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T. Kadono

Publications and source records attributed to T. Kadono.

15 recordsLinked to original sources

Fingerprints of Mott and Slater gaps in the core-level photoemission spectra of antiferromagnetic iridates

We present Ir $4f$ core-level hard-x-ray photoemission spectroscopy (HAXPES) experiments conducted across antiferromagnetic (AFM) ordering transition in Ruddlesden-Popper iridates Sr$_2$IrO$_4$ and Sr$_3$Ir$_2$O$_7$. The Ir $4f$ spectra exhibit distinct changes between the AFM and paramagnetic (PM) phases, with the spectral difference $I_\text{PM}-I_\text{AFM}$ showing a contrasting behavior in the two compounds. By employing computational simulations using the local-density approximation combined with the dynamical mean-field theory method, we elucidate that $I_\text{PM}-I_\text{AFM}$ primary reflects the Slater or Mott-Hubbard character of the AFM insulating state rather than material specific details. This sensitivity to fine low-energy electronic structure arises from the dependence of charge-transfer responses to the sudden creation of a localized core hole on both metal-insulator transitions and long-range AFM ordering. Our result broadens the applications of core-level HAXPES as a tool for characterization of electronic structure.

cond-mat.str-el

Effect of projectile shape and interior structure on crater size in strength regime

Experiments on crater formation in the strength regime were conducted using projectiles of various shapes with an aspect ratio of ~1, including both solid and hollow interiors. The surface diameter, inner (pit) diameter, and depth of the craters on basalt and porous gypsum targets were measured. Using the bulk density of the projectile, the surface diameter and depth for basalt and the pit diameter and depth for porous gypsum were scaled using the pi-scaling law for crater formation in the strength regime. The numerical code iSALE was used to simulate the impact of projectiles of various shapes and interior structure with similar bulk densities. Results show that the distributions of the maximum (peak) pressure experienced and particle velocity in the targets were similar regardless of projectile shape and interior structure, implying that the dimensions of the final craters were almost identical. This is consistent with the experimental results. Thus, we conclude that the size of the craters formed by the impact of projectiles with different shape and interior structure can be scaled using a conventional scaling law in the strength regime, using bulk density as projectile density.

astro-ph.EP

Cr doping-induced ferromagnetism in the spin-glass Cd1-xMnxTe studied by x-ray magnetic circular dichroism

The prototypical diluted magnetic semiconductor Cd1-xMnxTe is a spin glass (x<0.6) or an antiferromagnet (x>0.6), but becomes ferromagnetic upon doping with a small amount of Cr atoms substituting for Mn. In order to investigate the origin of the ferromagnetism in Cd1-x-yMnxCryTe, we have studied its element specific magnetic properties by x-ray absorption spectroscopy (XAS) and x-ray magnetic circular dichroism (XMCD) at the Cr and Mn L2,3 edges. Thin films were grown by molecular beam epitaxy with a fixed Mn content of x = 0.2 and varying Cr content in the range of y = 0 - 0.04. Measured XAS and XMCD spectra indicate that both Cr and Mn atoms are divalent and that the ferromagnetic or superparamagnetic components of Cr and Mn are aligned in the same directions. The magnetization of Mn increases with increasing Cr content. These results can be explained if ferromagnetic interaction exists between neighboring Mn and Cr ions although interaction between Mn atoms is largely antiferromagnetic. We conclude that each ferromagnetic or superparamagnetic cluster consists of ferromagnetically coupled several Cr and a much larger number of Mn ions.

cond-mat.str-el

Anisotropic spin-density distribution and magnetic anisotropy of strained La$_{1-x}$Sr$_x$MnO$_3$ thin films: Angle-dependent x-ray magnetic circular dichroism

Magnetic anisotropies of ferromagnetic thin films are induced by epitaxial strain from the substrate via strain-induced anisotropy in the orbital magnetic moment and that in the spatial distribution of spin-polarized electrons. However, the preferential orbital occupation in ferromagnetic metallic La$_{1-x}$Sr$_x$MnO$_3$ (LSMO) thin films studied by x-ray linear dichroism (XLD) has always been found out-of-plane for both tensile and compressive epitaxial strain and hence irrespective of the magnetic anisotropy. In order to resolve this mystery, we directly probed the preferential orbital occupation of spin-polarized electrons in LSMO thin films under strain by angle-dependent x-ray magnetic circular dichroism (XMCD). Anisotropy of the spin-density distribution was found to be in-plane for the tensile strain and out-of-plane for the compressive strain, consistent with the observed magnetic anisotropy. The ubiquitous out-of-plane preferential orbital occupation seen by XLD is attributed to the occupation of both spin-up and spin-down out-of-plane orbitals in the surface magnetic dead layer.

cond-mat.mtrl-sci

Magnetic anisotropy of $L1_0$-ordered FePt thin films studied by Fe and Pt $L_{2,3}$-edges x-ray magnetic circular dichroism

The strong perpendicular magnetic anisotropy of $L{\rm1_0}$-ordered FePt has been the subject of extensive studies for a long time. However, it is not known which element, Fe or Pt, mainly contributes to the magnetic anisotropy energy (MAE). We have investigated the anisotropy of the orbital magnetic moments of Fe 3$d$ and Pt 5$d$ electrons in $L{\rm1_0}$-ordered FePt thin films by Fe and Pt $L_{2,3}$-edge x-ray magnetic circular dichroism (XMCD) measurements for samples with various degrees of long-range chemical order $S$. Fe $L_{2,3}$-edge XMCD showed that the orbital magnetic moment was larger when the magnetic field was applied perpendicular to the film than parallel to it, and that the anisotropy of the orbital magnetic moment increased with $S$. Pt $L_{2,3}$-edge XMCD also showed that the orbital magnetic moment was smaller when the magnetic field was applied perpendicular to the film than parallel to it, opposite to the Fe $L_{2,3}$-edge XMCD results although the anisotropy of the orbital magnetic moment increases with $S$ like the Fe edge. These results are qualitatively consistent with the first-principles calculation by Solovyev ${\it et\ al.}$ [Phys. Rev. B $\bf{52}$, 13419 (1995).], which also predicts the dominant contributions of Pt 5$d$ to the magnetic anisotropy energy rather than Fe 3$d$ due to the strong spin-orbit coupling and the small spin splitting of the Pt 5$d$ bands in $L{\rm1_0}$-ordered FePt.

cond-mat.mtrl-sci

Thickness-dependent magnetic properties and strain-induced orbital magnetic moment in SrRuO3 thin films

Thin films of the ferromagnetic metal SrRuO3 (SRO) show a varying easy magnetization axis depending on the epitaxial strain and undergo a metal-to-insulator transition with decreasing film thickness. We have investigated the magnetic properties of SRO thin films with varying thicknesses fabricated on SrTiO3(001) substrates by soft x-ray magnetic circular dichroism (XMCD) at the Ru M2,3 edge. Results have shown that, with decreasing film thickness, the film changes from ferromagnetic to non-magnetic around 3monolayer thickness, consistent with previous magnetization and magneto-optical Kerr effect measurements. The orbital magnetic moment perpendicular to the film was found to be ~ 0.1μB/Ru atom, and remained nearly unchanged with decreasing film thickness while the spin magnetic moment decreases. Mechanism for the formation of the orbital magnetic moment is discussed based on the electronic structure of the compressively strained SRO film.

cond-mat.str-el

Photoemission System with Polarized Hard X-rays for Probing Ground State Symmetry of Strongly Correlated Materials

We have developed a polarized hard X-ray photoemission (HAXPES) system to study the ground-state symmetry of strongly correlated materials. The linear polarization of the incoming X-ray beam is switched by the transmission-type phase retarder composed of two diamond (100) crystals. The best degree of the linear polarization $P_L$ is $-0.96$, containing the vertical polarization component of 98%. A newly developed low temperature two-axis manipulator enables easy polar and azimuthal rotations to select the detection direction of photoelectrons. The lowest temperature achieved is 9 K, offering us a chance to access the ground state even for the strongly correlated electron systems in cubic symmetry. The co-axial sample monitoring system with the long-working-distance microscope enables us to keep measuring the same region on the sample surface before and after rotation procedures. Combining this sample monitoring system with a micro-focused X-ray beam by means of an ellipsoidal Kirkpatrick-Baez mirror (25 $μ$m $\times$ 25 $μ$m (FWHM)), we have demonstrated the polarized valence-band HAXPES on NiO for voltage application as resistive random access memories to reveal the origin of the metallic spectral weight near the Fermi level.

cond-mat.str-el

Spin and orbital magnetic moments of Fe in the $n$-type ferromagnetic semiconductor (In,Fe)As

The electronic and magnetic properties of Fe atoms in the ferromagnetic semiconductor (In,Fe)As codoped with Be have been studied by x-ray absorption spectroscopy (XAS) and x-ray magnetic circular dichroism (XMCD) at the Fe $L_{2,3}$ edge. The XAS and XMCD spectra showed simple spectral line shapes similar to Fe metal, but the ratio of the orbital and spin magnetic moments ($M_\mathrm{orb}$/$M_\mathrm{spin}$) estimated using the XMCD sum rules was significantly larger than that of Fe metal, indicating a significant orbital moment of Fe $3d$ electrons in (In,Fe)As:Be. The positive value of $M_\mathrm{orb}$/$M_\mathrm{spin}$ implies that the Fe $3d$ shell is more than half-filled, which arises from the hybridization of the Fe$^{3+}$ ($d^5$) state with the charge-transfer $d^6\underline{L}$ states, where $\underline{L}$ is a ligand hole in the host valence band. The XMCD intensity as a function of magnetic field indicated hysteretic behavior of the superparamagnetic-like component due to discrete ferromagnetic domains.

cond-mat.mtrl-sci

Spectroscopic studies on the electronic and magnetic states of Co-doped perovskite manganite Pr0.8Ca0.2Mn1-yCoyO3 thin films

We have investigated the electronic and magnetic properties of Co-doped Pr0.8Ca0.2MnO3 thin films using various spectroscopic techniques. X-ray absorption and hard x-ray photoemission spectroscopy revealed that the substituted Co ions are in the divalent state, resulting in hole doping on the Mn atoms. Studies of element-selective magnetic properties by x-ray magnetic circular dichroism found a large orbital magnetic moment for the Co ions. These spectroscopic studies reveal that the substituted Co ions play several roles of hole doping for Mn, ferromagnetic superexchange coupling between the Co2+ and Mn4+ ions, and orbital magnetism of the Co2+ ions. Competition among these complex interactions produces the unique electronic and magnetic behaviors including enhanced coercivity of the Co-doped Pr0.8Ca0.2MnO3.

cond-mat.str-el

Orbital magnetic moment and coercivity of SiO$_{2}$-coated FePt nanoparticles studied by x-ray magnetic circular dichroism

We have investigated the spin and orbital magnetic moments of Fe in FePt nanoparticles in the $L$1$_{0}$-ordered phase coated with SiO$_{2}$ by x-ray absorption spectroscopy (XAS) and x-ray magnetic circular dichroism (XMCD) measurements at the Fe $L_{\rm 2,3}$ absorption edges. Using XMCD sum rules, we evaluated the ratio of the orbital magnetic moment ($M_{\rm orb}$) to the spin magnetic moment ($M_{\rm spin}$) of Fe to be $M_{\rm orb}/M_{\rm spin}$ = 0.08. This $M_{\rm orb}/M_{\rm spin}$ value is comparable to the value (0.09) obtained for FePt nanoparticles prepared by gas phase condensation, and is larger than the values ($\sim$0.05) obtained for FePt thin films, indicating a high degree of $L$1$_{0}$ order. The hysteretic behavior of the FePt component of the magnetization was measured by XMCD. The magnetic coercivity ($H_{\rm c}$) was found to be as large as 1.8 T at room temperature, $\sim$3 times larger than the thin film value and $\sim$50 times larger than that of the gas phase condensed nanoparticles. The hysteresis curve is well explained by the Stoner-Wohlfarth model for non-interacting single-domain nanoparticles with the $H_{\rm c}$ distributed from 1 T to 5 T.

cond-mat.mtrl-sci

Phase diagram of Ca$_{1-x}$Ce$_x$MnO$_3$ thin films studied by X-ray magnetic circular dichroism

In the perovskite-type Ca$_{1-x}$Ce$_{x}$MnO$_{3}$ (CCMO), one can control the transport and magnetic properties through varying Ce content. In the case of thin films, the properties can also be controlled by epitaxial strain from the substrate through changing it such as YAlO$_{3}$ (YAO), NdAlO$_{3}$ (NAO), and LaSrAlO$_{4}$ (LSAO). However, one cannot measure the magnetization of thin films on NAO substrates by conventional magnetization measurements because of the strong paramagnetic signals from the Nd$^{3+}$ ions. In order to eliminate the influence of Nd$^{3+}$ and to identify magnetic phases of the CCMO thin films, we have performed element-selective X-ray magnetic circular dichroism (XMCD) measurements of the Mn 2{\it p} core level. By studying the anisotropy of the XMCD intensity, we could unambiguously determine the magnetic phase diagram of the CCMO thin films.

cond-mat.str-el

Role of doped Ru in coercivity-enhanced La$_{0.6}$Sr$_{0.4}MnO$_3$ thin film studied by x-ray magnetic circular dichroism

The coercivity of La$_{1-x}$Sr$_x$MnO$_3$ thin films can be enhanced by Ru substitution for Mn. In order to elucidate its mechanism, we performed soft x-ray absorption and magnetic circular dichroism measurements at the Ru M$_{2,3}$ and Mn L$_{2,3}$ edges. We found that the spin direction of Ru and Mn are opposite and that Ru has a finite orbital magnetic moment. Cluster-model analysis indicated that the finite orbital magnetic moment as well as the reduced spin moment of Ru result from local lattice distortion caused by epitaxial strain from the SrTiO$_3$ substrate in the presence of spin-orbit interaction.

cond-mat.mtrl-sci

Absence of Superconductivity in the "hole-doped" Fe pnictide Ba(Fe$_{1-x}$Mn$_{x}$)$_{2}$As$_{2}$: Photoemission and X-ray Absorption Spectroscopy Studies

We have studied the electronic structure of Ba(Fe$_{1-x}$Mn$_{x}$)$_{2}$As$_{2}$ ($x$=0.08), which fails to become a superconductor in spite of the formal hole doping like Ba$_{1-x}$K$_{x}$Fe$_{2}$As$_{2}$, by photoemission spectroscopy and X-ray absorption spectroscopy (XAS). With decreasing temperature, a transition from the paramagnetic phase to the antiferromagnetic phase was clearly observed by angle-resolved photoemission spectroscopy. XAS results indicated that the substituted Mn atoms form a strongly hybridized ground state. Resonance-photoemission spectra at the Mn $L_{3}$ edge revealed that the Mn 3d partial density of states is distributed over a wide energy range of 2-13 eV below the Fermi level ($E_F$), with little contribution around $E_F$. This indicates that the dopant Mn 3$d$ states are localized in spite of the strong Mn 3d-As $4p$ hybridization and split into the occupied and unoccupied parts due to the on-site Coulomb and exchange interaction. The absence of superconductivity in Ba(Fe$_{1-x}$Mn$_{x}$)$_{2}$As$_{2}$ can thus be ascribed both to the absence of carrier doping in the FeAs plane, and to the strong stabilizaiton of the antiferromagnetic order by the Mn impurities.

cond-mat.supr-con

Observation of magnetically hard grain boundaries in double-perovskite Sr$_{2}$FeMoO$_{6}$

Unusual low temperature magneto-resistance (MR) of ferromagnetic Sr$_{2}$FeMoO$_{6}$ polycrystals has been attributed to magnetically hard grain boundaries which act as spin valves. We detected the different magnetic hysteresis curves for the grains and the grain boundaries of polycrystalline Sr$_{2}$FeMoO$_{6}$ by utilizing the different probing depths of the different detection modes of x-ray absorption spectroscopy (XAS) and x-ray magnetic circular dichroism (XMCD), namely, the total electron yield (TEY) mode (probing depth $\sim$5 nm) and the total fluorescence yield (TFY) mode (probing depth $\sim$100 nm). At 20 K, the magnetic coercivity detected in the TEY mode ($H_{\rm c,TEY}$) was several times larger than that in the TFY mode ($H_{\rm c,TFY}$), indicating harder ferromagnetism of the grain boundaries than that of the grains. At room temperature, the grain boundary magnetism became soft and $H_{\rm c,TEY}$ and $H_{\rm c,TFY}$ were nearly the same. From line-shape analysis of the XAS and XMCD spectra, we found that in the grain boundary region the ferromagnetic component is dominated by Fe$^{2+}$ or well-screened signals while the non-magnetic component is dominated by Fe$^{3+}$ or poorly-screened signals.

cond-mat.str-el

Laser-Shock Compression and Hugoniot Measurements of Liquid Hydrogen to 55 GPa

The principal Hugoniot for liquid hydrogen was obtained up to 55 GPa under laser-driven shock loading. Pressure and density of compressed hydrogen were determined by impedance-matching to a quartz standard. The shock temperature was independently measured from the brightness of the shock front. Hugoniot data of hydrogen provide a good benchmark to modern theories of condensed matter. The initial number density of liquid hydrogen is lower than that for liquid deuterium, and this results in shock compressed hydrogen having a higher compression and higher temperature than deuterium at the same shock pressure.

cond-mat.mtrl-sci