Enhancement of superconducting transition temperature of FeSe by intercalation of a molecular spacer layer
| Autor: | Burrard-Lucas, Matthew, Free, David G., Sedlmaier, Stefan J., Wright, Jack D., Cassidy, Simon J., Hara, Yoshiaki, Corkett, Alex J., Lancaster, Tom, Baker, Peter J., Blundell, Stephen J., Clarke, Simon J. |
|---|---|
| Rok vydání: | 2012 |
| Předmět: | |
| Druh dokumentu: | Working Paper |
| DOI: | 10.1038/nmat3464 |
| Popis: | The recent discovery of high temperature superconductivity in a layered iron arsenide has led to an intensive search to optimize the superconducting properties of iron-based superconductors by changing the chemical composition of the spacer layer that is inserted between adjacent anionic iron arsenide layers. Until now, superconductivity has only been found in compounds with a cationic spacer layer consisting of metal ions: Li+, Na+, K+, Ba2+ or a PbO-type or perovskite-type oxide layer. Electronic doping is usually necessary to control the fine balance between antiferromagnetism and superconductivity. Superconductivity has also been reported in FeSe, which contains neutral layers similar in structure to those found in the iron arsenides but without the spacer layer. Here we demonstrate the synthesis of Lix(NH2)y(NH3)1-yFe2Se2 (x ~0.6 ; y ~ 0.2), with lithium ions, lithium amide and ammonia acting as the spacer layer, which exhibits superconductivity at 43(1) K, higher than in any FeSe-derived compound reported so far and four times higher at ambient pressure than the transition temperature, Tc, of the parent Fe1.01Se. We have determined the crystal structure using neutron powder diffraction and used magnetometry and muon-spin rotation data to determine the superconducting properties. This new synthetic route opens up the possibility of further exploitation of related molecular intercalations in this and other systems in order to greatly optimize the superconducting properties in this family. Comment: 9 pages, 4 figures; updated and with supplementary information |
| Databáze: | arXiv |
| Externí odkaz: |
|