Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 132, Issue 37, Pages 13000-13007Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja105279p
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- U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
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Single crystal and powder samples of the series of iron chalcogenide superconductors with nominal composition, Fe1.15Te1-ySy, 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, Fe1+xTe (x approximate to 0.12(1)) is nonsuperconducting and undergoes a tetragonal (P4/nmm) to monoclinic (P2(1)/m) structural transition at similar to 65 K, associated with the onset of commensurate antiferromagnetic order at q = (0.5 0 0.5). We show that on sulfur substitution, Fe1+xTe1-ySy becomes orthorhombic (Pmmn) at low temperature for 0 <= y <= 0.15, where the greatly suppressed magnetic scattering is now incommensurate at q = (0.5-delta 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 Fe1.123(5)Te0.948(4)S0.052(4) confirms the presence of compositional variation within the crystals, rationalizing the observed phase separation.
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