Journal of the American Chemical Society · 2010 · 66 citations · 28 references
Natural SciencesMaterials SciencePhysicsCondensed Matter PhysicsCrystal StructureSolid State PhysicsAntiferromagnetismMagnetic Properties Of SolidsMagnetism In SolidsPhase ChangePhase TransitionsSuperconducting MaterialsAntiferromagnetic OrderAntiferromagnetic OrderingAntiferromagnetic TransitionsMagnetic Ordering TransitionsMagnetic Phase TransitionsMagnetostructural TransitionsSuperconducting Critical TemperatureSuperconducting Properties
Single crystal and powder samples of the series of iron chalcogenide superconductors with nominal composition, Fe((1.15))Te((1-)y)S(y), are found to form for 0 ≤ y ≤ 0.15. They crystallize in the tetragonal anti-PbO structure, which is composed of layers of edge-shared Fe(Te, S)(4) tetrahedra. For y = 0, Fe(1+x)Te (x ≈ 0.12(1)) is nonsuperconducting and undergoes a tetragonal (P4/nmm) to monoclinic (P2(1)/m) structural transition at ∼65 K, associated with the onset of commensurate antiferromagnetic order at q = (0.5 0 0.5). We show that on sulfur substitution, Fe(1+x)Te(1-y)S(y) becomes orthorhombic (Pmmn) at low temperature for 0 ≤ y ≤ 0.015, where the greatly suppressed magnetic scattering is now incommensurate at q = (0.5-δ 0 0.5) and possesses short ranged magnetic correlations that are well fitted with a two-dimensional Warren peak shape. At much higher concentrations of S (y ≥ 0.075), there is suppression of both the structural and magnetic transitions and a superconducting transition at 9 K is observed. Between these two composition regimes, there exists a region of phase separation (0.025 ≤ y ≤ 0.05), where the low temperature neutron diffraction data is best refined with a model containing both the tetragonal and orthorhombic phases. The increase in the amount of sulfur is found to be associated with a reduction in interstitial iron, x. Microprobe analysis of a single crystal of composition Fe((1.123(5)))Te((0.948(4)))S((0.052(4))) confirms the presence of compositional variation within the crystals, rationalizing the observed phase separation.
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