THE 110 K SUPERCONDUCTING TRANSITION IN Bi-Ca-Sr-Cu-O SYSTEM

1988 ◽  
Vol 02 (07) ◽  
pp. 915-922 ◽  
Author(s):  
S.M. GREEN ◽  
YU MEI ◽  
C. JIANG ◽  
H.L. LUO ◽  
C. POLlTIS

Large resistive transitions with strong diamagnetic signals have been achieved in the Bi-Ca-Sr-Cu-O system. The fractional drop in resistivity at 110K is found not to correlate with the strength of the diamagnetic signal. For samples with nominal composition BiCaSrCu 2 O y containing two superconducting phases, greater than 50% of the susceptive transition can be associated with the 110K phase.

1992 ◽  
Vol 7 (2) ◽  
pp. 115-116 ◽  
Author(s):  
Terry L. Aselage ◽  
Michael O. Eatough

High temperature superconducting phases in the Tl-Ca-Ba-Cu-O system are ideally represented by the formula TlmCan−1Ba2CunO2(n+1)+m, with m either 1 or 2 and n = 1 to at least 3 (Parkin et at., 1988). Each of these phases contains one or more of the nearly planar CuO2sheets common to the cuprate superconductors. A single Ca atom separates adjacent CuO2sheets (n > 1). Single or double rock salt-like Tl-O layers are separated from the Can−1CunO2nregions by single Ba-O layers. Each of the Ca-containing members of this family crystallizes in a tetgragonal unit cell, with space group 14/mmm for the m = 2 series and P4/mmm for the m = 1 series.Despite the general interest in this family of superconductors, little has been reported about the m = 1, n = 2 member, TlCaBa2Cu2O7−δ, hereafter called 1122. This lack of work is due at least in part to the difficulty in synthesizing the pure compound (Michel et at., 1991). Additionally, technological interest has focused on members of the family with higher superconducting transition temperatures, particularly Tl2Ca2Ba2Cu3Oywith Tcup to 125 K. The critical temperature of 1122 has been reported from as low as 50 K (Hervieu et al., 1988) to as high as 103 K (Morosin et al., 1988), and at several values in between (Ganguli et al., 1988; Liang et al., 1988). Most of the samples had other superconducting phases in addition to 1122. Because of the nearly identical a axis lengths of the unit cells of the Tl-family of superconductors, syntactic intergrowths may be present in such multiphase samples.


Crystals ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 288 ◽  
Author(s):  
Maarten R. van Delft ◽  
Sergio Pezzini ◽  
Markus König ◽  
Paul Tinnemans ◽  
Nigel E. Hussey ◽  
...  

The motivation to search for signatures of superconductivity in Weyl semi-metals and other topological phases lies in their potential for hosting exotic phenomena such as nonzero-momentum pairing or the Majorana fermion, a viable candidate for the ultimate realization of a scalable quantum computer. Until now, however, all known reports of superconductivity in type-I Weyl semi-metals have arisen through surface contact with a sharp tip, focused ion-beam surface treatment or the application of high pressures. Here, we demonstrate the observation of superconductivity in single crystals, even an as-grown crystal, of the Weyl semi-metal tantalum phosphide (TaP), at ambient pressure. A superconducting transition temperature, T c , varying between 1.7 and 5.3 K, is observed in different samples, both as-grown and microscopic samples processed with focused ion beam (FIB) etching. Our data show that the superconductivity present in the as-grown crystal is inhomogeneous yet three-dimensional. For samples fabricated with FIB, we observe, in addition to the three-dimensional superconductivity, a second superconducting phase that resides on the sample surface. Through measurements of the characteristic fields as a function of temperature and angle, we are able to confirm the dimensionality of the two distinct superconducting phases.


1995 ◽  
Vol 09 (11n12) ◽  
pp. 731-736
Author(s):  
Y. CAO ◽  
R. L. MENG ◽  
C. W. CHU

The pressure effect on the superconducting transition temperature (T c ) of the newly discovered compound with a nominal composition La 3 Ni 2 B 2 N x with a T c ~14 K has been determined up to 1.5 GPa. T c was found to decrease linearly at a rate of –0.9 K/GPa, which is much greater than that of similar superconducting compounds, LuNi 2 B 2 C and Lu 2 Ni 2 B 2 C 2, while the compound resistivity remains unchanged. Reasons for the observation remain unknown.


1988 ◽  
Vol 02 (05) ◽  
pp. 1313-1319 ◽  
Author(s):  
S. Pekker ◽  
J. Sasvári ◽  
Gy. Hutiray

Bi 2 Sr 2 CuO 6 – CaCuO 2 system is studied in a wide range of compositions by electrical resistivity and X-ray diffraction measurements. The T c = 80 K phase can be observed in all compositions except the Ca free Bi 2 Sr 2 CuO 6, while the T c = 110 K phase is characteristic to the high CaCuO 2 concentration range, with maximum intensity at the nominal composition of Bi 2 Sr 2 Ca 2 Ca 5 Cu 6 O 16. The distribution of 20 K, 80 K and 110 K T c phases is estimated from powder X-ray measurements.


1993 ◽  
Vol 58 (7) ◽  
pp. 1548-1554 ◽  
Author(s):  
Olga Smrčková ◽  
Dagmar Sýkorová ◽  
Pavel Svoboda ◽  
Petr Vašek

Changes of magnetic susceptibility and electrical resistivity of ceramic superconductors of nominal composition YBa2Cu3O7-y and Bi1.4Pb0.6Sr2Ca2Cu3.6Ox observed during their soaking in water are reported. It was found that the YBa2Cu3O7-y superconductor is destroyed in few minutes by boiling water. At lower temperatures the hydrolysis reduces the volume of the superconductive phase, as seen from the susceptibility measurements. Reaction of Bi1.4Pb0.6Sr2Ca2Cu3.6Ox with water causes a decrease of the relative volume of both superconducting phases at a rate substantially higher for the high temperature one (Tc = 110 K).


2017 ◽  
Vol 268 ◽  
pp. 305-310 ◽  
Author(s):  
Nurhidayah Mohd Hapipi ◽  
Abdul Halim Shaari ◽  
Mohd Mustafa Awang Kechik ◽  
Kar Ban Tan ◽  
Roslan Abd-Shukor ◽  
...  

Polycrystalline samples with the nominal composition YBa2Cu3O7-δ (Y-123) were prepared using the co-precipitation method. The effect of the calcination process (single and multiple calcinations) on the samples was investigated by using the four-point temperature-resistance measurement, x-ray diffraction (XRD) and field-emission scanning electron microscope (FESEM). This study is divided into two parts. For the first part, the obtained oxalate powder underwent two calcination processes at 900 °C for 12 h and 900 °C for 24 h, respectively. Then, the powders were pressed into pellets and sintered at 920 °C for 15 h with oxygen flow during the entire heat treatment. In the second part, only one calcination process was undertaken at 900 °C for 24 h before the sintering process in oxygen flow at 920 °C for 15 h. From the XRD patterns, all of the peaks were indexed to the Y-123 phase showing that this superconducting phase was already formed after the first calcination. The volume fraction of Y-123 of the samples with single calcination process was higher compared to multiple calcination processes. From the temperature-resistance measurement, all the samples showed metallic behavior in the normal state and a superconducting transition to zero resistance. The superconducting transition temperature, Tc, for the samples prepared in a single calcination process is higher than that of the multiple calcination processes.


1989 ◽  
Vol 156 ◽  
Author(s):  
E. L. Venturini ◽  
B. Morosin ◽  
D. S. Ginley ◽  
J. F. Kwak ◽  
J. E. Schirber ◽  
...  

ABSTRACTSuperconducting transition temperatures (Tc'S) in the Tl-Ba-Ca-Cu-O system are shown to be a function of processing for both single crystals and bulk ceramics. Crystals with the identical structural phase and nominal composition but slightly different lattice constants can have significant differences in Tc. We report the effects of high temperature annealing in vacuum or flowing oxygen on Tc for single crystal plates of two common phases with nominal stochiometries Tl2Ba2Ca1Cu2O8 and Tl2Ba2Ca2Cu3O10. Contradictory results on nominally similar crystals suggest that strain, Tl content and TI/Ca site disorder are as important as the oxygen stoichiometry in determining Tc This interpretation is supported by complementary annealing studies in bulk ceramic, including a powder where Tc increased by 5 K following high-pressure shock loading which introduced substantial residual strain.


1988 ◽  
Vol 02 (02) ◽  
pp. 543-549 ◽  
Author(s):  
R.L. MENG ◽  
P.H. HOR ◽  
Y.Y. SUN ◽  
Z.J. HUANG ◽  
L. GAO ◽  
...  

The formation of the high temperature superconducting phases in the quinary Bi-Ca-Sr-Cu-O compound system has been investigated. The 120K-superconducting transition appears in samples prepared between 850 and 900°C. A certain homogeneity range is found to exist in this superconducting system, suggesting that higher Tc may be achievable in the same system.


1990 ◽  
Vol 04 (03) ◽  
pp. 195-199 ◽  
Author(s):  
R. SURYANARAYANAN ◽  
S. B. BALIGA ◽  
A. L. JAIN ◽  
O. GOROCHOV

Preparation, X-ray diffraction (XRD), resistivity (ρ) and magnetic susceptibility (χ) of YSrCuO y (nominal composition) synthesized at 1200°C are reported. XRD data indicate more than one phase. Zero resistivity is observed at 72 K. The field cooled χ indicates a superconducting transition at 68 K and also an anti-ferromagnetic transition at 15 K which could be due to Y 2 Cu 2 O 5. These data confirm the earlier observations of Wu et al.5 who have, however, observed a higher T c at 85 K which could be due to a higher temperature used for synthesis.


1989 ◽  
Vol 156 ◽  
Author(s):  
John B. Parise ◽  
Pratibha L. Gai ◽  
M. K. Crawford ◽  
Eugene M. McCarron

ABSTRACTSubstitution of Ca(II) for Y(III) into tetragonal YBa2Cu3O6 has been achieved and a superconducting transition has been observed for a material of nominal composition (Y0.5Ca0.5) Ba2Cu3O6 (Tc (onset) ˜50K) [1]. Observations using high resolution electron microscopy show samples with x < 0.3 consist of a complex mixture, including (Y, Ca) Ba2Cu3O6+δ, YBa2Cu3O6+δ, and BaCuO2. Further, structural refinement using neutron diffraction data provide evidence of a solid solution limit at x ˜ 0.3. A direct analogy can be drawn between superconducting (Y1−xCax)Ba2Cu3O6 (0.1 < x < 0.3) and superconductors of the type (Y1−xCax)Pb2Sr2Cu3O8 and (La2−xM(II)x)CuO4. Substitution of the Ca(II) for Y(III) effectively increases the formal copper oxidation state. The refined structural model is fully consistent with partially oxidized CuO2 sheets separated by linear O-Cu(I)-O units.


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