unresolved issue concerning the Co valence in the superconducting bilayer hydrated Na(x)CoO(2) · yH(2)O (x∼0.35, y∼1.3) using soft x-ray absorption spectroscopy at the Co-L(2,3) and O-K edges. We find that the valence state of the Co lies in a narrow range from +3.3 to +3.4 for all studied Na(x)CoO(2) · yH(2)O samples and their deuterated analogue with T(c)'s ranging from 3.8 to 4.7 K. These valence values are far from the often claimed +3.7, the number based on the Na content only. We propose to modify the phase diagram accordingly, where the basic electronic structure of the superconducting phase is very close to that of the Na(0.7)CoO(2) system, suggesting that the presence of in-plane spin fluctuations could play an important role for the superconductivity.

We addressed the so-far unresolved issue concerning the Co valence in the superconducting bilayer hydrated Na(x)CoO(2) · yH(2)O (x∼0.35, y∼1.3) using soft x-ray absorption spectroscopy at the Co-L(2,3) and O-K edges. We find that the valence state of the Co lies in a narrow range from +3.3 to +3.4 for all studied Na(x)CoO(2) · yH(2)O samples and their deuterated analogue with T(c)'s ranging from 3.8 to 4.7 K. These valence values are far from the often claimed +3.7, the number based on the Na content only. We propose to modify the phase diagram accordingly, where the basic electronic structure of the superconducting phase is very close to that of the Na(0.7)CoO(2) system, suggesting that the presence of in-plane spin fluctuations could play an important role for the superconductivity.

Using $\mathrm{Co}\mathrm{\text{\ensuremath{-}}}{L}_{2,3}$ and $\mathrm{O}\mathrm{\text{\ensuremath{-}}}K$ x-ray absorption spectroscopy, we reveal that the charge ordering in ${\mathrm{La}}_{1.5}{\mathrm{Sr}}_{0.5}{\mathrm{CoO}}_{4}$ involves high spin ($S=3/2$) ${\mathrm{Co}}^{2+}$ and low spin ($S=0$) ${\mathrm{Co}}^{3+}$ ions. This provides evidence for the spin-blockade phenomenon as a source for the extremely insulating nature of the ${\mathrm{La}}_{2\ensuremath{-}x}{\mathrm{Sr}}_{x}{\mathrm{CoO}}_{4}$ series. The associated ${e}_{g}^{2}$ and ${e}_{g}^{0}$ orbital occupation accounts for the large contrast in the Co-O bond lengths and, in turn, the high charge ordering temperature. Yet, the low magnetic ordering temperature is naturally explained by the presence of the nonmagnetic ($S=0$) ${\mathrm{Co}}^{3+}$ ions. From the identification of the bands we infer that ${\mathrm{La}}_{1.5}{\mathrm{Sr}}_{0.5}{\mathrm{CoO}}_{4}$ is a narrow band material.

Using Co-L2,3 and O-K x-ray absorption spectroscopy, we reveal that the charge ordering in La1.5Sr0.5CoO4 involves high spin (S=3/2) Co2+ and low spin (S=0) Co3+ ions. This provides evidence for the spin-blockade phenomenon as a source for the extremely insulating nature of the La2-xSrxCoO4 series. The associated e{g}{2} and e{g}{0} orbital occupation accounts for the large contrast in the Co-O bond lengths and, in turn, the high charge ordering temperature. Yet, the low magnetic ordering temperature is naturally explained by the presence of the nonmagnetic (S=0) Co3+ ions. From the identification of the bands we infer that La1.5Sr0.5CoO4 is a narrow band material.

We infer that soft-x-ray absorption spectroscopy is a versatile method for the determination of the crystal-field ground state symmetry of rare earth heavy fermion systems, complementing neutron scattering. Using realistic and universal parameters, we provide a theoretical mapping between the polarization dependence of Ce ${M}_{4,5}$ spectra and the charge distribution of the Ce $4f$ states. The experimental resolution can be orders of magnitude larger than the $4f$ crystal-field splitting itself. To demonstrate the experimental feasibility of the method, we investigated ${\mathrm{CePd}}_{2}{\mathrm{Si}}_{2}$, thereby settling an existing disagreement about its crystal-field ground state.

We describe a possible pathway to new magnetic materials with no conventional magnetic elements present. The substitution of nitrogen for oxygen in simple nonmagnetic oxides leads to holes in N 2p states which form local magnetic moments. Because of the very large Hund's rule coupling of Nitrogen and O 2p electrons and the rather extended spatial extent of the wave functions these materials are predicted to be ferromagnetic metals or small band gap insulators. Experimental studies support the theoretical calculations with regard to the basic electronic structure and the formation of local magnetic moments. It remains to be seen if these materials are magnetically ordered and, if so, below what temperature.

We present a detailed study of the valence and conduction bands of VO2 across the metal-insulator transition using bulk-sensitive photoelectron and O K x-ray absorption spectroscopies. We observe a giant transfer of spectral weight with distinct features that require an explanation which goes beyond the Peierls transition model as well as the standard single-band Hubbard model. Analysis of the symmetry and energies of the bands reveals the decisive role of the V 3d orbital degrees of freedom. Comparison to recent realistic many body calculations shows that much of the k dependence of the self-energy correction can be cast within a dimer model.

Using x-ray absorption spectroscopy at the Ru-L2,3 edge we reveal that the Ru4+ ions remain in the S=1 spin state across the rare 4d-orbital ordering transition and spin-gap formation. We find using local spin density approximation + Hubbard U band structure calculations that the crystal fields in the low-temperature phase are not strong enough to stabilize the S=0 state. Instead, we identify a distinct orbital ordering with a significant anisotropy of the antiferromagnetic exchange couplings. We conclude that La4Ru2O10 appears to be a novel material in which the orbital physics drives the formation of spin-singlet dimers in a quasi-two-dimensional S=1 system.

We found direct experimental evidence for an orbital switching in the V $3d$ states across the metal-insulator transition in ${\mathrm{VO}}_{2}$. We have used soft-x-ray absorption spectroscopy at the V ${L}_{2,3}$ edges as a sensitive local probe and have determined quantitatively the orbital polarizations. These results strongly suggest that, in going from the metallic to the insulating state, the orbital occupation changes in a manner that charge fluctuations and effective bandwidths are reduced, that the system becomes more one dimensional and more susceptible to a Peierls-like transition, and that the required massive orbital switching can only be made if the system is close to a Mott insulating regime.

Utilizing a sum rule in a spin-resolved photoelectron spectroscopic experiment with circularly polarized light, we show that the orbital moment in ${\mathrm{L}\mathrm{a}\mathrm{T}\mathrm{i}\mathrm{O}}_{3}$ is strongly reduced from its ionic value, both below and above the N\'eel temperature. Using Ti ${L}_{2,3}$ x-ray absorption spectroscopy as a local probe, we found that the crystal-field splitting in the ${t}_{2g}$ subshell is about 0.12--0.30 eV. This large splitting does not facilitate the formation of an orbital liquid.

Using soft-x-ray absorption spectroscopy at the Co ${L}_{2,3}$ and O $K$ edges, we demonstrate that the ${\mathrm{Co}}^{3+}$ ions with the ${\mathrm{CoO}}_{5}$ pyramidal coordination in the layered ${\mathrm{Sr}}_{2}{\mathrm{CoO}}_{3}\mathrm{Cl}$ compound are unambiguously in the high spin state. Our result questions the reliability of the spin state assignments made so far for the recently synthesized layered cobalt perovskites and calls for a reexamination of the modeling for the complex and fascinating properties of these new materials.

Using soft-x-ray absorption spectroscopy at the Co L(2,3) and O K edges, we demonstrate that the Co3+ ions with the CoO5 pyramidal coordination in the layered Sr2CoO3Cl compound are unambiguously in the high spin state. Our result questions the reliability of the spin state assignments made so far for the recently synthesized layered cobalt perovskites and calls for a reexamination of the modeling for the complex and fascinating properties of these new materials.

We find that Ni ${L}_{2}$ edge x-ray magnetic linear dichroism is fully reversed for NiO(001) films on materials with reversed lattice mismatch. We relate this phenomenon to a preferential stabilization of magnetic $S$ domains with main spin component either in or out of the plane, via dipolar interactions. This suggests a way to selectively control spin structures in $3d$ systems with small spin-orbit coupling.

We investigated ferromagnetism of a newly discovered ferromagnetic semiconductor Co-doped anatase ${\mathrm{T}\mathrm{i}\mathrm{O}}_{2}$ thin film, using the magnetic circular dichroism (MCD) at the Co ${L}_{2,3}$ absorption edges. The magnetic moment was observed to be $\ensuremath{\sim}0.1{\ensuremath{\mu}}_{B}/\mathrm{C}\mathrm{o}$ in the measurements, but the MCD spectral line shape is nearly identical to that of Co metal, showing that the ferromagnetism is induced by a small amount of clustered Co. With thermal treatments at $\ensuremath{\sim}400\text{ }\ifmmode^\circ\else\textdegree\fi{}\mathrm{C}$, the MCD signal increases, and the moment reaches up to $\ensuremath{\sim}1.55{\ensuremath{\mu}}_{B}/\mathrm{C}\mathrm{o}$, which is $\ensuremath{\sim}90%$ of the moment in Co metal. In the latter case, the cluster size was observed to be 20--60 nm.

We investigated ferromagnetism of a newly discovered ferromagnetic semiconductor Co-doped anatase TiO2 thin film, using the magnetic circular dichroism (MCD) at the Co L(2,3) absorption edges. The magnetic moment was observed to be approximately 0.1 micro(B)/Co in the measurements, but the MCD spectral line shape is nearly identical to that of Co metal, showing that the ferromagnetism is induced by a small amount of clustered Co. With thermal treatments at approximately 400 degrees C, the MCD signal increases, and the moment reaches up to approximately 1.55 micro(B)/Co, which is approximately 90% of the moment in Co metal. In the latter case, the cluster size was observed to be 20-60 nm.

Using soft x-ray absorption spectroscopy and magnetic circular dichroism at the Co-L(2,3) edge, we reveal that the spin state transition in LaCoO3 can be well described by a low-spin ground state and a triply degenerate high-spin first excited state. From the temperature dependence of the spectral line shapes, we find that LaCoO3 at finite temperatures is an inhomogeneous mixed-spin state system. It is crucial that the magnetic circular dichroism signal in the paramagnetic state carries a large orbital momentum. This directly shows that the currently accepted low- or intermediate-spin picture is at variance. Parameters derived from these spectroscopies fully explain existing magnetic susceptibility, electron spin resonance, and inelastic neutron data.