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51.
Shiro Kubuki Hitomi Masuda Koken Matsuda Kazuhiko Akiyama Ayuko Kitajo Shigeto Okada Péter Zsabka Zoltán Homonnay Ernõ Kuzmann Tetsuaki Nishida 《Hyperfine Interactions》2014,226(1-3):765-770
Charge-discharge capacity and cyclicity of lithium ion battery (LIB) was evaluated in which 15Li2O·10Fe2O3·xSnO2·5P2O5·(70–x)V2O5 glass (x?=?0 and 20 in mol%, abbreviated as xLFSPV) was used as a cathode. A local structure of xLFSPV glass before and after charging was investigated by 57Fe- and 119Sn-Mössbauer spectroscopies. 57Fe-Mössbauer spectrum of xLFSPV glass with ‘x’ of 20 was composed of a doublet with isomer shift (δ) of 0.35±0.02 mm s???1 and quadrupole splitting (Δ) of 0.88±0.03 mm s???1 due to distorted FeIIIO4 tetrahedra. 119Sn-Mössbauer spectrum of this glass consisted of a doublet with δ of 0.08±0.01 and Δ of 0.52±0.01 mms???1 due to distorted SnVIO6 octahedra. After discharging the battery from 4.5 to 1.0 V, larger δ of 0.40±0.03 mm s???1 and Δ of 0.94±0.04 mm s???1 were obtained, indicating that both iconicity of Fe-O bonds and local distortion of FeIIIO4 tetrahedra were increased. On the contrary, identical δ of 0.09±0.01 mm s???1 and Δ of 0.50±0.01 mm s???1 were observed in the 119Sn-Mössbauer spectrum of 20LFSPV glass after the discharge, indicating that chemical environment of SnIVO6 octahedra was not affected after the discharge. Charge-discharge curve of LIB containing 20LFSPV glass as a cathode active material recorded under the current density of 8.3 mA g???1 (0.011 mA cm???2) between 1.0 and 4.5 V showed a large initial charge capacity of 431.1 mAh g???1 and discharge capacity of 382.3 mAh g???1, respectively. These results indicate that 20LFSPV glass could be a new cathode active material for LIB. 相似文献
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Kohei Takechi Kyo Yoshida Toshihico Arimitsu 《Central European Journal of Physics》2012,10(3):684-691
Numerical simulations of two-dimensional granular flows under uniform mean shear and external body torque were performed following
the setting of the authors’ previous study [10]. Convergence of the stresses with the increase of coarse-graining length is
investigated. Difference R between vorticity field and spin field is controlled by the external torque and the stresses for the region R > 0 is obtained as well as those for R < 0. The symmetry of the stresses under the change of the sign of R is discussed. 相似文献
56.
Shiro Kubuki Jun Iwanuma Kazuhiko Akiyama Akira Mikuni Tetsuaki Nishida 《Hyperfine Interactions》2012,211(1-3):173-180
In order to enhance the mechanical strength of Hagi Porcelain (Hagiyaki), one of the oldest and famous potteries in Japan, new preparation condition was examined. Tempered Hagi porcelain, denominated as ‘Hagi Porcelain B’, was prepared with the Porcelain clay originating from Daido district, Yamaguchi Prefecture, Japan. Structural change of ‘Hagi Porcelain B’ was investigated by means of 57Fe-Mössbauer spectroscopy, X-ray diffractometry (XRD) and three-point bending test. Mechanical strength of the ‘original Hagi Porcelain B’ was estimated to be 43.1 MPa by means of the three-point bending test, while much larger value of 104.5 MPa could be achieved when tempered by a chemical modification. Mössbauer spectrum of the ‘original Hagi porcelain B’ was composed of a paramagnetic doublet and a magnetic sextet due to Fe(III) of γ-Fe2O3(maghemite), while only one paramagnetic doublet due to to octahedral Fe(II)O6 was observed for the ‘tempered Hagi Porcelain B’ with isomer shift and quadrupole splitting values of 1.13 and 2.15 mm s?1, respectively. It is considered that the absence of magnetic phase causes an increase of the mechanical strength because the maghemite phase has a defect spinel structure. These results indicate that mechanical strength of the ‘Hagi porcelain B’ could be enhanced by controlling the sintering condition. 相似文献
57.
Dr. Tatsuya Nishimaru Dr. Kohei Eto Dr. Keita Komine Prof. Dr. Jun Ishihara Prof. Dr. Susumi Hatakeyama 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(33):7927-7934
The first total synthesis of lajollamycin B, a structurally novel nitro-tetraene spiro-β-lactone/γ-lactone antibiotic, is described. The convergent synthesis involves the construction of the C8′–C11′ nitrodienylstannane and its coupling with the segment prepared from the C1′–C7′ ω-iodoheptadienoic acid and the right-hand heterocyclic fragment, which has been utilized for our previous syntheses of oxazolomycin A. The revision of the geometry of the terminal Δ10′, 11′-double bond from E to Z is also described for the structure of natural lajollamycin B. 相似文献
58.
Shunsuke Shimo Dr. Kohei Takahashi Prof. Nobuharu Iwasawa 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(15):3790-3794
A new chiral probe molecule for mono-alcohols is developed by using 1,2-dihydro-1-hydroxy-2,3,1-benzodiazaborine (DAB) bearing an acridine moiety 1 . In the presence of mono-alcohols, DAB 1 forms borate 2 by boronic ester formation, followed by coordination of the acridine moiety to the boron atom. Borate 2 has a chiral center on the boron atom and works as a stereodynamic circular dichroism (CD) probe molecule for chiral mono-alcohols based on the π–π interaction between the acridine moiety and the carbon–carbon unsaturated moiety on mono-alcohols. 相似文献
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