Nature Communications · 2015 · 202 citations · 29 references
Natural SciencesMaterials SciencePhysicsCondensed Matter PhysicsSolid State PhysicsSpectroscopyElectronic Band StructureMagnetism In SolidsStrongly Correlated Electron SystemsSuperconducting MaterialsSurface PhysicsAngle-resolved Photoelectron SpectroscopyAngle-resolved Photoemission SpectroscopyAngle-resolved X-ray Photoelectron SpectroscopyElectron Correlation EffectsFermi SurfaceIron-based AlloysIron-based SuperconductorsUnconventional Superconductivity
Establishing the appropriate theoretical framework for unconventional superconductivity in the iron-based materials requires correct understanding of both the electron correlation strength and the role of Fermi surfaces. This fundamental issue becomes especially relevant with the discovery of the iron chalcogenide superconductors. Here, we use angle-resolved photoemission spectroscopy to measure three representative iron chalcogenides, FeTe0.56Se0.44, monolayer FeSe grown on SrTiO3 and K0.76Fe1.72Se2. We show that these superconductors are all strongly correlated, with an orbital-selective strong renormalization in the dxy bands despite having drastically different Fermi surface topologies. Furthermore, raising temperature brings all three compounds from a metallic state to a phase where the dxy orbital loses all spectral weight while other orbitals remain itinerant. These observations establish that iron chalcogenides display universal orbital-selective strong correlations that are insensitive to the Fermi surface topology, and are close to an orbital-selective Mott phase, hence placing strong constraints for theoretical understanding of iron-based superconductors.
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Superconductivity in the PbO-type structure α-FeSe
Fong-Chi Hsu, Jiu-Yong Luo, K. C. Yeh et al. · Proceedings of the National Academy of Sciences · 2008 · 2.9K citations · Full text
Interfacial mode coupling as the origin of the enhancement of Tc in FeSe films on SrTiO3
J. J. Lee, F. Schmitt, R. G. Moore et al. · Nature · 2014 · 700 citations · Full text