First-order transition in the itinerant ferromagnet CoS1.9_{1.9}Se0.1_{0.1}

Undoped CoS$_2$ is an isotropic itinerant ferromagnet with a continuous or nearly continuous phase transition at $T_{\rm C} = 122$ K. In the doped CoS$_{1.9}$Se$_{0.1}$ system, the Curie temperature is lowered to $T_{\rm C} = 90$ K, and the transition becomes clearly first order in nature. In particular we find a discontinuous evolution of the spin dynamics as well as strong time relaxation in the ferromagnetic Bragg intensity and small angle neutron scattering in vicinity of the ferromagnetic transition. In the ordered state the long-wavelength spin excitations were found to be conventional ferromagnetic spin-waves with negligible spin-wave gap ($< 0.04$ meV), indicating that this system is also an excellent isotropic (soft) ferromagnet. In a wide temperature range up to $0.9T_{\rm C}$, the spin-wave stiffness $D(T)$ follows the prediction of the two-magnon interaction theory, $D(T) = D(0)(1 - AT^{5/2})$, with $D(0) = 131.7 \pm 2.8$ meV-\AA$^{2}$. The stiffness, however, does not collapse as $T \to T_{\rm C}$ from below. Instead a quasielastic central peak abruptly develops in the excitation spectrum, quite similar to results found in the colossal magnetoresistance oxides such as (La-Ca)MnO$_3$.Comment: 8pages, 8figure

Magnetic Order and Spin Dynamics in Ferroelectric HoMnO3_{3}

Hexagonal HoMnO$_{3}$ is a frustrated antiferromagnet (T$_{N}$=72 K) ferroelectric (T$_{C}$=875 K) in which these two order parameters are coupled. Our neutron measurements of the spin wave dispersion for the S=2 Mn$^{3+}$ on the layered triangular lattice are well described by a two-dimensional nearest-neighbor Heisenberg exchange J=2.44 meV, and an anisotropy $D$ that is 0.093 meV above the spin reorientation transition at 40 K, and 0.126 meV below. For $H\parallel c$ the magnetic structures and phase diagram have been determined, and reveal additional transitions below 8 K where the ferroelectrically displaced Ho$^{3+}$ ions are ordered magnetically.Comment: To be published in Physical Review Letter

Nonfrustrated magnetoelectric with incommensurate magnetic order in magnetic field

We discuss a model nonfrustrated magnetoelectric in which strong enough magnetoelectric coupling produces incommensurate magnetic order leading to ferroelectricity. Properties of the magnetoelectric in magnetic field directed perpendicular to wave vector describing the spin helix are considered in detail. Analysis of classical energy shows that in contrast to naive expectation the onset of ferroelectricity takes place at a field $H_{c1}$ that is lower than the saturation field $H_{c2}$. One has $H_{c1}=H_{c2}$ at strong enough magnetoelectric coupling. We show that at H=0 the ferroelectricity appears at $T=T_{FE}<T_N$. Qualitative discussion of phase diagram in $H-T$ plane is presented within mean field approach.Comment: 12 pages, 3 figures, accepted in JET

Uncorrelated and correlated nanoscale lattice distortions in the paramagnetic phase of magnetoresistive manganites

Neutron scattering measurements on a magnetoresistive manganite La$_{0.75}$(Ca$_{0.45}$Sr$_{0.55}$)$_{0.25}$MnO$_3$ show that uncorrelated dynamic polaronic lattice distortions are present in both the orthorhombic (O) and rhombohedral (R) paramagnetic phases. The uncorrelated distortions do not exhibit any significant anomaly at the O-to-R transition. Thus, both the paramagnetic phases are inhomogeneous on the nanometer scale, as confirmed further by strong damping of the acoustic phonons and by the anomalous Debye-Waller factors in these phases. In contrast, recent x-ray measurements and our neutron data show that polaronic correlations are present only in the O phase. In optimally doped manganites, the R phase is metallic, while the O paramagnetic state is insulating (or semiconducting). These measurements therefore strongly suggest that the {\it correlated} lattice distortions are primarily responsible for the insulating character of the paramagnetic state in magnetoresistive manganites.Comment: 10 pages, 8 figures embedde

First-order nature of the ferromagnetic phase transition in (La-Ca)MnO_3 near optimal doping

Neutron scattering has been used to study the nature of the ferromagnetic transition in single crystals of La_0.7Ca_0.3MnO_3 and La_0.8Ca_0.2MnO_3, and polycrystalline samples of La_0.67Ca_0.33MnO_3 and La_5/8Ca_3/8MnO_3 where the naturally occurring O-16 can be replaced with the O-18 isotope. Small angle neutron scattering on the x=0.3 single crystal reveals a discontinuous change in the scattering at the Curie temperature for wave vectors below ~0.065 A^-1. Strong relaxation effects are observed for this domain scattering, for the magnetic order parameter, and for the quasielastic scattering, demonstrating that the transition is not continuous in nature. There is a large oxygen isotope effect observed for the T_C in the polycrystalline samples. For the optimally doped x=3/8 sample we observed T_C(O-16)=266.5 K and T_C(O-18)=261.5 K at 90% O-18 substitution. The temperature dependence of the spin-wave stiffness is found to be identical for the two samples despite changes in T_C. Hence, T_C is not solely determined by the magnetic subsystem, but instead the ferromagnetic phase is truncated by the formation of polarons which cause an abrupt transition to the paramagnetic, insulating state. Application of uniaxial stress in the x=0.3 single crystal sharply enhances the polaron scattering at room temperature. Measurements of the phonon density-of-states show only modest differences above and below T_C and between the two different isotopic samples.Comment: 13 pages, 16 figures, submitted to Phys. Rev.