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排序方式: 共有260条查询结果,搜索用时 15 毫秒
1.
Motofumi Suzuki Kohei Kinoshita Shinji Jomori Hidehiko Harada Kaoru Nakajima Kenji Kimura 《Thin solid films》2007,515(22):8281-8284
The initial stage of iron silicide formation is investigated by high-resolution Rutherford backscattering spectroscopy. During the Fe deposition on Si(001) at 470 °C, the formation of FeSi2 is confirmed by the surface peak analysis. Initially, FeSi2 grows epitaxially so that one of the major crystallographic axes is parallel to the <111> axis of the Si substrate. With increasing Fe deposition, the deviation between the major crystallographic axis of the silicide region and Si<111> increases although the electron diffraction pattern is independent of the amount of Fe deposition. Therefore, the subsurface crystallographic structure of iron silicide is transformed from a cubic-like to a low-symmetry structure. 相似文献
2.
Takashi Mitamura Hiroyuki Ogino Hidehiko Kobayashi Toshiyuki Mori Hiroshi Yamamura 《Journal of the American Ceramic Society》1993,76(8):2127-2128
Preparation of BaLa2 O4 , Ba3 ,Y4 O9 , Ba ,In2 O5 , and Ba3 Ga2 O6 powders and their sintering were investigated in Ar or air. These sintered bodies with perovskite-related structure were synthesized by reaction sintering, using mixed powders in the atomic ratios of Ba/La = 1, Ba/Y = 0.75, Ba/In = 1, and Ba/Ga = 1.5. The order-disorder transition temperatures of the BaLa2 O4 , Ba3 Y4 O9 , Ba2 In2 O5 , and Ba3 Ga2 O6 sintered bodies were 270°, 350°, 880°, and 123Oo C, respectively. It was found that the temperatures were influenced by the ionic radius of cations in B sites, and the transition temperatures decreased with increasing ionic radius. 相似文献
3.
Motoi Takahashi Toshiyuki Mori Fei Ye Ajayan Vinu Hidehiko Kobayashi John Drennan 《Journal of the American Ceramic Society》2007,90(4):1291-1294
A Pt on nano-sized CeO2 particles that in turn are supported on carbon black (CB) was synthesized using the co-impregnation method. This potential anode material for fuel cell applications was synthesized in a stepwise process. The pure CeO2 was synthesized using an ammonium carbonate precipitation method, and the Pt particles dispersed on the CeO2 in such a way that a uniform dispersion with the CB was obtained (Pt–CeO2 /CB). The electrochemical activity of the methanol (CH3 OH) oxidation reaction on the Pt–CeO2 /CB was investigated using cyclic voltammetry and chronoamperometry experimentation. The onset potential of CH3 OH oxidation reaction on the Pt–CeO2 /CB anode was shifted to a lower potential as compared with that on commercially available Pt–Ru/carbon (C) alloy anode. In addition, the activation energy of the Pt–CeO2 /CB anode was much lower than that of the Pt–Ru/C alloy anode. Moreover, the current density of the Pt–CeO2 /CB anode was much higher than that of the Pt–Ru/C alloy anode at temperatures between 28° and 60°C. These results suggest that the anode performance of the Pt–CeO2 /CB anode at the operating temperature of typical fuel cells (80°C) is superior to that of the more usual Pt–Ru/C alloy anode. Importantly, the rare metal, Ru, is not required in the present anode material and the amount of Pt required is also significantly reduced. As a consequence, we report a promising candidate Pt–CeO2 /CB composite anode for application in the development of direct methanol fuel cells. 相似文献
4.
Hidehiko Kobayashi Kenichi Shimosaka Miki Saitoh Takashi Mitamura 《Journal of the American Ceramic Society》1993,76(9):2389-2392
We investigated the conditions for low-temperature synthesis of ZrC fine powder from ZrO2 –Mg–CH4 . The synthesis utilizes a thermite-type reaction, with Mg as the reducing agent, and a reaction between Mg and CH4 gas as a carbon source. The Mg/ZrO2 molar ratio as well as the heating rate were varied. Because C can be continuously fed into the reaction group by the cyclic reaction of Mg through the formation and decomposition of Mg2 C3 (2Mg + 3CH4 → Mg2 C3 + 6H2 → 2Mg + 3C), a molar ratio of 2.2 for Mg/ZrO2 was sufficient for the synthesis of single-phase ZrC. ZrC powders were synthesized under the following conditions: Mg/ZrO2 molar ratio = 2.2, heating rate = 20°C/min, and temperature maintained at 750°C for 30 min. The amount of reaction heat produced in the reduction reaction of ZrO2 by Mg depended on the Mg/ZrO2 molar ratio, specifically, the amount of ZrO2 contained. Moreover, the cyclic reaction of Mg-Mg2 C3 –Mg was influenced by the amount of reaction heat described above and by the heating rate. The ZrC fine powder showed little aggregation and high dispersibility. 相似文献
5.
It is of great importance in propene polymerization to control molecular weight and molecular weight distribution as well as isotacticity. Propene polymerization was carried out with an isospecific MgCl2/TiCl4-Cp2TiMe2 catalyst in the presence of various kinds of external Lewis bases. It was found that the molecular weight distribution of the isotactic polymer could be controlled while retaining high activity, high isospecificity and high molecular weight only by changing the kind and/or amount of the Lewis bases. © 1997 Elsevier Science Ltd. 相似文献
6.
Kazushi Yawata Daisuke Ito Hiroki Ikegami Hidehiko Ishimoto Hiroshi Fukuyama 《Journal of Low Temperature Physics》1998,113(5-6):769-774
Experimental methods and preliminary results of high-precision measurements of the
3
He melting curve in high magnetic fields have been described. The purpose of this work is twofold. One is to establish a reliable millikelvin temperature scale in high fields (T 10 mK, B 15 T), The other is to investigate a high field region of the magnetic phase diagram of solid
3
He by measuring the melting pressure down to temperatures below 1 mK. Besides the two superfluid transitions, the phase transition temperatures between the spin ordered solid and the paramagnetic solid, T
HFP
, were determined at B = 12 and 10 T with good accuracy, which is an extension of previous measurements up to 8 T. The present T
HFP
(B) line can not be scaled to that at a higher density with a single Grüneisen parameter, indicating a variation of density dependencies of the multiple-spin exchange interactions. 相似文献
7.
Takeda K Mori H Yamaguchi A Ishimoto H Nakamura T Kuriki S Hozumi T Ohkoshi S 《The Review of scientific instruments》2008,79(3):033909
We have developed a high temperature superconductor (HTS) micrometer-sized dc superconducting quantum interference device (SQUID) magnetometer for high field and high temperature operation. It was fabricated from YBa2Cu3O7-delta of 92 nm in thickness with photolithography techniques to have a hole of 4x9 microm2 and 2 microm wide grain boundary Josephson junctions. Combined with a three dimensional magnetic field coil system, the modulation patterns of critical current Ic were observed for three different field directions. They were successfully used to measure the magnetic properties of a molecular ferrimagnetic microcrystal (23x17x13 microm3), [Mn2(H2O)2(CH3COO)][W(CN)8]2H2O. The magnetization curve was obtained in magnetic field up to 0.12 T between 30 and 70 K. This is the first to measure the anisotropy of hysteresis curve in the field above 0.1 T with an accuracy of 10(-12) J T(-1) (10(-9) emu) with a HTS micro-SQUID magnetometer. 相似文献
8.
Effects of Gd Substitution on Sintering and Optical Properties of Highly Transparent (Y0.95−xGdxEu0.05)2O3 Ceramics
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Bin Lu Ji‐Guang Li Hidehiko Tanaka Xudong Sun Yoshio Sakka 《Journal of the American Ceramic Society》2015,98(8):2480-2487
Highly transparent (Y0.95?xGdxEu0.05)2O3 (x = 0.15–0.55) ceramics have been fabricated by vacuum sintering at the relatively low temperature of 1700°C for 4 h with the in‐line transmittances of 73.6%–79.5% at the Eu3+ emission wavelength of 613 nm (~91.9%–99.3% of the theoretical transmittance of Y1.34Gd0.6Eu0.06O3 single crystal), whereas the x = 0.65 ceramic undergoes a phase transformation at 1650°C and has a transparency of 53.4% at the lower sintering temperature of 1625°C. The effects of Gd3+ substitution for Y3+ on the particle characteristics, sintering kinetics, and optical performances of the materials were systematically studied. The results show that (1) calcining the layered rare‐earth hydroxide precursors of the ternary Y–Gd–Eu system yielded rounded oxide particles with greatly reduced hard agglomeration and the particle/crystallite size slightly decreases along with increasing Gd3+ incorporation; (2) in the temperature range 1100°C–1480°C, the sintering kinetics of (Y0.95?xGdxEu0.05)2O3 is mainly controlled by grain‐boundary diffusion with similar activation energies of ~230 kJ/mol; (3) Gd3+ addition promotes grain growth and densification in the temperature range 1100°C–1400°C; (4) the bandgap energies of the (Y0.95?xGdxEu0.05)2O3 ceramics generally decrease with increasing x; however, they are much lower than those of the oxide powders; (5) both the oxide powders and the transparent ceramics exhibit the typical red emission of Eu3+ at ~613 nm (the 5D0→7F2 transition) under charge transfer (CT) excitation. Gd3+ incorporation enhances the photoluminescence and shortens the fluorescence lifetime of Eu3+. 相似文献
9.
Chikara Tsutsumi Ryouji Watanabe Ayaka Tokumaru Nao Kuwaoka Yuushou Nakayama Takeshi Shiono 《应用聚合物科学杂志》2016,133(39)
Synthetic l ‐lactide random copolymers can be employed as controlled release materials when prepared using supercritical carbon dioxide (scCO2), since they are biodegradable via hydrolysis. To determine the effects of thermal properties on polymer performance following scCO2 processing, three types of poly(l ‐lactide) having different properties were assessed. The Tm of one poly(l ‐lactide) sample (H‐100) was found to be approximately 170 °C over the processing pressure range from 8 to 18 MPa, while a second sample (H‐440) also showed a constant value of approximately 152 °C. In contrast, the poly(l ‐lactide) REVODE exhibited a Tm of 146 °C prior to processing but a higher value of 147 °C following treatment at 8 MPa. Unlike the H‐100 and H‐440, the Tm value of the REVODE tended to decrease with increasing pressure. The Tg values increased greatly under mild conditions of 8 MPa pressure and a temperature of 40 °C. In particular, the Tg values for the H‐440 and REVODE increased by 4 °C and 5 °C, respectively. All Tg values were lowest at 12 MPa and increased with increasing processing pressure, although the effect of processing temperature was minimal. The Χc DSC of the H‐100 was 18% initially but increased to 20% upon scCO2 processing at 40 °C and 14 MPa, and showed further increases at higher processing temperatures. Although the relationship between processing temperature and Χc DSC values for the H‐440 showed the same trend as observed with the H‐100, a different trend was seen for the REVODE. The Χc XRD values obtained from the XRD analyses differed from the values generated by DSC analysis, and showed a maximum degree of crystallinity following processing at 80 °C both with and without scCO2 treatment. ATR FT‐IR analyses identified peaks due to semicrystalline regions in poly(l ‐lactide) samples treated with scCO2, even when applying low temperatures. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44006. 相似文献
10.
Xin Xu Toshiyuki Nishimura Qing Huang Rong-Jun Xie Naoto Hirosaki Hidehiko Tanaka 《Journal of the American Ceramic Society》2007,90(12):4047-4049
A feasible doping strategy is introduced to synthesize Eu2+ -doped α-Si3 N4 nanowires coated with a thin BN film. The nanowires were characterized by X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, and a fluorescence spectrophotometer. The Eu2+ -doped α-Si3 N4 nanowires emitted strong yellow light, which is related to the 4 f 6 5 d –4 f 7 transition of Eu2+ , upon a broad excitation wavelength range between 250 and 450 nm. The obtained nanowires provided a potential candidate for application in optical nanodevices, as well as in white LEDs. 相似文献