We report neutron inelastic scattering experiments on single-crystal PbMg1/3Nb2/3O3 doped with 32% PbTiO3, a relaxor ferroelectric that lies close to the morphotropic phase boundary. When cooled under an electric field E∥ [001] into tetragonal and monoclinic phases, the scattering cross section from transverse acoustic (TA) phonons polarized parallel to E weakens and shifts to higher energy relative to that under zero-field-cooled conditions. Likewise, the scattering cross section from transverse optic (TO) phonons polarized parallel to E weakens for energy transfers 4≤ω≤9 meV. However, TA and TO phonons polarized perpendicular to E show no change. This anisotropic field response is similar to that of the diffuse scattering cross section, which, as previously reported, is suppressed when polarized parallel to E but not when polarized perpendicular to E. Our findings suggest that the lattice dynamics and dynamic short-range polar correlations that give rise to the diffuse scattering are coupled.

We report neutron scattering measurements on low-energy (â.,ωâ5 meV) magnetic excitations from a series of Fe1+yâz(Ni/Cu)zTe1âxSex samples which belong to the “11†Fe-chalcogenide family. Our results suggest a strong correlation between the magnetic excitations near (0.5,0.5,0) and the superconducting properties of the system. The low-energy magnetic excitations are found to gradually move away from (0.5,0.5,0) to incommensurate positions when superconductivity is suppressed, either by heating or chemical doping, confirming previous observations. © 2014 American Physical Society.

Spin nematics break spin-rotational symmetry while maintaining time-reversal symmetry, analogous to liquid crystal nematics that break spatial rotational symmetry while maintaining translational symmetry. Although several candidate spin nematics have been proposed, the identification and characterization of such a state remain challenging because the spin-nematic order parameter does not couple directly to experimental probes. KFe_{0.8}Ag_{1.2}Te_{2} (K_{5}Fe_{4}Ag_{6}Te_{10}, KFAT) is a local-moment magnet consisting of well-separated 2×2 Fe clusters, and in its ground state the clusters order magnetically, breaking both spin-rotational and time-reversal symmetries. Using uniform magnetic susceptibility and neutron scattering measurements, we find a small strain induces sizable spin anisotropy in the paramagnetic state of KFAT, manifestly breaking spin-rotational symmetry while retaining time-reversal symmetry, resulting in a strain-induced spin-nematic state in which the 2×2 clusters act as the spin analog of molecules in a liquid crystal nematic. The strain-induced spin anisotropy in KFAT allows us to probe its nematic susceptibility, revealing a divergentlike increase upon cooling, indicating the ordered ground state is driven by a spin-orbital entangled nematic order parameter.

We present neutron scattering measurements on low-energy phonons from a superconducting (Tc=2.7K) Sn0.8In0.2Te single-crystal sample. The longitudinal acoustic phonon mode and one transverse acoustic branch have been mapped out around the (002) Bragg peak for temperatures of 1.7 and 4.2 K. We observe a substantial energy width of the transverse phonons at energies comparable to twice the superconducting gap; however, there is no change in this width between the superconducting and normal states, and the precise origin of this energy width anomaly is not entirely clear. We also confirm that the compound is well ordered, with no indications of structural instability.

We report inelastic neutron scattering measurements of low-energy (ω10 meV) magnetic excitations in the "11" system Fe1+yTe1-xSex. The spin correlations are two-dimensional (2D) in the superconducting samples at low temperature, but appear much more three-dimensional (3D) when the temperature rises well above Tc∼15 K, with a clear increase of the (dynamic) spin correlation length perpendicular to the Fe planes. This behavior is extremely unusual; typically, the suppression of thermal fluctuations at low temperature would favor the enhancement of 3D correlations, or even ordering, and the reversion to 2D cannot be naturally explained when only the spin degree of freedom is considered. Our results suggest that the low temperature physics in the 11 system, in particular the evolution of low-energy spin excitations towards superconducting pairing, intrinsically involves changes in orbital correlations.

In as-grown bulk crystals of Fe1+yTe1-xSex with x≲0.3, excess Fe (y>0) is inevitable and correlates with a suppression of superconductivity. At the same time, there remains the question as to whether the character of the antiferromagnetic correlations associated with the enhanced anion height above the Fe planes in Te-rich samples is compatible with superconductivity. To test this, we have annealed as-grown crystals with x=0.1 and 0.2 in Te vapor, effectively reducing the excess Fe and inducing bulk superconductivity. Inelastic neutron scattering measurements reveal low-energy magnetic excitations consistent with short-range correlations of the double-stripe type; nevertheless, cooling into the superconducting state results in a spin gap and a spin resonance, with the extra signal in the resonance being short range with a mixed single-stripe/double-stripe character, which is different than other iron-based superconductors. The mixed magnetic character of these superconducting samples does not appear to be trivially explainable by inhomogeneity.

We report neutron diffraction studies of FeS single crystals obtained from Rb _x Fe_2-y S₂ single crystals via a hydrothermal method. While no 5 × 5 iron vacancy order or block antiferromagnetic order typical of Rb _x Fe_2-y S₂ is found in our samples, we observe C-type short-range antiferromagnetic order with moments pointed along the c axis hosted by a different phase of FeS with an expanded interlayer spacing. The Néel temperature for this magnetic order is determined to be 170 ± 4 K. Our finding of a variant FeS structure hosting this C-type antiferromagnetic order demonstrates that the known FeS phase synthesized in this method is in the vicinity of a magnetically ordered ground state, providing insights into understanding a variety of phenomena observed in FeS and the related FeSe_1-x S _x iron chalcogenide system.

It has recently been demonstrated that dynamical magnetic correlations measured by neutron scattering in iron chalcogenides can be described with models of short-range correlations characterized by particular choices of four-spin plaquettes, where the appropriate choice changes as the parent material is doped towards superconductivity. Here we apply such models to describe measured maps of magnetic scattering as a function of two-dimensional wave vectors obtained for optimally superconducting crystals of FeTe1-xSex. We show that the characteristic antiferromagnetic wave vector evolves from that of the bicollinear structure found in underdoped chalcogenides (at high temperature) to that associated with the stripe structure of antiferromagnetic iron arsenides (at low temperature); these can both be described with the same local plaquette, but with different interplaquette correlations. While the magnitude of the low-energy magnetic spectral weight is substantial at all temperatures, it actually weakens somewhat at low temperature, where the charge carriers become more itinerant. The observed change in spin correlations is correlated with the dramatic drop in the electronic scattering rate and the growth of the bulk nematic response upon cooling. Finally, we also present powder neutron diffraction results for lattice parameters in FeTe1-xSex indicating that the tetrahedral bond angle tends to increase towards the ideal value upon cooling, in agreement with the increased screening of the crystal field by more itinerant electrons and the correspondingly smaller splitting of the Fe 3d orbitals.

We have studied the structure, magnetic, and transport properties of copper-substituted iron telluride. Our results extend the range of copper substitution to 60% substitution per formula unit, which is far beyond previously stated solubility limits. Substitution of copper into antiferromagnetic iron telluride is found to suppress the signatures of the low-temperature transitions in susceptibility and resistance measurements, giving rise to an insulating, spin-glass state. Upon increasing the copper substitution from 4% to 6%, short-range antiferromagnetic order appears followed by the combined magnetic and structural transition at a lower temperature, although the magnetic order is ultimately not resolution limited with a correlation length of 250 Å in the 6% Cu-substituted sample, in contrast to the magnetic order of the 4% copper-substituted sample, which is resolution limited. Upon warming the 6% Cu-substituted sample in the presence of a 5 T magnetic field oriented along the b axis, magnetic and structural phase transitions are observed at a temperature much lower than those of the magnetic and structural transitions which occur in zero field. Furthermore, these transitions are absent upon cooling in this field. We discuss the field results in the most general terms possible, including possible random field effects.

We report experimental studies of a series of BaFe₂S_3-x Se _x (0 ⩽ x ⩽ 3) single crystals and powder specimens using x-ray diffraction, neutron-diffraction, muon-spin-relaxation, and electrical transport measurements. A structural transformation from Cmcm (BaFe₂S₃) to Pnma (BaFe₂Se₃) was identified around x = 0.7 - 1. Neutron-diffraction measurements on the samples with x = 0.2, 0.4, and 0.7 reveal that the Néel temperature of the stripe antiferromagnetic order is gradually suppressed from ~120 to 85 K, while the magnitude of the ordered Fe²⁺ moments shows very little variation. Similarly, the block antiferromagnetic order in BaFe₂Se₃ remains robust for 1.5 ⩽ x ⩽ 3 with negligible variation in the ordered moment and a slight decrease of the Néel temperature from 250 K (x = 3) to 225 K (x = 1.5). The sample with x = 1 near the Cmcm and Pnma border shows coexisting, two-dimensional, short-range stripe- and block-type antiferromagnetic correlations. The system remains insulating for all x, but the thermal activation gap shows an abrupt increase when traversing the boundary from the Cmcm stripe phase to the Pnma block phase. The results demonstrate that the crystal structure, magnetic order, and electronic properties are strongly coupled in the BaFe₂S_3-x Se _x system.