arXiv subjects

Ryo Misawa

Publications and source records attributed to Ryo Misawa.

7 recordsLinked to original sources

arXiv2026

Observation of g-wave altermagnetic multipole

Over the past few years, altermagnets have emerged as a new class of collinear magnets with broken time-reversal symmetry, offering novel opportunities for spintronics beyond conventional magnets. Rather than from net magnetization, as in ferromagnets, the unconventional time-reversal symmetry breaking of altermagnets originates from antiferroic magnetic dipoles locked to higher-order multipoles. Here we report the direct visualization of a $g$-wave altermagnetic multipole in the canonical altermagnet CrSb. Combining high-energy synchrotron X-ray diffraction with valence electron density (VED) analysis, we uncover a pronounced directional anisotropy of the VED distribution alternating between Cr sublattices. This evidences the antiferroic order of electric hexadecapoles predicted in $g$-wave altermagnets. Its coexistence with antiferroic magnetic dipoles induces ferroic magnetic multipoles, as probed by polarized neutron diffraction. We further identify a microscopic model of altermagnetism that directly relates the $g$-wave multipole and the $g$-wave spin splitting. Through direct observation and quantification of multipoles, this study provides a real-space fingerprint of altermagnetism and establishes a general probe of hidden multipole order in quantum materials.

cond-mat.str-el↗

arXiv2026

Bond-density-wave orders induced by geometric frustration in the kagome metal CeRu3Si2

Geometric frustration gives rise to vast manifolds of degenerate ground states and competing orders in spin and charge systems. Typically, classical ground states are governed by a local ``zero-sum constraint" that relieves frustrated antiferromagnetic interactions or Coulomb repulsion. To date, the paradigm of geometric frustration has yielded a rich landscape of emergent phases, from spin ices and quantum spin liquids to charge glasses. However, an analogous phase rooted in chemical bonding has yet to be firmly demonstrated. Here we report the discovery of bond-density-wave orders induced by geometric frustration in the kagome metal CeRu$_3$Si$_2$ above room temperature. Through synchrotron X-ray diffraction, real-space transmission electron microscopy, and model calculations, we observe two distinct long-period superlattices with harmonic and anharmonic structural modulations. Crucially, interlayer bonds between kagome planes modulate in a sublattice-selective manner to fulfill the zero-sum constraint on the kagome lattice. We demonstrate the potential of kagome metals to host complex bond-ordered states constrained by geometric frustration and establish chemical bonding as a distinct pathway to frustration physics in quantum materials even above room temperature.

cond-mat.str-el↗

arXiv2026

Polar, checkerboard charge order in bilayer nickelate La3Ni2O7

Competing charge and spin orders are central to uncovering the nature of unconventional superconductivity. Here we utilize synchrotron X-ray diffraction on a high-quality single crystal to reveal the charge order of La$_3$Ni$_2$O$_7$ at ambient pressure, which competes with the high-temperature superconducting phase under pressure. Enabled by the high synchrotron photon flux and a large dynamic range, we resolve faint reflections -- nearly four orders of magnitude weaker than the main Bragg reflections -- that were overlooked in prior diffraction studies. This observation evidences a broken glide-mirror symmetry, leading to a polar crystal structure, rather than the widely used centrosymmetric structure model. The polarity is induced by checkerboard charge order on nickel sites in combination with octahedral tilting, reminiscent of bilayer manganese oxides. Our results provide a foundation for understanding phase competition and the mechanism of pressure-induced superconductivity in bilayer nickelates.

cond-mat.supr-con↗

arXiv2026

Stripe antiferromagnetism in van der Waals metal HoTe3 decoupled from charge density wave order

The $R\mathrm{Te}_3$ ($R = \text{rare earth}$) family of layered van der Waals (vdW) compounds hosts coexisting magnetic and charge density wave (CDW) orders, yet the interplay between these degrees of freedom remains little explored. Combining polarized and unpolarized neutron diffraction on single-crystal $\mathrm{HoTe}_3$, we identify two distinct antiferromagnetic (AFM) phases, both exhibiting a collinear $\uparrow\uparrow\downarrow\downarrow$ motif within individual vdW layers. The two phases are distinguished by the vdW stacking of magnetic layers: ferromagnetic (FM) stacking in the higher-temperature AFM-II phase, here termed ``vertical-stripe'', and AFM stacking in the AFM-I ground state, here termed ``tilted-stripe''; the two phases have propagation vectors $\boldsymbol{q}_{\mathrm{m2}} = (0.48, 0, 0)$ and $\boldsymbol{q}_{\mathrm{m1}} = (0.5, 0.5, 0)$, respectively. In contrast to the CDW-driven exotic magnetism in $\mathrm{DyTe}_3$, $\mathrm{TbTe}_3$, and $\mathrm{GdTe}_3$, we find no evidence for coupling between magnetism and CDW in $\mathrm{HoTe}_3$. The relative alignment between AFM and CDW propagation vectors, as well as single-ion anisotropy, are likely essential for generating coupled spin/charge orders in layered vdW systems.

cond-mat.str-el↗

arXiv2025

Bulk superconductivity in the kagome metal YRu3B2

Materials with a kagome sublattice have been heavily studied recently for their exotic electronic band structure, structural frustration, high-temperature charge order transitions, and unconventional electron-phonon coupling. In LaRu3Si2, it was proposed that electronic flat bands conspire with the characteristic phonon spectrum of the kagome lattice to drive enhanced superconductivity at Tc = 7 K. Here, we report bulk superconductivity in the structural analogue YRu3B2, which hosts a structurally pristine kagome lattice. We observe a superconducting transition at Tc = 0.7 K through magnetization, resistivity, and heat-capacity measurements in this novel kagome metal.

cond-mat.supr-con↗

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

Chemical enhancement of superconductivity in LaRu3Si2 with mode-selective coupling between kagome phonons and flat bands

In kagome metals, flat electronic bands induced by frustrated hopping are a platform for strong electron correlations. In particular, a selective coupling of flat band states to certain kagome phonon modes is proposed as a universal origin of superconductivity in this material class. Here, we investigate the superconductivity in the kagome system LaRu$_3$(Si$_{1-x}$Ge$_x$)$_2$ by chemical pressure tuning while preserving the Ru-$4d$ states that constitute the kagome flat bands. We observe a sizable enhancement in the density of states up to $x = 0.07$, as determined by the specific heat, with a concomitant increase in the superconducting transition temperature $T_\mathrm{c}$. Ge-dopants induce a uniaxial lattice expansion along the $c$-axis. Our first-principles calculations suggest that this mitigates the detrimental effect of hybridization between kagome layers and reduces the dispersion of the Ru-$4d_{x^2-y^2}$ flat band. The calculated chemical potential moves closer to the maximum in the energy-dependent density of states. Our result is consistent with a theoretical prediction of tunable flat band superconductivity in LaRu$_3$Si$_2$ by mode-selective coupling between specific kagome phonons and the Ru-$d_{x^2-y^2}$ orbitals.

cond-mat.supr-con↗