Optimization of a non-arsenic iron-based superconductor for wire fabrication
We report on the optimization of synthesis of iron selenide-based superconducting powders and the fabrication of selenide-based wire. The powders were synthesized by an ammonothermal method, whereby Ba is intercalated between FeSe layers to produce Bax(NH3)yFe2Se2, with tetragonal structure similar...
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Published in | Superconductor science & technology Vol. 28; no. 4; pp. 45018 - 45025 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
IOP Publishing
13.03.2015
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Subjects | |
Online Access | Get full text |
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Summary: | We report on the optimization of synthesis of iron selenide-based superconducting powders and the fabrication of selenide-based wire. The powders were synthesized by an ammonothermal method, whereby Ba is intercalated between FeSe layers to produce Bax(NH3)yFe2Se2, with tetragonal structure similar to AFe2X2 (X: As, Se), '122', superconductors. The optimal Tc (up to 38 K) and Meissner and shielding superconducting fractions are obtained from the shortest reaction time (t) of reactants in liquid ammonia (30 min). With the increase of t, a second crystalline 122 phase, with a smaller unit cell, emerges. A small amount of NH3 is released from the structure above ∼200 °C, which results in loss of superconductivity. However, in the confined space of niobium Monel tubing, results indicate there is enough pressure for some of NH3 to remain in the crystal lattice, and thermal annealing can be performed at temperatures of up to 780 °C, increasing wire density and yielded a reasonable Tc 16 K. Here, we report of the first successful wire fabrication of non-arsenic high-Tc iron-based superconductor. Although bulk materials are estimated to carry critical current densities >100 kA cm−2 (4 K, self-field), the current transport within wires need to be optimized (Jc ∼ 1 kA cm−2). |
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Bibliography: | USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22) AC05-00OR22725 |
ISSN: | 0953-2048 1361-6668 |
DOI: | 10.1088/0953-2048/28/4/045018 |