Lix(C5H5N)yFe2–zSe2: A Defect-Resilient Expanded-Lattice High-Temperature Superconductor

Le résumé fourni par la source

Two-dimensional iron chalcogenide intercalates display a remarkable correlation of the interlayer spacing with enhancement of the superconducting critical temperature ( T c ). In this work, synchrotron X-ray absorption (XAS; at the Fe and Se K-edges) and emission (XES; at the Fe Κβ) spectroscopies allow one to discuss how the important rise of T c (∼44 K) in the molecule-intercalated Li x (C 5 H 5 N) y Fe 2– z Se 2 relates to the electronic and local structural changes felt by the inorganic host upon doping ( x ). XES shows that widely separated layers of edge-sharing FeSe 4 tetrahedra carry low-spin moieties, with a local Fe magnetic moment slightly reduced compared to the parent β-Fe 2– z Se 2 . Pre-edge XAS expresses the progressively reduced mixing of metal 3d–4p states upon lithiation. Doping-mediated local lattice modifications, probed by conventional T c optimization measures (cf. the anion height and FeSe 4 tetrahedra regularity), become less relevant when layers are spaced far away. On the basis of extended X-ray absorption fine structure, such distortions are compensated by a softer Fe network that relates to Fe-site vacancies, alleviating electron–lattice correlations and superconductivity. Density functional theory (DFT) guided modification of the isolated Fe 2– z Se 2 ( z, vacant sites) planes, resembling the host layers, identify that Fe-site deficiency occurs at low energy cost, giving rise to stretched Fe sheets, in accordance with experiments. The robust high- T c in Li x (C 5 H 5 N) y Fe 2– z Se 2, arises from the interplay of electron-donating spacers and the iron selenide layer’s tolerance to defect chemistry, a tool to favorably tune its Fermi surface properties.

Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.