Koji Kimoto

Characterization and properties of green-emitting β-SiAlON:Eu2+ powder phosphors for white light-emitting diodes

This letter reports a β-SiAlON:Eu2+ green phosphor with the composition of Eu0.00296Si0.41395Al0.01334O0.0044N0.56528. The phosphor powder exhibits a rod-like morphology with the length of ∼4μm and the diameter of ∼0.5μm. It can be excited efficiently over a broad spectral range between 280 and 480 nm, and has an emission peak at 535 nm with a full width at half maximum of 55 nm. It has a superior color chromaticity of x=0.32 and y=0.64. The internal and external quantum efficiencies of this phosphor is 70% and 61% at λex=303nm, respectively. This newly developed green phosphor has potential applications in phosphor-converted white LEDs.

Near room-temperature formation of a skyrmion crystal in thin-films of the helimagnet FeGe.

The skyrmion, a vortex-like spin-swirling object, is anticipated to play a vital role in quantum magneto-transport processes such as the quantum Hall and topological Hall effects. The existence of the magnetic skyrmion crystal (SkX) state was recently verified experimentally for MnSi and Fe(0.5)Co(0.5)Si by means of small-angle neutron scattering and Lorentz transmission electron microscopy. However, to enable the application of such a SkX for spintronic function, materials problems such as a low crystallization temperature and low stability of SkX have to be overcome. Here we report the formation of SkX close to room temperature in thin-films of the helimagnet FeGe. In addition to the magnetic twin structure, we found a magnetic chirality inversion of the SkX across lattice twin boundaries. Furthermore, for thin crystal plates with thicknesses much smaller than the SkX lattice constant (as) the two-dimensional SkX is quite stable over a wide range of temperatures and magnetic fields, whereas for quasi-three-dimensional films with thicknesses over as the SkX is relatively unstable and observed only around the helical transition temperature. The room-temperature stable SkX state as promised by this study will pave a new path to designing quantum-effect devices based on the controllable skyrmion dynamics.

Skyrmion flow near room temperature in an ultralow current density

The manipulation of spin textures with electric currents is an important challenge in the field of spintronics. Many attempts have been made to electrically drive magnetic domain walls in ferromagnets, yet the necessary current density remains quite high (~10(7) A cm(-2)). A recent neutron study combining Hall effect measurements has shown that an ultralow current density of J~10(2) A cm(-2) can trigger the rotational and translational motion of the skyrmion lattice in MnSi, a helimagnet, within a narrow temperature range. Raising the temperature range in which skyrmions are stable and reducing the current required to drive them are therefore desirable objectives. Here we demonstrate near-room-temperature motion of skyrmions driven by electrical currents in a microdevice composed of the helimagnet FeGe, by using in-situ Lorentz transmission electron microscopy. The rotational and translational motions of skyrmion crystal begin under critical current densities far below 100 A cm(-2).

Element-selective imaging of atomic columns in a crystal using STEM and EELS

Microstructure characterization has become indispensable to the study of complex materials, such as strongly correlated oxides, and can obtain useful information about the origin of their physical properties. Although atomically resolved measurements have long been possible, an important goal in microstructure characterization is to achieve element-selective imaging at atomic resolution. A combination of scanning transmission electron microscopy (STEM) and electron energy-loss spectroscopy (EELS) is a promising technique for atomic-column analysis. However, two-dimensional analysis has not yet been performed owing to several difficulties, such as delocalization in inelastic scattering or instrumentation instabilities. Here we demonstrate atomic-column imaging of a crystal specimen using localized inelastic scattering and a stabilized scanning transmission electron microscope. The atomic columns of La, Mn and O in the layered manganite La1.2Sr1.8Mn2O7 are visualized as two-dimensional images.

Direct observation of single dopant atom in light-emitting phosphor of β-SiAlON:Eu2+

Rare-earth doped nitride attracts considerable attention because of its application as a light-emitting phosphor. The atomic site of dopants in a crystal is important for the development of advanced materials. Here, we directly observe a single Eu dopant atom in phosphor β-SiAlON using scanning transmission electron microscopy (STEM). A STEM annular dark-field image reveals that a Eu dopant exists in a continuous atomic channel in a β-Si3N4 structure. The image contrast of the single Eu dopant is confirmed based on the comparison of experimental and simulation results.

Carbon nanofilm with a new structure and property

We have prepared a carbon film of nanometer thickness, which is called here a carbon nanofilm (CNF), starting from the oxidation of graphite. The structure and thickness of the CNF are determined by high-resolution transmission electron microscopy and electron diffraction. The structure is of a new type (S.G.: P3), in which carbon six-membered-ring planes are stacked with the sequence of ...AA.... According to electron energy loss spectroscopy, a substantial amount of oxygen is detected but the molar ratio of oxygen to carbon is possibly decreased to less than 0.1. The CNF changes from an insulator to a semiconductor when reduced on heating at 250°C.

Towards control of the size and helicity of skyrmions in helimagnetic alloys by spin-orbit coupling

K. Shibata, X. Z. Yu, T. Hara, D. Morikawa, N. Kanazawa, K. Kimoto, S. Ishiwata, Y. Matsui and Y. Tokura 1 Department of Applied Physics and Quantum-Phase Electronics Center (QPEC), University of Tokyo, Tokyo 113-8656, Japan, 2 RIKEN Center for Emergent Matter Science (CEMS), Wako 351-0198, Japan, 3 Surface Physics and Structure Unit, National Institute for Materials Science, Tsukuba 305-0044, Japan.Chirality--that is, left- or right-handedness--is an important concept in a broad range of scientific areas. In condensed matter, chirality is found not only in molecular or crystal forms, but also in magnetic structures. A magnetic skyrmion is a topologically stable spin vortex structure, as observed in chiral-lattice helimagnets, and is one example of such a structure. The spin swirling direction (skyrmion helicity) should be closely related to the underlying lattice chirality via the relativistic spin-orbit coupling. Here, we report on the correlation between skyrmion helicity and crystal chirality in alloys of helimagnets Mn(1-x)Fe(x)Ge with varying compositions by Lorentz transmission electron microscopy and convergent-beam electron diffraction over a broad range of compositions (x = 0.3-1.0). The skyrmion lattice constant shows non-monotonous variation with composition x, with a divergent behaviour around x = 0.8, where the correlation between magnetic helicity and crystal chirality changes sign. This originates from continuous variation of the spin-orbit coupling strength and its sign reversal in the metallic alloys as a function of x. Controllable spin-orbit coupling may offer a promising way to tune skyrmion size and helicity.

Magnetic stripes and skyrmions with helicity reversals

It was recently realized that topological spin textures do not merely have mathematical beauty but can also give rise to unique functionalities of magnetic materials. An example is the skyrmion—a nano-sized bundle of noncoplanar spins—that by virtue of its nontrivial topology acts as a flux of magnetic field on spin-polarized electrons. Lorentz transmission electron microscopy recently emerged as a powerful tool for direct visualization of skyrmions in noncentrosymmetric helimagnets. Topologically, skyrmions are equivalent to magnetic bubbles (cylindrical domains) in ferromagnetic thin films, which were extensively explored in the 1970s for data storage applications. In this study we use Lorentz microscopy to image magnetic domain patterns in the prototypical magnetic oxide–M-type hexaferrite with a hint of scandium. Surprisingly, we find that the magnetic bubbles and stripes in the hexaferrite have a much more complex structure than the skyrmions and spirals in helimagnets, which we associate with the new degree of freedom—helicity (or vector spin chirality) describing the direction of spin rotation across the domain walls. We observe numerous random reversals of helicity in the stripe domain state. Random helicity of cylindrical domain walls coexists with the positional order of magnetic bubbles in a triangular lattice. Most unexpectedly, we observe regular helicity reversals inside skyrmions with an unusual multiple-ring structure.

Spontaneous Formation of Wurzite-CdS/Zinc Blende-CdTe Heterodimers through a Partial Anion Exchange Reaction

Ion exchange of ionic semiconductor nanoparticles (NPs) is a facile method for the synthesis of type-II semiconductor heterostructured NPs with staggered alignment of band edges for photoelectric applications. Through consideration of the crystallographic orientation and strain at the heterointerface, well-designed heterostructures can be constructed through ion exchange reactions. Here we report the selective synthesis of anisotropically phase-segregated cadmium sulfide (CdS)/ cadmium telluride (CdTe) heterodimers via a novel anion exchange reaction of CdS NPs with an organic telluride precursor. The wurtzite-CdS/zinc blende-CdTe heterodimers in this study resulted from spontaneous phase segregation induced by the differences in the crystal structures of the two phases, accompanying a centrosymmetry breaking of the spherical CdS NPs. The CdS/CdTe heterodimers exhibited photoinduced spatial charge separation because of their staggered band-edge alignment.

Coordination and interface analysis of atomic-layer-deposition Al2O3 on Si(001) using energy-loss near-edge structures

The coordination and interface of Al2O3 formed on Si(001) by atomic layer deposition (ALD) were studied using electron energy-loss spectroscopy in a transmission electron microscope. Al energy-loss near-edge structures (ELNESs) were interpreted using first-principles calculations. The Al L23 ELNESs show two peaks at 78.2 and 79.7 eV, which originate from tetrahedrally and octahedrally coordinated aluminum, respectively. The depth profile of coordination in ALD Al2O3/Si was investigated. While both tetrahedrally and octahedrally coordinated Al atoms exist in the ALD Al2O3, the former is dominant near the interface. Aluminum silicate was detected near the interface, and it may cause the difference in aluminum coordination.