Author
V. P. S. Awana
Other affiliations: National Institute for Materials Science, Tokyo Institute of Technology, Tata Institute of Fundamental Research ...read more
Bio: V. P. S. Awana is an academic researcher from Council of Scientific and Industrial Research. The author has contributed to research in topics: Superconductivity & Magnetization. The author has an hindex of 34, co-authored 465 publications receiving 5491 citations. Previous affiliations of V. P. S. Awana include National Institute for Materials Science & Tokyo Institute of Technology.
Papers published on a yearly basis
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TL;DR: In this paper, the authors reported synthesis and superconductivity at 3.7 K in REO0.5F 0.5BiS2 using vacuum encapsulation technique.
Abstract: We report synthesis and superconductivity at 3.7 K in PrO0.5F0.5BiS2. The newly discovered material belongs to the layered sulfide based REO0.5F0.5BiS2 compounds having a ZrCuSiAs-type structure. The bulk polycrystalline compound is synthesized by the vacuum encapsulation technique at 780 ∘C in a single step. Detailed structural analysis has shown that the as synthesized PrO0.5F0.5BiS2 is crystallized in a tetragonal P4/nmm space group with lattice parameters a=4.015(5) A, c=13.362(4) A. Bulk superconductivity is observed in PrO0.5F0.5BiS2 below 4 K from magnetic and transport measurements. Electrical transport measurements showed superconducting transition temperature (Tc) onset at 3.7 K and Tc(ρ=0) at 3.1 K. The hump at Tc related to the superconducting transition is not observed in the heat capacity measurement and rather a Schottky-type anomaly is observed at below ∼6 K. The compound is slightly semiconducting in a normal state. Isothermal magnetization (MH) exhibited typical type II behavior with a lower critical field (Hc1) of around 8 Oe.
194 citations
TL;DR: Mizuguchi et al. as mentioned in this paper reported the synthesis of a superconductor with a transition temperature of 4.4 K at 500 °C by a vacuum encapsulation technique.
Abstract: A very recent report on the observation of superconductivity in Bi(4)O(4)S(3) [Mizuguchi, Y.; http://arxiv.org/abs/1207.3145] could potentially reignite the search for superconductivity in a broad range of layered sulfides. We report here the synthesis of Bi(4)O(4)S(3) at 500 °C by a vacuum encapsulation technique and its basic characterizations. The as-synthesized Bi(4)O(4)S(3) was contaminated with small amounts of Bi(2)S(3) and Bi impurities. The majority phase was found to be tetragonal (space group I4/mmm) with lattice parameters a = 3.9697(2) A and c = 41.3520(1) A. Both AC and DC magnetization measurements confirmed that Bi(4)O(4)S(3) is a bulk superconductor with a superconducting transition temperature (T(c)) of 4.4 K. Isothermal magnetization (M-H) measurements indicated closed loops with clear signatures of flux pinning and irreversible behavior. The lower critical field (H(c1)) at 2 K for the new superconductor was found to be ~15 Oe. Magnetotransport measurements showed a broadening of the resistivity (ρ) and a decrease in T(c) (ρ = 0) with increasing magnetic field. The extrapolated upper critical field H(c2)(0) was ~31 kOe with a corresponding Ginzburg-Landau coherence length of ~100 A . In the normal state, the ρ ~ T(2) dependence was not indicated. Hall resistivity data showed a nonlinear magnetic field dependence. Our magnetization and electrical transport measurements substantiate the appearance of bulk superconductivity in as-synthesized Bi(4)O(4)S(3). On the other hand, Bi heat-treated at the same temperature is not superconducting, thus excluding the possibility of impurity-driven superconductivity in the newly discovered superconductor Bi(4)O(4)S(3).
178 citations
Posted Content•
TL;DR: In this article, the authors reported synthesis and superconductivity at 3.7K in PrO0.5F 0.5BiS2 using vacuum encapsulation technique at 7800C in single step.
Abstract: We report synthesis and superconductivity at 3.7K in PrO0.5F0.5BiS2. The newly discovered material belongs to the layered sulfide based REO0.5F0.5BiS2 compounds having ZrCuSiAs type structure. The bulk polycrystalline compound is synthesized by vacuum encapsulation technique at 7800C in single step. Detailed structural analysis has shown that the as synthesized PrO0.5F0.5BiS2 is crystallized in tetragonal P4/nmm space group with lattice parameters a = 4.015(5) {\AA}, c = 13.362(4) {\AA}. Bulk superconductivity is observed in PrO0.5F0.5BiS2 below 4K from magnetic and transport measurements. Electrical transport measurements showed superconducting transition temperature (Tc) onset at 3.7K and Tc ({\rho}=0) at 3.1K. Hump at Tc related to superconducting transition is not observed in heat capacity measurement and rather a Schottky-type anomaly is observed at below ~6K. The compound is slightly semiconducting in normal state. Isothermal magnetization (MH) exhibited typical type II behavior with lower critical field (Hc1) of around 8Oe.
127 citations
TL;DR: In this article, a frequency-dependent cusp was observed in polycrystalline Ru-1222 vs T measurements, which was interpreted as a spin glass transition, which is commonly accepted to describe a spin-glass with magnetically interacting clusters.
Abstract: The dynamics of the magnetic properties of polycrystalline ${\mathrm{RuSr}}_{2}{\mathrm{Gd}}_{1.5}{\mathrm{Ce}}_{0.5}{\mathrm{Cu}}_{2}{\mathrm{O}}_{10\ensuremath{-}\ensuremath{\delta}}$ (Ru-1222) have been studied by ac susceptibility and dc magnetization measurements, including relaxation and ageing studies. Ru-1222 is a reported magnetosuperconductor with Ru spins magnetic ordering at temperatures near 100 K and superconductivity in $\mathrm{Cu}\ensuremath{-}{\mathrm{O}}_{2}$ planes below ${T}_{c}\ensuremath{\sim}40\mathrm{K}.$ The exact nature of Ru spins magnetic ordering is still being debated, and no conclusion has been reached yet. In this work, a frequency-dependent cusp was observed in ${\ensuremath{\chi}}_{\mathrm{ac}}$ vs T measurements, which is interpreted as a spin glass transition. The change in the cusp position with frequency follows the Vogel-Fulcher law, which is commonly accepted to describe a spin-glass with magnetically interacting clusters. Such an interpretation is supported by thermoremanent magnetization (TRM) measurements at $T=60\mathrm{K}.$ TRM relaxations are well described by a stretched exponential relation, and present significant aging effects.
123 citations
TL;DR: In this article, phase pure samples of LaOBiS 2 and LaO 0.5 F0.5 BiS 2 were synthesized by conventional solid state reaction route via vacuum encapsulation technique at 800°C for 12h.
109 citations
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Journal Article•
28,685 citations
TL;DR: In this article, the reactivity of a class of high-capacity oxides with a single redox cation has been investigated and it has been shown that these oxides exhibit sustainable reversible capacities as high as 230 mAh/g−1 and good cycling behavior with no signs of voltage decay.
Abstract: Li-ion batteries have contributed to the commercial success of portable electronics and may soon dominate the electric transportation market provided that major scientific advances including new materials and concepts are developed. Classical positive electrodes for Li-ion technology operate mainly through an insertion-deinsertion redox process involving cationic species. However, this mechanism is insufficient to account for the high capacities exhibited by the new generation of Li-rich (Li1+xNiyCozMn(1−x−y−z)O2) layered oxides that present unusual Li reactivity. In an attempt to overcome both the inherent composition and the structural complexity of this class of oxides, we have designed structurally related Li2Ru1−ySnyO3 materials that have a single redox cation and exhibit sustainable reversible capacities as high as 230 mA h g−1. Moreover, they present good cycling behaviour with no signs of voltage decay and a small irreversible capacity. We also unambiguously show, on the basis of an arsenal of characterization techniques, that the reactivity of these high-capacity materials towards Li entails cumulative cationic (Mn+→M(n+1)+) and anionic (O2−→O22−) reversible redox processes, owing to the d-sp hybridization associated with a reductive coupling mechanism. Because Li2MO3 is a large family of compounds, this study opens the door to the exploration of a vast number of high-capacity materials.
1,109 citations
TL;DR: The magnetocaloric effect and its most straightforward application, magnetic refrigeration, are topics of current interest due to the potential improvement of energy efficiency of cooling and temperature control systems, in combination with other environmental benefits associated to a technology that does not rely on the compression/expansion of harmful gases.
941 citations
16 Mar 1993
TL;DR: Giant and isotropic magnetoresistance as huge as −53% was observed in magnetic manganese oxide La0.72Ca0.25MnOz films with an intrinsic antiferromagnetic spin structure as discussed by the authors.
Abstract: Giant and isotropic magnetoresistance as huge as −53% was observed in magnetic manganese oxide La0.72Ca0.25MnOz films with an intrinsic antiferromagnetic spin structure. We ascribe this magnetoresistance to spin‐dependent electron scattering due to spin canting of the manganese oxide.
924 citations
TL;DR: The migration of cations between metal layers and Li layers is an intrinsic feature of the charge-discharge process that increases the trapping of metal ions in interstitial tetrahedral sites and provides insights into new chemistry to be explored for developing high-capacity layered electrodes that evade voltage decay.
Abstract: Although Li-rich layered oxides (Li1+xNiyCozMn1−x−y−zO2 > 250 mAh g−1) are attractive electrode materials providing energy densities more than 15% higher than today’s commercial Li-ion cells, they suffer from voltage decay on cycling. To elucidate the origin of this phenomenon, we employ chemical substitution in structurally related Li2RuO3 compounds. Li-rich layered Li2Ru1−yTiyO3 phases with capacities of ~240 mAh g−1 exhibit the characteristic voltage decay on cycling. A combination of transmission electron microscopy and X-ray photoelectron spectroscopy studies reveals that the migration of cations between metal layers and Li layers is an intrinsic feature of the charge–discharge process that increases the trapping of metal ions in interstitial tetrahedral sites. A correlation between these trapped ions and the voltage decay is established by expanding the study to both Li2Ru1−ySnyO3 and Li2RuO3; the slowest decay occurs for the cations with the largest ionic radii. This effect is robust, and the finding provides insights into new chemistry to be explored for developing high-capacity layered electrodes that evade voltage decay.
723 citations