Takuo Ohkochi

Electronic structure and magnetism of the diluted magnetic semiconductor Fe-doped ZnO nanoparticles

We have studied the electronic structure of Fe-doped ZnO nanoparticles, which have been reported to show ferromagnetism at room temperature, by x-ray photoemission spectroscopy, resonant photoemission spectroscopy, x-ray absorption spectroscopy, and x-ray magnetic circular dichroism (XMCD). From the experimental and cluster-model calculation results, we find that Fe atoms are predominantly in the Fe3+ ionic state with mixture of a small amount of Fe2+ and that Fe3+ ions are dominant in the surface region of the nanoparticles. It is shown that the room temperature ferromagnetism in the Fe-doped ZnO nanoparticles primarily originated from the antiferromagnetic coupling between unequal amounts of Fe3+ ions occupying two sets of nonequivalent positions in the region of the XMCD probing depth of ∼2–3 nm.

Structural, magnetic and electronic state characterization of L1 0-type ordered FeNi alloy extracted from a natural meteorite

To understand the hard magnetism of L10-type ordered FeNi alloy, we extracted the L10-FeNi phase from a natural meteorite, and evaluated its fundamental solid-state properties: sample composition, magnetic hysteresis, crystal structure and electronic structure. We executed multidirectional analyses using scanning electron microscopy with an electron probe micro-analyzer (SEM-EPMA), a superconducting quantum interference device (SQUID), x-ray diffraction (XRD) and magnetic circular dichroism (MCD). As a result, we found that the composition was Fe: 50.47 ± 1.98 at.%, Ni: 49.60 ± 1.49 at.%, and an obvious superlattice peak is confirmed. The estimated degree of order was 0.608, with lattice constants a = b = 3.582 Å and c = 3.607 Å. The obtained coercivity was more than 500 Oe. MCD analysis using the K absorption edge suggests that the magnetic anisotropy could originate from the orbital magnetic moment of 3d electrons in Fe; this result is consistent with that in a previous report obtained with synthetic L10-FeNi.

Formation of FeNi with L10-ordered structure using high-pressure torsion

FeNi with the L10-ordered structure is formed over an astronomical timescale in meteorites. In this study, severe plastic deformation using high-pressure torsion (HPT) is employed for the production of the L10 structure in the laboratory. Its formation is confirmed by X-ray diffraction analysis and transmission electron microscopy. Processing of elemental nanopowders by HPT is an effective method for the formation of the L10 phase, which is enhanced by the addition of Co to FeNi or annealing after HPT. The formation of the phase must be associated with enhanced diffusion through HPT.

Ferromagnetism in ZnO co-doped with Mn and N studied by soft x-ray magnetic circular dichroism

We have investigated the electronic structure of ZnO:Mn and ZnO:Mn,N thin films using x-ray magnetic circular dichroism (XMCD) and resonance-photoemission spectroscopy. From the Mn 2p -> 3d XMCD ...

4f-derived Fermi surfaces of CeRu2(Si1-xGex)2 near the quantum critical point: resonant soft-X-ray ARPES study.

Angle-resolved photoelectron spectroscopy in the Ce 3d-->4f excitation region was measured for the paramagnetic state of CeRu2Si2, CeRu2(Si0.82Ge0.18)2, and LaRu2Si2 to investigate the changes of the 4f electron Fermi surfaces around the quantum critical point. While the difference of the Fermi surfaces between CeRu2Si2 and LaRu2Si2 was experimentally confirmed, a strong 4f-electron character was observed in the band structures and the Fermi surfaces of CeRu2Si2 and CeRu2(Si0.82Ge0.18)2, consequently indicating a delocalized nature of the 4f electrons in both compounds. The absence of Fermi surface reconstruction across the critical composition suggests that SDW quantum criticality is more appropriate than local quantum criticality in CeRu2(Si1-xGex)2.

Electronic configuration of Mn ions in the π-d molecular ferromagnet β-Mn phthalocyanine studied by soft X-ray magnetic circular dichroism

Abstract We have studied the electronic structure of the molecular ferromagnet β -Mn phthalocyanine ( β -MnPc) in a polycrystalline form, which has been reported to show ferromagnetism at T 8.6 K , by X-ray absorption spectroscopy (XAS) and X-ray magnetic circular dichroism (XMCD). From the experimental results and subsequent cluster-model calculation, we find that the ferromagnetic Mn ion in β -MnPc is largely in the 4 E g ground state arising from the ( e g ) 3 ( b 2 g ) 1 ( a 1 g ) 1 [ ( d x z , y z ) 3 ( d x y ) 1 ( d z 2 ) 1 ] configuration of the Mn2+ state. Considering that the highest occupied molecular orbital (HOMO) of MnPc with the 4 E g ground state originates from the a 1 g orbital of the Mn2+ ion, it is proposed that a 1 g – a 1 g exchange coupling via the π orbitals of the phthalocyanine ring plays a crucial role in the ferromagnetism of β -MnPc.

Electronic Structure of Heavy Fermion Uranium Compounds Studied by Core-Level Photoelectron Spectroscopy

High-energy-resolution core-level and valence-band photoelectron spectroscopic studies were performed for the heavy fermion uranium compounds UGe 2 , UCoGe, URhGe, URu 2 Si 2 , UNi 2 Al 3 , UPd 2 Al 3 , and UPt 3 as well as typical localized and itinerant uranium compounds to understand the relationship between the uranium valence state and their core-level spectral line shapes. In addition to the main line and high-binding energy satellite structure recognized in the core-level spectra of uranium compounds, a shoulder structure on the lower binding energy side of the main lines of localized and nearly localized uranium compounds was also found. The spectral line shapes show a systematic variation depending on the U 5 f electronic structure. The core-level spectra of UGe 2 , UCoGe, URhGe, URu 2 Si 2 , and UNi 2 Al 3 are rather similar to those of itinerant compounds, suggesting that U 5 f electrons in these compounds are well hybridized with ligand states. On the other hand, the core-level spectra of UPd ...

Nature of magnetic coupling between Mn ions in As-grown Ga1-xMnxAs studied by X-ray magnetic circular dichroism.

The magnetic properties of as-grown Ga1-xMnxAs have been investigated by the systematic measurements of temperature and magnetic field dependent soft x-ray magnetic circular dichroism (XMCD). The intrinsic XMCD intensity at high temperatures obeys the Curie-Weiss law, but a residual spin magnetic moment appears already around 100 K, significantly above the Curie temperature (T_{C}), suggesting that short-range ferromagnetic correlations are developed above T_{C}. The present results also suggest that the antiferromagnetic interaction between the substitutional and interstitial Mn (Mn_{int}) ions exists and that the amount of the Mn_{int} affects T_{C}.

Depth Profile of Induced Spin Polarization in Au Layers of Fe/Au(001) Superlattices by Resonant X-ray Magnetic Scattering

The depth distribution of the induced spin polarization in the Au layers of epitaxitial Fe/Au(001) superlattices has been estimated by resonant X-ray magnetic scattering, using circularly polarized...

Itinerant nature of U 5 f states in uranium mononitride revealed by angle-resolved photoelectron spectroscopy

The electronic structure of the antiferromagnet uranium nitride (UN) has been studied by angle-resolved photoelectron spectroscopy (ARPES) using soft x-rays (