Competing spin density wave, collinear, and helical magnetism in Fe1+xTe

C. Stock, E. E. Rodriguez, P. Bourges, R. A. Ewings, H. Cao, S. Chi, J. A. Rodriguez-Rivera, M. A. Green

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    15 Scopus citations

    Abstract

    The Fe1+xTe phase diagram consists of two distinct magnetic structures with collinear order present at low interstitial iron concentrations and a helical phase at large values of x with these phases separated by a Lifshitz point. We use unpolarized single-crystal diffraction to confirm the helical phase for large interstitial iron concentrations and polarized single-crystal diffraction to demonstrate the collinear order for the iron-deficient side of the Fe1+xTe phase diagram. Polarized neutron inelastic scattering shows that the fluctuations associated with this collinear order are predominately transverse at low-energy transfers, consistent with a localized magnetic moment picture. We then apply neutron inelastic scattering and polarization analysis to investigate the dynamics and structure near the boundary between collinear and helical orders in the Fe1+xTe phase diagram. We first show that the phase separating collinear and helical orders is characterized by a spin density wave with a single propagation wave vector of (∼0.45, 0, 0.5). We do not observe harmonics or the presence of a charge density wave. The magnetic fluctuations associated with this wave vector are different from the collinear phase, being strongly longitudinal in nature and correlated anisotropically in the (H,K) plane. The excitations preserve the C4 symmetry of the lattice but display different widths in momentum along the two tetragonal directions at low-energy transfers. While the low-energy excitations and minimal magnetic phase diagram can be understood in terms of localized interactions, we suggest that the presence of the density wave phase implies the importance of electronic and orbital properties.

    Original languageEnglish
    Article number144407
    JournalPhysical Review B
    Volume95
    Issue number14
    DOIs
    StatePublished - Apr 7 2017

    Funding

    This work was funded by the Carnegie Trust for the Universities of Scotland, the Royal Society of Edinburgh, and the EPSRC and through the National Science Foundation (Grant No. DMR-09447720). Research at Oak Ridge National Laboratory's HFIR was sponsored by the Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy.

    FundersFunder number
    Scientific User Facilities Division
    National Science FoundationDMR-09447720
    National Science Foundation
    U.S. Department of Energy
    Basic Energy Sciences
    Oak Ridge National Laboratory
    Engineering and Physical Sciences Research CouncilEP/M01052X/1
    Engineering and Physical Sciences Research Council
    Royal Society of Edinburgh
    Carnegie Trust for the Universities of Scotland

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