Increasing dissipation-free supercurrent has been the primary issue for practical application of superconducting wires. For magnesium diboride, MgB 2 , carbon is known to be the most effective dopant to enhance high-field properties. However, the critical role of carbon remains elusive, and also low-field critical current density has not been improved. Here, we have undertaken malic acid doping of MgB 2 and find that the microscopic origin for the enhancement of high-field properties is due to boron vacancies and associated stacking faults, as observed by high-resolution transmission electron microscopy and electron energy loss spectroscopy. The carbon from the malic acid almost uniformly encapsulates boron, preventing boron agglomeration and reducing porosity, as observed by three-dimensional X-ray tomography. The critical current density either exceeds or matches that of niobium titanium at 4.2 K. Our findings provide atomic-level insights, which could pave the way to further enhancement of the critical current density of MgB 2 up to the theoretical limit.

Carbon‐encapsulated crystalline boron nanopowder and coarse magnesium powder are used as inexpensive tailored starting materials for the fabrication of high‐performance MgB2 superconducting wire. A low sintering temperature leads to a high critical current density, as a result of nanometer‐sized boron powder, surface oxidation preclusion by carbon encapsulation, and grain alignment by elongated magnesium coarse powder.

We studied the effects of sintering temperature on the phase transformation, lattice parameters, full width at half-maximum (FWHM), strain, critical temperature (Tc), critical current density (Jc) and resistivity (ρ) in MgB2/Fe wires. All samples were fabricated by the in situ powder-in-tube method (PIT) and sintered within a temperature range of 650–900 °C. It was observed that wires sintered at low temperature, 650 °C, resulted in higher Jc up to 12 T and lower Tc. The best transport Jc value reached 4200 A cm−2 at 4.2 K and 10 T. This is related to the grain boundary pinning due to small grain size. On the other hand, wires sintered at 900 °C had a lower Jc in combination with a higher Tc.

The urgent need for nanoporous metal oxides with highly crystallized frameworks is motivating scientists to try to discover new preparation methods, because of their wide use in practical applications. Recent work has demonstrated that two-dimensional (2D) cyanide-bridged coordination polymers (CPs) are promising materials and appropriate for this purpose (Angew. Chem. Int. Ed.- 2013, 52, 1235). After calcination, 2D CPs can be transformed into nanoporous metal oxides with a highly accessible surface area. Here, this strategy is adopted in order to form 2D nanoporous nickel oxide (NiO) with tunable porosity and crystallinity, using trisodium citrate dihydrate as a controlling agent. The presence of trisodium citrate dihydrate plays a key role in the formation of 2D nanoflakes by controlling the nucleation rate and the crystal growth. The size of the nanoflakes gradually increases by augmenting the amount of trisodium citrate dihydrate in the reaction. After heating the as-prepared CPs in air at different temperatures, nanoporous NiO can be obtained. During this thermal treatment, organic units (carbon and nitrogen) are completely removed and only the metal content remains to take part in the formation of nanoporous NiO. In the case of large-sized 2D CP nanoflakes, the original 2D flake-shapes are almost retained, even after thermal treatment at low temperature, but they are completely destroyed at high temperature because of further crystallization in the framework. Nanoporous NiO with high surface area shows significant efficiency and interesting results for supercapacitor application.

High-performance superconducting joints are essential for realizing persistent-mode magnets. Herein, we propose a concept and fabrication of such superconducting joints, which yielded reliable performance in the operating temperature range of 4.2-25 K. MgB 2 -MgB 2 joints in magnets are known to result in deterioration of localized electrical, thermal, and mechanical properties. To overcome these problems, the ends of the two wires are inserted into a pellet press, which is then filled with a mixture of unreacted magnesium and boron powders, followed by heat treatment. The critical current capacity and joint resistance were precisely evaluated by the standard four-probe method in open-circuit and by field-decay measurements in a closed-loop, respectively. These joints demonstrated up to 66% of the current-carrying capacity of unjoined wire at 20 K, 2 T and joint resistance of 1.4 x 10 −12 Ω at 4.2 K in self-field. AbstractHigh-performance superconducting joints are essential for realizing persistent-mode magnets.Herein, we propose a new process and fabrication of such superconducting joints, which yielded reliable performance in the operating temperature range of 4.2 K to 25 K. MgB 2 -MgB 2 joints in magnets, are known to result in deterioration of localized electrical, thermal, and mechanical properties. To overcome these problems, the ends of the two wires are inserted into a pellet press, which is then filled with a mixture of unreacted magnesium and boron powders, followed by heat treatment. The critical current capacity and joint resistance were precisely evaluated by the standard four-probe method in open-circuit and by fielddecay measurements in a closed-loop, respectively. These joints demonstrated up to 66% of the current-carrying capacity of unjoined wire at 20 K, 2 T and joint resistance of < 1.4 x 10 -12 Ω at 4.2 K in self-field.

No abstract

No abstract

In this work, we report on significantly enhanced critical current density (Jc) in MgB2 superconductor that was easily obtained by doping with a hydrocarbon, highly active pyrene (C16H10), and using a sintering temperature as low as ∼600°C. The processing advantages of the C16H10 additive include production of a highly active carbon (C) source, an increased level of disorder, and the introduction of small grain size, resulting in enhancement of Jc.