We report the synthesis and physical property characterization of PrFe1-xCoxAsO with x = 0.0 to 1.0. The studied samples are synthesized by solid state reaction route via vacuum encapsulation method. The pristine compound PrFeAsO does not show superc
onductivity, but rather exhibits a metallic step like transition due to spin density wave ordering of Fe moments below 150 K, followed by another upward step due to anomalous ordering of Pr moments at 12 K. Both the Fe-SDW and Pr-TN temperatures decrease monotonically with Co substitution at Fe site. Superconductivity appears in a narrow range of x from 0.07 to 0.25 with maximum Tc at 11.12 K for x = 0.15. Samples, with x = 0.25 exhibit metallic behavior right from 300 K down to 2 K, without any Fe-SDW or Pr-TN steps in resistivity. In fact, though Fe-SDW decreases monotonically, the Pr-TN is disappeared even with x = 0.02. The magneto transport measurements below 14 Tesla on superconducting polycrystalline Co doped PrFeAsO lead to extrapolated values of the upper critical fields [Hc2(0)] of up to 60 Tesla.
We report high field (up to 13 Tesla) magneto transport R(T)H] of YBa2Cu3O7 (YBCO):Agx (x= 0.0, 0.1 and 0.2) composites. The transport properties are significantly improved by Ag doping on the insulating grain boundaries of YBCO. Pure and Ag diffused
YBCO superconducting samples are synthesized through solid state reaction route. Both pure and Ag doped YBCO are superconducting at below 90K. Though, the Tc (R=0) of YBCO:Ag samples under applied field of 13 Tesla is around 65K, the same is 45K for pure YBCO under same applied field. The upper critical field [Hc2(0)], being estimated from R(T)H is around 70Tesla for pristine sample, and is above 190Tesla for Ag doped samples. The boarding of the resistive transition under applied magnetic field is comparatively less and nearly single step for Ag doped samples, while the same is clearly two step and relatively much larger for the pristine YBCO. The resistive broadening is explained on the basis of changed inter-granular coupling and thermally activated flux flow (TAFF). The TAFF activation energy (U0) is found to be linear with applied magnetic field for all the samples, but with nearly an order of magnitude less value for the Ag doped samples. Summarily, it is shown that inclusion of Ag significantly improves the superconducting performance of YBCO:Ag composites, in particular under applied field.
We report synthesis, structure, electrical transport and heat capacity of SmFeAsO. The title compound is synthesized by one-step encapsulation of stoichiometric FeAs, Sm, and Sm2O3 in an evacuated (10-5 Torr) quartz tube by prolong (72 hours) anneali
ng at 1100oC. The as synthesized compound is crystallized in tetragonal structure with P4/nmm space group having lattice parameters a = 3.93726(33) A and c = 8.49802(07) A. The resistance (R-T) measurements on the compound exhibited ground state spin-density-wave (SDW)-like metallic steps below 140 K. Heat capacity CP(T) measurements on the title compound, showed an anomaly at around 140 K, which is reminiscent of the SDW ordering of the compound. At lower temperatures the CP(T) shows a clear peak at around 4.5 K. At lower temperature below 20 K, Cp(T) is also measured under an applied field of 7 Tesla. It is concluded that the CP(T) peak at 4.5 K is due to the anti-ferromagnetic(AFM) ordering of Sm3+ spins. These results are in confirmation with ordering of Sm in Sm2-xCexCuO4.
We report high field magneto transport of Sm/PrFeAsO. Below spin density wave transition (TSDW), the magneto-resistance (MR) of Sm/PrFeAsO is positive and increasing with decreasing temperature. The MR of SmFeAsO, is found 16%, whereas the same is 21
.5% in case of PrFeAsO, at 2.5 K under applied magnetic field of 14 Tesla (T). In case of SmFeAsO, the variation of isothermal MR with field below 20 K is nonlinear at lower magnetic fields (< 2 Tesla) and the same is linear at moderately higher magnetic fields (H geq 3.5 T). On the other hand PrFeAsO shows almost linear MR at all temperatures below 20 K. The anomalous behavior of MR being exhibited in PrFeAsO is originated from Dirac cone states. The stronger interplay of Fe and Pr ordered moments is responsible for this distinct behavior. PrFeAsO also shows a hump in resistivity (R-T) with possible conduction band (FeAs) mediated ordering of Pr moments at around 12 K. However the same is absent in SmFeAsO even down to 2 K. Our results of high field magneto-transport of up to 14 Tesla brings about clear distinction between ground states of SmFeAsO and PrFeAsO.
We present detailed magnetization and magneto-transport studies on the title compound SmCoAsO. In a recent paper we reported [1] the complex magnetism of this compound. SmCoAsO undergoes successive paramagnetic (PM) - ferro-magnetic (FM) - anti-ferro
-magnetic (AFM) transitions with decrease in temperature. This is mainly driven via the c-direction interaction of Sm4f (SmO layer) spins with adjacent (CoAs layer) ordered Co3d spins. In this article we present an evidence of kinetic arrest for FM-AFM transition. The isothermal magnetization (MH) loops for SmCoAsO exhibited the meta-magnetic transitions at 6, 8 and 10K at around 80, 60 and 50kOe fields respectively with characteristic hysteresis shoulders along with the non-zero moment at origin, thus suggesting the possibility of kinetic arrest. Suggested kinetic arrest is further evident in zero field-cooled (ZFC) and field-cooled (FC) hysteresis under high fields of up to 140kOe magnetization (MT) and the magneto-transport measurements R(T)H during FM-AFM transition. The time dependent moment experiments exhibited very small (~2-3%) increase of the same below 20kO and decrease for 30kOe at 15K.
We report the electrical, magneto transport and specific heat of the layered polycrystalline RECoPO (RE = La, Nd and Sm) samples. These compounds are iso-structural to recently discovered superconductor LaFeAs(O/F). Bulk polycrystalline samples are s
ynthesized by solid state reaction route in an evacuated sealed quartz tube. All these compounds are crystallized in a tetragonal structure with space group P4/nmm. The Cobalt in these compounds is in itinerant state with its paramagnetic moment above 1.4muB and the same orders ferromagnetically (FM) with saturation moment of around 0.20muB below say 80K. Though, LaCoPO shows single paramagnetic (PM) to ferromagnetic (FM) transition near 35K, the NdCoPO and SmCoPO exhibit successive PM-FM-AFM transitions. Both FM and AFM transition temperatures vary with applied field. Although the itinerant ferromagnetism occurs with small saturation moment, typical anti-ferromagnetic (AFM) transitions (TN1, TN2) are observed at 69K and 14K for Nd and 57K and 45K for Sm. This FM-AFM transition of Co spins in NdCoPO and SmCoPO is both field and temperature dependent. The Magneto-transport of NdCoPO and SmCoPO distinctly follows their successive PM-FM-AFM transitions. It is clear that Sm/Nd (4f) interacts with the Co (3d) in first time synthesized Sm/NdCoPO.
The bulk polycrystalline sample FeSe1/2Te1/2 is synthesized by solid state reaction route in an evacuated sealed quartz tube at 750 oC. The presence of superconductivity is confirmed through magnetization/thermoelectric/resistivity studies. It is fou
nd that the superconducting transition temperature (Tc) is around 12 K. Heat capacity (Cp) of superconducting FeSe1-xTex exhibited a hump near Tc, instead of well defined Lambda transition. X-ray Photo electron spectroscopy (XPS) studies revealed well defined positions for divalent Fe, Se and Te but with sufficient hybridization of Fe (2p) and Se/Te (3d) core levels. In particular divalent Fe is shifted to higher BE (binding energy) and Se and Te to lower. The situation is similar to that as observed earlier for famous Cu based HTSc (High Tc superconductors), where Cu (3d) orbital hybridizes with O (2p). We also found the satellite peak of Fe at 712.00 eV, which is attributed to charge carrier localization induced by Fe at 2c site.
We synthesized bulk polycrystalline samples of RECoAsO (RE=La, Nd and Sm) by solid state reaction route in an evacuated sealed quartz tube. All these compounds are crystallized in a tetragonal structure with space group P4/nmm. The Co, in these compo
unds is in itinerant ferromagnetic state with its paramagnetic moment above 1.5 microB and the same orders ferromagnetically (FM) with small saturation moment of around 0.20 microB below say 80K. This bulk intrinsic magnetism of Co changes dramatically when nonmagnetic La is changed by magnetic Sm and Nd. Although the itinerant ferromagnetism occurs below 80-100K with small saturation moment, typical anti-ferromagnetic (AFM) transitions (TN1, TN2) are observed at 57K and 45K for Sm and at 69K and 14K for Nd. The transition of Co spins from FM to AFM, for magnetic Sm and Nd in RECoAsO is both field and temperature dependent. For applied fields below 100Oe, both TN1 and TN2 are seen, with intermediate fields below 1-2kOe only TN1 and above say 5kOe the AFM transition is not observed. This is evidenced in isothermal magnetization (MH) plots as well. It is clear that Sm/Nd magnetic moments interact with the ordered Co spins in adjacent layer and thus transforms the FM ordering to AFM. All the studied compounds are metallic in nature, and their magneto-transport R(T)H follows the temperature and field dependent FM-AFM transition of ordered Co spins.
Here, we report the synthesis and characterization of sulphur-substituted iron telluride i.e. FeTe1-xSx; (x = 0-30 %) system and study the impact of low temperature oxygen (O2) annealing as well. Rietveld analysis of room temperature x-ray diffractio
n (XRD) patterns shows that all the compounds are crystallized in a tetragonal structure (space group P4/nmm) and no secondary phases are observed. Lattice constants are decreased with increasing S concentration. The parent compound of the system i.e. FeTe does not exhibit superconductivity but shows an anomaly in the resistivity measurement at around 78 K, which corresponds to a structural phase transition. Heat capacity Cp(T) measurement also confirms the structural phase transition of FeTe compound. Superconductivity appears by S substitution; the onset of superconducting transition temperature is about 8 K for FeTe0.75S0.25 sample. Thermoelectric power measurements S(T) also shows the superconducting transition at around 7 K for FeTe0.75S0.25 sample. The upper critical fields Hc2(10%), Hc2(50%) and Hc2(90%) are estimated to be 400, 650 and 900 kOe respectively at 0 K by applying Ginzburg Landau (GL) equation. Interestingly, superconducting volume fraction is increased with low temperature (200 oC) O2 annealing at normal pressure. Detailed investigations related to structural (XRD), transport [S(T), R(T)H], magnetization (AC and DC susceptibility) and thermal [Cp(T)] measurements for FeTe1-xS:O2 system are presented and discussed.
We report an easy single step synthesis route of title compound NdFeAsO0.80F0.20 superconductor having bulk superconductivity below 50 K. The title compound is synthesized via solid-state reaction route by encapsulation in an evacuated (10-3 Torr) qu
artz tube. Rietveld analysis of powder X-ray diffraction data shows that compound crystallized in tetragonal structure with space group P4/nmm. R(T)H measurements showed superconductivity with Tc (R=0) at 48 K and a very high upper critical field (Hc2) of up to 345 Tesla. Magnetic measurements exhibited bulk superconductivity in terms of diamagnetic onset below 50 K. The lower critical field (Hc1) is around 1000 Oe at 5 K. In normal state i.e., above 60 K, the compound exhibited purely paramagnetic behavior and thus ruling out the presence of any ordered FeOx impurity in the matrix. In specific heat measurements a jump is observed in the vicinity of superconducting transition (Tc) along with an upturn at below T=4 K due to the AFM ordering of Nd+3 ions in the system. The Thermo-electric power (TEP) is negative down to Tc, thus indicating dominant carriers to be of n-type in NdFeAsO0.80F0.20 superconductor. The granularity of the bulk superconducting NdFeAsO0.8F0.2 sample is investigated and the intra and inter grain contributions have been individuated by looking at various amplitude and frequencies of the applied AC drive magnetic field.
