A new 1223-type high Tc cuprate (Tl,V) Sr2Ca2Cu3O9

A new 1223-type (Tl, V)-based superconducting layered cuprate (Tl_1–x V _x ) Sr₂Ca₂Cu₃O₉ withx=0.25 and 0.50 has been successfully synthesized in the nearly-pure form and identified by powder X-ray diffration analyses. An excessive quantity of Tl is necessary for the preparation of the (Tl, V)-based 1223-type compound. Resistance and ac susceptibility measurements showed that the new (Tl, V)-based 1223 cuprate exhibits T_c above 110 K.     

A new (Hg,V)-based 1212-type cuprate (Hg,V) Sr2(Y,Ca) Cu2Oz with Tc(onset) up to 110 K

We have successfully synthesized a new (Hg, V)-based 1212-type cuprate (Hg_1?x V _x )Sr₂(Y_1?y Ca _y )Cu₂O _z . The electrical resistance measurements showed that some of the as-synthesized materials with proper Hg/V and Y/Ca ratios exhibit weak superconductivity. Oxygen-annealing significantly improved their superconducting behavior, andT _c(onset) up to 110 K was observed. The lattice parameters of (Hg,V)-1212 were found to be in the order ofa=3.8415(1) Å andc=11.8514(6) Å. Substitu ting mercury atoms by vanadium ones results in an important increase of thea parameter and an important decrease of thec parameter compared to the known Hg-based Sr-bearing compounds. The crystal structure of (Hg, V)-1212 was refined by Rietveld refinement against X-ray powder data using the tetragonal symmetry of space groupP4/mmm. The V and Cu valence states and superconductivity in this new (Hg, V)-1212 cuprate are briefly discussed.     

A new (Hg,V)-based 1212-type cuprate (Hg,V) Sr2(Y,Ca) Cu2Oz with Tc(onset) up to 110 K

We have successfully synthesized a new (Hg, V)-based 1212-type cuprate (Hg_1?x V _x )Sr₂(Y_1?y Ca _y )Cu₂O _z . The electrical resistance measurements showed that some of the as-synthesized materials with proper Hg/V and Y/Ca ratios exhibit weak superconductivity. Oxygen-annealing significantly improved their superconducting behavior, andT _c(onset) up to 110 K was observed. The lattice parameters of (Hg,V)-1212 were found to be in the order ofa=3.8415(1) Å andc=11.8514(6) Å. Substitu ting mercury atoms by vanadium ones results in an important increase of thea parameter and an important decrease of thec parameter compared to the known Hg-based Sr-bearing compounds. The crystal structure of (Hg, V)-1212 was refined by Rietveld refinement against X-ray powder data using the tetragonal symmetry of space groupP4/mmm. The V and Cu valence states and superconductivity in this new (Hg, V)-1212 cuprate are briefly discussed.     

Novel 1122 thallium cuprates showing high Tc superconductivity: TlCa1-xY,Ba2Cu2O y,T,1-xPb x CaSr2Cu2O y and TlCa0.5Ln0.5Sr2Cu2O y

Substitution of Ca by Y in TlCaBa₂Cu₂O _y does not favour superconductivity, but substitution of Tl by Pb or of Ca by Ln (Ln = Y or rare earth) in TlCaSr₂Cu₂O _y results in high T_c superconductivity (T_c π 60–90 K). TlCa_1-xLn _x Sr₂Cu₂O _y is a new series of high T_c superconductors, but the x = 0.0 composition does not exhibit bulk superconductivity.     

Magnetization scaling in the ruthenate-cuprate RuSr2Eu1.4Ce 0.6Cu2O10-δ (Ru-1222)

The magnetic properties of the superconducting ruthenate-cuprate RuSr₂Eu _1.4Ce_0.6Cu₂O_10-δ (Ru-1222) have been studied by a scaling analysis of the dc magnetization and ac susceptibility measurements. Non-linear M(H) curves reveal the presence of nano-size clusters with a net magnetic moment of ∼10² μ_B at 180 K, near the deviation from a Curie-Weiss behavior. On cooling, no scaling was observed down to 90 K, discarding the possibility of magnetic phase separation of collinear ferromagnetic particles. We explain this result in terms of a variable number of contributing particles, with a temperature dependent net magnetic moment. For 70 K ≤T≤ 90 K the scaling plots evidence the emergence of a system of non-interacting particles, which couple on further cooling. The observed cluster-glass features are preserved down to the lowest measured temperature (10 K); no signature of long-range order was detected. The frequency shift of the peak in the real part of the ac susceptibility does not follow the Vogel-Fulcher type dependence, as previously reported. The puzzling temperature dependence of the coercive field, H_C(T), is correlated with the changes in the scaling factors.     

在氧-水蒸气存在下单相Sr2(Gd,Ce)2Cu2RuO10的合成及其电学性质

传统固相反应所合成的锶系钌铜氧化物,通常总伴有少量铁磁性SrRuO3杂相.采用氧(或空气)-水蒸气混合气氛下的新型固相反应,既能成功合成锶系钌铜氧化物的前驱物纯相Sr2GdRuO6(211相), 也能进一步在相对低的温度下成功合成锶系钌铜氧1222纯相化合物RuSr2(Gd,Ce)2Cu2O10 (Ru-1222),使其中SrRuO3杂相含量大大减少.详细讨论了新型固相反应下产物的形成及其机理,并涉及SrRuO3杂相的存在对RuSr2(Gd,Ce)2Cu2O10产物电学性质的影响.结果表明,水蒸气的作用能抑制前驱物合成中SrRuO3杂相的形成,进而控制反应产物Ru-1222相中SrRuO3杂相的存在,而后者又有利于Ru-1222相超导电性的获得.     

Synthesis and superconducting properties of Nd0.33Eu0.08Gd0.58Ba2Cu3O z materials

We have studied the effect of the ratio of different rare-earth element on the superconducting properties and phase formation of (Nd_0.33Eu_0.08Gd_0.58)Ba₂Cu₃O _z ceramic. Bulk NEG samples were prepared using the solid-state reaction process. The superconducting transition for Nd_0.33Eu_0.08Gd_0.58Ba₂Cu₃O _z is T _c ≈90 K and the value of the critical current density (J _c ) is 13.9 A/cm² at 77 K under zero magnetic fields. This value is twice as high when compared with the (J _c ) value of YBCO systems (J _c = 7.31 A/cm²). The obtained bulk sample was used for the production of superconducting Ag-sheathed tapes by OPIT method including hot rolling. The critical current density of the obtained tape (337 A/cm²) is one order higher than the one of the bulk sample.      

Electronic structure of the trilayer cuprate superconductor Bi(2)Sr(2)Ca(2)Cu(3)O(10+delta)

The low-energy electronic structure of the nearly optimally doped trilayer cuprate superconductor Bi(2)Sr(2)Ca(2)Cu(3)O(10+delta) is investigated by angle-resolved photoemission spectroscopy. The normal state quasiparticle dispersion and Fermi surface and the superconducting d-wave gap and coherence peak are observed and compared with those of single- and bilayer systems. We find that both the superconducting gap magnitude and the relative coherence-peak intensity scale linearly with T(c) for various optimally doped materials.     

HRTEM study of new superconducting lead cuprate (Pb, Cu) (Eu, Ce)2(Eu, Sr)2Cu2Oz

Crystallographic properties of a new lead cuprate superconducting material (Pb, Cu) (Eu, Ce)₂(Eu, Sr)₂Cu₂O_z are examined by electron probe micro-analysis and transmission electron microscopy. It is confirmed that although the sample examined here is not of single-phase, the composition of the superconducting phase is close to the nominal composition. From TEM observations, it follows that the crystal structure of the new phase is similar to that of Tl-1222 which consists of a fluorite type block, a rock salt type layer and a perovskite block.     

Pressure tuning of magnetic interactions in layered (La0.6Nd0.4)1. 2Sr1.8Mn2O7 manganite

The effect of pressure of up to 9 GPa on the magnetic and structural properties of layered (La0.6Nd0.4)1.2Sr1.8Mn2O7 manganite has been investigated. Pressure shifts the Mn atoms from the center of each bilayer towards the adjacent bilayer. The observed shift of the Mn atoms involves mainly a charge redistribution within the d(3z(2)-r(2)) axial orbital. The decrease in the interbilayer spacing and the shift of the Mn atoms away from the center of each bilayer result in increased magnetic and electronic coupling between the adjacent bilayers along the c axis.     

Effect of Sb substitution on the superconductivity of Bi2(Ca,Sr) n+1Cu n O4n+2 (n=1, 2 and 3) systems

Effect of incorporation of Sb in place of Bi in the bismuth cuprate superconductors has been examined. The nominal compositions studied are MCa_1·5Sr_1·5Cu₂O_8+δ and MCa₂Sr₂Cu₃O_10+δ, whereM=Bi_2−x Sb _x or Bi_1·5−x Sb _x Pb_0·5. Different preparative routes such as the ceramic method, the matrix route as well as the melt route were employed to prepare the materials. No indication of either Sb entering the lattice or enhancement ofT _c is noted from resistivity, magnetic susceptibility and microwave absorption measurements. Communication No. 162 from Materials Research Centre.     

Atomic structure of Sr0.75Ba0.25Nb2O6 single crystal and composition-structure-property relationin (Sr,Ba)Nb2O6 solid solutions

The structure of the Sr_0.75Ba_0.25Nb₂O₆ single crystal has been investigated by x-ray diffraction. The occupancies of the Ba and Sr sites in two structural channels are determined. It is found that these sites are split in the large (pentagonal) channel. A qualitative correlation is revealed between the smearing of the phase transition and the displacement of the Sr atom from the m symmetry plane in the pentagonal channel at different [Sr]/[Ba] ratios. The degree of acentricity of the NbO₆ octahedra is analyzed as a function of the [Sr]/[Ba] ratio.     

Magnetic and superconducting properties of doped (Sr,Ca)10Cu17O29-type single crystals

Magnetization, resistivity and electron spin resonance (ESR) measurements have been performed on single crystals of A₁₀Cu₁₇O₂₉ (A=Ca_5.9, Sr_3.5, Bi_0.3, Pb_0.1, Y_0.1, Al_0.1) of the S=1/2 quasi-one-dimensional system, which has both simple chains and two-leg ladders of copper ions. Substantial hole doping has been achieved in the studied crystals, which led to superconductivity with a high critical temperature (T_c≈80 K). The values of the penetration depth have been estimated for temperatures in the range 30–60 K using the reversible magnetization data. A rough estimation of the Ginzburg–Landau parameter, κ, indicates that the superconductivity in the investigated ladder material should be described as an extreme type-II limit. It has been suggested that the superconductivity in the studied system should be related to the two-leg ladders rather than to the chains.     

Colossal magnetoresistance in layered manganite Nd2−2x Sr1+2x Mn2O7 (0 ≤ x ≤ 0.5)

The layered manganite Nd_2−2x Sr_1+2x Mn₂O₇, with x varying between 0 and 0.5, has been synthesized using solid-state reaction method. We have found that Nd_2−2x Sr_1+2x Mn₂O₇ do not form the single-phase layered compound with A₃B₂O₇ structure. Instead, mixtures of various phases, such as, orthorhombic perovskite, i.e., Nd_1−z Sr _z MnO₃, layered manganite and unreacted starting compounds, have been obtained. Except for x=0.4, which is found to be an antiferromagnetic insulator, all other x values yielded metal-insulator transition and ferromagnetic ordering.     

Magnetism and superconductivity in R1.5Ce0.5MSr2Cu2O10‐δ (M=Ru and Fe) compounds

It is shown here, that the superconducting (SC) R_1.5Ce_0.5RuSr₂Cu₂O_10-δ (RCeRuSCO, R= Eu and Gd) materials (T_c ～ 32 and 42 K) are also antiferromagnetically (AFM) ordered at T _N(Ru) ～ 122 and 180 K, respectively, thus, T_N ? T_c, a trend which is contrary to that obtained in “magnetic‐SC” intermetallic systems. Mössbauer spectroscopy (MS) on 0.5% ⁵⁷Fe doped samples shows that all Fe ions reside in the Ru site which is magnetically ordered, whereas SC is confined to the CuO₂ planes. On the other hand, for Y_1.5Ce_0.5FeSr₂Cu₂O₉ (YCeFSCO) no SC is found and the Cu–O planes order AFM at T _N(Cu)=31 K. MS studies reveal two in equivalent Fe sites, and that Fe resides predominantly (60%) in the Cu(1) site. In both sites, the Fe does not order magnetically, and the low T _N(Cu) obtained is due to frustration of the Cu moments by the presence of Fe. T _N is sensitive to oxygen concentration and shifts toward 260 K when oxygen is depleted.