A. Bombardi

Charge density wave fluctuations in La2-x Srx CuO4 and their competition with superconductivity

We report hard (14 keV) x-ray diffraction measurements on three compositions (x=0.11,0.12,0.13) of the high-temperature superconductor La2-xSrxCuO4. All samples show charge-density-wave (CDW) order with onset temperatures in the range 51-80 K and ordering wavevectors close to (0.23,0,0.5). The CDW is strongest with the longest in-plane correlation length near 1/8 doping. On entering the superconducting state the CDW is suppressed, demonstrating the strong competition between the charge order and superconductivity. CDW order coexists with incommensurate magnetic order and wavevectors of the two modulations have the simple relationship

X-Ray Imaging and Multiferroic Coupling of Cycloidal Magnetic Domains in Ferroelectric Monodomain BiFeO 3

\delta_{charge}= 2\delta_{spin}

Slow magnetic order-order transition in the spin chain antiferromagnet Ca3Co2O6.

. The intensity of the CDW Bragg peak tracks the intensity of the low-energy (quasi-elastic) spin fluctuations. We present a phase diagram of La2-xSrxCuO4 including the pseudogap phase, CDW and magnetic order.

Incommensurate magnetic ground state revealed by resonant x-ray scattering in the frustrated spin system Ca3Co2O6

Magnetic domains at the surface of a ferroelectric monodomain BiFeO(3) single crystal have been imaged by hard x-ray magnetic scattering. Magnetic domains up to several hundred microns in size have been observed, corresponding to cycloidal modulations of the magnetization along the wave vector k=(δ,δ,0) and symmetry equivalent directions. The rotation direction of the magnetization in all magnetic domains, determined by diffraction of circularly polarized light, was found to be unique and in agreement with predictions of a combined approach based on a spin-model complemented by relativistic density-functional simulations. Imaging of the surface shows that the largest adjacent domains display a 120° vortex structure.

Dimerization-induced cross-layer quasi-two-dimensionality in metallic IrTe 2

Using powder neutron diffraction, we have discovered an unusual magnetic order-order transition in the Ising spin chain compound Ca3Co2O6. On lowering the temperature, an antiferromagnetic phase with a propagation vector k=(0.5,-0.5,1) emerges from a higher temperature spin density wave structure with k=(0,0,1.01). This transition occurs over an unprecedented time scale of several hours and is never complete.

Symmetry Switching of Negative Thermal Expansion by Chemical Control

We have performed a resonant x-ray scattering study at the Co pre-K edge on a single crystal of Ca3Co2O6. The measurements reveal an abrupt transition to a magnetically ordered state immediately below T-N=25 K, with a magnetic correlation length in excess of 5500 A along the c axis chains. There is no evidence for modifications to the Co3+ spin state. A temperature dependent modulation in the magnetic order along the c axis and an unusual decrease in the magnetic correlation lengths on cooling are observed. The results are compatible with the onset of a partially disordered antiferromagnetic structure in Ca3Co2O6.

Cu3Nb2O8: A Multiferroic with Chiral Coupling to the Crystal Structure

The crystal structure of layered metal IrTe2 is determined using single-crystal x-ray diffraction. At T=220 K, it exhibits Ir and Te dimers forming a valence-bond crystal. Electronic structure calculations reveal an intriguing quasi-two-dimensional electronic state, with planes of reduced density of states cutting diagonally through the Ir and Te layers. These planes are formed by the Ir and Te dimers, which exhibit a signature of covalent bonding character development. Evidence for significant charge disproportionation among the dimerized and non-dimerized Ir (charge order) is also presented.

Modulated spin helicity stabilized by incommensurate orbital density waves in a quadruple perovskite manganite

The layered perovskite Ca3-xSrxMn2O7 is shown to exhibit a switching from a material exhibiting uniaxial negative to positive thermal expansion as a function of x. The switching is shown to be related to two closely competing phases with different symmetries. The negative thermal expansion (NTE) effect is maximized when the solid solution is tuned closest to this region of phase space but is switched off suddenly on passing though the transition. Our results show for the first time that, by understanding the symmetry of the competing phases alone, one may achieve unprecedented chemical control of this unusual property.

Direct observation of charge order in triangular metallic AgNiO2 by single-crystal resonant X-ray scattering.

By combining bulk properties, neutron diffraction, and nonresonant x-ray diffraction measurements, we demonstrate that the new multiferroic Cu(3)Nb(2)O(8) becomes polar simultaneously with the appearance of generalized helicoidal magnetic ordering. The electrical polarization is oriented perpendicularly to the common plane of rotation of the spins-an observation that cannot be reconciled with the conventional theory developed for cycloidal multiferroics. Our results are consistent with coupling between a macroscopic structural rotation, which is allowed in the paramagnetic group, and magnetically induced structural chirality.

Resonant x-ray scattering investigation of the multipolar ordering in Ca3CO2O6

Through a combination of neutron diffraction and Landau theory we describe the spin ordering in the ground state of the quadruple perovskite manganite CaMn7O12 - a magnetic multiferroic supporting an incommensurate orbital density wave that onsets above the magnetic ordering temperature, TN1 = 90 K. The multi-k magnetic structure in the ground state was found to be a nearly-constant-moment helix with modulated spin helicity, which oscillates in phase with the orbital occupancies on the Mn3+ sites via trilinear magneto-orbital coupling. Our phenomenological model also shows that, above TN2 = 48 K, the primary magnetic order parameter is locked into the orbital wave by an admixture of helical and collinear spin density wave structures. Furthermore, our model naturally explains the lack of a sharp dielectric anomaly at TN1 and the unusual temperature dependence of the electrical polarisation.