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Oba, Yojiro; Morooka, Satoshi; Oishi, Kazuki*; Suzuki, Junichi*; Tsuchiyama, Toshihiro*
ISIJ International, 62(1), p.173 - 178, 2022/01
Fujita, Yoshitaka; Seki, Misaki; Namekawa, Yoji*; Nishikata, Kaori; Daigo, Fumihisa; Ide, Hiroshi; Tsuchiya, Kunihiko; Sano, Tadafumi*; Fujihara, Yasuyuki*; Hori, Junichi*; et al.
KURNS Progress Report 2020, P. 136, 2021/08
no abstracts in English
Miura, Daisuke*; Kumada, Takayuki; Sekine, Yurina; Motokawa, Ryuhei; Nakagawa, Hiroshi; Oba, Yojiro; Ohara, Takashi; Takata, Shinichi; Hiroi, Kosuke; Morikawa, Toshiaki*; et al.
Journal of Applied Crystallography, 54(2), p.454 - 460, 2021/04
Times Cited Count:0 Percentile:0.02(Chemistry, Multidisciplinary)We developed a spin-contrast-variation neutron powder diffractometry technique that extracts the structure factor of hydrogen atoms, namely, the contribution of hydrogen atoms to a crystal structure factor. Crystals of L-glutamic acid were dispersed in a dpolystyrene matrix containing 4-methacryloyloxy-2,2,6,6,-tetramethyl-1-piperidinyloxy (TEMPO methacrylate) to polarize their proton spins dynamically. The intensities of the diffraction peaks of the sample changed according to the proton polarization, and the structure factor of the hydrogen atoms was extracted from the proton-polarization dependent intensities. This technique is expected to enable analyses of the structures of hydrogen-containing materials that are difficult to determine with conventional powder diffractometry.
Fujita, Yoshitaka; Seki, Misaki; Namekawa, Yoji*; Nishikata, Kaori; Kato, Yoshiaki; Sayato, Natsuki; Tsuchiya, Kunihiko; Sano, Tadafumi*; Fujihara, Yasuyuki*; Hori, Junichi*; et al.
KURNS Progress Report 2019, P. 157, 2020/08
no abstracts in English
Fujita, Yoshitaka; Seki, Misaki; Namekawa, Yoji*; Nishikata, Kaori; Kimura, Akihiro; Shibata, Akira; Sayato, Natsuki; Tsuchiya, Kunihiko; Sano, Tadafumi*; Fujihara, Yasuyuki*; et al.
KURNS Progress Report 2018, P. 155, 2019/08
no abstracts in English
Taminato, So*; Hirayama, Masaaki*; Suzuki, Kota*; Kim, K.-S.*; Tamura, Kazuhisa; Kanno, Ryoji*
Journal of Physical Chemistry C, 122(29), p.16607 - 16612, 2018/07
Times Cited Count:6 Percentile:37.83(Chemistry, Physical)Lithium-rich layered rocksalt oxides are promising cathode materials for lithium-ion batteries. We investigate the effects of surface modification by amorphous LiPO
on the structures and electrochemical reactions in the surface region of an epitaxial Li
RuO
(010) film electrode. Structural characterization using SXRD, HAXPES, and NR shows that surface modification by Li
PO
resulted in the partial substitution of P for Li in the surface region of Li
RuO
. The modified (010) surface exhibits better rate capability at 20 C compared to the unmodified surface.
surface XRD confirmed that highly reversible structural changes occurred at the modified surface during lithium (de)intercalation. These results demonstrate that this surface modification stabilizes the crystal structure in the surface region, and it can improve the rate capability of lithium-rich layered rocksalt oxide cathodes.
Suzuki, Yoshitaka; Kitagawa, Tomoya*; Namekawa, Yoji*; Matsukura, Minoru*; Nishikata, Kaori; Mimura, Hitoshi*; Tsuchiya, Kunihiko
Transactions of the Materials Research Society of Japan, 43(2), p.75 - 80, 2018/04
no abstracts in English
Nakajima, Kenji; Kawakita, Yukinobu; Ito, Shinichi*; Abe, Jun*; Aizawa, Kazuya; Aoki, Hiroyuki; Endo, Hitoshi*; Fujita, Masaki*; Funakoshi, Kenichi*; Gong, W.*; et al.
Quantum Beam Science (Internet), 1(3), p.9_1 - 9_59, 2017/12
The neutron instruments suite, installed at the spallation neutron source of the Materials and Life Science Experimental Facility (MLF) at the Japan Proton Accelerator Research Complex (J-PARC), is reviewed. MLF has 23 neutron beam ports and 21 instruments are in operation for user programs or are under commissioning. A unique and challenging instrumental suite in MLF has been realized via combination of a high-performance neutron source, optimized for neutron scattering, and unique instruments using cutting-edge technologies. All instruments are/will serve in world-leading investigations in a broad range of fields, from fundamental physics to industrial applications. In this review, overviews, characteristic features, and typical applications of the individual instruments are mentioned.
Oba, Yojiro*; Morooka, Satoshi; Oishi, Kazuki*; Suzuki, Junichi*; Takata, Shinichi; Sato, Nobuhiro*; Inoue, Rintaro*; Tsuchiyama, Toshihiro*; Gilbert, E. P.*; Sugiyama, Masaaki*
Journal of Applied Crystallography, 50(2), p.334 - 339, 2017/04
Times Cited Count:2 Percentile:26.99(Chemistry, Multidisciplinary)Abe, Machiko*; Iba, Hideki*; Suzuki, Kota*; Minamishima, Hiroaki*; Hirayama, Masaaki*; Tamura, Kazuhisa; Mizuki, Junichiro*; Saito, Tomohiro*; Ikuhara, Yuichi*; Kanno, Ryoji*
Journal of Power Sources, 345, p.108 - 119, 2017/03
Times Cited Count:9 Percentile:44.85(Chemistry, Physical)The surface structure of the Li(Ni, Co, Mn)O electrode was studied during charge/discharge process using electrochemical methods and X-ray/Neutron scattering techniques. It was found that during charge/discharge process the coverage of spinel structure increased. The spinel structure has low electrochemical activity and is not involved in Li insertion/extraction. After the surface modification, it was found that the coverage of the spinel structure did not increase. Further, it was also found out that the Li concentration at the electrode/electrolyte interface increased.
Oba, Yojiro; Morooka, Satoshi; Oishi, Kazuki*; Suzuki, Junichi*; Tsuchiyama, Toshihiro*; Gilbert, E. P.*
Proceedings of 5th International Symposium on Steel Science (ISSS 2017), p.151 - 154, 2017/00
Small-angle neutron scattering and neutron diffraction are powerful tools to characterize microstructures in steels. Several new experimental techniques such as Bragg edge transmission analysis and energy-resolved small-angle neuron scattering have been recently developed with the opening of new-generation pulsed neutron sources. In this talk, the combined use of these diffraction and small-angle scattering techniques are discussed for the total characterization of the microstructures in steels.
Oba, Yojiro*; Morooka, Satoshi; Oishi, Kazuki*; Sato, Nobuhiro*; Inoue, Rintaro*; Adachi, Nozomu*; Suzuki, Junichi*; Tsuchiyama, Toshihiro*; Gilbert, E. P.*; Sugiyama, Masaaki*
Journal of Applied Crystallography, 49(5), p.1659 - 1664, 2016/10
Times Cited Count:9 Percentile:63.8(Chemistry, Multidisciplinary)Ikeda, Yoshimasa*; Taketani, Atsushi*; Takamura, Masato*; Sunaga, Hideyuki*; Kumagai, Masayoshi*; Oba, Yojiro*; Otake, Yoshie*; Suzuki, Hiroshi
Nuclear Instruments and Methods in Physics Research A, 833, p.61 - 67, 2016/10
Times Cited Count:29 Percentile:97.29(Instruments & Instrumentation)A compact accelerator-based neutron source has been lately discussed on engineering applications such as transmission imaging and small angle scattering as well as reflectometry. However, nobody considers using it for neutron diffraction experiment because of its low neutron flux. In this study, therefore, the neutron diffraction experiments are carried out using Riken Accelerator-driven Compact Neutron Source (RANS), to clarify the capability of the compact neutron source for neutron engineering diffraction. The diffraction pattern from a ferritic steel was successfully measured by suitable arrangement of the optical system to reduce the background noise, and it was confirmed that the recognizable diffraction pattern can be measured by the large sampling volume with 10 mm in cubic for an acceptable measurement time, i.e. 10 minutes. The minimum resolution of the 110 reflection for RANS is approximately 2.5 % at 8 s of the proton pulse width, which is insufficient to perform the strain measurement by neutron diffraction. The moderation time width at the wavelength corresponding to the 110 reflection is estimated to be approximately 30
s, which is the most dominant factor to determine the resolution. Therefore, refinements of the moderator system to decrease the moderation time are important to improve the resolution of the diffraction experiment using the compact neutron source. In contrast, the texture evolution due to plastic deformation was successfully observed by measuring a change in the diffraction peak intensity by RANS. Furthermore, the volume fraction of the austenite phase was also successfully evaluated by fitting the diffraction pattern using a Rietveld code. Consequently, RANS was proved to be capable for neutron engineering diffraction aiming for the easy access measurement of the texture and the amount of retained austenite.
Takamura, Masato*; Ikeda, Yoshimasa*; Sunaga, Hideyuki*; Taketani, Atsushi*; Otake, Yoshie*; Suzuki, Hiroshi; Kumagai, Masayoshi*; Hama, Takayuki*; Oba, Yojiro*
Journal of Physics; Conference Series, 734(Part B), p.032047_1 - 032047_4, 2016/08
Times Cited Count:4 Percentile:87.32Neutron diffraction is well known to be a useful technique for measuring a bulk texture of metallic materials taking advantage of a large penetration depth of the neutron beam. However, this technique has not been widely utilized for the texture measurement because large facilities like a reactor or a large accelerator are required in general. In contrast, RANS (Riken Accelerator-driven Compact Neutron Source) has been developed as a neutron source which can be used easily in laboratories. In this study, texture evolution in steel sheets with plastic deformation was successfully measured using RANS. The results show the capability of the compact neutron source for the analysis of the crystal structure of metallic materials, which leads us to a better understanding of plastic deformation behavior.
Taminato, So*; Hirayama, Masaaki*; Suzuki, Kota*; Tamura, Kazuhisa; Minato, Taketoshi*; Arai, Hajime*; Uchimoto, Yoshiharu*; Ogumi, Zempachi*; Kanno, Ryoji*
Journal of Power Sources, 307, p.599 - 603, 2016/03
Times Cited Count:26 Percentile:73.4(Chemistry, Physical)An epitaxial-film model electrode of LiCoO(104) was fabricated on SrRuO
(100)/Nb:SrTiO
(100) using pulsed laser deposition. The 50 nm thick LiCoO
(104) film exhibited lithium (de-)intercalation activity with a first discharge capacity of 119 mAh g
between 3.0 and 4.4 V, followed by a gradual capacity fading with subsequent charge-discharge cycles. In contrast, a 3.2 nm thick Li
PO
-coated film exhibited a higher intercalation capacity of 148 mAh g
with superior cycle retention than the uncoated film. In situ surface X-ray diffraction measurements revealed a small lattice change at the coated surface during the (de-)intercalation processes compared to the uncoated surface. The surface modification of LiCoO
by the Li
PO
coating could lead to improvement of the structural stability at the surface region during lithium (de-)intercalation at high voltage.
Kanno, Ryoji*; Hirayama, Masaaki*; Suzuki, Kota*; Tamura, Kazuhisa
Hyomen Kagaku, 37(2), p.52 - 59, 2016/02
Batteries are a key technology in today's society. Since the lithium-ion configuration has been widely accepted, significant efforts have been devoted to attain high energy and power densities to produce an excellent energy storage system without any safety issue. To improve the reliability and power characteristics of batteries, deep insights into the reactions at the electrode/electrolyte interface are necessary. The model systems with epitaxial thin-film electrodes might be suitable for understanding these reactions. The in situ techniques for directly observing surface structural changes of the electrodes have been developed for surface X-ray scattering and neutron reflectivity techniques. These techniques are reviewed and future studies on the interfacial reaction in batteries will be discussed.
Suzuki, Kota*; Hirayama, Masaaki*; Kim, K.-S.*; Taminato, So*; Tamura, Kazuhisa; Son, J.-Y.*; Mizuki, Junichiro; Kanno, Ryoji*
Journal of the Electrochemical Society, 162(13), p.A7083 - A7090, 2015/08
Times Cited Count:8 Percentile:33.81(Electrochemistry)The effects of surface coatings on LiMnO
were investigated using LiMn
O
epitaxial thin films with a thickness of 30 nm. Bare and surface-coated LiMn
O
epitaxial thin films were synthesized on SrTiO
(111) substrates using a pulsed laser deposition method. The surface coating, which was formed using the solid electrolyte Li
PO
and had a thickness of 3 nm, improved the reversibility of the electrochemical reactions undergone by the LiMn
O
epitaxial thin films. The changes induced in the surface structure were maintained during battery operation; in contrast, the bare LiMn
O
thin film exhibited structural degradation and Mn dissolution. The structural changes induced in the coated electrode and the increase in its surface stability were intrinsic effects of the Li
PO
coating and improved the electrochemical performance of the LiMn
O
thin-film electrode.
Taminato, So*; Hirayama, Masaaki*; Suzuki, Kota*; Kim, K.-S.*; Zheng, Y.*; Tamura, Kazuhisa; Mizuki, Junichiro; Kanno, Ryoji*
Journal of Materials Chemistry A, 2(34), p.17875 - 17882, 2014/11
Times Cited Count:20 Percentile:60.96(Chemistry, Physical)The surface structure of a lithium-rich layered material and its relation to intercalation properties were investigated by synchrotron X-ray surface structural analyses using LiRuO
epitaxial-film model electrodes with different lattice planes of (010) and (001). Electrochemical charge-discharge measurements confirmed reversible lithium intercalation activity through both planes, corresponding to three-dimensional lithium diffusion within the Li
RuO
. The (001) plane exhibited higher discharge capacities compared to the (010) plane under high rate operation (over 5 C). Direct observations of surface structural changes by
surface X-ray diffraction (XRD) and surface X-ray absorption near edge structure (XANES) established that an irreversible phase change occurs at the (010) surface during the first (de)intercalation process, whereas reversible structural changes take place at the (001) surface.
Hirose, Takanori; Someya, Yoji; Tanigawa, Hisashi; Suzuki, Satoshi
Yosetsu Gakkai-Shi, 83(1), p.70 - 77, 2014/01
no abstracts in English
Daido, Hiroyuki; Suzuki, Yoji; Kawachi, Tetsuya; Fukuda, Takeshi*; Nakagiri, Toshio; Kaku, Masanori*; Kubodera, Masakazu*
Optics Express (Internet), 21(23), p.28182 - 28188, 2013/11
Times Cited Count:1 Percentile:7.96(Optics)We describe the direct measurement of actual transmittance of sodium samples with thickness of a 2 mm and 3 mm in a spectral range 115 nm, resulting in
50% transmittance of 3 mm thick solid and liquid sodium samples including transmission of a pair of the windows at the wavelength of 120 nm, giving an extinction coefficient of
10
to
10
which represents the sodium with a few cm thickness to be partially transparent for this wavelength. To confirm the measurement, we perform simple imaging experiments by the ultra-violet light passing through a 8 mm-thick sodium sample to illuminate a mesh as an object, resulting in obtaining a clear image.