arXiv subjects

Hidenori Takagi

Publications and source records attributed to Hidenori Takagi.

At least 37 records · Page 2Linked to original sources

arXiv2022

Magnetic and Electrical Properties of high-entropy rare-earth manganites

Detailed investigations of structural, magnetic and electronic transport properties of hole-doped high-entropy rare-earth manganites are presented. The high-entropy samples (LaNdPrSmEu)$_{1-x}$Sr$_x$MnO$_3$ (0$\leq$\textit{x}$\leq$0.5), synthesized using the solid-state technique, show a change in the crystal structure from \textit{Pbnm} to \textit{R-3c} with increasing Sr substitution, attributed to the change in the tolerance factor. Prominent ferromagnetic ordering is observed in the sample with a rhombohedral structure (\textit{x}$\geq$0.3), originating from the dominant double exchange mechanism mediated by itinerant electrons. Further, the Curie temperature is smaller for the high-entropy sample with \textit{x}=0.3, as compared to La$_{0.7}$Sr$_{0.3}$MnO$_3$, suggesting a strong relation between the Curie temperature and the Mn-O-Mn bond angle associated with the reduced ionic radii at the rare-earth site. The electrical resistivity of the high-entropy samples is larger than those of La$_{1-x}$Sr$_x$MnO$_3$, which can be ascribed to the reduced bandwidth due to the enhanced structural distortion. A concomitant rise in magnetoresistance is observed for high-entropy samples with the increase in Sr concentration. These findings considering the configurational complexity of different rare-earths advance the understanding of high-entropy rare earth manganites.

cond-mat.str-el↗

arXiv2022

Terahertz spin-to-charge current conversion in stacks of ferromagnets and the transition-metal dichalcogenide NbSe$_2$

Transition-metal dichalcogenides (TMDCs) are an aspiring class of materials with unique electronic and optical properties and potential applications in spin-based electronics. Here, we use terahertz emission spectroscopy to study spin-to-charge current conversion (S2C) in the TMDC NbSe$_2$ in ultra-high-vacuum-grown F|NbSe$_2$ thin-film stacks, where F is a layer of ferromagnetic Fe or Ni. Ultrafast laser excitation triggers an ultrafast spin current that is converted into an in-plane charge current and, thus, a measurable THz electromagnetic pulse. The THz signal amplitude as a function of the NbSe$_2$ thickness shows that the measured signals are fully consistent with an ultrafast optically driven injection of an in-plane-polarized spin current into NbSe$_2$. Modeling of the spin-current dynamics reveals that a sizable fraction of the total S2C originates from the bulk of NbSe$_2$ with the same, negative, sign as the spin Hall angle of pure Nb. By quantitative comparison of the emitted THz radiation from F|NbSe$_2$ to F|Pt reference samples and the results of ab-initio calculations, we estimate that the spin Hall angle of NbSe$_2$ for an in-plane polarized spin current lies between -0.2% and -1.1%, while the THz spin-current relaxation length is of the order of a few nanometers.

cond-mat.mes-hall↗

arXiv2022

Magnetic Excitations and Interactions in the Kitaev Hyperhoneycomb Iridate $β$-Li$_2$IrO$_3$

We present a thorough experimental study of the three-dimensional hyperhoneycomb Kitaev magnet $β$-Li$_2$IrO$_3$, using a combination of inelastic neutron scattering (INS), time-domain THz spectroscopy, and heat capacity measurements. The main results include a massive low-temperature reorganization of the INS spectral weight that evolves into a broad peak centered around 12 meV, and a distinctive peak in the THz data at 2.8(1) meV. A detailed comparison to powder-averaged spin-wave theory calculations reveals that the positions of these two features are controlled by the anisotropic $Γ$ coupling and the Heisenberg exchange $J$, respectively. The refined microscopic spin model places $β$-Li$_2$IrO$_3$ in close proximity to the Kitaev spin liquid phase.

cond-mat.str-el↗

arXiv2022

Observation of ultrafast interfacial Meitner-Auger energy transfer in a van der Waals heterostructure

Atomically thin layered van der Waals heterostructures feature exotic and emergent optoelectronic properties. With growing interest in these novel quantum materials, the microscopic understanding of fundamental interfacial coupling mechanisms is of capital importance. Here, using multidimensional photoemission spectroscopy, we provide a layer- and momentum-resolved view on ultrafast interlayer electron and energy transfer in a monolayer-WSe$_2$/graphene heterostructure. Depending on the nature of the optically prepared state, we find the different dominating transfer mechanisms: while electron injection from graphene to WSe$_2$ is observed after photoexcitation of quasi-free hot carriers in the graphene layer, we establish an interfacial Meitner-Auger energy transfer process following the excitation of excitons in WSe$_2$. By analysing the time-energy-momentum distributions of excited-state carriers with a rate-equation model, we distinguish these two types of interfacial dynamics and identify the ultrafast conversion of excitons in WSe$_2$ to valence band transitions in graphene. Microscopic calculations find interfacial dipole-monopole coupling underlying the Meitner-Auger energy transfer to dominate over conventional Förster- and Dexter-type interactions, in agreement with the experimental observations. The energy transfer mechanism revealed here might enable new hot-carrier-based device concepts with van der Waals heterostructures.

cond-mat.mtrl-sci↗

arXiv2021

Unveiling the underlying interactions in Ta2NiSe5 from photo-induced lifetime change

We present a generic procedure for quantifying the interplay of electronic and lattice degrees of freedom in photo-doped insulators through a comparative analysis of theoretical many-body simulations and time- and angle-resolved photoemission spectroscopy (TR-ARPES) of the transient response of the candidate excitonic insulator Ta2NiSe5. Our analysis demonstrates that the electron-electron interactions dominate the electron-phonon ones. In particular, a detailed analysis of the TRARPES spectrum enables a clear separation of the dominant broadening (electronic lifetime) effects from the much smaller bandgap renormalization. Theoretical calculations show that the observed strong spectral broadening arises from the electronic scattering of the photo-excited particle-hole pairs and cannot be accounted for in a model in which electron-phonon interactions are dominant. We demonstrate that the magnitude of the weaker subdominant bandgap renormalization sensitively depends on the distance from the semiconductor/semimetal transition in the high-temperature state, which could explain apparent contradictions between various TR-ARPES experiments. The analysis presented here indicates that electron-electron interactions play a vital role (although not necessarily the sole one) in stabilizing the insulating state.

cond-mat.str-el↗

arXiv2021

Charge Order Stabilized Quantum Spin Liquid in Hollandite K$_2$V$_8$O$_{16}$

Quantum spin liquid is an elusive state that display strong many-body entanglement with potential applications in future quantum computing. This study reports muon spin relaxation ($μ^+$SR) measurements on a novel high-pressure synthesized material, the Hollandite K$_{2}$V$_8$O$_{16}$. In this quasi-one-dimensional compound, charge ordering (CO) at $T_{\rm MIT}\approx160$~K effectively isolates half of the vanadium chains and model-like Heisenberg spin-1/2 chains are realized. Our zero field $μ^+$SR measurements show exponential like relaxation down to the lowest temperature $T=100$~mK and the absence of long range ordering is confirmed. The relaxation rate is found to be temperature independent below $T_{\rm QSL}\approx2$~K and measurements in longitudinal field confirms a highly dynamic ground state. These results represents the first confirmation of quantum spin liquid (QSL) behavior within the Hollandite family, stabilized by the CO. Finally, the presence of strong local electron correlation and one dimensional Fermi surface suggest this QSL to be a gapless Tomonaga-Luttinger liquid (TLL), which here uniquely presents itself in a stoichiometric compound under zero applied magnetic field and at ambient pressure.

cond-mat.str-el↗

arXiv2021

Real-space visualization of quasiparticle dephasing near the Planckian limit in the Dirac line node material ZrSiS

Dirac line node (DLN) materials are topological semimetals wherein a set of symmetry protected crossing points forms a one-dimensional (1D) line in reciprocal space. Not only are the linearly dispersing bands expected to give rise to exceptional electronic properties, but the weak screening of the Coulomb interaction near the line node may enhance electronic correlations, produce new many-body ground states, or influence the quasiparticle lifetime. We investigate the quasiparticle dynamics in the DLN material ZrSiS via spectroscopic imaging scanning tunneling microscopy (SI-STM). By studying the spatial decay of quasiparticle interference patterns (QPI) from point scatterers, we were able to directly and selectively extract the phase coherence length $l_{\textrm{QPI}}$ and lifetime $τ_{\textrm{QPI}}$ for the bulk DLN excitations, which are dominated by inelastic electron-electron scattering. We find that the experimental $τ_{\textrm{QPI}}(E)$ values below $-$40 meV are very short, likely due to the stronger Coulomb interactions, and lie at the Planckian limit $\hbar/|E|$. Our results corroborate a growing body of experimental reports demonstrating unusual electronic correlation effects near a DLN.

cond-mat.str-el↗

arXiv2021

Nearly room temperature ferromagnetism in pressure-induced correlated metallic state of van der Waals insulator CrGeTe$_3$

A complex interplay of different energy scales involving Coulomb repulsion, spin-orbit coupling and Hund's coupling energy in two-dimensional (2D) van der Waals (vdW) material produces novel emerging physical state. For instance, ferromagnetism in vdW charge transfer insulator CrGeTe$_3$, that provides a promising platform to simultaneously manipulate the magnetic and electrical properties for potential device implementation using few layers thick materials. Here, we show a continuous tuning of magnetic and electrical properties of CrGeTe$_3$ single crystal using pressure. With application of pressure, CrGeTe$_3$ transforms from a FM insulator with Curie temperature, $T_{\rm{C}} \sim $ 66 K at ambient condition to a correlated 2D Fermi metal with $T_{\rm{C}}$ exceeding $\sim$ 250 K. Notably, absence of an accompanying structural distortion across the insulator-metal transition (IMT) suggests that the pressure induced modification of electronic ground states are driven by electronic correlation furnishing a rare example of bandwidth-controlled IMT in a vdW material.

cond-mat.str-el↗

arXiv2021

Discovery of Superconductivity in (Ba,K)SbO$_{3}$

Superconducting bismuthates (Ba,K)BiO$_{3}$ (BKBO) constitute an interesting class of superconductors in that superconductivity with a remarkably high $T_\mathrm{c}$ of 30 K arises in proximity to charge density wave (CDW) order. Prior understanding on the driving mechanism of the CDW and superconductivity emphasizes the role of either bismuth (negative $U$ model) or oxygen ions (ligand hole model). While holes in BKBO presumably reside on oxygen owing to their negative charge transfer energy, so far there has been no other comparative material studied. Here, we introduce (Ba,K)SbO$_{3}$ (BKSO) in which the Sb 5$s$ orbital energy is higher than that of the Bi 6$s$ orbitals enabling tuning of the charge transfer energy from negative to slightly positive. The parent compound BaSbO$_{3-δ}$ shows a larger CDW gap compared to the undoped bismuthate BaBiO$_{3}$. As the CDW order is suppressed via potassium substitution up to 65 %, superconductivity emerges, rising up to $T_\mathrm{c}$ = 15 K. This value is lower than the maximum $T_\mathrm{c}$ of BKBO, but higher by more than a factor of two at comparable potassium concentrations. The discovery of an enhanced CDW gap and superconductivity in BKSO indicates that the sign of the charge transfer energy may not be crucial, but instead strong metal-oxygen covalency plays the essential role in constituting a CDW and high-$T_\mathrm{c}$ superconductivity in the main-group perovskite oxides.

cond-mat.supr-con↗

arXiv2021

Hybridization-gap Formation and Superconductivity in the Pressure-induced Semimetallic Phase of the Excitonic Insulator Ta$_2$NiSe$_5$

The excitonic insulator Ta$_2$NiSe$_5$ experiences a first-order structural transition under pressure from rippled to flat layer-structure at Ps = 3 GPa, which drives the system from an almost zero-gap semiconductor to a semimetal. The pressure-induced semimetal, with lowering temperature, experiences a transition to another semimetal with a partial-gap of 0.1-0.2 eV, accompanied with a monoclinic distortion analogous to that occurs at the excitonic transition below Ps. We argue that the partial-gap originates primarily from a symmetry-allowed hybridization of Ta-conduction and Ni-valence bands due to the lattice distortion, indicative of the importance of electron-lattice coupling. The transition is suppressed with increasing pressure to Pc = 8 GPa. Superconductivity with a maximum Tsc = 1.2 K emerges around Pc, likely mediated by strongly electron-coupled soft phonons. The electron-lattice coupling is as important ingredient as the excitonic instability in Ta2NiSe5.

cond-mat.str-el↗

arXiv2021

Electronic Structure of the Bond Disproportionated Bismuthate Ag$_2$BiO$_3$

We present a comprehensive study on the silver bismuthate Ag$_2$BiO$_3$, synthesized under high-pressure high-temperature conditions, which has been the subject of recent theoretical work on topologically complex electronic states. We present X-ray photoelectron spectroscopy results showing two different bismuth states, and X-ray absorption spectroscopy results on the oxygen $K$-edge showing holes in the oxygen bands. These results support a bond disproportionated state with holes on the oxygen atoms for Ag$_2$BiO$_3$. We estimate a band gap of $\sim$1.25~eV for Ag$_2$BiO$_3$ from optical conductivity measurements, which matches the band gap in density functional calculations of the electronic band structure in the non-symmorphic space group $Pnn2$, which supports two inequivalent Bi sites. In our band structure calculations the disproportionated Ag$_2$BiO$_3$ is expected to host Weyl nodal chains, one of which is located $\sim$0.5~eV below the Fermi level. Furthermore, we highlight similarities between Ag$_2$BiO$_3$ and the well-known disproportionated bismuthate BaBiO$_3$, including breathing phonon modes with similar energy. In both compounds hybridization of Bi-$6s$ and O-$2p$ atomic orbitals is important in shaping the band structure, but in contrast to the Ba-$5p$ in BaBiO$_3$, the Ag-$4d$ bands in Ag$_2$BiO$_3$ extend up to the Fermi level.

cond-mat.mtrl-sci↗

arXiv2021

Design of opposed-anvil-type high-pressure cell for precision magnetometry and its application to quantum magnetism

We have developed a much sensitve technique to conduct magnetometry under ultrahigh pressures up to 6.3~GPa, which can detect a weak volume susceptibilities as small as $\sim 10^{-4}$. An opposed-anvil-type high-pressure cell is designed by numerical analysis to give nearly zero magnetic response, in a commercial SQUID magnetometer. We introduced procedures for subtracting background contributions from a high-pressure cell by taking displacements of the cell parts into account, and found a way of resolving tiny magnetism of a sample from given magnetometer response curves. A non-magnetic material, binderless tungsten carbide ceramic, is employed. To increase sample-signal-to-background ratio further, a conical shaped gasket and cupped anvils are introduced, yielding nearly ten times better space efficiency. The new set-up and analysis are applied to measure the paramagnetic susceptibilities of spin orbit entangled moment under pressures.

cond-mat.str-el↗

arXiv2021

Positive Seebeck coefficient in highly doped La$_{2-x}$Sr$_x$CuO$_4$ ($x$=0.33); its origin and implication

We present a study of the thermoelectric (Seebeck and Nernst) response in heavily overdoped, non-superconducting La$_{1.67}$Sr$_{0.33}$CuO$_4$. In spite of the electron-like curvature of the Fermi surface, the Seebeck coefficient is positive at low temperatures. Such a feature, previously observed in copper, silver, gold and lithium, is caused by a non-trivial energy dependence of the scattering time. We argue that this feature implies a strong asymmetry between the lifetime of occupied and unoccupied states along the zone diagonals and such an electron-hole asymmetry impedes formation of Cooper pairs along the nodal direction in the superconducting ground state emerging at lower doping levels.

cond-mat.supr-con↗

arXiv2021

Thermal transport signatures of the excitonic transition and associated phonon softening in the layered chalcogenide Ta$_2$NiSe$_5$

The layered compound $\mathrm{Ta_2NiSe_5}$ is a quasi-one-dimensional and narrow-gap semiconductor, which is proposed to undergo a transition to an excitonic insulator at $T_\mathrm{c}=326$ K. We found a clear anomaly at $T_\mathrm{c}$ in the in-plane thermal conductivities both parallel ($\parallel$ $a$) and perpendicular ($\parallel$ $c$) to the one-dimensional chains, $κ_\mathrm{a}$ and $κ_\mathrm{c}$. While $κ_\mathrm{a}$ shows a rapid decrease below $T_\mathrm{c}$, $κ_\mathrm{c}$ shows a pronounced V-shaped suppression centered at $T_\mathrm{c}$. We argue that the decrease of $κ_\mathrm{a}$ represents the suppression of the quasiparticle contribution below $T_\mathrm{c}$ due to excitonic condensation. On the other hand, the V-shaped suppression of $κ_\mathrm{c}$ comes from the enhanced phonon scattering by soft phonons associated with the monoclinic transition with momentum $\mathbf{q}\parallel c$. The continued suppression of $κ_\mathrm{c}$ up to an extremely high temperature above $T_\mathrm{c}$ suggests the persistence of phonon softening likely coupled to electronic, presumably excitonic, fluctuations.

cond-mat.str-el↗

arXiv2021

Phononic soft mode and strong electronic background behavior across the structural phase transition in the excitonic insulator Ta$_2$NiSe$_5$ (with Erratum)

Ta$_2$NiSe$_5$ became one of the most investigated candidate materials for hosting an excitonic insulator ground state. Many studies describe the corresponding phase transition as a condensation of excitons breaking a continuous symmetry. This view got challenged recently pointing out the importance of the loss of two mirror symmetries at a structural phase transition that occurs together with the semiconductor-excitonic insulator transition. For such a scenario an unstable optical zone-center phonon at low energy is proposed to drive the transition. Here we report on the experimental observation of such a soft mode behavior using Raman spectroscopy. In addition we find a novel spectral feature, likely of electronic or joint electronic and phononic origin, that is clearly distinct from the lattice dynamics and that becomes dominant at Tc. This suggests a picture of joint structural and electronic order driving the phase transition.

cond-mat.str-el↗

arXiv2021

Spin-orbit-entangled electronic phases in 4$d$ and 5$d$ transition-metal compounds

Complex oxides with $4d$ and $5d$ transition-metal ions recently emerged as a new paradigm in correlated electron physics, due to the interplay between spin-orbit coupling and electron interactions. For $4d$ and $5d$ ions, the spin-orbit coupling, $ζ$, can be as large as 0.2-0.4 eV, which is comparable with and often exceeds other relevant parameters such as Hund's coupling $J_{\rm H}$, noncubic crystal field splitting $Δ$, and the electron hopping amplitude $t$. This gives rise to a variety of spin-orbit-entangled degrees of freedom and, crucially, non-trivial interactions between them that depend on the $d$-electron configuration, the chemical bonding, and the lattice geometry. Exotic electronic phases often emerge, including spin-orbit assisted Mott insulators, quantum spin liquids, excitonic magnetism, multipolar orderings and correlated topological semimetals. This paper provides a selective overview of some of the most interesting spin-orbit-entangled phases that arise in $4d$ and $5d$ transition-metal compounds.

cond-mat.str-el↗

arXiv2021

Lattice dynamics and structural transition of the hyperhoneycomb iridate $β$-Li$_2$IrO$_3$ investigated by high-pressure Raman scattering

We report a polarized Raman scattering study of the lattice dynamics of $β$-Li$_2$IrO$_3$ under hydrostatic pressures up to 7.62 GPa. At ambient pressure, $β$-Li$_2$IrO$_3$ exhibits the hyperhoneycomb crystal structure and a magnetically ordered state of spin-orbit entangled Jeff = 1/2 moments that is strongly influenced by bond-directional (Kitaev) exchange interactions. At a critical pressure of ~ 4.1 GPa, the phonon spectrum changes abruptly consistent with the reported structural transition into a monoclinic, dimerized phase. A comparison to the phonon spectra obtained from density functional calculations shows reasonable overall agreement. The calculations also indicate that the high-pressure phase is a nonmagnetic insulator driven by the formation of Ir-Ir dimer bonds. Our results thus indicate a strong sensitivity of the electronic properties of $β$-Li$_2$IrO$_3$ to the pressure-induced structural transition.

cond-mat.str-el↗

arXiv2020

The spontaneous symmetry breaking in Ta$_2$NiSe$_5$ is structural in nature

The excitonic insulator is an electronically-driven phase of matter that emerges upon the spontaneous formation and Bose condensation of excitons. Detecting this exotic order in candidate materials is a subject of paramount importance, as the size of the excitonic gap in the band structure establishes the potential of this collective state for superfluid energy transport. However, the identification of this phase in real solids is hindered by the coexistence of a structural order parameter with the same symmetry as the excitonic order. Only a few materials are currently believed to host a dominant excitonic phase, Ta$_2$NiSe$_5$ being the most promising. Here, we test this scenario by using an ultrashort laser pulse to quench the broken-symmetry phase of this transition metal chalcogenide. Tracking the dynamics of the material's electronic and crystal structure after light excitation reveals surprising spectroscopic fingerprints that are only compatible with a primary order parameter of phononic nature. We rationalize our findings through state-of-the-art calculations, confirming that the structural order accounts for most of the electronic gap opening. Not only do our results uncover the long-sought mechanism driving the phase transition of Ta$_2$NiSe$_5$, but they also conclusively rule out any substantial excitonic character in this instability.

cond-mat.str-el↗