arXiv subjects

H. Takagi

Publications and source records attributed to H. Takagi.

At least 73 records · Page 4Linked to original sources

arXiv2017

Pressure-tuning of bond-directional exchange interactions and magnetic frustration in hyperhoneycomb iridate $β$-$\mathrm{Li_2IrO_3}$

We explore the response of Ir $5d$ orbitals to pressure in $β$-$\mathrm{Li_2IrO_3}$, a hyperhoneycomb iridate in proximity to a Kitaev quantum spin liquid (QSL) ground state. X-ray absorption spectroscopy reveals a reconstruction of the electronic ground state below 2 GPa, the same pressure range where x-ray magnetic circular dichroism shows an apparent collapse of magnetic order. The electronic reconstruction, which manifests a reduction in the effective spin-orbit (SO) interaction in $5d$ orbitals, pushes $β$-$\mathrm{Li_2IrO_3}$ further away from the pure $J_{\rm eff}=1/2$ limit. Although lattice symmetry is preserved across the electronic transition, x-ray diffraction shows a highly anisotropic compression of the hyperhoneycomb lattice which affects the balance of bond-directional Ir-Ir exchange interactions driven by spin-orbit coupling at Ir sites. An enhancement of symmetric anisotropic exchange over Kitaev and Heisenberg exchange interactions seen in theoretical calculations that use precisely this anisotropic Ir-Ir bond compression provides one possible route to realization of a QSL state in this hyperhoneycomb iridate at high pressures.

cond-mat.str-el↗

arXiv2017

Nearly-free-electron system of monolayer Na on the surface of single-crystal HfSe$_2$

The electronic structure of a single Na monolayer on the surface of single-crystal HfSe$_2$ is investigated using angle-resolved photoemission spectroscopy. We find that this system exhibits an almost perfect "nearly-free-electron" behavior with an extracted effective mass of $\sim\!1m_e$, in contrast to heavier masses found previously for alkali metal monolayers on other substrates. Our density-functional-theory calculations indicate that this is due to the large lattice constant, causing both exchange and correlation interactions to be suppressed, and to the weak hybridization between the overlayer and the substrate. This is therefore an ideal model system for understanding the properties of two-dimensional materials.

cond-mat.mtrl-sci↗

arXiv2017

Giant exciton Fano resonance in quasi-one-dimensional Ta$_2$NiSe$_5$

We report the complex dielectric function of the quasi-one-dimensional chalcogenide Ta$_2$NiSe$_5$, which exhibits a structural phase transition that has been attributed to exciton condensation below $T_c = 326$ K, and of the isostructural Ta$_2$NiS$_5$ which does not exhibit such a transition. Using spectroscopic ellipsometry, we have detected exciton doublets with pronounced Fano lineshapes in both the compounds. The exciton Fano resonances in Ta$_2$NiSe$_5$ display an order of magnitude higher intensity than those in Ta$_2$NiS$_5$. In conjunction with prior theoretical work by E. Rashba, we attribute this observation to the giant oscillator strength of spatially extended exciton-phonon bound states in Ta$_2$NiSe$_5$. The formation of exciton-phonon complexes in Ta$_2$NiS$_5$ and Ta$_2$NiSe$_5$ is confirmed by the pronounced temperature dependence of sharp interband transitions in the optical spectra, whose peak energies and widths scale with the thermal population of optical phonon modes. The description of the optically excited states in terms of strongly overlapping exciton complexes is in good agreement with the hypothesis of an EI ground state.

cond-mat.str-el↗

arXiv2016

Long-range interactions in the effective low energy Hamiltonian of Sr2IrO4: a core level resonant inelastic x-ray scattering study

We have investigated the electronic structure of Sr2IrO4 using core level resonant inelastic x-ray scattering. The experimental spectra can be well reproduced using ab initio density functional theory based multiplet ligand field theory calculations, thereby validating these calculations. We found that the low-energy, effective Ir t2g orbitals are practically degenerate in energy. We uncovered that covalency in Sr2IrO4, and generally in iridates, is very large with substantial oxygen ligand hole character in the Ir t2g Wannier orbitals. This has far reaching consequences, as not only the onsite crystal-field energies are determined by the long range crystal-structure, but, more significantly, magnetic exchange interactions will have long range distance dependent anisotropies in the spin direction. These findings set constraints and show pathways for the design of d^5 materials that can host compass-like magnetic interactions.

cond-mat.str-el↗

arXiv2016

Three-dimensional electronic structures and the metal-insulator transition in Ruddlesden-Popper iridates

In this study, we systematically investigate 3D momentum($\hbar k$)-resolved electronic structures of Ruddlesden-Popper-type iridium oxides Sr$_{n+1}$Ir$_n$O$_{3n+1}$ using soft-x-ray (SX) angle-resolved photoemission spectroscopy (ARPES). Our results provide direct evidence of an insulator-to-metal transition that occurs upon increasing the dimensionality of the IrO$_2$-plane structure. This transition occurs when the spin-orbit-coupled $j_{\rm eff}$=1/2 band changes its behavior in the dispersion relation and moves across the Fermi energy. In addition, an emerging band along the $Γ$(0,0,0)-R($π$,$π$,$π$) direction is found to play a crucial role in the metallic characteristics of SrIrO$_3$. By scanning the photon energy over 350 eV, we reveal the 3D Fermi surface in SrIrO$_3$ and $k_z$-dependent oscillations of photoelectron intensity in Sr$_3$Ir$_2$O$_7$. In contrast to previously reported results obtained using low-energy photons, folded bands derived from lattice distortions and/or magnetic ordering make significantly weak (but finite) contributions to the $k$-resolved photoemission spectrum. At the first glance, this leads to the ambiguous result that the observed $k$-space topology is consistent with the unfolded Brillouin zone (BZ) picture derived from a non-realistic simple square or cubic Ir lattice. Through careful analysis, we determine that a superposition of the folded and unfolded band structures has been observed in the ARPES spectra obtained using photons in both ultraviolet and SX regions. To corroborate the physics deduced using low-energy ARPES studies, we propose to utilize SX-ARPES as a powerful complementary technique, as this method surveys more than one whole BZ and provides a panoramic view of electronic structures.

cond-mat.str-el↗

arXiv2016

Origin of the metal-to-insulator crossover in cuprate superconductors

Superconductivity in cuprates peaks in the doping regime between a metal at high p and an insulator at low p. Understanding how the material evolves from metal to insulator is a fundamental and open question. Early studies in high magnetic fields revealed that below some critical doping an insulator-like upturn appears in the resistivity of cuprates at low temperature, but its origin has remained a puzzle. Here we propose that this 'metal-to-insulator crossover' is due to a drop in carrier density n associated with the onset of the pseudogap phase at a critical doping p*. We use high-field resistivity measurements on LSCO to show that the upturns are quantitatively consistent with a drop from n=1+p above p* to n=p below p*, in agreement with high-field Hall data in YBCO. We demonstrate how previously reported upturns in the resistivity of LSCO, YBCO and Nd-LSCO are explained by the same universal mechanism: a drop in carrier density by 1.0 hole per Cu atom.

cond-mat.supr-con↗

arXiv2016

Critical Doping for the Onset of Fermi-Surface Reconstruction by Charge-Density-Wave Order in the Cuprate Superconductor La$ _{2-x} $Sr$_{x} $CuO$ _{4}$

The Seebeck coefficient $S$ of the cuprate superconductor La$ _{2-x} $Sr$_{x} $CuO$ _{4}$ (LSCO) was measured in magnetic fields large enough to access the normal state at low temperatures, for a range of Sr concentrations from $x = 0.07$ to $x = 0.15$. For $x = 0.11$, 0.12, 0.125 and 0.13, $S/T$ decreases upon cooling to become negative at low temperatures. The same behavior is observed in the Hall coefficient $R_{H}(T)$. In analogy with other hole-doped cuprates at similar hole concentrations $p$, the negative $S$ and $R_{H}$ show that the Fermi surface of LSCO undergoes a reconstruction caused by the onset of charge-density-wave modulations. Such modulations have indeed been detected in LSCO by X-ray diffraction in precisely the same doping range. Our data show that in LSCO this Fermi-surface reconstruction is confined to $0.085 < p < 0.15$. We argue that in the field-induced normal state of LSCO, charge-density-wave order ends at a critical doping $p_{\rm CDW} = 0.15 \pm 0.005$, well below the pseudogap critical doping $p^\star \simeq 0.19$.

cond-mat.supr-con↗

arXiv2016

Optical anisotropy of the Jeff = 1/2 Mott insulator Sr2IrO4

We report the complex dielectric function along and perpendicular to the IrO2 planes in the layered perovskite Sr2IrO4 determined by spectroscopic ellipsometry in the spectral range from 12 meV to 6 eV. Thin high quality single crystals were stacked to measure the c-axis optical conductivity. In the phonon response we identified 10 infrared-active modes polarized within the basal plane and only four modes polarized along the c-axis, in full agreement with first-principle lattice dynamics calculations. We also observed a strong optical anisotropy in the near-infrared spectra arising from direct transitions between Ir 5d t2g Jeff = 1/2 and Jeff = 3/2 bands, which transition probability is highly suppressed for light polarized along the c-axis. The spectra are analyzed and discussed in terms of relativistic LSDA+U band structure calculations.

cond-mat.str-el↗

arXiv2015

S=1/2 quantum critical spin ladders produced by orbital ordering in Ba2CuTeO6

The ordered hexagonal perovskite Ba2CuTeO6 hosts weakly coupled S=1/2 spin ladders produced by an orbital ordering of Cu2+. The magnetic susceptibility chi(T) of Ba2CuTeO6 is well described by that expected for isolated spin ladders with exchange coupling of J~86 K but shows a deviation from the expected thermally activated behavior at low temperatures below T*~25 K. An anomaly in chi(T), indicative of magnetic ordering, is observed at T_mag=16 K. No clear signature of long-range ordering, however, is captured in NMR, specific heat or neutron diffraction measurements at and below T_mag. The marginal magnetic transition, indicative of strong quantum fluctuations, is evidence that Ba2CuTeO6 is in very close proximity to a quantum critical point between a magnetically ordered phase and a gapped spin liquid controlled by inter-ladder couplings.

cond-mat.str-el↗

arXiv2015

Electron scattering, charge order, and pseudogap physics in La$_{1.6-x}$Nd$_{0.4}$Sr$_x$CuO$_4$: An angle resolved photoemission spectroscopy study

We report an angle-resolved photoemission study of the charge stripe ordered La$_{1.6-x}$Nd$_{0.4}$Sr$_x$CuO$_4$ system. A comparative and quantitative line shape analysis is presented as the system evolves from the overdoped regime into the charge ordered phase. On the overdoped side ($x=0.20$), a normal state anti-nodal spectral gap opens upon cooling below ~ 80 K. In this process spectral weight is preserved but redistributed to larger energies. A correlation between this spectral gap and electron scattering is found. A different lineshape is observed in the antinodal region of charge ordered Nd-LSCO $x=1/8$. Significant low-energy spectral weight appears to be lost. These observations are discussed in terms of spectral weight redistribution and gapping %of spectral weight originating from charge stripe ordering.

cond-mat.supr-con↗

arXiv2015

Imaging ambipolar two-dimensional carriers induced by the spontaneous electric polarization of a polar semiconductor BiTeI

Two-dimensional (2D) mobile carriers are a wellspring of quantum phenomena. Among various 2D-carrier systems, such as field effect transistors and heterostructures, polar materials hold a unique potential; the spontaneous electric polarization in the bulk could generate positive and negative 2D carriers at the surface. Although several experiments have shown ambipolar carriers at the surface of a polar semiconductor BiTeI, their origin is yet to be specified. Here we provide compelling experimental evidences that the ambipolar 2D carriers at the surface of BiTeI are induced by the spontaneous electric polarization. By imaging electron standing waves with spectroscopic imaging scanning tunneling microscopy, we find that positive or negative carriers with Rashba-type spin splitting emerge at the surface correspondingly to the polar directions in the bulk. The electron densities at the surface are constant independently of those in the bulk, corroborating that the 2D carriers are induced by the spontaneous electric polarization. We also successfully image that lateral $p$-$n$ junctions are formed along the boundaries of submicron-scale domains with opposite polar directions. Our study presents a novel means to endow non-volatile, spin-polarized, and ambipolar 2D carriers as well as, without elaborate fabrication, lateral $p$-$n$ junctions of those carriers at atomically-sharp interfaces.

cond-mat.mtrl-sci↗

arXiv2015

Evidence for ordered magnetic moments at oxygen sites in antiferromagnetic Sr$_2$IrO$_4$ and Sr$_3$Ir$_2$O$_7$

In this study, the magnetic ground state of iridium perovskites (Sr$_{n+1}$Ir$_{n}$O$_{3n+1}$, where $n=1$, 2, and $\infty$) was considered using muon spin spectroscopy ($μ$SR). When probed by muons in Sr$_2$IrO$_4$ and Sr$_3$Ir$_2$O$_7$ ($n=1,2$), the internal field ($B_{\rm loc}$) showed clear sign of a magnetic order in two stages at transition temperatures $T_{\rm N}\simeq 230$ K and $T_{\rm m}\simeq 90$ K in Sr$_2$IrO$_4$ and $T_{\rm N}\simeq 280$ K and $T_{\rm m}\simeq 70$ K in Sr$_3$Ir$_2$O$_7$, respectively. In contrast, no long-range magnetic order was observed in orthorhombic SrIrO$_3$ ($n=\infty$). Based on the known magnetic structure in Sr$_2$IrO$_4$ and Sr$_3$Ir$_2$O$_7$, we successfully identified muon sites in these compounds from the magnitude of $B_{\rm loc}$ in the first stage ($T_{\rm m}\le T\le T_{\rm N}$). Below $T_{\rm m}$, $B_{\rm loc}$ probed by a fraction of muons occupying sites near the apical oxygen of IrO$_6$ octahedra exhibited a further increase but remained mostly unchanged for sites close to the in-plane oxygen. While such behavior cannot be explained by the alteration of the Ir spin structure, it is consistent with the selective appearance of ordered magnetic moments on the apical oxygen. The oxygen polarization was also in line with the reported magnetization anomalies in these compounds below $\sim T_{\rm m}$. A possible link between the oxygen polarization and ferroelectric (multiferroic) behavior in Sr$_2$IrO$_4$ was considered.

cond-mat.str-el↗

arXiv2015

Two distinct kinetic regimes for the relaxation of light-induced superconductivity in La$_{1.675}$Eu$_{0.2}$Sr$_{0.125}$CuO$_{4}$

We address the kinetic competition between charge striped order and superconductivity in La$_{1.675}$Eu$_{0.2}$Sr$_{0.125}$CuO$_{4}$. Ultrafast optical excitation is tuned to a mid-infrared vibrational resonance that destroys charge order and promptly establishes transient coherent interlayer coupling in this material. This effect is evidenced by the appearance of a longitudinal plasma mode reminiscent of a Josephson plasma resonance. We find that coherent interlayer coupling can be generated up to the charge order transition $T_{CO} \approx$ 80 K, far above the equilibrium superconducting transition temperature of any lanthanide cuprate. Two key observations are extracted from the relaxation kinetics of the interlayer coupling. Firstly, the plasma mode relaxes through a collapse of its coherence length and not its density. Secondly, two distinct kinetic regimes are observed for this relaxation, above and below spin order transition $T_{SO} =$ 25 K. Especially, the temperature independent relaxation rate observed below $T_{SO}$ is anomalous and suggests coexistence of superconductivity and stripes rather than competition. Both observations support arguments that a low temperature coherent stripe (or pair density wave) phase suppresses c-axis tunnelling by disruptive interference rather than by depleting the condensate.

cond-mat.supr-con↗

arXiv2014

Thermal conductivity across the metal-insulator transition in single crystalline hyperkagome Na$_{3+x}$Ir$_3$O$_8$

The hyperkagome antiferromagnet Na$_{4}$Ir$_3$O$_8$ represents the first genuine candidate for the realisation of a three-dimensional quantum spin-liquid. It can also be doped towards a metallic state, thus offering a rare opportunity to explore the nature of the metal-insulator transition in correlated, frustrated magnets. Here we report thermodynamic and transport measurements in both metallic and weakly insulating single crystals down to 150 mK. While in the metallic sample the phonon thermal conductivity ($κ^{ph}$) is almost in the boundary scattering regime, in the insulating sample we find a large reduction $κ^{ph}$ over a very wide temperature range. This result can be ascribed to the scattering of phonons off nanoscale disorder or off the gapless magnetic excitations that are seen in the low-temperature specific heat. This works highlights the peculiarity of the metal-insulator transition in Na$_{3+x}$Ir$_3$O$_8$ and demonstrates the importance of the coupling between lattice and spin degrees of freedom in the presence of strong spin-orbit coupling.

cond-mat.str-el↗

arXiv2014

Commensurate structural modulation in the charge- and orbitally-ordered phase of the quadruple perovskite (NaMn$_3$)Mn$_4$O$_{12}$

By means of synchrotron x-ray and electron diffraction, we studied the structural changes at the charge order transition $T_{CO}$=176 K in the mixed-valence quadruple perovskite (NaMn$_3$)Mn$_4$O$_{12}$. Below $T_{CO}$ we find satellite peaks indicating a commensurate structural modulation with the same propagation vector q =(1/2,0,-1/2) of the CE magnetic order that appears at low temperature, similarly to the case of simple perovskites like La$_{0.5}$Ca$_{0.5}$MnO$_3$. In the present case, the modulated structure together with the observation of a large entropy change at $T_{CO}$ gives evidence of a rare case of full Mn$^{3+}$/Mn$^{4+}$ charge and orbital order consistent with the Goodenough-Kanamori model.

cond-mat.str-el↗

arXiv2014

Excitonic Bose-Einstein condensation in Ta2NiSe5 above room temperature

We show that finite temperature variational cluster approximation (VCA) calculations on an extended Falicov-Kimball model can reproduce angle-resolved photoemission spectroscopy (ARPES) results on Ta2NiSe5 across a semiconductor-to-semiconductor structural phase transition at 325 K. We demonstrate that the characteristic temperature dependence of the flat-top valence band observed by ARPES is reproduced by the VCA calculation on the realistic model for an excitonic insulator only when the strong excitonic fluctuation is taken into account. The present calculations indicate that Ta2NiSe5 falls in the Bose-Einstein condensation regime of the excitonic insulator state.

cond-mat.str-el↗

arXiv2014

Direct observation of spin-polarised bulk bands in an inversion-symmetric semiconductor

Methods to generate spin-polarised electronic states in non-magnetic solids are strongly desired to enable all-electrical manipulation of electron spins for new quantum devices. This is generally accepted to require breaking global structural inversion symmetry. In contrast, here we present direct evidence from spin- and angle-resolved photoemission spectroscopy for a strong spin polarisation of bulk states in the centrosymmetric transition-metal dichalcogenide WSe$_2$. We show how this arises due to a lack of inversion symmetry in constituent structural units of the bulk crystal where the electronic states are localised, leading to enormous spin splittings up to $\sim\!0.5$ eV, with a spin texture that is strongly modulated in both real and momentum space. As well as providing the first experimental evidence for a recently-predicted `hidden' spin polarisation in inversion-symmetric materials, our study sheds new light on a putative spin-valley coupling in transition-metal dichalcogenides, of key importance for using these compounds in proposed valleytronic devices.

cond-mat.mtrl-sci↗

arXiv2014

Imaging two-component nature of Dirac-Landau levels in the topological surface state of Bi2Se3

Massless Dirac electrons in condensed matter have attracted considerable attention. Unlike conventional electrons, Dirac electrons are described in the form of two-component wave functions. In the surface state of topological insulators, these two components are associated with the spin degrees of freedom, hence governing the magnetic properties. Therefore, the observation of the two-component wave function provides a useful clue for exploring the novel spin phenomena. Here we show that the two-component nature is manifested in the Landau levels (LLs) whose degeneracy is lifted by a Coulomb potential. Using spectroscopic-imaging scanning tunneling microscopy, we visualize energy and spatial structures of LLs in a topological insulator Bi2Se3. The observed potential-induced LL splitting and internal structures of Landau orbits are distinct from those in a conventional electron system and are well reproduced by a two-component model Dirac Hamiltonian. Our model further predicts non-trivial energy-dependent spin-magnetization textures in a potential variation. This provides a way to manipulate spins in the topological surface state.

cond-mat.mes-hall↗