Field induced hysteretic structural phase switching and possible CDW in Re-doped MoTe2.

Novel electronic systems displaying exotic physical properties can be derived from complex topological materials through chemical doping. MoTe2, the candidate type-II Weyl semimetal shows dramatically enhanced superconductivity up to 4.1 K upon Re doping in Mo sites. Based on bulk transport and local scanning tunnelling microscopy here we show that Re doping also leads to the emergence of a possible charge density wave phase in Re0.2Mo0.8Te2. In addition, the tunnellingI-Vcharacteristics display non-linearity and hysteresis which is commensurate with a hysteresis observed in the change in tip-height (z) as a function of applied voltageV. The observations indicate an electric field induced hysteretic switching consistent with piezoelectricity and possible ferroelectricity.

Nodeless s-wave superconductivity in the [Formula: see text]-Mn structure type noncentrosymmetric superconductor TaOs: a [Formula: see text]SR study.

Noncentrosymmetric superconductors can lead to a variety of exotic properties in the superconducting state such as line nodes, multigap behavior, and time-reversal symmetry breaking. In this paper, we report the properties of a new noncentrosymmetric superconductor TaOs, using muon spin relaxation and rotation measurements. It is shown using the zero-field muon experiment that TaOs preserve the time-reversal symmetry in the superconducting state. From the transverse field muon measurements, we extract the temperature dependence of [Formula: see text], which is proportional to the superfluid density. This data can be fit with a fully gapped s-wave model for [Formula: see text] = 2.01 [Formula: see text] 0.02. Furthermore, the value of magnetic penetration depth is found to be 5919 [Formula: see text] 45 [Formula: see text], which is consistent with the value obtained from the bulk measurements.

Low Dimensional Magnetic Lattice and Room Temperature Magneto(di)electric Effect in Polyanion Ruddlesden-Popper Iron Oxides.

We have shown a new design strategy which exploits different oxyanions in a Ruddlesden-Popper (RP)-type phase to modulate the local crystal structure and magnetic lattice. Material (Sr4Fe2(SO4)0.5O6.5) with the larger voluminous oxyanion (SO4, S-O distance = 1.49 Å) as separating blocks between magnetic FeO layers shows a two-dimensional magnetic lattice. A three-dimensional magnetic lattice and spin reorientation transition is observed for the Sr4Fe2(CO3)O6, having CO3 (C-O distance = 1.25 Å), a smaller oxyanion, as a separating layer. Using mixed oxyanions (SO4 and CO3) in the central perovskite block of the RP3 phase, we have demonstrated a facile strategy to modulate the local crystal structure. The modulated displacement of the magnetic cations, which can break the local centrosymmetry, is suggested to originate the magnetodielectric effect near the magnetic ordering temperatures (higher than room temperature). Further, all CO3 containing samples show magnetodielectric coupling below room temperature due to the spin reorientation transition. The room temperature magnetodielectric effect coupled to the targeted local modulation of the crystal structure by oxyanions (in the absence of second-order Jahn-Teller active "distortion centers") opens a new door to the design of new multifunctional materials with the possibility for the room temperature application.

Tetrahedral chain ordering and low dimensional magnetic lattice in a new brownmillerite Sr2ScFeO5.

We report the synthesis, structure and physical properties of a hitherto unreported brownmillerite compound Sr2ScFeO5. We have shown a new ordering sequence of the interlayer iron tetrahedral chains. Reduced dimensionality of the magnetic lattice and the frustration in the two dimensional iron tetrahedral chains originate complex magnetic and magneto-dielectric effects. Our study highlights a novel approach to tailor the magnetic lattice in bulk oxides.

Effect of Co Substitution on the Crystal and Magnetic Structure of SrFeO2.75-δ: Stabilization of the "314-Type" Oxygen Vacancy Ordered Structure without A-Site Ordering.

A study of the structure-composition-properties correlation is reported for the oxygen-deficient SrFe1-xCoxO2.75-δ (x = 0.1-0.85) materials. The introduction of Co in the parent SrFeO2.75 (Sr4Fe4O11) structure revealed an interesting structural transformation. At room temperature (RT), an orthorhombic (space group Cmmm, 2√2ap × 2ap × âˆš2ap type, ap = lattice parameter of the cubic perovskite) → tetragonal (space group P4/mmm, ap × ap × 2ap type) → tetragonal (space group I4/mmm, 2ap × 2ap × 4ap type) structural transformation is observed in parallel with increasing Co content and decreasing oxygen content in the structure. At the same time, a rich variation in the magnetic properties is explored. The samples with x = 0.25, 0.3 show temperature-induced magnetization reversal. With increasing Co content in the structure, magnetic interactions start to weaken due to the random distribution of Fe and Co in the structure; the x = 0.5 sample shows frustration in the magnetic behavior with much smaller magnetization value. With a further increase in the Co content in the structure, RT ferrimagnetic-type behavior is observed for the sample with x = 0.85. The nuclear and magnetic structure refinements using RT and low-temperature neutron powder diffraction (NPD, 10 K) patterns confirm the formation of a "314-type" novel oxygen vacancy ordered phase for the sample with x = 0.85, which is the first case of "314-type" novel oxygen vacancy ordering without A-site (ABO3-δ type perovskite) ordering. The magnetic structure is G-type antiferromagnetic starting at room temperature. Further, the stabilization of the "314-type" complex superstructure is related to the ordering of oxygen vacancies in the oxygen-deficient Co-O layers, and the same assists in building a network of Co ions with different coordination environments, each with different spin states, and forms the spin-state ordering.

Core-level photoemission spectra of Mo0.3Cu0.7Sr2ErCu2Oy, a superconducting perovskite derivative. Unconventional structure-property relationships.

Detailed studies of the electronic states for Mo(0.3)Cu(0.7)Sr(2)ErCu(2)Oy samples with different oxygen contents are presented here. The influence of oxygenation on the electronic states for the Mo(0.3)Cu(0.7)Sr(2)ErCu(2)Oy system from the semiconducting to the superconducting state has been investigated by means of X-ray photoelectron spectroscopy (XPS). The XPS studies show that Mo is in a mixed Mo(V) and Mo(VI) oxidation state and Mo(V) is predominant over the Mo(VI) in the as-prepared (AP) sample. Yet annealing under an oxygen atmosphere enhances the Mo(VI) state. At the same time, a reduction in the copper species is observed. In the Cu 2p spectra, a larger energy separation between the satellite and main peaks (E(S)-E(M)) and a lower intensity ratio (I(S)/I(M)) are found to correlate with higher values of the superconducting transition temperature (T(C)). Analysis of these spectra within the Configuration Interaction (CI) model suggests that higher values of TC are related to lower values of the O 2p-Cu 3d charge transfer energy. The change in the Sr 3d and O 1s core level spectra correlates with the oxygen insertion in the (Mo/Cu)O(1+δ) chain site, after oxygenation. The hole concentration (Ph) in the copper plane has been obtained using the room temperature thermoelectric power (TEP) value; this shows an increasing tendency with increasing T(C), after oxygenation. From these experimental results, one observes that T(C)increases with decreasing charge transfer energy. This is, indeed, opposite to the accepted views and occurs in parallel with the shortening of the apical copper-oxygen distance (Cu(2)-O(2)) and the increasing of the CuO(2) plane buckling angle.

Spin glass to superconducting phase transformation by oxidation of a molybdo-cuprate: Mo0.3Cu0.7Sr2TmCu2Oy.

A detailed study of the structure and properties for the as-prepared and oxygen annealed Mo0.3Cu0.7Sr2TmCu2Oy material is reported. The Cu/Mo cationic distribution is established using a combination of x-ray/neutron powder diffraction refinement. The chemical substitution of the Mo ions for the Cu ions in the CuYSr2Cu2O(7-δ) structure is found to occur in both of the copper sites for the as-prepared sample. Interestingly, no trace of Mo substitution in the copper plane site is found to occur after oxygenation. The as-prepared Mo0.3Cu0.7Sr2TmCu2Oy material is found to be a spin glass (SG) system and explained on the basis of the cluster-by-cluster freezing model. On the other hand, the oxygen annealed material is superconducting (SC) (T(SC,onset) = 31 K). A peak has been observed in the critical current density plot and can be explained on the basis of field induced pins. The influence of oxygen annealing in the structure and properties of this material are presented and discussed. This seems to be the first case of a SG-SC transformation following an oxidation reaction in cuprates.