arXiv subjects

Shunsuke Kitou

Publications and source records attributed to Shunsuke Kitou.

At least 37 records · Page 2Linked to original sources

arXiv2025

A rutile-based homologous series Na(PtO$_2$)$_{2\it{n}+1}$ discovered by computationally assisted high-pressure synthesis

Layered transition metal oxides typified by the Ruddlesden-Popper phase have been extensively studied for its applications in high-temperature superconductivity, catalysis, and battery technologies. Despite the remarkable structural diversity and catalytic functionality of platinum oxides, the exploration of layered polymorphs has remained significantly constrained mainly due to the high inertness of platinum. Here, we discover a new homologous series of layered ternary oxides, Na(PtO$_2$)$_{2\it{n}+1}$, by a combination of highly oxidizing high-pressure methods and density functional theory (DFT) calculations. This series features unprecedented layered structural motifs, rutile-based PtO$_6$ octahedra and one-dimensional PtO$_4$ square-planar columns, which enables systematic control of dimensionality. Furthermore, we demonstrate a computationally-assisted identification of isomeric and putative members of this homologous series as confirmed by controlled synthesis and quantitative analysis of diffuse scattering data. This approach provides an effective platform for the exhaustive exploration of metastable transition metal oxides with rich structural variations.

cond-mat.mtrl-sci↗

arXiv2025

Unraveling a chemical-bond-driven root of topology in three-dimensional chiral crystals

Chirality manifests across multiple scales, yielding unique phenomena that break mirror symmetry. In chiral materials, unexpectedly large spin-filtering or photogalvanic effects have been observed even in materials composed of light elements, implying crucial influence of their topological electronic states. However, an underlying framework that links chemical bonding and electronic topology remains elusive, preventing the rational design of quantum chiral properties. Here we identify the chiral bonding network responsible for multifold topological fermions by combining synchrotron X-ray diffraction and first-principles calculations on cubic chiral crystals, CoSi and FeSi. Based on the observations of asymmetric valence electron distributions around the transition metals, together with analyses of their bonding to sevenfold-coordinated silicon atoms, we develop a three-dimensional Su-Schrieffer-Heeger model, showing that inter-site hopping on this chiral network creates multifold fermions with doubled topological invariants. Topological features can be switched by reversing the crystalline chirality or tuning electron filling. Our results highlight that implementing strong spin-orbit coupling is not the sole route to realize robust topological phases at elevated temperatures and offer a practical design principle for exploiting chiral topology. Moreover, this real-space framework naturally extends to other elementary excitations or artificial metamaterials, enabling various quantum functionalities through an intuitive approach to chirality engineering.

cond-mat.mtrl-sci↗

arXiv2025

Successive orthorhombic distortions in kagome metals by molecular orbital formation

The kagome lattice, with its inherent frustration, hosts a plethora of exotic phenomena, including the emergence of $3\mathbf{q}$ charge density wave order. The high rotational symmetry, required to realize such an unconventional charge order, is broken in many kagome materials by orthorhombic distortions at high temperature, the origin of which is much less discussed despite their ubiquity. In this study, synchrotron X-ray diffraction reveals a structural phase transition from a parent hexagonal phase to an orthorhombic ground state, mediated by a critical regime of diffuse scattering in the prototypical kagome metals $R$Ru$_3$Si$_2$ ($R$=rare-earth). Structural analysis uncovers an interlayer dimerization of kagome atoms in the low-temperature phase. Accordingly, a dimer model with one-dimensional disorder on kagome layers successfully reproduces the diffuse scattering. The observations point to molecular orbital formation between kagome $4d_{z^2}$ orbitals as the driving force behind the transition, consistent with \textit{ab initio} calculations. A framework based on electronegativity and atomic radii is proposed to evaluate the stability of the hexagonal phase in kagome metals, guiding the design of highly symmetric materials.

cond-mat.str-el↗

arXiv2025

Ferroaxial order of the monolayer ice in martyite

Ice Ih, the most stable phase of water at ambient pressure, is a stacking of the honeycomb network of water molecules H2O. What if one layer of ice is exfoliated and confined to a two-dimensional (2D) sheet? Martyite Zn3(V2O7)(OH)2 2H2O, a mineral with the honeycomb lattice of H2O in the porous framework, is an ideal system for studying such monolayer ice. Due to the geometrical frustration and 2D nature, H2O molecules are dynamically disordered at room temperature. In this study, we reveal disorder-order transitions of H2O in martyite using single-crystal x-ray diffraction (XRD). The XRD results visualize the formation of hydrogen-bonded toroidal H2O hexamers, leading to the ferroaxial order below 200 K. Combined with the molecular dynamics simulations, we discuss the formation process of the H2O hexamers and how they compromise the molecular arrangement towards lower temperatures. Our results unveil the ground state of monolayer ice, a fundamental knowledge to understand the polymorphism of H2O.

cond-mat.mtrl-sci↗

arXiv2025

Current-induced successive structural phase transitions beyond thermal equilibrium in single-crystal VO2

Nonequilibrium systems driven by external energy sources host unexplored physics; yet phase transitions beyond thermal equilibrium remain elusive. Here, we demonstrate that electric current induces structural phase transitions in single-crystal VO2, a prototypical strongly correlated material. At room temperature, synchrotron X-ray diffraction shows that a current density of 6.5 A/cm2 disrupts V-V dimers, driving a monoclinic-to-tetragonal insulator-to-metal transition, independent of Joule heating. Increasing the current to 10 A/cm2 triggers a discontinuous isotropic lattice expansion, stabilizing a novel tetragonal structure that does not exist in thermal equilibrium. Optical microscopy and microscopic Raman spectroscopy reveal dynamic domain motion and metastable phases, reminiscent of dissipative structures. These findings establish direct pathways to access hidden phases and symmetry changes beyond thermal equilibrium, broadening the frontiers of nonequilibrium thermodynamics.

cond-mat.str-el↗

arXiv2025

Piezoelectric Transition in a Nonpyroelectric Gyroidal Metal-Organic Framework

Among the thirty-two crystallographic point groups, 432 is the only one that lacks an inversion center but does not exhibit piezoelectricity. A gyroidal structure belongs to point group 432 and shows characteristic physical properties attributed to its distinctive strong isotropic network. Here, we investigate a gyroidal cobalt oxalate metal-organic framework (MOF) with disordered orientations of SO4 tetrahedra. Synchrotron X-ray diffraction experiments using a single crystal reveal a cubic-to-cubic structural phase transition at TS = 120 K. This transition involves a change in the point group from nonpiezoelectric 432 to piezoelectric 23. The symmetry change arises from the ordering of distorted SO4 molecules, leading to a three-dimensional helical arrangement of electric dipole moments. Furthermore, pyroelectric current measurements using polycrystalline pellet samples reveal that electric polarization emerges below TS depending on the magnitude of the pelletizing pressure, demonstrating piezoelectricity. The gyroidal MOF offers an opportunity to explore unique dielectric properties induced by the helical ordering of molecules and structural flexibility.

cond-mat.mtrl-sci↗

arXiv2025

Entropy-assisted, long-period stacking of honeycomb layers in an AlB2-type silicide

Configurational entropy can impact crystallization processes, tipping the scales between structures of nearly equal internal energy. Using alloyed single crystals of Gd2PdSi3 in the AlB2-type structure, we explore the formation of complex layer sequences made from alternating, two-dimensional triangular and honeycomb slabs. A four-period and an eight-period stacking sequence are found to be very close in internal energy, the latter being favored by entropy associated with covering the full configuration space of interlayer bonds. Possible consequences of polytype formation on magnetism in Gd2PdSi3 are discussed.

cond-mat.mtrl-sci↗

arXiv2025

Canted antiferromagnetism in a spin-orbit coupled $S_{\text{eff}} = 3/2$ triangular-lattice magnet DyAuGe

Exploration of nontrivial magnetic states induced by strong spin-orbit interaction is a central topic of frustrated magnetism. Extensive studies are concentrated on rare-earth-based magnets and 4d/5d transition metal compounds, which are mostly described by an effective spin $S_{\text{eff}} = 1/2$ for the Kramers doublet of the lowest crystal-electric-field levels. Variety of magnetic orderings may be greatly enhanced when magnetic dipolar moments intertwined with multipolar degrees of freedom which are described by higher-rank tensors and often require the magnetic ions with $S_{\text{eff}} > 1/2$. Here, our synchrotron x-ray diffraction near the Dy $L_3$ edge has unveiled a canted antiferromagnetic ground state arising from a quasi-quartet ($S_{\text{eff}} = 3/2$) of 4f electrons in a triangular-lattice (TL) rare-earth intermetallics DyAuGe. Magnetic moment and electric-quadrupole moment are closely interlocked and noncollinear magnetic-dipole alignment is induced by antiferroic electric-quadrupole (AFQ) ordering in the TL layers. The correlation between the AFQ and canted magnetic structures is further confirmed by phase transitions in an in-plane magnetic field. These findings offer insights into the emergence of nontrivial magnetic states in frustrated TL systems described beyond the $S_{\text{eff}} = 1/2$.

cond-mat.str-el↗

arXiv2024

Contrasting magnetothermal conductivity in sibling Co-based honeycomb-lattice antiferromagnets

Honeycomb-lattice antiferromagnets have attracted wide attention for exploration of exotic heat transport and their interplay with magnetic excitations. In this work, we have revealed a contrasting behavior in the magneto-thermal conductivity (MTC) between two Co-based honeycomb-lattice magnets Co4M2O9 (M = Nb, Ta), despite their identical lattice structures and quite similar magnetism. Co4Ta2O9 exhibits enhanced MTC of about 550% at 9 T of an in-plane magnetic field, comparable to other honeycomb-magnets, while MTC for Co4Nb2O9 reaches only ~30%. This marked difference is ascribed to distinct features in the field-induced evolution of magnetic excitations that resonantly scatter phonons. This finding sheds light on implicit impacts of non-magnetic ions on thermal transport, and hints at the potential for broad heat-transport tunability while preserving magnetism and lattice structures.

cond-mat.str-el↗

arXiv2024

Metamagnetic multiband Hall effect in Ising antiferromagnet ErGa$_2$

Frustrated rare-earth-based intermetallics provide a promising platform for emergent magnetotransport properties through exchange coupling between conduction electrons and localized rare-earth magnetic moments. Metamagnetism, the abrupt change of magnetization under an external magnetic field, is a signature of first-order magnetic phase transitions; recently, metamagnetic transitions in frustrated rare earths intermetallics have attracted interest for their accompanying nontrivial spin structures (e.g. skyrmions) and associated non-linear and topological Hall effects. Here, we present metamagnetism-induced Hall anomalies in single-crystalline ErGa$_2$, which recalls features arising from the topological Hall effect but wherein the strong Ising type anisotropy of Er moments prohibit noncoplanar spin structures. We show that the observed anomalies are neither due to anomalous Hall effect nor topological Hall effect, instead, can be accounted for via 4f-5d interactions which produce a band-dependent mobility modulation. This leads to a pronounced multiband Hall response across the magnetization process -- a metamagnetic multiband Hall effect that resembles a topological-Hall-like response but without nontrivial origins. The present findings may be of general relevance in itinerant metamagnetic systems regardless of coplanar/non-coplanar nature of spins and are important for the accurate identification of Hall signals due to emergent magnetic fields.

cond-mat.str-el↗

arXiv2024

Metamagnetism and anomalous magnetotransport properties in rare-earth-based polar semimetals $R$AuGe ($R =$ Dy, Ho, and Gd)

We report the magnetic, magnetoelastic, and magnetotransport properties of single crystals of polar magnets $R$AuGe ($R=$ Dy, Ho, and Gd), grown by Au-Ge self-flux. Magnetization and magnetostriction measurements reveal multi-step metamagnetic transitions for the $c$-axis magnetic field ($H\parallel c$) for DyAuGe and HoAuGe, suggesting magnetic frustration in the triangular lattice of $R$ ions. The magnetic phase diagrams have clarified a close connection between the magnetoelastic property and the emergence of the intermediate metamagentic phase. The magnetic-field dependence of the resistivity and Hall resistivity reveal the semimetallic transport dominated by hole-type carriers, consistent with the behavior in a nonmagnetic analogue YAuGe. We also identify a signature of an anomalous Hall effect (AHE) proportional to the field-induced magnetization in $R=$ Dy, Ho, and Gd. GdAuGe shows magnetic and transport behavior as reported in a previous study using Bi-flux grown single crystals, while the self-flux grown crystal shows larger magnetoresistance ($\sim$ 345\%, at 1.8 K and 9 T) due to higher hole-type carrier mobility ($\sim$ 6400 cm$^2$/Vs). Using the two-band model analysis considering the mobility change during the magnetization process, we extract the anomalous Hall conductivity: $\sim 1200$ S/cm and $\sim 530$ S/cm for $R=$ Dy and Ho, respectively, at 1.8 K with 9 T for $H\parallel c$. The magnitude of conductivity suggests a contribution of intrinsic origin, possibly related to the Berry curvature in the electron bands induced by the time-reversal symmetry breaking and the polar lattice.

cond-mat.str-el↗

arXiv2024

Cluster rearrangement by chiral charge order in lacunar spinel GaNb$_4$Se$_8$

Transition-metal atoms with d electrons sometimes form clusters in crystals, which significantly affects the physical properties. Such a cluster formation frequently accompanies a change in the crystal system, leading to the presence of domains with different crystal orientations. In particular, the cubic symmetry is rarely retained after the cluster formation. Here, we identify a cubic-to-cubic phase transition in lacunar spinel GaNb$_4$Se$_8$, where the change in the lattice parameter is less than 0.0001%. Each Nb$^{3.25+}$ tetramer with seven 4d electrons is distorted into a Nb$^{3+}$ trimer and a Nb$^{4+}$ monomer induced by charge disproportionation among Nb ions. While the Nb$^{3+}$ trimer with six 4d electrons forms spin-singlets in the sigma-bonding orbitals for three Nb-Nb bonds, a localized S=1/2 spin remains on the Nb$^{4+}$ ion. Furthermore, a local electric dipole moment is induced along the three-fold rotation axis of each distorted tetramer by the cluster rearrangement. The electric dipole moments are regularly arranged to maintain the cubic symmetry, giving rise to chiral order.

cond-mat.str-el↗

arXiv2024

Molecular orbital formation and metastable short-range ordered structure in VO$_2$

The metal-insulator transition (MIT) in vanadium dioxide VO$_2$ due to V-V dimerization has been extensively discussed for decades. While it is widely acknowledged that electron correlations, Peierls instabilities, and molecular orbital formations are crucial for understanding the MIT of VO$_2$, the primary origin of the MIT remains controversial. In this study, we delve into the crystal structure and orbital state of VO$_2$ through synchrotron x-ray diffraction experiments. The molecular orbital formation corresponding to the V-V dimerization is directly observed in the low-temperature insulating monoclinic phase, called the M1 phase, as indicated by the valence electron density distribution. Moreover, diffuse scattering observed in the high-temperature metal phase of rutile structure suggests the presence of short-range correlation of V displacements, which is not directly attributed to the structural fluctuation of the M1 phase. The short-range order in the rutile phase will be the key to understanding the MIT in this system.

cond-mat.str-el↗

arXiv2023

Real-Space Observation of Ligand Hole State in Cubic Perovskite SrFeO$_3$

An anomalously high valence state sometimes shows up in transition-metal oxide compounds. In such systems, holes tend to occupy mainly the ligand $p$ orbitals, giving rise to interesting physical properties such as superconductivity in cuprates and rich magnetic phases in ferrates. However, no one has ever observed the distribution of ligand holes in real space. Here, we report a successful observation of the spatial distribution of valence electrons in cubic perovskite SrFeO$_3$ by high-energy X-ray diffraction experiments and precise electron density analysis using a core differential Fourier synthesis method. A real-space picture of ligand holes formed by the orbital hybridization of Fe 3$d$ and O 2$p$ is revealed. The anomalous valence state in Fe is attributed to the considerable contribution of the ligand hole, which is related to the metallic nature and the absence of Jahn-Teller distortions in this system.

cond-mat.str-el↗

arXiv2023

Rhombic skyrmion lattice coupled with orthorhombic structural distortion in EuAl$_{4}$

The centrosymmetric tetragonal itinerant magnet EuAl$_{4}$ exhibits an intricate magnetic phase diagram including rhombic and square skyrmion-lattice (SkL) phases in the external magnetic field. Here, we report a multi-axis dilatometric investigation of EuAl$_{4}$ by means of a newly designed fiber-Bragg-grating technique complemented by a resonant x-ray scattering experiment, revealing anisotropic magnetostriction and magnetovolume effect associated with successive phase transitions. The rhombic and square SkL phases are found to possess $\sim$0.10% and $\sim$0.03% orthorhombic structural distortion within the $ab$ plane, respectively. We propose that the coupling between the spin system and the lattice deformation should be essential for the structural instability in EuAl$_{4}$, yielding a rich variety of topological spin textures with spontaneous rotational-symmetry breaking as well as a potential controllability of the SkL phases by uniaxial stress or pressure.

cond-mat.str-el↗

arXiv2023

Single crystal growths and magnetic properties of hexagonal polar semimetals RAuGe (R = Y, Gd-Tm, and Lu)

We study structural and magnetic properties of rare-earth based semimetals RAuGe (R = Y, Gd-Tm, and Lu) using flux-grown single crystals. These compounds belong to the noncentrosymmetric polar space group P63mc. We confirm the systematic structural evolution at room temperature as a function of ionic radius of rare earths to clarify the isopointal crossover between two polar structures: three-dimensional LiGaGe-type and quasi-two-dimensional NdPtSb-type. Magnetism shows a characteristic anisotropy in reasonable agreement with the crystal electric field (CEF) theory; the easy-plane-type anisotropy for R = Tb and Dy turns into the Ising-type anisotropy for R = Er and Tm. We evaluate the CEF parameters based on the Stevens operators to reasonably reproduce the temperature dependence of magnetic susceptibilities and specific heat for RAuGe (R = Tb-Tm). The estimated energy scale of the Ising gap (~ 11 meV) in TmAuGe is consistent with an excitation observed in an inelastic neutron scattering experiment. These findings suggest an opportunity for interplay between conduction electrons and nontrivial spin structures in the family of magnetic polar semimetals RAuGe.

cond-mat.mtrl-sci↗

arXiv2022

Anisotropic magnetotransport properties coupled with spiral spin modulation in a triangular-lattice magnet EuZnGe

We investigate the thermodynamic, magnetic, and electrical transport properties of a triangular-lattice antiferromagnet EuZnGe using single crystals grown from Eu-Zn flux in sealed tantalum tubes. Magnetic properties are found to be isotropic in the paramagnetic state while we observe an enhancement of in-plane magnetic susceptibility at the temperature near T* =11.3 K, suggesting an easy-plane anisotropy at low temperatures. Magnetic transition temperature is lower than T* as specific heat shows a peak at TN =7.6 K. We reveal the magnetic modulation along the c axis by resonant x-ray scattering at Eu L2 edge, which suggests competing magnetic interaction among Eu triangular-lattice layers. We observe a double-peak structure in the intensity profile along (0, 0, L) below TN, which is mainly composed of a dominant helical modulation with q ~ (0, 0, 0.4) coexisting with a secondary contribution from q ~ (0, 0, 0.5). We reproduce the intensity profile with a random mixture of five- and four-sublattice helices with spin rotation skipping due to hexagonal in-plane anisotropy. The metallic conductivity is highly anisotropic with the ratio rho_zz/rho_xx exceeding 10 over the entire temperature range and additionally exhibits a sharp enhancement of rho_zz at TN giving rise to rho_zz/rho_xx ~ 50, suggesting a coupling between out-of-plane electron conduction and the spiral magnetic modulations. In-plane magnetic field induces a spin-flop like transition, where the q = 0.4 peak disappears and an incommensurate peak of approximately qICM ~ 0.47 emerges, while the q = 0.5 modulation retains a finite intensity. This transition correlates with non-monotonic magnetoresistance and Hall resistivity, suggesting a significant interplay between electrons and spin structures through Ruderman-Kittel-Kasuya-Yosida (RKKY) interaction.

cond-mat.str-el↗

arXiv2022

Experimental signatures of versatile Weyl semimetal in pyrochlore iridate with spin-ice like magnetic orders

We report experimental signatures of topological transitions among the Weyl semimetal states of pyrochlore Pr2Ir2O7, where the Kondo coupling between the Ir topological electrons and the spin-ice like orders of Pr moments plays a decisive role. The magnetic-field dependence of resistivity and the Hall conductivity exhibits a plateau and a sharp jump associated with a magnetic-field hysteresis, similar to a liquid-gas-like transition in dipolar spin ice system. Furthermore, the Kondo coupling is controlled by the hydrostatic pressure, revealing that the field-induced displacement of Weyl points in the momentum space strongly depends on the respective electronic state as well as on the Kondo coupling strength. These observations pave a route toward the engineering of band topology in hybrid quantum materials with relativistic conduction electrons and localized magnetic moments.

cond-mat.str-el↗