arXiv subjects

S. Ishiwata

Publications and source records attributed to S. Ishiwata.

43 records · Page 3Linked to original sources

arXiv2009

Perovskite Manganites Hosting Versatile Multiferroic Phases with Symmetric and Antisymmetric Exchange Strictions

Complete magnetoelectric (ME) phase diagrams of orthorhombic $R$MnO$_{3}$ with and without magnetic moments on the $R$ ions have been established. Three kinds of multiferroic ground states, the $ab$-cycloidal, the $bc$-cycloidal, and the collinear $E$-type phases, have been identified by the distinct ME responses. The electric polarization of the $E$-type phase dominated by the symmetric spin exchange ($bm{S}_{i} cdot bm{S}_{j}$) is more than 10 times as large as that of the $bc$-cycloidal phase dominated by the antisymmetric one ($bm{S}_{i} times bm{S}_{j}$), and the ME response is enhanced near the bicritical phase boundary between these multiferroic phases of different origins. These findings will provide an important clue for the development of the magnetically induced multiferroics.

cond-mat.str-el↗

arXiv2007

Two-Staged Magnetoresistance Driven by Ising-like Spin Sublattice in SrCo6O11

A two-staged, uniaxial magnetoresistive effect has been discovered in SrCo6O11 having a layered hexagonal structure. Conduction electrons and localized Ising spins are in different sublattices but their interpenetration makes the conduction electrons sensitively pick up the stepwise field-dependence of magnetization. The stepwise field-dependence suggests two competitive interlayer interactions between ferromagnetic Ising-spin layers, i.e., a ferromagnetic nearest-layer interaction and an antiferromagnetic next-nearest-layer interaction. This oxide offers a unique opportunity to study nontrivial interplay between conduction electrons and Ising spins, the coupling of which can be finely controlled by a magnetic field of a few Tesla.

cond-mat.str-el↗

arXiv2006

Crystal Structure and Elementary Properties of NaxCoO2 (x = 0.32, 0.5, 0.6, 0.75, and 0.92) in the Three-Layer NaCoO2 Family

The crystal structures of the NaxCoO2 phases based on three-layer NaCoO2, with x=0.32, x=0.51, x=0.60, x=0.75 and x=0.92, determined by powder neutron diffraction, are reported. The structures have triangular CoO2 layers interleaved by sodium ions, and evolve with variation in Na content in a more complex way than has been observed in the two-layer NaxCoO2 system. The highest and lowest Na containing phases studied (x=0.92 and x=0.32) are trigonal, with three CoO2 layers per cell and octahedral Na ion coordination. The intermediate compositions have monoclinic structures. The x=0.75 compound has one CoO2 layer per cell, with Na in octahedral coordination and an incommensurate superlattice. The x=0.6 and x=0.5 phases are also single-layer, but the Na is found in trigonal prismatic coordination. The magnetic behavior of the phases is similar to that observed in the two-layer system. Both the susceptibility and the electronic contribution to the specific heat are largest for x=0.6.

cond-mat.str-el↗

arXiv2006

Room-temperature ferromagnetism in Sr_(1-x)Y_xCoO_(3-delta) (0.2 < x < 0.25)

We have measured magnetic susceptibility and resistivity of Sr$_{1-x}$Y$_x$CoO$_{3-δ}$ ($x=$ 0.1, 0.15, 0.2, 0.215, 0.225, 0.25, 0.3, and 0.4), and have found that Sr$_{1-x}$Y$_x$CoO$_{3-δ}$ is a room temperature ferromagnet with a Curie temperature of 335 K in a narrow compositional range of 0.2 $\leq x\leq$ 0.25. This is the highest transition temperature among perovskite Co oxides. The saturation magnetization for $x=$ 0.225 is 0.25 $μ_B$/Co at 10 K, which implies that the observed ferromagnetism is a bulk effect. We attribute this ferromagnetism to a peculiar Sr/Y ordering.

cond-mat.str-el↗

arXiv2005

Valence changes associated with the metal-insulator transition in Bi$_{1-x}$La$_x$NiO$_3$

Perovskite-type BiNiO$_3$ is an insulating antiferromagnet in which a charge disproportionation occurs at the Bi site. La substitution for Bi suppresses the charge disproportionation and makes the system metallic. We have measured the photoemission and x-ray absorption (XAS) spectra of Bi$_{1-x}$La$_{x}$NiO$_{3}$ to investigate how the electronic structure changes with La doping. From Ni $2p$ XAS, we observed an increase of the valence of Ni from 2+ toward 3+. Combined with the core-level photoemission study, it was found that the average valence of Bi remains $\sim 4+$ and that the Ni valence behaves as $\sim (2+x)+$, that is, La substitution results in hole doping at the Ni sites. In the valence-band photoemission spectra, we observed a Fermi cutoff for $x>0$, consistent with the metallic behavior of the La-doped compounds. The Ni $2p$ XAS, Ni $2p$ core-level photoemission, and valence-band photoemission spectra were analyzed by configuration-interaction cluster-model calculation, and the spectral line shapes were found to be consistent with the gradual Ni$^{2+} \to$ Ni$^{3+}$ valence change.

cond-mat.str-el↗

arXiv2005

Pressure/temperature/substitution-induced melting of A-site charge disproportionation in Bi_(1-x)La_(x)NiO_3 (0 =< x =< 0.5)

Metal-insulator transitions strongly coupled with lattice were found in Bi1-xLaxNiO3. Synchrotron X-ray powder diffraction revealed that pressure (P ~ 3 GPa, T = 300 K), temperature (T ~ 340 K, x = 0.05), and La-substitution (x ~ 0.075, T = 300 K) caused the similar structural change from a triclinic (insulating) to an orthorhombic (metallic) symmetry, suggesting melting of the A-site charge disproportionation. Comparing crystal structure and physical properties with the other ANiO3 series, an electronic state of the metallic phase can be described as [A3+Ld, Ni2+L1-d], where a ligand-hole L contributes to a conductivity. We depicted a schematic P-T phase diagram of BiNiO3 including a critical point (3 GPa, 300 K) and an inhomogeneous region, which implies universality of ligand-hole dynamics in ANiO3 (A = Bi, Pr, Nd,...).

cond-mat.str-el↗

arXiv2002

Spin-Trimer Antiferromagnetism in La$_4$Cu$_3$MoO$_{12}$

La$_4$Cu$_3$MoO$_{12}$ is a cluster antiferromagnet where copper spin-1/2 form a network of st rongly coupled spin-trimers. The magnetic properties of this material have bee n examined using magnetic neutron scattering. At low temperatures, excitations from the ground state are observed at 7.5(3) meV and 132.5(5) meV. An additio nal peak in the neutron scattering spectrum, which appears at 125.0(5) meV on heating is ascribed to a transition between excited states. The wave-vector an d temperature-dependence of the inelastic magnetic scattering cross section is consistent with intra-trimer transitions. Magnetic neutron diffraction reveal s antiferromagnetic order below T$_N$=2.6 K that doubles the unit cell along t he {\bf a} direction. The ordered magnetic structure is described as inter-tri mer order where spin correlations within trimers are controlled by the strong intra-trimer interactions. Combining the information derived from elastic and inelastic magnetic neutron scattering with group theoretical analysis, a consi stent set of intra-trimer interactions and ordered magnetic structures are der ived. The experiment provides a simple worked example of magnetism associated with inter-atomic composite degrees of freedom in the extreme quantum limit.

cond-mat.str-el↗