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排序方式: 共有322条查询结果,搜索用时 15 毫秒
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I. Tsukada M. Hanawa Seiki Komiya A. Ichinose T. Akiike Y. Imai A. Maeda 《Physica C: Superconductivity and its Applications》2011,471(21-22):625-629
The Hall effect is investigated in thin-film samples of iron–chalcogenide superconductors in detail. The Hall coefficient (RH) of FeTe and Fe(Se1–xTex) exhibits a similar positive value around 300 K, indicating that the high-temperature normal state is dominated by hole-channel transport. FeTe exhibits a sign reversal from positive to negative across the transition to the low-temperature antiferromagnetic state, indicating the occurrence of drastic reconstruction in the band structure. The mobility analysis using the carrier density theoretically calculated reveals that the mobility of holes is strongly suppressed to zero, and hence the electric transport looks to be dominated by electrons. The Se substitution to Te suppresses the antiferromagnetic long-range order and induces superconductivity instead. The similar mobility analysis for Fe(Se0.4Te0.6) and Fe(Se0.5Te0.5) thin films shows that the mobility of electrons increases with decreasing temperature even in the paramagnetic state, and keeps sufficiently high values down to the superconducting transition temperature. From the comparison between FeTe and Fe(Se1–xTex), it is suggested that the coexistence of ‘itinerant’ carriers both in electron and hole channels is indispensable for the occurrence of superconductivity. 相似文献
3.
H. Matsui K. Tsukada T. Tsuchiya M. Sohma I. Yamaguchi T. Kumagai T. Manabe 《Physica C: Superconductivity and its Applications》2011,471(21-22):960-962
We have studied the crystallization time dependence of the epitaxial YBCO films (t = 0.8 μm) grown on CeO2-buffered SrTiO3 substrates by fluorine-free metal–organic deposition using uv-lamp irradiation (uv-MOD). As increasing the time (T0) for heat treatment at the reaction temperature (760 °C) from 0 to 90 min, Jc and the YBCO 0 0 l XRD intensity are steeply increased and reach their maximum values at T0 = 10 min. This suggests that the heat treatment required for YBCO crystallization is significantly shortened in uv-MOD compared to conventional all-pyrolytic F-free MOD processes, which consume T0 = 90–150 min for crystallizing 0.4–0.5-μm-thick films. Scanning electron microscope measurement revealed a drastic change in surface morphology between T0 = 8 and 10 min, showing a good correspondence to the Jc and XRD data which suggest that the epitaxial growth reaches the film surface at the very early stage in the heat treatment. 相似文献
4.
Development of a New Benzylating Reagent Spontaneously Releasing Benzyl Cation Equivalents at Room Temperature 下载免费PDF全文
Dr. Kohei Yamada Yuichi Tsukada Yukiko Karuo Dr. Masanori Kitamura Prof. Dr. Munetaka Kunishima 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(38):12274-12278
A new O‐benzylating reagent, that is, 4‐(4,6‐diphenoxy‐1,3,5‐triazin‐2‐yl)‐4‐benzylmorpholinium trifluoromethanesulfonate (DPT‐BM), has been developed. Benzyl cation equivalents are generated from DPT‐BM by dissolving the compound in a solvent at room temperature under non‐acidic conditions. The benzylation of various alcohols by using a combination of DPT‐BM and magnesium oxide provided the benzyl ethers in good yields. 相似文献
5.
Takahiro Gunji Kengo Hirama Satoru Tsukada Yoshimoto Abe 《Journal of Sol-Gel Science and Technology》2014,72(1):80-84
An organic–inorganic hybrid was prepared by simply mixing a fullerene derivative with polymethoxysiloxane. First, C60 was subjected to a radical addition reaction with 4,4′-azobis(4-cyanovaleric acid) to provide a C60 derivative. Polymethoxysiloxane was prepared by a controlled hydrolytic condensation of tetramethoxysilane. These two compounds were mixed and heated to provide hybrid bulk body. The hybrid bulk body showed high mechanical strength and elastic modulus compared with polymethoxysiloxane or the C60/polymethoxysiloxane hybrid. The formation of a dense siloxane network was established by a homogeneous mixing of the C60 derivative with polymethoxysiloxane. 相似文献
6.
Naofumi Tsukada Makiko Wada Naoki Takahashi Yoshio Inoue 《Journal of organometallic chemistry》2009,694(9-10):1333-1338
Novel dinuclear palladium complexes having two isocyanide ligands were synthesized by using a binucleating ligand, N,N′-bis[2-(diphenylphsphino)phenyl]formamidinate (dpfam). The structure of [Pd2(μ-dpfam)(tert-BuNC)2]Cl was confirmed by X-ray analysis, showing that the Pd–Pd bond length of 2.5824(3) Å falls well within the range of those for known dipalladium complexes having the edge-sharing structure and two isocyanides coordinate to palladium in almost parallel and in close proximity. The dinuclear complex [Pd2(μ-dpfam)(tert-BuNC)2]PF6 served as catalyst for pyrrole formation from tert-butylisocyanide and various alkynes. 相似文献
7.
K. Hirose M. Ejima T. Fujibayashi Y. Fujii K. Futatsukawa O. Hashimoto T. Ishikawa S. Kameoka H. Kanda F. Kato S. Kinoshita T. Kinoshita T. Kon O. Konno K. Maeda A. Matsumura Y. Miura F. Miyahara H. Miyase T. Nakabayashi S.N. Nakamura H. Nomura K. Nonaka A. Ohtani Y. Okayasu M. Oyamada A. Sasaki H. Shimizu T. Takahashi T. Tamae H. Tamura T. Terasawa H. Tsubota K. Tsukada D. Uchida M. Ukai M. Wakamatsu T. Watanabe H. Yamauchi H. Yamazaki K. Yawata 《Physics letters. [Part B]》2009
8.
Tae-Ho Kim Masakazu Saito Masaya Matsuoka Shinya Tsukada Kiyohisa Wada Masakazu Anpo 《Research on Chemical Intermediates》2010,36(5):453-461
It was found that the photoelectrochemical performance and photocatalytic activity of rod-type TiO2 electrodes were affected by various post-calcination treatments, for example, calcination in NH3 or under vacuum. Post-calcination treatment in NH3 at 773 K was particularly effective in increasing the photoelectrochemical performance and photocatalytic activity of rod-type
TiO2 electrodes. A unique photoelectrochemical circuit was constructed by connecting a rod-type TiO2 electrode to a Pt electrode through a silicon solar cell in which the negative bias was applied on the rod-type TiO2 electrode. It was found that the photoelectrochemical circuit can effectively oxidize ethanethiol in water into CO2. 相似文献
9.
10.
Tadashi Nishio Rie Suzuki Yuko Tsukada Hideko Kanazawa Teruo Okano Takako Miyabe-Nishiwaki 《Journal of chromatography. A》2009,1216(44):7427-7432
A new method for the quantitative analysis of monkey serum propofol, which is widely used as an anaesthetic agent, was developed by utilizing a temperature-responsive polymer of N-isopropylacrylamide (NIPAAm) and butyl methacrylate (BMA) as the stationary phase of HPLC–fluorescence detection. This poly(NIPAAm-co-BMA) copolymer undergoes a reversible phase transition from a hydrophilic to a hydrophobic microstructure when triggered by change in the temperature. Also this chromatographic system is possible to separate the analytes by using only water as a mobile phase. A pretreatment of the serum (80 μL) was only solid-phase extraction, and the recovery rate of propofol and internal standard was more than 77%, respectively. This method covered the calibration range from 0.5 μg/mL to 10 μg/mL and allowed a reproducible quantification of the serum propofol in administrated monkey serum. The intra- and inter-assay relative standard deviations were less than 14.1%. In addition, there was good relationship of the quantification values between the developed method and the widely used reversed-phase HPLC method. Our developed method has proven to be useful for a simple analysis of propofol in clinical practice, because the avoidance of complicated mobile phase preparation was possible, and only temperature changing could regulate the retention time of the analyte. In addition, by using water instead of fossil fuel, it is the ideal analytical method according to green chemistry. 相似文献