arXiv subjects

T. Arima

Publications and source records attributed to T. Arima.

At least 55 records · Page 3Linked to original sources

arXiv2011

Magnetically-Driven Ferroelectric Atomic Displacements in perovskite like YMnO3

Magnetically-driven ferroelectric atomic displacements of the order of 10$^{-3} Angstrom have been observed in orthorhombic (perovskite like) YMnO$_3$ by a single-crystal synchrotron x-ray diffraction. The refined polar structure shows the characteristic bond alternation driven by the exchange striction in staggered Mn-O-Mn arrays with $\uparrow\uparrow\downarrow\downarrow$ type ordering, giving rise to a spontaneous polarization along a-axis. First-principles calculations based on the Berry phase method as well as on the experimentally refined crystal structure can reproduce the observed polarization value.

cond-mat.str-el↗

arXiv2011

Ultrafast Spectral Weight Transfer in RBaCo2O6-delta (R=Sm, Gd, and Tb): A Role of Electronic Correlation in Photoinduced Phase Transition

We performed femtosecond reflection spectroscopy on a series of perovskite-type cobalt oxide $R$BaCo$_2$O$_{6-δ}$ ($R$=Sm, Gd, and Tb) crystals, in which the electronic transfer was controlled by $R$. The transient reflectivity and the optical conductivity ($σ^{\rm PI}(ω)$) obtained by Kramers-Kronig analysis showed an ultrafast change within a time resolution ($\approx 150$ fs) at room temperature and the appearance of signals of a hidden state different from the high temperature metallic state. The transferred spectral weight in $σ^{\rm PI}(ω)$ upon photoexcitation sensitively depended on the $R$-species, indicating an important role of electronic correlation in the photoexcited state.

cond-mat.str-el↗

arXiv2010

Electronic structure and anomalous band-edge absorption feature in multiferroic MnWO4: An optical spectroscopic study

We investigated the electronic structure and lattice dynamics of multiferroic MnWO4 by optical spectroscopy. With variation of polarization, temperature, and magnetic field, we obtained optical responses over a wide range of photon energies. The electronic structure of MnWO4 near to the Fermi level was examined, with inter-band transitions identified in optical conductivity spectra above a band-gap of 2.5 eV. As for the lattice dynamics, we identified all the infrared transverse optical phonon modes available according to the group-theory analysis. Although we did not observe much change in global electronic structure across the phase transition temperatures, an optical absorption at around 2.2 eV showed an evident change depending upon the spin configuration and magnetic field. The behavior of this band-edge absorption indicates that spin-orbit coupling plays an important role in multiferroic MnWO4.

cond-mat.str-el↗

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↗

arXiv2009

Epitaxial-strain effect on charge/orbital order in Pr0.5Ca0.5MnO3 films

Effect of growth orientation on charge- and orbital-ordering (CO-OO) phenomena has been studied for Pr0.5Ca0.5MnO3 epitaxial thin films fabricated on (LaAlO3)0.3-(SrAl0.5Ta0.5O3)0.7 (LSAT) substrates by means of resistivity, synchrotron x-ray diffraction, and polarized optical microscopy measurements. CO-OO transition is observed around 220 K for a film grown on an LSAT (011) substrate ((011)-film), similarly to a bulk sample, while a film grown on a (001) plane of LSAT ((001)-film) shows much higher transition temperature around 300 K. The domain size of OO is approximately 3 times as large in the (011)-film as in the (001)-film. These results demonstrate that various properties of CO-OO phenomena can be controlled with the growth orientation via the epitaxial strain from the substrate.

cond-mat.str-el↗

arXiv2009

Lattice-form dependent orbital shape and charge disproportionation in charge- and orbital-ordered manganites

The orbital shapes and charge disproportionations at nominal Mn$^{3+}$ and Mn$^{4+}$ sites for the charge- and orbital-ordered phases have been studied on half-doped manganites Pr(Sr$_{0.1}$Ca$_{0.9}$)$_2$Mn$_2$O$_7$ and Eu$_{0.5}$Ca$_{1.5}$MnO$_4$ with double-layer and single-layer Mn-O networks, respectively, by means of x-ray structural analyses, in comparison with Pr$_{0.5}$Ca$_{0.5}$MnO$_3$ with the pseudo cubic network. In a single-layer Eu$_{0.5}$Ca$_{1.5}$MnO$_4$ system, the ($y^2-z^2$)/($z^2-x^2$)-type orbital shape is observed, while the ($3y^2-r^2$)/($3x^2-r^2$)-type orbital shape in a pseudo cubic Pr$_{0.5}$Ca$_{0.5}$MnO$_3$ system. In a double-layer Pr(Sr$_{0.1}$Ca$_{0.9}$)$_2$Mn$_2$O$_7$ system, the orbital shape is found to undergo a large change upon thermally induced rotation of orbital stripe. Furthermore, clear charge disproportionation is observed for the pseudo cubic and double-layer systems, while not in the single-layer system. These results indicate that the orbital shape and charge disproportionation are sensitive to the dimension of Mn-O network.

cond-mat.str-el↗

arXiv2009

Terahertz time-domain spectroscopy of electromagnons in multiferroic perovskite manganites

Recent spectroscopic studies at terahertz frequencies for a variety of multiferroics endowed with both ferroelectric and magnetic orders have revealed the possible emergence of a new collective excitation, frequently referred to as electromagnon. It is magnetic origin, but becomes active in response to the electric field component of light. Here we give an overview on our recent advance in the terahertz time-domain spectroscopy of electromagnons or electric-dipole active magnetic resonances, focused on perovskite manganites--$R$MnO$_3$ ($R$ denotes rare-earth ions). The respective electric and magnetic contributions to the observed magnetic resonance are firmly identified by the measurements of the light-polarization dependence using a complete set of the crystal orientations. We extract general optical features in a variety of the spin ordered phases, including the $A$-type antiferromagnetic, collinear spin ordered, and ferroelectric $bc$ and $ab$ spiral spin ordered phases, which are realized by tuning the chemical composition of $R$, temperature, and external magnetic field. In addition to the antiferromagnetic resonances of Mn ions driven by the magnetic field component of light, we clarify that the electromagnon appears only for light polarized along the a-axis even in the collinear spin ordered phase and grows in intensity with evolution of the spiral spin order, but independent of the direction of the spiral spin plane ($bc$ or $ab$) or equivalently the direction of the ferroelectric polarization $P_{\rm s}$ ($P_{\rm s}\| c$ or $P_{\rm s}\| a$). A possible origin of the observed magnetic resonances at terahertz frequencies is discussed by comparing the systematic experimental data presented here with theoretical considerations based on Heisenberg model.

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arXiv2009

Size of Orbital Ordering Domain Controlled by the Itinerancy of the 3d Electrons in a Manganite Thin Film

An electronic effect on a macroscopic domain structure is found in a strongly correlated half-doped manganite film Nd$_{0.5}$Sr$_{0.5}$MnO3 grown on a (011) surface of SrTiO3. The sample has a high-temperature (HT) phase free from distortion above 180K and two low-temperature (LT) phases with a large shear-mode strain and a concomitant twin structure. One LT phase has a large itinerancy (A-type), and the other has a small itinerancy (CE-type), while the lattice distortions they cause are almost equal. Our x ray diffraction measurement shows that the domain size of the LT phase made by the HT-CE transition is much smaller than that by the HT-A transition, indicating that the difference in domain size is caused by the electronic states of the LT phases.

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arXiv2008

Electric-dipole active two-magnon excitation in {\textit{ab}} spiral spin phase of a ferroelectric magnet Gd$_{\textbf{0.7}}$Tb$_{\textbf{0.3}}$MnO$_{\textbf 3}$

A broad continuum-like spin excitation (1--10 meV) with a peak structure around 2.4 meV has been observed in the ferroelectric $ab$ spiral spin phase of Gd$_{0.7}$Tb$_{0.3}$MnO$_3$ by using terahertz (THz) time-domain spectroscopy. Based on a complete set of light-polarization measurements, we identify the spin excitation active for the light $E$ vector only along the a-axis, which grows in intensity with lowering temperature even from above the magnetic ordering temperature but disappears upon the transition to the $A$-type antiferromagnetic phase. Such an electric-dipole active spin excitation as observed at THz frequencies can be ascribed to the two-magnon excitation in terms of the unique polarization selection rule in a variety of the magnetically ordered phases.

cond-mat.str-el↗

arXiv2008

Electrically driven spin excitation in a ferroelectric magnet DyMnO_3

Temperature (5--250 K) and magnetic field (0--70 kOe) variations of the low-energy (1--10 meV) electrodynamics of spin excitations have been investigated for a complete set of light-polarization configurations for a ferroelectric magnet DyMnO$_3$ by using terahertz time-domain spectroscopy. We identify the pronounced absorption continuum (1--8 meV) with a peak feature around 2 meV, which is electric-dipole active only for the light $E$-vector along the a-axis. This absorption band grows in intensity with lowering temperature from the spin-collinear paraelectric phase above the ferroelectric transition, but is independent of the orientation of spiral spin plane ($bc$ or $ab$), as shown on the original $P_{\rm s}$ (ferroelectric polarization) $\parallel c$ phase as well as the magnetic field induced $P_{\rm s}\parallel a$ phase. The possible origin of this electric-dipole active band is argued in terms of the large fluctuations of spins and spin-current.

cond-mat.mtrl-sci↗

arXiv2007

Coexistence of long-ranged charge and orbital order and spin-glass state in single-layered manganites with weak quenched disorder

The relationship between orbital and spin degrees of freedom in the single-crystals of the hole-doped Pr$_{1-x}$Ca$_{1+x}$MnO$_4$, 0.3 $\leq$ $x$ $\leq$ 0.7, has been investigated by means of ac-magnetometry and charge transport. Even though there is no cation ordering on the $A$-site, the quenched disorder is extremely weak in this system due to the very similar ionic size of Pr$^{3+}$ and Ca$^{2+}$. A clear asymmetric response of the system to the under- (respective over-) hole doping was observed. The long-ranged charge-orbital order established for half doping ($x$=0.5) subsists in the over-doping case ($x$ $>$ 0.5), albeit rearranged to accommodate the extra holes introduced in the structure. The charge-orbital order is however destabilized by the presence of extra localized electrons (under-doping, $x$ $<$ 0.5), leading to its disappearance below $x$=0.35. We show that in an intermediate under-doped region, with 0.35 $\leq$ $x$ $<$ 0.5, the ``orbital-master spin-slave'' relationship commonly observed in half-doped manganites does not take place. The long-ranged charge-orbital order is not accompanied by an antiferromagnetic transition at low temperatures, but by a frustrated short-ranged magnetic state bringing forth a spin-glass phase. We discuss in detail the nature and origin of this spin-glass state, which, as in the half-doped manganites with large quenched disorder, is not related to the macroscopic phase separation observed in crystals with minor defects or impurities.

cond-mat.mtrl-sci↗

arXiv2007

Variation of charge/orbital ordering in layered manganites Pr1-xCa1+xMnO4 investigated by transmission electron microscopy

Structural features of the charge/orbital ordering (CO/OO) in single-layered manganites Pr1-xCa1+xMnO4 have been investigated systematically by transmission electron microscopy. Analyses of electron diffraction patterns as well as dark-field images have revealed that the CO/OO shows a striking asymmetric behavior as the hole doping x deviates from x = 0.5. The modulation wavenumber linearly decreases with increasing x in the over-hole-doped (x > 0.5) crystals, while much less dependent on x in the under-hole-doped (x < 0.5) crystals. A temperature-induced incommensurate-commensurate crossover is observed in 0.35 < x < 0.5 and x = 0.65. The correlation length of CO/OO in x = 0.3 was proven to become shorter than that in x > 0.3.

cond-mat.str-el↗

arXiv2007

Electric Control of Spin Helicity in a Magnetic Ferroelectric

Magnetic ferroelectrics or multiferroics, which are currently extensively explored, may provide a good arena to realize a novel magnetoelectric function. Here we demonstrate the genuine electric control of the spiral magnetic structure in one of such magnetic ferroelectrics, TbMnO3. A spin-polarized neutron scattering experiment clearly shows that the spin helicity, clockwise or counter-clockwise, is controlled by the direction of spontaneous polarization and hence by the polarity of the small cooling electric field.

cond-mat.str-el↗

arXiv2006

Ferroelectric polarization flop in a frustrated magnet MnWO$_4$ induced by magnetic fields

The relationship between magnetic order and ferroelectric properties has been investigated for MnWO$_4$ with long-wavelength magnetic structure. Spontaneous electric polarization is observed in an elliptical spiral spin phase. The magnetic-field dependence of electric polarization indicates that the noncollinear spin configuration plays a key role for the appearance of ferroelectric phase. An electric polarization flop from the b direction to the a direction has been observed when a magnetic field above 10T is applied along the b axis. This result demonstrates that an electric polarization flop can be induced by a magnetic field in a simple system without rare-earth f-moments.

cond-mat.str-el↗

arXiv2006

Bandwidth-disorder phase diagram of half doped layered manganites

Phase diagrams in the plane of $r_A$ (the average ionic radius, related to one-electron bandwidth $W$) and $σ^2$ (the ionic radius variance, measuring the quenched disorder), or ``bandwidth-disorder phase diagrams'', have been established for perovskite manganites, with three-dimensional (3$D$) Mn-O network. Here we establish the intrinsic bandwidth-disorder phase diagram of half-doped layered manganites with the two-dimensional (2$D$) Mn-O network, examining in detail the ``mother state'' of the colossal magnetoresistance (CMR) phenomenon in crystals without ferromagnetic instability. The consequences of the reduced dimensionality, from 3$D$ to 2$D$, on the order-disorder phenomena in the charge-orbital sectors are also highlighted.

cond-mat.mtrl-sci↗

arXiv2006

In-plane anisotropy of the electronic structure for the charge/orbital-ordered state in half-doped manganite with layered structure

We report on the in-plane anisotropy of the electronic response in the spin/charge/orbital ordered phase of a half-doped layered-structure manganite. The optical conductivity spectra for a single domain of Eu$_{1/2}$% Ca$_{3/2}$MnO$_{4}$ unambiguously show the anisotropic charge dynamics which well corresponds to the theoretical calculation: the optical conductivity with the polarization along the zigzag ferromagnetic chain direction exhibits a smaller gap and a larger intensity at lower energies than that of the perpendicular polarization mostly due to the charge/orbital ordering and the associated quantum interference effect.

cond-mat.str-el↗

arXiv2006

Collinear-to-Spiral Spin Transformation without Changing Modulation Wavelength upon Ferroelectric Transition in Tb1-xDyxMnO3

Lattice modulation and magnetic structures in magnetoelectric compounds Tb1-xDyxMnO3 have been studied around the ferroelectric (FE) Curie temperature T_C by x-ray and neutron diffraction. Temperature-independent modulation vectors through T_C are observed for the compounds with 0.50< x < 0.68. This indicates that ferroelectricity with a polarization (P) along the c axis in the RMnO3 series cannot be ascribed to such an incommensurate-commensurate transition of an antiferromagnetic order as was previously anticipated. Neutron diffraction study of a single crystal with x=0.59 shows that the FE transition is accompanied by the transformation of the Mn-spin alignment from sinusoidal (collinear) antiferromagnetism into a transverse spiral structure. The observed spiral structure below T_C is expected to produce P along the c axis with the `inverse' Dzialoshinski-Moriya interaction, which is consistent with the observation.

cond-mat.str-el↗

arXiv2005

Impurity-induced transition to a Mott insulator in Sr$_3$Ru$_2$O$_7$

The electrical, magnetic, and structural properties of Sr$_3$(Ru$_{1-x}$Mn$_x$)$_2$O$_7$ (0 $\leq x \leq$ 0.2) are investigated. The parent compound Sr$_3$Ru$_2$O$_7$ is a paramagnetic metal, critically close to magnetic order. We have found that, with a Ru-site doping by only a few percent of Mn, the ground state is switched from a paramagnetic metal to an antiferromagnetic insulator. Optical conductivity measurements show the opening of a gap as large as 0.1 eV, indicating that the metal-to-insulator transition is driven by the electron correlation. The complex low-temperature antiferromagnetic spin arrangement, reminiscent of those observed in some nickelates and manganites, suggests a long range orbital order.

cond-mat.mtrl-sci↗