RESUMEN
Superconductivity in FeSe emerges from a nematic phase that breaks four-fold rotational symmetry in the iron plane. This phase may arise from orbital ordering, spin fluctuations or hidden magnetic quadrupolar order. Here we use inelastic neutron scattering on a mosaic of single crystals of FeSe, detwinned by mounting on a BaFe2As2 substrate to demonstrate that spin excitations are most intense at the antiferromagnetic wave vectors QAF = (±1, 0) at low energies E = 6-11 meV in the normal state. This two-fold (C2) anisotropy is reduced at lower energies, 3-5 meV, indicating a gapped four-fold (C4) mode. In the superconducting state, however, the strong nematic anisotropy is again reflected in the spin resonance (E = 3.6 meV) at QAF with incommensurate scattering around 5-6 meV. Our results highlight the extreme electronic anisotropy of the nematic phase of FeSe and are consistent with a highly anisotropic superconducting gap driven by spin fluctuations.
RESUMEN
SrLaMnO4 is a layered antiferromagnetic (AF) oxide with the tetragonal ( I4/ mmm) n = 1 Ruddlesden-Popper phase structure (also known as the K2NiF4 structure) with TN = 128 K. Remarkably, substitution of Sr2+ by Ba2+, forming the solid solution Ba1- xSr xLaMnO4, results in the destruction of long-range magnetic order and of the ordered moment on Mn3+ for x > 0.35, although the effective paramagnetic moment remains unchanged, an unprecedented behavior for this class of magnetic materials. Four members, x = 0.0, 0.25, 0.35, and 1.0, have been studied using XYZ neutron polarization analysis which permits isolation of the magnetic, nuclear and nuclear spin components of the scattering and the measurement of the absolute value of the magnetic cross section. Data analysis is done using model independent reverse Monte Carlo methods (SPINVERT). The results for x = 0.0 (SrLaMnO4), T > TN(128 K), show an asymmetric diffuse peak which evolves into resolution limited Bragg peaks below T N and a fully ordered AF ground state with a Mn3+ moment of 3.06 µB. For x = 0.25 the magnetic scattering below T N displays a remarkable phase separation-Bragg reflections coexisting with diffuse scattering. The ordered Mn3+ moment is 1.1 µB, much reduced from that obtained via unpolarized neutrons. There are no Bragg peaks for x = 0.35 at any measured temperature ( T > 3 K) but there is highly structured diffuse scattering indicating strong short-range order reminiscent of x = 0 and 0.25 above their respective transition temperatures. For x = 1.00 (BaLaMnO4) the diffuse scattering roughly follows a paramagnetic form-factor indicating no short or long-range magnetic correlations. It is argued that the observed phenomena are due to a competition between AF and ferromagnetic (F) superexchange interactions for the 180° Mn3+-O-Mn3+ geometry within the ab plane and that the changes in the local geometry of the Mn-O octahedron leads to reduction of the AF interaction with a likely enhancement of the F interaction with increasing Ba content, ultimately giving rise to a glassy ground state. Analysis of the diffuse magnetic components show clear 2D AF spin correlations above TN for x = 0.00, 0.25, and 0.35 with correlation lengths, ξ â¼ 14-7 Å and no spin correlations for x = 1.00.
RESUMEN
Samples of nanoscale hematite, α-Fe2O3, with different surface geometries and properties have been studied with inelastic time-of-flight neutron scattering. The 15 nm diameter nanoparticles previously shown to have two collective magnetic excitation modes in separate triple-axis neutron scattering studies have been studied in further detail using the advantage of a large detector area, high resolution, and large energy transfer range of the IN5 TOF spectrometer. A mesoporous hematite sample has also been studied, showing similarities to that of the nanoparticle sample and bulk α-Fe2O3. Analysis of these modes provides temperature dependence of the magnetic anisotropy coefficient along the c-axis, κ1. This is shown to remain negative throughout the temperature range studied in both samples, providing an explanation for the previously observed suppression of the Morin transition in the mesoporous material. The values of this anisotropy coefficient are found to lie between those of bulk and nano-particulate samples, showing the hybrid nature of the mesoporous 3-dimensional structure.
RESUMEN
We investigate low-temperature spin correlations in the metallic frustrated magnet ß-Mn1-xCox. Single-crystal polarized-neutron scattering experiments reveal the persistence of highly structured magnetic diffuse scattering and the absence of periodic magnetic order to T=0.05 K. We employ reverse Monte Carlo refinements and mean-field theory calculations to construct an effective Hamiltonian which accounts for the magnetic scattering. The interactions we identify describe an emergent spin structure which mimics the triangular lattice antiferromagnet, one of the canonical models of frustrated magnetism.
RESUMEN
The presence of spin-fluctuations deep within the ordered state of ferromagnetic [Formula: see text] alloy [Formula: see text] has long been suspected but seldom directly observed. Inhomogeneities of one type or another have been cited as important in stabilizing [Formula: see text] behaviour-either longitudinal spin-fluctuations associated with the [Formula: see text]-state (local environment) model or transverse magnetisation arising from non-collinear spin structures. In this study we employ small-angle neutron scattering with neutron polarization analysis to distinguish between the two possibilities. Surprisingly we in fact find evidence of dominant but uncorrelated longitudinal spin-fluctuations coexisting with transverse magnetisation which exists in short-range clusters of size ~[Formula: see text]. This finding supports recent first principles calculations of [Formula: see text] in which both longitudinal spin-fluctuations and magnetic short-range order are identified as important ingredients in reproducing the equilibrium [Formula: see text] lattice.
RESUMEN
We present a program (spinvert; http://spinvert.chem.ox.ac.uk) for refinement of magnetic diffuse scattering data for frustrated magnets, spin liquids, spin glasses, and other magnetically disordered materials. The approach uses reverse Monte Carlo refinement to fit a large configuration of spins to experimental powder neutron diffraction data. Despite fitting to spherically averaged data, this approach allows the recovery of the three-dimensional magnetic diffuse scattering pattern and the spin-pair correlation function. We illustrate the use of the spinvert program with two case studies. First, we use simulated powder data for the canonical antiferromagnetic Heisenberg model on the kagome lattice to discuss the sensitivity of spinvert refinement to both pairwise and higher-order spin correlations. The effect of limited experimental data on the results is also considered. Second, we re-analyse published experimental data on the frustrated system Y0.5Ca0.5BaCo4O7. The results from spinvert refinement indicate similarities between Y0.5Ca0.5BaCo4O7 and its parent compound YBaCo4O7, which were overlooked in previous analyses using powder data.