We report the results a comprehensive study of charge density wave (CDW) correlations in untwinned YBCO6+x single crystals with 0.4<x<0.99 using Cu-L3 edge resonant x-ray scattering (RXS). Evidence of CDW formation is found for 0.45<x<0.93, but not f
or samples with x<0.44 that exhibit incommensurate spin-density-wave order, and in slightly overdoped samples with x=0.99. This suggests the presence of two proximate zero-temperature CDW critical points at doping pc1~0.08 and pc2~0.18. The CDW reflections are observed at incommensurate in-plane wave vectors (d_a, 0) and (0, d_b). Both decrease linearly with increasing doping, in agreement with recent reports on Bi-based high-Tc superconductors, but in sharp contrast to the behavior of the 214 family. The CDW intensity and correlation length exhibit maxima at p~0.12, coincident with a plateau in the superconducting transition temperature Tc. The onset temperature of the CDW reflections depends non-monotonically on p, with a maximum of~160 K for p~0.12. The RXS reflections exhibit a uniaxial intensity anisotropy. We further observe a depression of CDW correlations upon cooling below Tc, and (for samples with p> 0.09) an enhancement of the signal when an external magnetic field up to 6 T is applied in the superconducting state. For samples with p~0.08, where prior work has revealed a field-enhancement of incommensurate magnetic order, the RXS signal is field-independent. This supports a previously suggested scenario in which incommensurate charge and spin orders compete against each other, in addition to individually competing against. We discuss the relationship of these results to stripe order 214, the pseudogap phenomenon, superconducting fluctuations, and quantum oscillations.
We report a detailed Raman scattering study of the lattice dynamics in detwinned single crystals of the underdoped high temperature superconductor YBa2Cu3O6+x (x=0.75, 0.6, 0.55 and 0.45). Whereas at room temperature the phonon spectra of these compo
unds are similar to that of optimally doped YBa2Cu3O6.99, additional Raman-active modes appear upon cooling below ~170-200 K in underdoped crystals. The temperature dependence of these new features indicates that they are associated with the incommensurate charge density wave state recently discovered using synchrotron x-ray scattering techniques on the same single crystals. Raman scattering has thus the potential to explore the evolution of this state under extreme conditions.
A charge modulation has recently been reported in (Y,Nd)Ba$_2$Cu$_3$O$_{6+x}$ [Ghiringhelli {em et al.} Science 337, 821 (2013)]. Here we report Cu $L_3$ edge soft x-ray scattering studies comparing the lattice modulation associated with the charge m
odulation in YBa$_2$Cu$_3$O$_{6.6}$ with that associated with the well known charge and spin stripe order in La$_{1.875}$Ba$_{0.125}$CuO$_4$. We find that the correlation length in the CuO$_2$ plane is isotropic in both cases, and is $259 pm 9$ AA for La$_{1.875}$Ba$_{0.125}$CuO$_4$ and $55 pm 15$ AA for YBa$_2$Cu$_3$O$_{6.6}$. Assuming weak inter-planar correlations of the charge ordering in both compounds, we conclude that the order parameters of the lattice modulations in La$_{1.875}$Ba$_{0.125}$CuO$_4$ and YBa$_2$Cu$_3$O$_{6.6}$ are of the same order of magnitude.
We have used resonant x-ray scattering to determine the momentum dependent charge correlations in YBa$_2$Cu$_3$O$_{6.55}$ samples with highly ordered chain arrays of oxygen acceptors (ortho-II structure). The results reveal nearly critical, biaxial c
harge density wave (CDW) correlations at in-plane wave vectors (0.315, 0) and (0, 0.325). The corresponding scattering intensity exhibits a strong uniaxial anisotropy. The CDW amplitude and correlation length are enhanced as superconductivity is weakened by an external magnetic field. Analogous experiments were carried out on a YBa$_2$Cu$_3$O$_{6.6}$ crystal with a dilute concentration of spinless (Zn) impurities, which had earlier been shown to nucleate incommensurate magnetic order. Compared to pristine crystals with the same doping level, the CDW amplitude and correlation length were found to be strongly reduced. These results indicate a three-phase competition between spin-modulated, charge-modulated, and superconducting states in underdoped YBa$_2$Cu$_3$O$_{6+delta}$.
The electron-phonon interaction is of central importance for the electrical and thermal properties of solids, and its influence on superconductivity, colossal magnetoresistance, and other many-body phenomena in correlated-electron materials is curren
tly the subject of intense research. However, the non-local nature of the interactions between valence electrons and lattice ions, often compounded by a plethora of vibrational modes, present formidable challenges for attempts to experimentally control and theoretically describe the physical properties of complex materials. Here we report a Raman scattering study of the lattice dynamics in superlattices of the high-temperature superconductor $bf YBa_2 Cu_3 O_7$ and the colossal-magnetoresistance compound $bf La_{2/3}Ca_{1/3}MnO_{3}$ that suggests a new approach to this problem. We find that a rotational mode of the MnO$_6$ octahedra in $bf La_{2/3}Ca_{1/3}MnO_{3}$ experiences pronounced superconductivity-induced lineshape anomalies, which scale linearly with the thickness of the $bf YBa_2 Cu_3 O_7$ layers over a remarkably long range of several tens of nanometers. The transfer of the electron-phonon coupling between superlattice layers can be understood as a consequence of long-range Coulomb forces in conjunction with an orbital reconstruction at the interface. The superlattice geometry thus provides new opportunities for controlled modification of the electron-phonon interaction in complex materials.
We report high-pressure x-ray diffraction and magnetization measurements combined with ab-initio calculations to demonstrate that the high-pressure optical and transport transitions recently reported in TiOCl, correspond in fact to an enhanced Ti3+-T
i3+ dimerization existing already at room temperature. Our results confirm the formation of a metal-metal bond between Ti3+ ions along the b-axis of TiOCl, accompanied by a strong reduction of the electronic gap. The evolution of the dimerization with pressure suggests a crossover from the spin-Peierls to a conventional Peierls situation at high pressures.
Electronic structure calculations for spinel vanadate ZnV$_2$O$_4$ show that partial electronic delocalization in this system leads to structural instabilities. These are a consequence of the proximity to the itinerant-electron boundary, not being re
lated to orbital ordering. We discuss how this mechanism naturally couples charge and lattice degrees of freedom in magnetic insulators close to such a crossover. For the case of ZnV$_2$O$_4$, this leads to the formation of V-V dimers along the [011] and [101] directions that readily accounts for the intriguing magnetic structure of ZnV$_2$O$_4$.
On the basis of experimental thermoelectric power results and ab initio calculations, we propose that a metal-insulator transition takes place at high pressure (approximately 6 GPa) in MgV_2O_4.
We report a systematic enhancement of the pressure dependence of TN in A2+[V2]O4 spinels as the V-V separation approaches the critical separation for a transition to itinerant-electron behavior. An intermediate phase between localized and itinerant e
lectron behavior is identified in Zn[V2]O4 and Mg[V2]O4 exhibiting mobile holes as large polarons. In Zn[V2]O4, cooperative ordering of V-V pairs below a Ts=TN does not totally suppress the V3+-ion spins at ambient pressure, but makes TN to decrease with pressure. Our results demonstrate that Zn[V2]O4 and Mg[V2]O4 are less localized than previously thought.
