No Arabic abstract
The clathrate compound Ce3Pd20Si6 is a heavy-fermion metal that exhibits magnetically hidden order at low temperatures. Reputedly, this exotic type of magnetic ground state, known as phase II, could be associated with the ordering of Ce 4f quadrupolar moments. In contrast to conventional (dipolar) order, it has vanishing Bragg intensity in zero magnetic field and, as a result, has escaped direct observation by neutron scattering until now. Here we report the observation of diffuse magnetic neutron scattering induced by an application of magnetic field along either the [110] or the [001] direction within phase II. The broad elastic magnetic signal that surrounds the (111) structural Bragg peak can be attributed to a short-range G-type antiferromagnetic arrangement of field-induced dipoles modulated by the underlying multipolar order on the simple-cubic sublattice of Ce ions occupying the 8c Wyckoff site. In addition, for magnetic fields applied along the [001] direction, the diffuse magnetic peaks in Ce3Pd20Si6 become incommensurate, suggesting a more complex modulated structure of the underlying multipolar order that can be continuously tuned by a magnetic field.
The magnetic properties of the layered oxypnictide LaMnAsO have been revisited using neutron scattering and magnetization measurements. The present measurements identify the N{e}el temperature $T_N$ = 360(1) K. Below $T_N$ the critical exponent describing the magnetic order parameter is $beta$ = 0.33$-$0.35, consistent with a three dimensional Heisenberg model. Above this temperature, diffuse magnetic scattering indicative of short-range magnetic order is observed, and this scattering persists up to $T_{SRO}$ = 650(10) K. The magnetic susceptibility shows a weak anomaly at $T_{SRO}$ and no anomaly at $T_N$. Analysis of the diffuse scattering data using a reverse Monte Carlo algorithm indicates that above $T_N$ nearly two- dimensional, short-range magnetic order is present with a correlation length of 9.3(3) {AA} within the Mn layers at 400 K. The inelastic scattering data reveal a spin-gap of 3.5 meV in the long-range ordered state, and strong, low-energy (quasi-elastic) magnetic excitations emerging in the short-range ordered state. Comparison with other related compounds correlates the distortion of the Mn coordination tetrahedra to the sign of the magnetic exchange along the layer-stacking direction, and suggests that short-range order above $T_N$ is a common feature in the magnetic behavior of layered Mn-based pnictides and oxypnictides.
The temperature dependence of charge order in Fe2OBO3 was investigated by resistivity and differential scanning calorimetry measurements, Mossbauer spectroscopy, and synchrotron x-ray scattering, revealing an intermediate phase between room temperature and 340 K, characterized by coexisting mobile and immobile carriers, and by incommensurate superstructure modulations with temperature-dependent propagation vector (1/2,0,tau). The incommensurate modulations arise from specific anti-phase boundaries with low energy cost due to geometrical charge frustration.
The origin of non-collinear magnetic order in UO$_{2}$ is studied by an ab initio dynamical-mean-field-theory framework in conjunction with a linear-response approach for evaluating inter-site superexchange interactions between U 5$f^{2}$ shells. The calculated quadrupole-quadruple superexchange interactions are found to unambiguously resolve the frustration of face-centered-cubic U sublattice toward stabilization of the experimentally observed non-collinear 3k-magnetic order. Therefore, the exotic 3k antiferromagnetic order in UO$_{2}$ can be accounted for by a purely electronic exchange mechanism acting in the undistorted cubic lattice structure. The quadrupolar short-range order above magnetic ordering temperature $T_N$ is found to qualitatively differ from the long-range order below $T_N$.
We report extensive measurements on a new compound (Yb0.24Sn0.76)Ru that crystallizes in the cubic CsCl structure. Valence band photoemission and L3 x-ray absorption show no divalent component in the 4f configuration of Yb. Inelastic neutron scattering (INS) indicates that the eight-fold degenerate J-multiplet of Yb3+ is split by the crystalline electric field (CEF) into a {Gamma}7 doublet ground state and a {Gamma}8 quartet at an excitation energy 20 meV. The magnetic susceptibility can be fit very well by this CEF scheme under the assumption that a {Gamma}6 excited state resides at 32 meV; however, the {Gamma}8/{Gamma}6 transition expected at 12 meV was not observed in the INS. The resistivity follows a Bloch- Gruneisen law shunted by a parallel resistor, as is typical of systems subject to phonon scattering with no apparent magnetic scattering. All of these properties can be understood as representing simple local moment behavior of the trivalent Yb ion. At 1 K, there is a peak in specific heat that is too broad to represent a magnetic phase transition, consistent with absence of magnetic reflections in neutron diffraction. On the other hand, this peak also is too narrow to represent the Kondo effect in the {Gamma}7 ground state doublet. On the basis of the field-dependence of the specific heat, we argue that antiferromagnetic shortrange order (possibly co-existing with Kondo physics) occurs at low temperatures. The long-range magnetic order is suppressed because the Yb site occupancy is below the percolation threshold for this disordered compound.
We report a combined neutron scattering and magnetization study on the multiferroic DyFeO3 which shows a very strong magnetoelectric effect. Applying magnetic field along the c-axis, the weak ferromagnetic order of the Fe ions is quickly recovered from a spin reorientation transition, and the long-range antiferromagnetic order of Dy becomes a short-range one. We found that the short-range order concurs with the multiferroic phase and is responsible for its sizable hysteresis. Our H-T phase diagram suggests that the strong magnetoelectric effect in DyFeO3 has to be understood with not only the weak ferromagnetism of Fe but also the short-range antiferromagnetic order of Dy.