Evaluation of microscopic structural randomness in SiO2 by analysis of photoluminescence decay profiles

Microscopic structural randomness in SiO₂, a typical electrical insulating material, was evaluated by observing the decay profile of the photoluminescence due to oxygen vacancies (≡Si-Si≡). As samples with different degrees of randomness, an ion-implanted thermal SiO₂ film, SiO₂ films formed by plasma-enhanced chemical vapor deposition of tetraethoxysilane with and without doped fluorine, a buried oxide film prepared by SIMOX (separation by ion-implanted oxygen), and a bulk silica glass prepared by the soot-remelting method were tested. By analyzing the decay profile with a stretched exponential function, it was found that the deviation of the decay profile from a single exponential function is larger in the samples whose infrared absorption properties and HF etch rate suggest greater structural randomness. © 1997 Scripta Technica, Inc. Electr Eng Jpn, 119 (3): 1–6, 1997     

Analysis of counter ions of cyanine dye in Langmuir–Blodgett films by PIXE

Langmuir–Blodgett (LB) films of 1-methyl-1^′-octadecylquinocyanine bromide, iodide and perchlorate were prepared from subphases containing NaClO₄, KBr and/or KI. Each sample consists of an arachidic cadmium layer and about 100 cyanine dye layers on a Si substrate. Anions incorporated into the film as counter ions from the subphase were analyzed by particle induced X-ray emission (PIXE) using a 2.5 MeV He²⁺ beam. It was found that the dissociation of the cationic dye molecule in the monolayer at the air/water interface leads to the substitution of counter anions of the dye molecules, and the subsequent incorporation of the counter anions in the LB films. Some of the dissociation constants of cyanine halide dyes were estimated.     

Substituent-Induced Supramolecular Aggregates of Edge Functionalized Nanographenes

Precisely controlled molecular assemblies often display intriguing morphologies and/or functions arising from their structures. The application of the concept of the self-assembly for controlling the aggregation of nanographenes (NGs) is challenging. The title NGs are those carrying both long alkyl chains and tris(phenylisoxazolyl)benzene (TPIB) on the edge. The former group secures the affinity of NGs for organic solvents, and the latter group drives the 1D arrangement of NGs through the interactions between the TPIB units. The concentration-dependent and temperature variable ¹H NMR, UV–vis, and PL spectra demonstrate the aggregation of NGs in 1,2-dichloroethane, and the aggregation is controllable by the regulation of the solvent polarity. AFM images give the stacked structures of the NGs, and these aggregates turn out to be network polymeric structures at a high concentration. These observations demonstrate that the synergy of the face-to-face interactions between the surfaces and the interactions between the TPIB units are effective for controlling the self-assembly of the NGs.     

Performance Evaluation of Magnetostrictive Small Wind Turbines Using Fe–Co Alloy–Based Clad Sheets

In this study, the Fe–Co alloy is combined with cobalt ferrite (CoFe₂O₄) and nickel (Ni) to form Fe–Co/CoFe₂O₄ and Fe–Co/Ni clad sheets and their energy-harvesting performance is evaluated. The Fe–Co/CoFe₂O₄ clad sheet exhibits an output voltage of 4.229 mV and an output power of 6.89 nW at a wind speed of 10 m s⁻¹. The energy-harvesting performance of both these clad sheets cannot be quantitatively compared owing to their different thicknesses, which result in varying volume and distance from the neutral plane. Nevertheless, the values of output voltage and power for Fe–Co/CoFe₂O₄ are higher than those for Fe–Co/Ni (2.107 mV and 0.294 nW).     

One-step fabrication of Li2TiO3 ceramic pebbles using pulsed YAG laser

A large amount of Li-containing ceramic breeder pebbles is packed in the solid breeding blanket of a nuclear fusion reactor. Several pebble fabrication technologies have been proposed in previous studies, including wet process, emulsion method, extrusion spheronization, additive manufacturing, and melt process. However, a simple, energy-effective, and scalable fabrication technology remains to be developed for the automated mass production and reprocessing of used radioactive pebbles post-operation. Selective laser melting potentially enables the quick and automated fabrication of breeder pebbles. Herein, we employ a high-power density pulse laser to produce ceramic breeder pebbles. A pulsed YAG laser was irradiated over a lithium metatitanate (Li₂TiO₃) powder bed in air, and the corresponding temperature was monitored using fiber-type infrared pyrometers. Spherical Li₂TiO₃ pebbles were successfully fabricated in a single step with an average diameter of 0.78 ± 0.13 μm and the sintering density of 87.4% ± 5.6% (input power: 7.9 J/pulse). The irradiated Li₂TiO₃ powder melted and turned spherical under surface tension and rapidly solidified, resulting in uniaxial fine grains and a decrease in the degree of long-range cation ordering.     

Bandgap Tunable Oxynitride LaNb2O7–xNx Nanosheets

Bandgap tunable lanthanum niobium oxynitride [LaNb₂O_7-xN_x]^(1+x)− nanosheet is prepared by the delamination of a Ruddlesden−Popper phase perovskite oxynitride via ion−exchange and two−step intercalation processes. The lanthanum niobium oxynitride nanosheets have a homogeneous thickness of 1.6 nm and exhibit a variety of chromatic colors depending on the nitridation temperature of the parent-layered oxynitride. The bandgap energy of the nanosheets is determined by ultraviolet photoemission spectroscopy, Mott–Schottky, and photoelectrochemical measurements and is found to be tunable in the range of 2.03–2.63 eV. Furthermore, the oxide/oxynitride superlattice structures are fabricated by face−to−face stacking of 2D crystals using oxynitride [LaNb₂O_7-xN_x]^(1+x)− and oxide [Ca₂Nb₃O₁₀]⁻ nanosheets as building blocks. Moreover, the superlattices-like restacked oxynitride/oxide nanosheets hybrid exhibits unique proton conductivity and dielectric properties strongly influenced by the oxynitride nanosheets and enhanced photocatalytic activity under visible light irradiation.     

Effects of nitridation temperature on properties of sintered reaction-bonded silicon nitride

We prepared sintered reaction-bonded silicon nitride ceramics by using yttria and magnesia as sintering additives and evaluated effects of the nitridation temperature on their microstructure, bending strength, fracture toughness, and thermal conductivity. The effects of the nitridation temperature were large, but different depending on the property. The ratio of β-phase in the nitrided compacts significantly increased with increasing the nitridation temperature, whereas their microstructures had no clear difference. Although the bending strength varied, it maintains a high value of 800 MPa. Fracture toughness was almost constant regardless the temperature. The thermal conductivity improved as the β-phase in the nitrided compact increases. This resulted in a decrease of the lattice oxygen content and increase of the thermal conductivity. Therefore, elevating the nitridation temperature and consequently the β-phase ratio should be a promising strategy for achieving compatibly high strength and high thermal conductivity, which are generally known to be in a trade-off relationship.