arXiv subjects

H. Murakawa

Publications and source records attributed to H. Murakawa.

23 records · Page 2Linked to original sources

arXiv2010

Cupric chloride CuCl2 as an S=1/2 chain multiferroic

Magnetoelectric properties were investigated for an S=1/2 chain antiferromagnet CuCl2, which turns out to be the first example of non-chalcogen based spiral-spin induced multiferroics. Upon the onset of helimagnetic order propagating along the b-axis under zero magnetic field (H), we found emergence of ferroelectric polarization along the c-axis. Application of H along the b-axis leads to spin-flop transition coupled with drastic suppression of ferroelectricity, and rotation of H around the b-axis induces the rotation of spin-spiral plane and associated polarization direction. These behaviors are explained well within the framework of the inverse Dzyaloshinskii-Moriya model, suggesting the robustness of this magnetoelectric coupling mechanism even under the strong quantum fluctuation.

cond-mat.str-el↗

arXiv2010

Ferroelectricity induced by spin-dependent metal-ligand hybridization in Ba$_2$CoGe$_2$O$_7$

We have investigated the variation of induced ferroelectric polarization under magnetic field with various directions and magnitudes in a staggered antiferromagnet Ba$_2$CoGe$_2$O$_7$. While the ferroelectric polarization cannot be explained by the well-accepted spin current model nor exchange striction mechanism, we have shown that it is induced by the spin-dependent $p$-$d$ hybridization between the transition-metal (Co) and ligand (O) via the spin-orbit interaction. On the basis of the correspondence between the direction of electric polarization and the magnetic state, we have also demonstrated the electrical control of the magnetization direction.

cond-mat.str-el↗

arXiv2009

Magnetic digital flop of ferroelectric domain with fixed spin chirality in a triangular lattice helimagnet

Ferroelectric properties in magnetic fields of varying magnitude and direction have been investigated for a triangular-lattice helimagnet CuFe1-xGaxO2 (x=0.035). The magnetoelectric phase diagrams were deduced for magnetic fields along [001], [110], and [1-10] direction, and the in-plane magnetic field was found to induce the rearrangement of six possible multiferroic domains. Upon every 60-degree rotation of in-plane magnetic field around the c-axis, unique 120-degree flop of electric polarization occurs as a result of the switch of helical magnetic q-vector. The chirality of spin helix is always conserved upon the q-flop. The possible origin is discussed in the light of the stable structure of multiferroic domain wall.

cond-mat.str-el↗

arXiv2009

Dynamics of Multiferroic Domain Wall in Spin-Cycloidal Ferroelectric DyMnO$_{3}$

We report the dielectric dispersion of the giant magnetocapacitance (GMC) in multiferroic DyMnO$_{3}$ over a wide frequency range. The GMC is found to be attributable not to the softened electromagnon but to the electric-field-driven motion of multiferroic domain wall (DW). In contrast to conventional ferroelectric DWs, the present multiferroic DW motion holds extremely high relaxation rate of $\sim$$10^{7}$ s$^{-1}$ even at low temperatures. This mobile nature as well as the model simulation suggests that the multiferroic DW is not atomically thin as in ferroelectrics but thick, reflecting its magnetic origin.

cond-mat.str-el↗

arXiv2006

Orbital Properties of Sr3Ru2O7 and Related Ruthenates Probed by 17O-NMR

We report a site-separated $^{17}$O-NMR study of the layered perovskite ruthenate Sr$_3$Ru$_2$O$_7$, which exhibits nearly two-dimensional transport properties and itinerant metamagnetism at low temperatures. The local hole occupancies and the spin densities in the oxygen $2p$ orbitals are obtained by means of tight-binding analyses of electric field gradients and anisotropic Knight shifts. These quantities are compared with two other layered perovskite ruthenates: the two-dimensional paramagnet Sr$_2$RuO$_4$ and the three-dimensional ferromagnet SrRuO$_3$. The hole occupancies at the oxygen sites are very large, about one hole per ruthenium atom. This is due to the strong covalent character of the Ru-O bonding in this compound. The magnitude of the hole occupancy might be related to the rotation or tilt of the RuO$_6$ octahedra. The spin densities at the oxygen sites are also large, 20-40% of the bulk susceptibilities, but in contrast to the hole occupancies, the spin densities strongly depend on the dimensionality. This result suggests that the density-of-states at the oxygen sites plays an essential role for the understanding of the complex magnetism found in the layered perovskite ruthenates.

cond-mat.str-el↗