The nature of the charge density waves in under-doped YBa2_2Cu3_3O6.54_{6.54} revealed by X-ray measurements of the ionic displacements

All underdoped high-temperature cuprate superconductors appear to exhibit charge density wave (CDW) order, but both the underlying symmetry breaking and the origin of the CDW remain unclear. We use X-ray diffraction to determine the microscopic structure of the CDW in an archetypical cuprate YBa$_2$Cu$_3$O$_{6.54}$ at its superconducting transition temperature Tc ~ 60 K. We find that the CDWs present in this material break the mirror symmetry of the CuO2 bilayers. The ionic displacements in a CDW have two components: one perpendicular to the CuO$_2$ planes, and another parallel to these planes, which is out of phase with the first. The largest displacements are those of the planar oxygen atoms and are perpendicular to the CuO$_2$ planes. Our results allow many electronic properties of the underdoped cuprates to be understood. For instance, the CDW will lead to local variations in the doping (or electronic structure) giving an explicit explanation of the appearance of density-wave states with broken symmetry in scanning tunnelling microscopy (STM) and soft X-ray measurements

Profile of the U 5f magnetization in U/Fe multilayers

Recent calculations, concerning the magnetism of uranium in the U/Fe multilayer system have described the spatial dependence of the 5f polarization that might be expected. We have used the x-ray resonant magnetic reflectivity technique to obtain the profile of the induced uranium magnetic moment for selected U/Fe multilayer samples. This study extends the use of x-ray magnetic scattering for induced moment systems to the 5f actinide metals. The spatial dependence of the U magnetization shows that the predominant fraction of the polarization is present at the interfacial boundaries, decaying rapidly towards the center of the uranium layer, in good agreement with predictions.Comment: 7 pages, 6 figure

Simultaneous dynamic electrical and structural measurements of functional materials

A new materials characterization system developed at the XMaS beamline, located at the European Synchrotron Radiation Facility in France, is presented. We show that this new capability allows to measure the atomic structural evolution (crystallography) of piezoelectric materials whilst simultaneously measuring the overall strain characteristics and electrical response to dynamically (ac) applied external stimuli

Temperature dependence of the spin and orbital magnetization density in Sm1−xGdxAl2Sm_{1-x}Gd_{x} Al_{2} around the spin-orbital compensation point

Non-resonant ferromagnetic x-ray diffraction has been used to separate the spin and orbital contribution to the magnetization density of the proposed zero-moment ferromagnet $Sm_{0.982}Gd_{0.018} Al_{2}$. The alignment of the spin and orbital moments relative to the net magnetization shows a sign reversal at 84K, the compensation temperature. Below this temperature the orbital moment is larger than the spin moment, and vice versa above it. This result implies that the compensation mechanism is driven by the different temperature dependencies of the $4f$ spin and orbital moments. Specific heat data indicate that the system remains ferromagnetically ordered throughout

Magnetic field induced effects on the electric polarization in RMnO3 R Dy,Gd

X-ray resonant magnetic scattering studies of rare earth magnetic ordering were performed on perovskite manganites RMnO3 (R = Dy, Gd) in an applied magnetic field. The data reveal that the field-induced three-fold polarization enhancement for H || a (H approx. 20 kOe) observed in DyMnO3 below 6.5 K is due to a re-emergence of the Mn-induced Dy spin order with propagation vector k(Dy) = k(Mn) = 0.385 b*, which accompanies the suppression of the independent Dy magnetic ordering, k(Dy) = 1/2 b*. For GdMnO3, the Mn-induced ordering of Gd spins is used to track the Mn-ordering propagation vector. The data confirm the incommensurate ordering reported previously, with k(Mn) varying from 0.245 to 0.16 b* on cooling from T_N(Mn) down to a transition temperature T'. New superstructure reflections which appear below T' suggest a propagation vector k(Mn) = 1/4 b* in zero magnetic field, which may coexist with the previously reported A-type ordering of Mn. The Gd spins order with the same propagation vector below 7 K. Within the ordered state of Gd at T = 1.8 K we find a phase boundary for an applied magnetic field H || b, H = 10 kOe, which coincides with the previously reported transition between the ground state paraelectric and the ferroelectric phase of GdMnO3. Our results suggest that the magnetic ordering of Gd in magnetic field may stabilize a cycloidal ordering of Mn that, in turn, produces ferroelectricity.Comment: 8 Figures, v2: improved figure layou

Antiferromagnetic order and domains in Sr3Ir2O7 probed by x-ray resonant scattering

This article reports a detailed x-ray resonant scattering study of the bilayer iridate compound, Sr3Ir2O7, at the Ir L2 and L3 edges. Resonant scattering at the Ir L3 edge has been used to determine that Sr3Ir2O7 is a long-range ordered antiferromagnet below TN 230K with an ordering wavevector, q=(1/2,1/2,0). The energy resonance at the L3 edge was found to be a factor of ~30 times larger than that at the L2. This remarkable effect has been seen in the single layer compound Sr2IrO4 and has been linked to the observation of a Jeff=1/2 spin-orbit insulator. Our result shows that despite the modified electronic structure of the bilayer compound, caused by the larger bandwidth, the effect of strong spin-orbit coupling on the resonant magnetic scattering persists. Using the programme SARAh, we have determined that the magnetic order consists of two domains with propagation vectors k1=(1/2,1/2,0) and k2=(1/2,-1/2,0), respectively. A raster measurement of a focussed x-ray beam across the surface of the sample yielded images of domains of the order of 100 microns size, with odd and even L components, respectively. Fully relativistic, monoelectronic calculations (FDMNES), using the Green's function technique for a muffin-tin potential have been employed to calculate the relative intensities of the L2,3 edge resonances, comparing the effects of including spin-orbit coupling and the Hubbard, U, term. A large L3 to L2 edge intensity ratio (~5) was found for calculations including spin-orbit coupling. Adding the Hubbard, U, term resulted in changes to the intensity ratio <5%.Comment: 9 pages, 9 figure

Non-uniform Gd distribution and magnetization profiles within GdCoFe alloy thin films

Rare earth (RE):transition metal (TM) ferrimagnetic alloys continue to attract significant attention for spintronics. This work focuses on the elemental distribution of RE and TM elements throughout the thickness of nominally uniform films and the resulting spatial variations of the magnetization within these layers. Samples of CoFe alloyed with Gd were studied using secondary ion mass spectroscopy, polarized neutron reflectometry, and x-ray resonant magnetic reflectivity. The samples were grown by magnetron co-sputtering to control the RE:TM alloy ratio of the ferrimagnetic layer, which was combined with W and Pt layers as either under or over-layers to create sample structures such as W/Gdx(Co70Fe30)100-x/Pt, wherex x=0,8, and 23 at. %. Results show that uniformly deposited thin-films have a significant variation in the distribution of the TM and RE through the film thickness, and this leads to a spatial distribution in the net magnetization profile and a non-uniform Gd magnetization profile within the layer. These findings have implications for the application RE:TM alloys in spintronics as they may impact the perpendicular magnetic anisotropy, the ferrimagnetic compensation temperature, and interfacial spin transport