Magnetic Structure and Excitations in CeCuxAl4-x System.

CeCuAl3 crystallizing in the tetragonal BaNiSn3-type structure and CeCuxAl4-x solid solutions were investigated by means of elastic and inelastic neutron scattering. Powder neutron diffraction brought information on both temperature evolution of crystallographic parameters and magnetic order at low temperatures. No structural change was observed in the investigated temperature range from 1.5 to 300 K. Weak magnetic peaks outside nuclear Bragg positions observed in solid solutions with 0.90 ≤ x ≤ 1.10 were described by the propagation vector k = (0.40 + δx, 0.60 + δy, 0), where δx ≈ 0.02 and δy ≈ 0.01. The magnetic structure of CeCu0.75Al3.25 consists of two components: an anti-ferromagnetic one described by the same k and a ferromagnetic one with k0 = (0, 0, 0) and magnetic moments lying within the tetragonal basal plane. The evolution of magnetic excitations as a function of Cu-Al concentration in CeCuxAl4-x was studied by inelastic neutron scattering. The measured spectra of CeCuAl3 and the solution with x = 0.95 point to a three-magnetic-peak energy scheme, while only two excitations are expected from the local symmetry conditions on Ce atoms. The standard two-peak spectrum of crystal electric field excitations was observed for Cu-Al substitutions further from the 1:1:3 stoichiometry (x = 0.75 and 1.10). The intermediate concentrations (x = 0.90 and 1.05) exhibit spectra on the border between the former cases with a less clear pronounced first inelastic magnetic peak. The observed behavior is discussed considering the evolution of structural parameters in the CeCuxAl4-x system and the coupling between the lattice vibrations and the crystal electric field excitations.

Incommensurate magnetic structure of CrAs at low temperatures and high pressures.

The magnetic structure of chromium arsenide CrAs is studied with neutron powder diffraction at ambient pressure in the temperature range 1.5-300 K as well as with neutron single-crystal diffraction at 2 K and 0.12 GPa. The material undergoes an anti-isostructural phase transition at TN = 267 K and atmospheric conditions, in which both orthorhombic phases have the same space-group symmetry (Pnma, Z = 4) but different distortions of the parent hexagonal structure of the NiAs type (P63/mmc, Z = 2). The magnetic structure below TN is incommensurate with the propagation vector k = (0, 0, kc). At ambient pressure, the component kc decreases from kc = 0.3807 (7) at 260 K to kc = 0.3531 (6) at 50 K. Below this temperature, it is basically constant. With increasing pressure at 2 K, kc is also constant within standard uncertainties [kc = 0.353 (2)]. For the analysis of the magnetic structure, a group-theoretical approach based on the space group of the nuclear structure and its subgroups is used. To avoid falling into false minima in the refinements, a random search for magnetic moments in the models is implemented. In the literature, the magnetic structure has been determined on the basis of powder diffraction data as a double helix propagating along the c axis. Although this double-helical model leads to satisfactory agreement factors for our powder data, it does not reproduce the intensities of the magnetic satellite reflections measured on single-crystal data in a satisfactory way and can therefore be discarded. Instead, several other models are found that lead to better agreement. Each of them is spiral-like with directional components in all three directions and with no spin-density wave character that would cause a non-constant magnetic moment. In all these models, the ordering of the spins is neither a pure helix nor a pure cycloid. Instead, the unit vectors of the spin rotation planes make an angle α, 0° < α < 90°, with respect to the c* direction. The model in superspace group P21.1'(α0γ)0s yields the best agreement factors in the refinements of the neutron single-crystal and powder diffraction data. This model is unique as it is the only one in which all the magnetic moments rotate with the same chirality.

Neutron diffraction investigation of the magnetic structure and magnetoelastic effects in NdMnO(3).

We investigated the evolution of the magnetic structure and magnetoelastic effects of NdMnO(3) by neutron powder diffraction. We confirmed the A-type antiferromagnetic (AF) structure of NdMnO(3) below T(N)≈82 K with magnetic moments parallel to the b axis of the orthorhombic crystal structure (space group Pbnm). We found that the magnetic moments of Nd order below about T(N)(Nd)≈20 K in a ferromagnetic structure with moments parallel to the c axis. At the same temperature the magnetic moments of Mn develop a ferromagnetic component parallel to the c axis. We found strong magnetoelastic effects associated with the AF transition at T(N)≈82 K. The effect is very prominent for the b lattice parameter. All three lattice parameters and therefore the unit cell volume contracts at T(N)≈82 K. We treated quantitatively the magnetoelastic effect of the b lattice parameter and found that the extra change in the lattice parameter Δb due to the magnetoelastic effect is proportional to the magnetic moment of the Mn ion. We also determined the critical exponent of the AF phase transition to be ß = 0.296 ± 0.008.

Preferred Orientation Contribution to the Anisotropic Normal State Resistivity in Superconducting Melt-Cast Processed Bi2Sr2CaCu2O8+δ.

We describe how the contribution of crystallographic texture to the anisotropy of the resistivity of polycrystalline samples can be estimated by averaging over crystallographic orientations through a geometric mean approach. The calculation takes into account the orientation distribution refined from neutron diffraction data and literature values for the single crystal resistivity tensor. The example discussed here is a melt-cast processed Bi2Sr2CaCu2O8+δ (Bi-2212) polycrystalline tube in which the main texture component is a <010> fiber texture with relatively low texture strength. Experimentally-measured resistivities along the longitudinal, radial, and tangential directions of the Bi-2212 tube were compared to calculated values and found to be of the same order of magnitude. Calculations for this example and additional simulations for various texture strengths and single crystal resistivity anisotropies confirm that in the case of highly anisotropic phases such as Bi-2212, even low texture strengths have a significant effect on the anisotropy of the resistivity in polycrystalline samples.

Field-induced magnetic instability within a superconducting condensate.

The application of magnetic fields, chemical substitution, or hydrostatic pressure to strongly correlated electron materials can stabilize electronic phases with different organizational principles. We present evidence for a field-induced quantum phase transition, in superconducting Nd0.05Ce0.95CoIn5, that separates two antiferromagnetic phases with identical magnetic symmetry. At zero field, we find a spin-density wave that is suppressed at the critical field µ0H* = 8 T. For H > H*, a spin-density phase emerges and shares many properties with the Q phase in CeCoIn5. These results suggest that the magnetic instability is not magnetically driven, and we propose that it is driven by a modification of superconducting condensate at H*.

Molecular-Based Magnetism in Bimetallic Two-Dimensional Oxalate-Bridged Networks. An X-ray and Neutron Diffraction Study.

Bimetallic, oxalate-bridged compounds with bi- and trivalent transition metals comprise a class of layered materials which express a large variety in their molecular-based magnetic behavior. Because of this, the availability of the corresponding single-crystal structural data is essential to the successful interpretation of the experimental magnetic results. We report in this paper the crystal structure and magnetic properties of the ferromagnetic compound {[N(n-C(3)H(7))(4)][Mn(II)Cr(III)(C(2)O(4))(3)]}(n)() (1), the crystal structure of the antiferromagnetic compound {[N(n-C(4)H(9))(4)][Mn(II)Fe(III)(C(2)O(4))(3)]}(n)() (2), and the results of a neutron diffraction study of a polycrystalline sample of the ferromagnetic compound {[P(C(6)D(5))(4)][Mn(II)Cr(III)(C(2)O(4))(3)]}(n)() (3). Crystal data: 1, rhombohedral, R3c, a = 9.363(3) Å, c = 49.207(27) Å, Z = 6; 2, hexagonal, P6(3), a = 9.482(2) Å, c = 17.827(8) Å, Z = 2. The structures consist of anionic, two-dimensional, honeycomb networks formed by the oxalate-bridged metal ions, interleaved by the templating cations. Single-crystal field dependent magnetization measurements as well as elastic neutron scattering experiments on the manganese(II)-chromium(III) samples show the existence of long-range ferromagnetic ordering behavior below T(c) = 6 K. The magnetic structure corresponds to an alignment of the spins perpendicular to the network layers. In contrast, the manganese(II)-iron(III) compound expresses a two-dimensional antiferromagnetic ordering.

Neutron diffraction study of triple-layered Sr4Ru3O10.

The magnetic properties of the triple-layered Sr(4)Ru(3)O(10) have been investigated by means of neutron scattering diffraction. At zero field we find that the magnetic moments are ferromagnetically coupled and oriented along the c-axis with no signatures of either long-range antiferromagnetic order or ferromagnetic components in the ab-plane. The field dependence of the reflection intensity points to a metamagnetic response involving only the planar magnetic moments. The structural refinement indicates a distinct rearrangement of the unit cell as a function of both temperature and in-plane applied field. We show that at the temperature T* ~/= 50 K, below which the metamagnetic behavior is observed, the c-axis lattice parameter exhibits a rapid increase while the in-plane amplitude saturates. A similar upturn of the in-plane lattice parameter after the quench of the c-axis amplitude occurs above a critical magnetic field.

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.

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.

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).

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.