Dynamic crystallography reveals spontaneous anisotropy in cubic GeTe.

Cubic energy materials such as thermoelectrics or hybrid perovskite materials are often understood to be highly disordered1,2. In GeTe and related IV-VI compounds, this is thought to provide the low thermal conductivities needed for thermoelectric applications1. Since conventional crystallography cannot distinguish between static disorder and atomic motions, we develop the energy-resolved variable-shutter pair distribution function technique. This collects structural snapshots with varying exposure times, on timescales relevant for atomic motions. In disagreement with previous interpretations3-5, we find the time-averaged structure of GeTe to be crystalline at all temperatures, but with anisotropic anharmonic dynamics at higher temperatures that resemble static disorder at fast shutter speeds, with correlated ferroelectric fluctuations along the <100>c direction. We show that this anisotropy naturally emerges from a Ginzburg-Landau model that couples polarization fluctuations through long-range elastic interactions6. By accessing time-dependent atomic correlations in energy materials, we resolve the long-standing disagreement between local and average structure probes1,7-9 and show that spontaneous anisotropy is ubiquitous in cubic IV-VI materials.

Hyperfine interaction in cobalt by high-resolution neutron spectroscopy.

We have investigated the ferromagnetic phase transition of elemental Co by high-resolution neutron backscattering spectroscopy. We monitored the splitting of the nuclear levels by the hyperfine field at the Co nucleus. The energy of this hyperfine splitting is identified as the order parameter of the ferromagnetic phase transition. By measuring the temperature dependence of the energy we determined the critical exponent [Formula: see text] and the ferromagnetic Curie temperature of [Formula: see text] K. The present result of the critical exponent agrees better with the predicted value (0.367) of the three-dimensional Heisenberg model than that determined previously by nuclear magnetic resonance.

A neutron tomography study: probing the spontaneous crystallization of randomly packed granular assemblies.

We study the spontaneous crystallization of an assembly of highly monodisperse steel spheres under shaking, as it evolves from localized icosahedral ordering towards a packing reaching crystalline ordering. Towards this end, real space neutron tomography measurements on the granular assembly are carried out, as it is systematically subjected to a variation of frequency and amplitude. As expected, we see a presence of localized icosahedral ordering in the disordered initial state (packing fraction ≈ 0.62). As the frequency is increased for both the shaking amplitudes (0.2 and 0.6 mm) studied here, there is a rise in packing fraction, accompanied by an evolution to crystallinity. The extent of crystallinity is found to depend on both the amplitude and frequency of shaking. We find that the icosahedral ordering remains localized and its extent does not grow significantly, while the crystalline ordering grows rapidly as an ordering transition point is approached. In the ordered state, crystalline clusters of both face centered cubic (FCC) and hexagonal close packed (HCP) types are identified, the latter of which grows from stacking faults. Our study shows that an earlier domination of FCC gives way to HCP ordering at higher shaking frequencies, suggesting that despite their coexistence, there is a subtle dynamical competition at play. This competition depends on both shaking amplitude and frequency, as our results as well as those of earlier theoretical simulations demonstrate. It is likely that this involves the very small free energy difference between the two structures.

Setup for polarized neutron imaging using in situ 3He cells at the Oak Ridge National Laboratory High Flux Isotope Reactor CG-1D beamline.

In the present study, we report a new setup for polarized neutron imaging at the ORNL High Flux Isotope Reactor CG-1D beamline using an in situ 3He polarizer and analyzer. This development is very important for extending the capabilities of the imaging instrument at ORNL providing a polarized beam with a large field-of-view, which can be further used in combination with optical devices like Wolter optics, focusing guides, or other lenses for the development of microscope arrangement. Such a setup can be of advantage for the existing and future imaging beamlines at the pulsed neutron sources. The first proof-of-concept experiment is performed to study the ferromagnetic phase transition in the Fe3Pt sample. We also demonstrate that the polychromatic neutron beam in combination with in situ 3He cells can be used as the initial step for the rapid measurement and qualitative analysis of radiographs.

Magnetic glass state and magnetoresistance in SrLaFeCoO6 double perovskite.

Unusual features in magnetization resembling the kinetic arrest of a magnetic glass state are observed in the La-doped double perovskite, SrLaFeCoO6. Neutron powder diffraction experiments confirm the presence of antisite disorder as well as a lack of long-range magnetic order down to 4 K in this double perovskite which displays spin glass-like features in dc and ac susceptibilities. Magnetic relaxation observed through cooling and heating under unequal fields (CHUF) point towards unusual domain dynamics which is supported by a broad memory effect. Among the two anomalies that are observed at [Formula: see text] 75 K and at [Formula: see text] 250 K in the magnetic measurements, the former is associated with a spin-freezing temperature below which the magnetic glass state is experimentally verified. The magnetometric experiments detailed in the paper bring out the non-equilibrium metastable magnetic states in this disordered magnetic system. The magnetic glass state described above manifests in the electrical resistivity [Formula: see text] through the formation of a 'hard gap' because of the spin-exchange energy following the formation of magnetic glass. It is observed that the combination of disorder and magnetic glass state leads to a large, negative magnetoresistance (MR) of ≈47[Formula: see text] at 5 K in 8 T.

Spin-driven symmetry breaking in the frustrated fcc pyrite MnS2.

We report the characterisation of natural samples of the cubic pyrite mineral MnS2 using very high resolution synchrotron x-ray diffraction techniques. At low temperatures we find a new low temperature polymorph, which results from coupling between magnetic and lattice degrees of freedom. Below the magnetic ordering temperature T(N) = 48 K, we detect a pseudo-tetragonal distortion with a tiny c/a ratio of 1.0006. The structure can be refined in the space group Pbca The symmetry lowering reduces magnetic frustration in the fcc Mn(2+) lattice and is likely responsible for the previously reported lock-in of the magnetic propagation vector. This behaviour is similar to the spin-Peierls phase transitions reported in other three-dimensional Heisenberg magnets like the chromate spinels.

Pressure control of magnetic clusters in strongly inhomogeneous ferromagnetic chalcopyrites.

Room-temperature ferromagnetism in Mn-doped chalcopyrites is a desire aspect when applying those materials to spin electronics. However, dominance of high Curie-temperatures due to cluster formation or inhomogeneities limited their consideration. Here we report how an external perturbation such as applied hydrostatic pressure in CdGeP2:Mn induces a two serial magnetic transitions from ferromagnet to non-magnet state at room temperature. This effect is related to the unconventional properties of created MnP magnetic clusters within the host material. Such behavior is also discussed in connection with ab initio density functional calculations, where the structural properties of MnP indicate magnetic transitions as function of pressure as observed experimentally. Our results point out new ways to obtain controlled response of embedded magnetic clusters.

Giant pressure-induced volume collapse in the pyrite mineral MnS2.

Dramatic volume collapses under pressure are fundamental to geochemistry and of increasing importance to fields as diverse as hydrogen storage and high-temperature superconductivity. In transition metal materials, collapses are usually driven by so-called spin-state transitions, the interplay between the single-ion crystal field and the size of the magnetic moment. Here we show that the classical S = 5/2 mineral hauerite (MnS2) undergoes an unprecedented (ΔV ~ 22%) collapse driven by a conceptually different magnetic mechanism. Using synchrotron X-ray diffraction we show that cold compression induces the formation of a disordered intermediate. However, using an evolutionary algorithm we predict a new structure with edge-sharing chains. This is confirmed as the thermodynamic ground state using in situ laser heating. We show that magnetism is globally absent in the new phase, as low-spin quantum S = 1/2 moments are quenched by dimerization. Our results show how the emergence of metal-metal bonding can stabilize giant spin-lattice coupling in Earth's minerals.

Effect of size reduction on the structural and magnetic order in LaMnO(3+δ) (δ ≈ 0:03) nanocrystals: a neutron diffraction study.

We report a structural transition from the orthorhombic to the rhombohedral phase upon size reduction in nanocrystalline LaMnO(3+δ) (δ ≈ 0:03) as revealed through neutron diffraction studies. The transition occurs when the average particle (crystallite) size is taken below ~50 nm without change of δ, which is fixed at around 0.03 as measured by a number of characterization tools. The change in the crystallographic structure is accompanied by a change in the magnetic order, where the canted antiferromagnetic order with moments in the basal (ab) plane for the bulk changes to collinear ferromagnetic order with spins along the c-axis for the nanocrystals. The spontaneous ferromagnetic moment ~3 µ(B) and the transition temperature of 260 K in LaMnO(3+δ) nanocrystals are similar to those found in La0:67Ca0:33MnO3 which has a much higher Mn(4+) content. The likely origin is traced to change in magnetic exchange interactions due to change in Mn-O bond lengths which become almost identical in the MnO6 octahedron in the rhombohedral structure in the absence of Jahn-Teller distortion. The study provides an example of structural and magnetic phase transition driven purely by size reduction and with no change in the chemical constituents.

Direct evidence for nuclear spin waves in Nd2CuO4 by high-resolution neutron-spin-echo spectroscopy.

The possibility of coupling through the hyperfine interaction of nuclear spins with the electronic spin system has given rise to hope for potential novel applications in spintronics and quantum computations. We investigated the dispersion of nuclear spin waves in such a coupled system, Nd2CuO4, by using neutron-spin-echo spectroscopy at millikelvin temperatures. Our results show the existence of dispersion of nuclear spin waves in Nd2CuO4 at T D 40 mK. A fit of the dispersion data with the spin wave dispersion formula gave the Suhl­Nakamura interaction range to be of the order of 10 A° , which is much smaller than that expected theoretically.

Low energy nuclear spin excitations in Ho metal investigated by high resolution neutron spectroscopy.

We have investigated the low energy excitations in metallic Ho by high resolution neutron spectroscopy. We found at T = 3 K clear inelastic peaks in the energy loss and energy gain sides, along with the central elastic peak. The energy of this low energy excitation, which is 26.59 ± 0.02 µeV at T = 3 K, decreased continuously and became zero at TN ≈ 130 K. By fitting the data in the temperature range 100-127.5 K with a power law we obtained the power-law exponent ß = 0.37 ± 0.02, which agrees with the expected value ß = 0.367 for a three-dimensional Heisenberg model. Thus the energy of the low energy excitations can be associated with the order parameter.

Magnetoelastic effects in multiferroic YMnO3.

We have investigated magnetoelastic effects in multiferroic YMnO(3) below the antiferromagnetic phase transition, T(N) ≈ 70 K, using neutron powder diffraction. The a lattice parameter of the hexagonal unit cell of YMnO(3) decreases normally above T(N), but decreases anomalously below T(N), whereas the c lattice parameter increases with decreasing temperature and then increases anomalously below T(N). The unit cell volume also undergoes an anomalous contraction below T(N). By fitting the background thermal expansion for a non-magnetic lattice with the Einstein-Grüneisen equation, we determined the lattice strains Δa, Δc and ΔV due to the magnetoelastic effects as a function of temperature. We have also determined the temperature variation of the ordered magnetic moment of the Mn ion by fitting the measured Bragg intensities of the nuclear and magnetic reflections with the known crystal and magnetic structure models and have established that the lattice strain due to the magnetoelastic effect in YMnO(3) couples with the square of the ordered magnetic moment or the square of the order parameter of the antiferromagnetic phase transition.

Magnetic ordering in double perovskites R2CoMnO6 (R = Y, Tb) investigated by high resolution neutron spectroscopy.

We have investigated low energy nuclear spin excitations in double perovskite compounds R(2)CoMnO(6) (R=Y, Tb) by inelastic neutron scattering with a high resolution back-scattering spectrometer. We observed inelastic signals at about 2.1 µeV for Y(2)CoMnO(6) and also for Tb(2)CoMnO(6) at T = 2 K in both energy-loss and energy-gain sides. We interpret these inelastic peaks to be due to the transitions between the hyperfine split nuclear levels of the (59)Co nucleus. The inelastic peaks move towards the central elastic peak and finally merge with it at the magnetic ordering temperature T(C). The energy of the low energy excitations decreases continuously and becomes zero at T(C) ≈ 75 K for Y(2)CoMnO(6) and T(C) ≈ 100 K for Tb(2)CoMnO(6). For Tb(2)CoMnO(6), which contains magnetic rare earth ions, additional quasielastic scattering due presumably to the fluctuations of large Tb magnetic moments was observed. The present study reveals the magnetic ordering of the Co sublattice. The results of this investigation along with that obtained by us for other compounds indicate the presence of unquenched orbital moments in some of the Co compounds.

Structural and thermal properties of LaMnO3 from neutron diffraction and first principles studies.

Neutron diffraction experiments have been performed on powder samples of LaMnO(3) below and above the Jahn-Teller transition temperature of 750 K. Experimental investigations are assisted by density functional theory calculations. Theoretical studies are carried out for the orbitally ordered state of LaMnO(3) which allows one to compare the behavior of the orbitally ordered and disordered structures as a function of temperature. The temperature dependences of the structural parameters characterizing the Jahn-Teller distortions are reported and discussed. A gradual departure of the experimental data from theoretical predictions is observed above 650 K. In this range of temperatures, anions surrounding the Jahn-Teller active cations perform more isotropic thermal motion. The onset of structural phase transition induces a reduction of the crystal volume by about 0.4% which follows from the structural transformations yielding more regular oxygen octahedra formed above the phase transformation. It is found that above the Jahn-Teller transition the distortions of the MnO(6) octahedra are not completely removed. The non-vanishing distortions are accompanied by the lifted degeneracy of the Mn e(g) states. Weak residual distortions can be assigned to the short-range orbital order that persists within a local scale but it seems quenched on average giving rise to a disappearance of the long-range order coherency of the Jahn-Teller effect.

Magnetoelastic effects in Jahn-Teller distorted CrF2 and CuF2 studied by neutron powder diffraction.

We have studied the temperature dependence of the crystal and magnetic structures of the Jahn-Teller distorted transition metal difluorides CrF2 and CuF2 by neutron powder diffraction in the temperature range 2-280 K. The lattice parameters and the unit cell volume show magnetoelastic effects below the Néel temperature. The lattice strain due to the magnetostriction effect couples with the square of the order parameter of the antiferromagnetic phase transition. We also investigated the temperature dependence of the Jahn-Teller distortion, which does not show any significant effect at the antiferromagnetic phase transition but increases linearly with increasing temperature for CrF2, and remains almost independent of temperature in CuF2. The magnitude of magnetovolume effect seems to increase with the low temperature saturated magnetic moment of the transition metal ions but the correlation is not at all perfect.

The magnetoelastic effect in CoF2 investigated by means of neutron powder diffraction.

We have investigated the magnetoelastic effects in CoF(2) associated with the antiferromagnetic phase transition temperature T(N)≈39 K by means of neutron powder diffraction. The temperature variation of the lattice parameters and the unit cell volume has been determined accurately with small temperature steps. From the temperature variation of the lattice parameter c we extracted the lattice strain Δc associated with the antiferromagnetic phase transition. Rietveld refinement of the crystal and magnetic structure from the diffraction data at 2.2 K gave a magnetic moment of 2.57 ± 0.02 µ(B) per Co ion. We determined the temperature variation of the intensity of the 100 magnetic Bragg reflection, which is proportional to the square of the order parameter of the phase transition. We established that the lattice strain Δc couples linearly with the square of the order parameter of the antiferromagnetic phase transition in CoF(2).

Magnetic lattice dynamics of the oxygen-free FeAs pnictides: how sensitive are phonons to magnetic ordering?

To shed light on the role of magnetism on the superconducting mechanism of the oxygen-free FeAs pnictides, we investigate the effect of magnetic ordering on phonon dynamics in the low-temperature orthorhombic parent compounds, which present a spin density wave. The study covers both the 122 (AFe(2)As(2); A = Ca, Sr, Ba) and 1111 (AFeAsF; A = Ca, Sr) phases. We extend our recent work on the Ca (122 and 1111) and Ba (122) cases by treating, computationally and experimentally, the 122 and 1111 Sr compounds. The effect of magnetic ordering is investigated through detailed non-magnetic and magnetic lattice dynamical calculations. The comparison of the experimental and calculated phonon spectra shows that the magnetic interactions/ordering have to be included in order to reproduce well the measured density of states. This highlights a spin-correlated phonon behavior which is more pronounced than the apparently weak electron-phonon coupling estimated in these materials. Furthermore, there is no noticeable difference between phonon spectra of the 122 Ba and Sr, whereas there are substantial differences when comparing these to CaFe(2)As(2) originating from different aspects of structure and bonding.

Magnetoelastic effect in MF2 (M = Mn, Fe, Ni) investigated by neutron powder diffraction.

We have investigated the magnetoelastic effects in MF(2) (M = Mn, Fe, Ni) associated with the antiferromagnetic phase transition temperature T(N) by neutron powder diffraction. The temperature variation of the lattice parameters and the unit cell volume has been determined accurately with small temperature steps. From the temperature variation of the lattice parameters a, c and V the lattice strains Δa, Δc and ΔV associated with the antiferromagnetic phase transition have been extracted. Rietveld refinement of the crystal and magnetic structures from the diffraction data at low temperature gave a magnetic moment of 5.12 ± 0.09 µ(B), 4.05 ± 0.05 µ(B) and 1.99 ± 0.05 µ(B) per Mn, Fe and Ni ions, respectively. The lattice strains Δa, Δc and ΔV couple linearly with the intensity of the 100 magnetic reflection, which is proportional to square of the order parameter of the antiferromagnetic phase transition. The volume strains in MF(2) (M = Mn, Fe, Co, Ni) due to the magnetostriction vary smoothly along the transition metal series and seem to be correlated with the strength of the exchange interaction and the moments of the magnetic ions.

Similarities between structural distortions under pressure and chemical doping in superconducting BaFe2As2.

The discovery of a new family of high-T(C) materials, the iron arsenides (FeAs), has led to a resurgence of interest in superconductivity. Several important traits of these materials are now apparent: for example, layers of iron tetrahedrally coordinated by arsenic are crucial structural ingredients. It is also now well established that the parent non-superconducting phases are itinerant magnets, and that superconductivity can be induced by either chemical substitution or application of pressure, in sharp contrast to the cuprate family of materials. The structure and properties of chemically substituted samples are known to be intimately linked; however, remarkably little is known about this relationship when high pressure is used to induce superconductivity in undoped compounds. Here we show that the key structural features in BaFe2As2, namely suppression of the tetragonal-to-orthorhombic phase transition and reduction in the As-Fe-As bond angle and Fe-Fe distance, show the same behaviour under pressure as found in chemically substituted samples. Using experimentally derived structural data, we show that the electronic structure evolves similarly in both cases. These results suggest that modification of the Fermi surface by structural distortions is more important than charge doping for inducing superconductivity in BaFe2As2.

Direct evidence for the Nd magnetic ordering in NdMnO(3) from the hyperfine field splitting of Nd nuclear levels.

We investigated the low energy excitations in NdMnO(3) in the µeV range by a backscattering neutron spectrometer. The energy spectra on polycrystalline NdMnO(3) samples revealed inelastic peaks at E = 2.15 ± 0.01 µeV at T = 2 K on both energy gain and energy loss sides. The inelastic peaks move gradually towards lower energy with increasing temperature and tend to merge with the elastic peak at the electronic magnetic ordering temperature of Nd, T(Nd)≈20 K. However, at temperatures higher than T(Nd)≈20 K the energy of the inelastic peak decreases at a much slower rate and remains finite up to T = 55 K, the highest temperature investigated. We interpret the inelastic peaks to be due to the transition between the hyperfine-split nuclear level of the (143)Nd and (145)Nd isotopes with spin I = 7/2 caused by the magnetic ordering of Nd electronic moment below T(Nd)≈20 K. We ascribe the finite energy of the inelastic peak and its much smaller temperature dependence at T>20 K to be due to the polarization of the Nd magnetic moment by the field of Mn moments that order below T(N)≈78 K.