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Journal Articles

Intercalative and non-intercalative photo-recharge using all-solid-state cells for solar energy conversion and storage

Yoshimoto, Masataka*; Tamura, Kazuhisa; Watanabe, Kenta*; Shimizu, Keisuke*; Horisawa, Yuhei*; Kobayashi, Takeshi*; Tsurita, Hanae*; Suzuki, Kota*; Kanno, Ryoji*; Hirayama, Masaaki*

Sustainable Energy & Fuels (Internet), 8(6), p.1236 - 1244, 2024/03

 Times Cited Count:0

Photo-rechargeable systems, which can efficiently convert and store solar energy into chemical energy within single devices, are essential to harness sunlight effectively. Photo-(de)intercalation plays a pivotal role in the functionality of photorechargeable systems. Nevertheless, the photo-(de)intercalation process has not been conclusively confirmed owing to potential interference from side reactions, such as the decomposition of liquid electrolytes and the elution of electrode materials. In this study, we successfully demonstrated photo-responsive Li$$^{+}$$-deintercalation using an all-solid-state thin-film battery comprised of epitaxially-grown anatase TiO$$_{2}$$ doped with Nb (a-TiO$$_{2}$$:Nb) as the cathode. Under light irradiation, Li$$^{+}$$-deintercalation occurred and was subsequently reversibly intercalated into a-TiO$$_{2}$$:Nb during discharge.

Journal Articles

Stable photoelectrochemical reactions at solid/solid interfaces toward solar energy conversion and storage

Watanabe, Kenta*; Horisawa, Yuhei*; Yoshimoto, Masataka*; Tamura, Kazuhisa; Suzuki, Kota*; Kanno, Ryoji*; Hirayama, Masaaki*

Nano Letters, 24(6), p.1916 - 1922, 2024/02

 Times Cited Count:1 Percentile:0.02(Chemistry, Multidisciplinary)

Electrochemistry has extended from reactions at solid/liquid interfaces to those at solid/solid interfaces. In this study, we achieve the stable photoelectrochemical reaction at the semiconductor-electrode/solid-electrolyte interface in Nb-doped anatase-TiO$$_{2}$$ (a-TiO$$_{2}$$:Nb)/Li$$_{3}$$PO$$_{4}$$ (LPO)/Li all-solid-state cell. The oxidative currents of a-TiO$$_{2}$$:Nb/LPO/Li increase upon light irradiation when a-TiO$$_{2}$$:Nb is located at a potential that is more positive than its flat-band potential. The photoelectrochemical reaction at the semiconductor/solid-electrolyte interface is driven by the same principle as that at semiconductor/liquid-electrolyte interfaces. Thus, we extend photoelectrochemistry to all-solid-state systems composed of solid/solid interfaces.

Journal Articles

Spontaneous topological Hall effect induced by non-coplanar antiferromagnetic order in intercalated van der Waals materials

Takagi, Hirotaka*; Takagi, Rina*; Minami, Susumu*; Nomoto, Takuya*; Oishi, Kazuki*; Suzuki, Michito*; Yanagi, Yuki*; Hirayama, Motoaki*; Khanh, N.*; Karube, Kosuke*; et al.

Nature Physics, 19(7), p.961 - 968, 2023/07

 Times Cited Count:8 Percentile:96.03(Physics, Multidisciplinary)

Journal Articles

Oxygen reduction activity and interfacial structures of La$$_{0.8}$$Sr$$_{0.2}$$CoO$$_{3}$$ at initial electrochemical process in an alkaline solution

Matsuzaki, Akira*; Hirayama, Masaaki*; Oguchi, Shoya*; Komo, Mamoru*; Ikezawa, Atsunori*; Suzuki, Kota*; Tamura, Kazuhisa; Arai, Hajime*; Kanno, Ryoji*

Electrochemistry (Internet), 90(10), p.107001_1 - 107001_8, 2022/10

 Times Cited Count:0 Percentile:0.01(Electrochemistry)

Oxygen reduction and evolution reactions (ORR and OER) of perovskite-type La$$_{0.8}$$Sr$$_{0.2}$$CoO$$_{3}$$ were characterized using two-dimensional model electrodes with different reaction planes. Synthesized by pulsed laser deposition, these thin and flat electrodes can reveal the reaction plane dependence of the ORR activity. From steady-state polarization measurements in KOH (aq.), the ORR activity was the highest on the (001) film during the first ORR/OER cycle, and it decreased significantly during the second cycle. In-situ synchrotron X-ray diffraction clarified crystal structure changes in the bulk and surface regions of La$$_{0.8}$$Sr$$_{0.2}$$CoO$$_{3}$$, and these changes are associated with forming oxygen defects during the initial electrochemical process. Furthermore, the La$$_{0.8}$$Sr$$_{0.2}$$CoO$$_{3}$$ surface partially decomposed upon reacting. Therefore, the interfacial structures formed in the electrochemical reaction field is important for enhancing ORR and OER activities.

Journal Articles

Reactions of the Li$$_{2}$$MnO$$_{3}$$ cathode in an all-solid-state thin-film battery during cycling

Hikima, Kazuhiro*; Hinuma, Yoyo*; Shimizu, Keisuke*; Suzuki, Kota*; Taminato, So*; Hirayama, Masaaki*; Masuda, Takuya*; Tamura, Kazuhisa; Kanno, Ryoji*

ACS Applied Materials & Interfaces, 13(6), p.7650 - 7663, 2021/02

 Times Cited Count:12 Percentile:67.96(Nanoscience & Nanotechnology)

We evaluated the structural change of the cathode material Li$$_{2}$$MnO$$_{3}$$ that was deposited as an epitaxial film with an (001) orientation in an all-solid-state battery. In case of the electrode with LiPO$$_{4}$$ coating. Experiments revealed a structural change to a high-capacity (activated) phase that proceeded gradually and continuously with cycling. The activated phase barely showed any capacity fading. We propose a mechanism of structural change with cycling: charging to a high voltage at a sufficiently low Li concentration typically induces irreversible transition to a phase detrimental to cycling that could, but not necessarily, be accompanied by the dissolution of Mn and/or the release of O into the electrolyte, while a gradual irreversible transition to an activated phase happens at a similar Li concentration under a lower voltage.

Journal Articles

Reversible structural changes and high-rate capability of Li$$_{3}$$PO$$_{4}$$-modified Li$$_{2}$$RuO$$_{3}$$ for lithium-rich layered rocksalt oxide cathodes

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:8 Percentile:31.15(Chemistry, Physical)

Lithium-rich layered rocksalt oxides are promising cathode materials for lithium-ion batteries. We investigate the effects of surface modification by amorphous Li$$_{3}$$PO$$_{4}$$ on the structures and electrochemical reactions in the surface region of an epitaxial Li$$_{2}$$RuO$$_{3}$$(010) film electrode. Structural characterization using SXRD, HAXPES, and NR shows that surface modification by Li$$_{3}$$PO$$_{4}$$ resulted in the partial substitution of P for Li in the surface region of Li$$_{2}$$RuO$$_{3}$$. The modified (010) surface exhibits better rate capability at 20 C compared to the unmodified surface. ${it In situ}$ 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.

Journal Articles

Materials and Life Science Experimental Facility (MLF) at the Japan Proton Accelerator Research Complex, 2; Neutron scattering instruments

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.

Journal Articles

Study on the deterioration mechanism of layered rock-salt electrodes using epitaxial thin films; Li(Ni, Co, Mn)O$$_{2}$$ and their Zr-O surface modified electrodes

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:11 Percentile:38.74(Chemistry, Physical)

The surface structure of the Li(Ni, Co, Mn)O$$_{2}$$ 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.

Journal Articles

Lithium intercalation and structural changes at the LiCoO$$_{2}$$ surface under high voltage battery operation

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:34 Percentile:71.85(Chemistry, Physical)

An epitaxial-film model electrode of LiCoO$$_{2}$$(104) was fabricated on SrRuO$$_{3}$$(100)/Nb:SrTiO$$_{3}$$(100) using pulsed laser deposition. The 50 nm thick LiCoO$$_{2}$$(104) film exhibited lithium (de-)intercalation activity with a first discharge capacity of 119 mAh g$$^{-1}$$ 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$$_{3}$$PO$$_{4}$$-coated film exhibited a higher intercalation capacity of 148 mAh g$$^{-1}$$ 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$$_{2}$$ by the Li$$_{3}$$PO$$_{4}$$ coating could lead to improvement of the structural stability at the surface region during lithium (de-)intercalation at high voltage.

Journal Articles

Structural analysis of electrode-electrolyte interface in lithium batteries

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.

Journal Articles

Interfacial analysis of surface-coated LiMn$$_{2}$$O$$_{4}$$ epitaxial thin film electrode for lithium batteries

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:11 Percentile:36.55(Electrochemistry)

The effects of surface coatings on LiMn$$_{2}$$O$$_{4}$$ were investigated using LiMn$$_{2}$$O$$_{4}$$ epitaxial thin films with a thickness of 30 nm. Bare and surface-coated LiMn$$_{2}$$O$$_{4}$$ epitaxial thin films were synthesized on SrTiO$$_{3}$$(111) substrates using a pulsed laser deposition method. The surface coating, which was formed using the solid electrolyte Li$$_{3}$$PO$$_{4}$$ and had a thickness of 3 nm, improved the reversibility of the electrochemical reactions undergone by the LiMn$$_{2}$$O$$_{4}$$ epitaxial thin films. The changes induced in the surface structure were maintained during battery operation; in contrast, the bare LiMn$$_{2}$$O$$_{4}$$ 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$$_{3}$$PO$$_{4}$$ coating and improved the electrochemical performance of the LiMn$$_{2}$$O$$_{4}$$ thin-film electrode.

Journal Articles

Mechanistic studies on lithium intercalation in a lithium-rich layered material using Li$$_{2}$$RuO$$_{3}$$ epitaxial film electrodes and ${{it in situ}}$ surface X-ray analysis

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:21 Percentile:55.49(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 Li$$_{2}$$RuO$$_{3}$$ 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$$_{2}$$RuO$$_{3}$$. 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 ${{it in situ}}$ 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.

Journal Articles

Characterization of nano-sized epitaxial Li$$_{4}$$Ti$$_{5}$$O$$_{12}$$(110) film electrode for lithium batteries

Kim, K.-S.*; Tojigamori, Takeshi*; Suzuki, Kota*; Taminato, So*; Tamura, Kazuhisa; Mizuki, Junichiro; Hirayama, Masaaki*; Kanno, Ryoji*

Denki Kagaku Oyobi Kogyo Butsuri Kagaku, 80(10), p.800 - 803, 2012/10

 Times Cited Count:12 Percentile:29.96(Electrochemistry)

Electrochemical properties and structure changes of nano-sized Li$$_{4}$$Ti$$_{5}$$O$$_{12}$$ during lithium (de)intercalation wereinvestigated using a two-dimensional thin film electrode. Li$$_{4}$$Ti$$_{5}$$O$$_{12}$$ thin films were deposited on a Nb:SrTiO$$_{3}$$(110)substrate by a pulsed laser deposition technique. In situ X-ray diffraction measurements clarified the drastic structural changes of the Li$$_{4}$$Ti$$_{5}$$O$$_{12}$$film upon soaking in the electrolyte and during the first intercalation and deintercalation processes. The surfaceregion of Li$$_{4}$$Ti$$_{5}$$O$$_{12}$$ had a different structure from the bulk during electrochemical cycling and could cause the nanosizedLi$$_{4}$$Ti$$_{5}$$O$$_{12}$$ electrodes to have high capacities and poor stabilities.

Journal Articles

Numerical consideration for multiscale statistical process control method applied to nuclear material accountancy

Suzuki, Mitsutoshi; Hori, Masato; Aso, Ryoji; Usuda, Shigekazu

Journal of Nuclear Science and Technology, 43(10), p.1270 - 1279, 2006/10

 Times Cited Count:3 Percentile:24.11(Nuclear Science & Technology)

The multiscale statistical process control (MSSPC) method is applied to explain material unaccounted for (MUF) in large scale reprocessing plants using numerical calculations. Continuous wavelet functions are used to decompose the process data, which simulate batch operation superimposed by various types of disturbance, and the disturbance components included in the data are divided into time and frequency spaces. The diagnosis of MSSPC is applied to distinguish abnormal events from the process data and shows how to detect abrupt and protracted diversions using principle component analysis. Quantitative performance of MSSPC for the time series data is shown with average run lengths given by Monte-Carlo simulation to compare to the non-detection probability B. Recent discussion about bias corrections in material balances is introduced and another approach is presented to evaluate MUF without assuming the measurement error model.

Journal Articles

Numerical consideration for multiscale statistical process control method applied to nuclear material accountancy

Suzuki, Mitsutoshi; Hori, Masato; Aso, Ryoji; Usuda, Shigekazu

Proceedings of INMM 47th Annual Meeting (CD-ROM), 8 Pages, 2006/00

The multiscale statistical process control (MSSPC) method is applied to explain material unaccounted for (MUF) in a large scale reprocessing plant using numerical calculations. Increasing the amount of nuclear material throughput per year, which is more than 5000kgPu in commercial reprocessing plant, the accumulated annual measurement errors will exceed 1SQ (=8kgPu) and frequent Near Real Time Accountancy (NRTA) and process monitoring measures are required to satisfy the IAEA safeguard criteria. In this study, continuous wavelet functions are used to decompose the process data, which is simulated batch operation mode superimposed by various types of disturbance, and the disturbance components constituting the data are divided into both time and frequency region. Because MSSPC based on wavelet decomposition provides efficient performance over a wide range of abnormal events, the protracted or abrupt diversion loss, not known a priori, can be detected for nuclear safeguards purpose. The diagnosis for MSSPC is applied to distinguish an abnormal event from the normal data and shows how to detect both types of diversion loss using principle component analysis (PCA). MUF data is generally supposed to be autocorrelated time series data. Quantitative performance of MSSPC for the time series data is shown with the average run lengths simulated by Monte-Calro calculation to compare the nondetection probability B. Recent discussion about bias corrections (BC) in material balances is introduced and other approach is presented to evaluate MUF in an explanatory manner without an adoption of BC.

Journal Articles

Experimental validation of beam particle self interaction in JT-60U by use of N-NB

Okano, Kunihiko*; Suzuki, Takahiro; Umeda, Naotaka; Hiwatari, Ryoji*; Masaki, Kei; Tobita, Kenji; Fujita, Takaaki

Purazuma, Kaku Yugo Gakkai-Shi, 81(8), p.579 - 580, 2005/08

In a toroidal system, circulating fast ions generated by neutral beam injection affect the beam stopping cross-section of the neutral beam itself. This effect is called "beam particle self-interaction (BPSI)". In a recent experiment in JT-60U with 350 keV H$$^{0}$$ beam, an indication of this BPSI effect has been found for the first time. In a low density discharge at about 1$$times$$10$$^{19}$$m$$^{-3}$$, the beam shine-through decreased by about 35% within several hundred msec after beam injection. This result is consistent with a prediction by the BPSI theory.

Journal Articles

Desulfurization reaction of high sulfur content flue gas treated by electron beam

Hirosawa, Shojiro*; Kojima, Takuji; Hashimoto, Shoji; Suzuki, Ryoji*; Aoki, Shinji*

Radioisotopes, 51(8), p.285 - 295, 2002/08

Experiments of flue gas treatment by electron beam were carried out, using simulated lignite-burning flue gas containing SO$$_{2}$$(5500ppm), NO(390ppm) and H$$_{2}$$O(22%). Removal efficiency of SO$$_{2}$$ was more than 90% at a dose of 1-2kGy. It shows applicability of electron beam for treatment of lignite-burning flue gas. Another removal reaction besides the radiation-induced radical reaction and the thermal reaction occurring without irradiation was suggested by the facts that removal of SO$$_{2}$$ by the radical reaction is only a few hundreds of ppm and the removal amounts by thermal reaction under irradiation is lower than a half of total desulfurization. The mechanism similar to thermal reaction was proposed, assuming simultaneous uptake reaction of SO$$_{2}$$ and NH$$_{3}$$ on the surface of liquid aerosol. It was suggested that ammonium nitrate having deliquescence relative humidity(DRH) of 60% at 25$$^{circ}C$$ plays an important role in producing liquid aerosols. Decrease of DRH of ammonium nitrate with increasing temperature and with formation of double salt of ammonium sulfate results in enhancement of formation of liquid aerosols.

Journal Articles

Detailed magnetic field measurement on a hybrid undulator for the JAERI FEL

Nagai, Ryoji; Minehara, Eisuke; Sasaki, Shigemi; Sawamura, Masaru; Sugimoto, Masayoshi; Takao, Masaru*; ; Okubo, Makio; Suzuki, Yasuo; *; et al.

Journal of Nuclear Science and Technology, 32(8), p.715 - 718, 1995/08

 Times Cited Count:1 Percentile:17.54(Nuclear Science & Technology)

no abstracts in English

JAEA Reports

A Proposal for the formation of a plasma micro-undulator by combined techniques of laser interference and resonant photoionization

*; Suzuki, Yasuo; Nagai, Ryoji; *; *; *

JAERI-Research 95-028, 20 Pages, 1995/03

JAERI-Research-95-028.pdf:0.92MB

no abstracts in English

Journal Articles

Status of the JAERI free electron laser facility driven by a super conducting rf linac

Minehara, Eisuke; Nagai, Ryoji; Sawamura, Masaru; Takao, Masaru*; Sugimoto, Masayoshi; Sasaki, Shigemi; Okubo, Makio; Kikuzawa, Nobuhiro; *; Suzuki, Yasuo; et al.

Nuclear Instruments and Methods in Physics Research A, 358, p.ABS30 - ABS31, 1995/00

 Times Cited Count:0 Percentile:0.01(Instruments & Instrumentation)

no abstracts in English

32 (Records 1-20 displayed on this page)