Intense paramagnon excitations in a large family of high-temperature superconductor

Using soft x-ray absorption spectroscopy and magnetic circular dichroism at the Co-L2,3 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 lineshapes we find that LaCoO3 at finite temperatures is an inhomogeneous mixed-spinstate system. Crucial is that the magnetic circular dichroism signal in the paramagnetic state carries a large orbital momentum. This directly shows that the currently accepted low-/intermediate-spin picture is at variance. Parameters derived from these spectroscopies fully explain existing magnetic susceptibility, electron spin resonance and inelastic neutron data.PACS numbers: 71.28.+d, 71.70.Ch, 78.70.Dm LaCoO 3 shows a gradual non-magnetic to magnetic transition with temperature, which has been interpreted originally four decades ago as a gradual population of high spin (HS, t 4 2g e 2 g , S = 2) excited states starting from a low spin (LS, t 6 2g , S = 0) ground state [1,2,3,4,5,6,7,8]. This interpretation continued to be the starting point for experiments carried out up to roughly the first half of the 1990's [9,10,11,12]. All this changed with the theoretical work in 1996 by Korotin et al., who proposed on the basis of local density approximation + Hubbard U (LDA+U) band structure calculations, that the excited states are of the intermediate spin (IS, t 5 2g e 1 g , S = 1) type [13]. Since then many more studies have been carried out on LaCoO 3 with the majority of them [14,15,16,17,18,19,20,21,22,23,24,25,26,27] claiming to have proven the presence of this IS mechanism. In fact, this LDA+U work is so influential [28] that it forms the basis of most explanations for the fascinating properties of the recently synthesized layered cobaltate materials, which show giant magneto resistance as well as metal-insulator and ferroferri-antiferro-magnetic transitions with various forms of charge, orbital and spin ordering [29,30].In this paper we critically re-examine the spin state issue in LaCoO 3 . There has been several attempts made since 1996 in order to revive the LS-HS scenario [31,32,33,34,35], but these were overwhelmed by the above mentioned flurry of studies claiming the IS mechanism [14,15,16,17,18,19,20,21,22,23,24,25,26,27]. Moreover, a new investigation using inelastic neutron scattering (INS) has recently appeared in Phys. Rev. Lett.[36] making again the claim that the spin state transition involves the IS states. Here we used soft xray absorption spectroscopy (XAS) and magnetic circular dichroism (MCD) at the Co-L 2,3 edge and we revealed that the spin state transition in LaCoO 3 can be well described by a LS ground state and a triply degenerate HS excited state, and that an inhomogeneous mixed-spinstate system is formed. Parameters derived from these spectroscopies fully explain existing magnetic susceptibility and electron spin resonance (ESR) data, and provide support for an alternative interpretation of the INS [37]. C...

When viewed as an elementary particle, the electron has spin and charge. When binding to the atomic nucleus, it also acquires an angular momentum quantum number corresponding to the quantized atomic orbital it occupies. Even if electrons in solids form bands and delocalize from the nuclei, in Mott insulators they retain their three fundamental quantum numbers: spin, charge and orbital. The hallmark of one-dimensional physics is a breaking up of the elementary electron into its separate degrees of freedom. The separation of the electron into independent quasi-particles that carry either spin (spinons) or charge (holons) was first observed fifteen years ago. Here we report observation of the separation of the orbital degree of freedom (orbiton) using resonant inelastic X-ray scattering on the one-dimensional Mott insulator Sr2CuO3. We resolve an orbiton separating itself from spinons and propagating through the lattice as a distinct quasi-particle with a substantial dispersion in energy over momentum, of about 0.2 electronvolts, over nearly one Brillouin zone.

We demonstrate how ab initio cluster calculations including the full Coulomb vertex can be done in the basis of the localized, generalized Wannier orbitals which describe the low-energy density functional (LDA) band structure of the infinite crystal, e.g. the transition metal 3d and oxygen 2p orbitals. The spatial extend of our 3d Wannier orbitals (orthonormalized Nth order muffin-tin orbitals) is close to that found for atomic Hartree-Fock orbitals. We define Ligand orbitals as those linear combinations of the O 2p Wannier orbitals which couple to the 3d orbitals for the chosen cluster. The use of ligand orbitals allows for a minimal Hilbert space in multiplet ligand-field theory calculations, thus reducing the computational costs substantially. The result is a fast and simple ab initio theory, which can provide useful information about local properties of correlated insulators. We compare results for NiO, MnO and SrTiO3 with x-ray absorption, inelastic x-ray scattering, and photoemission experiments. The multiplet ligand field theory parameters found by our ab initio method agree within ~10% to known experimental values

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.