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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 Percentile:0.01(Chemistry, Physical)

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

Experimental visualization of water/ice phase distribution at cold start for practical-sized polymer electrolyte fuel cells

Higuchi, Yuki*; Yoshimune, Wataru*; Kato, Satoru*; Hibi, Shogo*; Setoyama, Daigo*; Isegawa, Kazuhisa*; Matsumoto, Yoshihiro*; Hayashida, Hirotoshi*; Nozaki, Hiroshi*; Harada, Masashi*; et al.

Communications Engineering (Internet), 3, p.33_1 - 33_7, 2024/02

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:2 Percentile:95.46(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

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:66.55(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

Development and application of a $$^3$$He neutron spin filter at J-PARC

Okudaira, Takuya; Oku, Takayuki; Ino, Takashi*; Hayashida, Hirotoshi*; Kira, Hiroshi*; Sakai, Kenji; Hiroi, Kosuke; Takahashi, Shingo*; Aizawa, Kazuya; Endo, Hitoshi*; et al.

Nuclear Instruments and Methods in Physics Research A, 977, p.164301_1 - 164301_8, 2020/10

 Times Cited Count:11 Percentile:78.21(Instruments & Instrumentation)

Journal Articles

Horizontal line nodes in Sr$$_2$$RuO$$_4$$ proved by spin resonance

Iida, Kazuki*; Kofu, Maiko; Suzuki, Katsuhiro*; Murai, Naoki; Kawamura, Seiko; Kajimoto, Ryoichi; Inamura, Yasuhiro; Ishikado, Motoyuki*; Hasegawa, Shunsuke*; Masuda, Takatsugu*; et al.

Journal of the Physical Society of Japan, 89(5), p.053702_1 - 053702_5, 2020/05

 Times Cited Count:19 Percentile:80.6(Physics, Multidisciplinary)

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:30.74(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

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:38.39(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:72.4(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

Development status of the NMR system for the polarized $$^{3}$$He Neutron Spin Filter (NSF) in the MLF at J-PARC

Sakai, Kenji; Oku, Takayuki; Hayashida, Hirotoshi*; Kira, Hiroshi*; Hiroi, Kosuke; Ino, Takashi*; Oyama, Kenji*; Okawara, Manabu*; Kakurai, Kazuhisa; Shinohara, Takenao; et al.

JPS Conference Proceedings (Internet), 8, p.036015_1 - 036015_6, 2015/09

The polarized $$^{3}$$He filter, which polarizes neutrons due to a large neutron absorption cross section of $$^{3}$$He with strong spin selectivity, becomes a convenient neutron spin filter (NSF) because it is operated immediately after its installation in beam lines without any neutron beam adjustments. For realizing such the NSF, a nuclear magnetic resonance (NMR) system is indispensable for monitoring $$^{3}$$He nuclear spin polarization ${it P}$ of the NSF. We have developed the flexible NMR system based on adiabatic fast passage (AFP) and pulse NMR methods by using their complementary features. In comparing with the values of ${it P}$ obtained by neutron transmission measurement at the beam line 10 of the J-PARC, we measured the correlations between the AFP and pulse NMR signals as changing condition of temperature, amplitude and applying period of the radio frequency field for the pulse NMR, and so on. As the results, we confirmed that our system would function enough as the ${it P}$ monitor.

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:12 Percentile:39.14(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:55.29(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

Development of portable polarized $$^{3}$$He neutron spin filter and its application to magnetic field imaging at J-PARC

Sakai, Kenji; Oku, Takayuki; Hayashida, Hirotoshi; Kira, Hiroshi*; Shinohara, Takenao; Oikawa, Kenichi; Harada, Masahide; Kakurai, Kazuhisa; Aizawa, Kazuya; Arai, Masatoshi; et al.

Journal of Physics; Conference Series, 528, p.012016_1 - 012016_7, 2014/07

 Times Cited Count:2 Percentile:69.14(Optics)

In polarized neutron experiments, it is interested in expanding measurable neutron energy region up to epithermal neutrons. For realizing this situation, a Polarized $$^{3}$$He Spin Flipper (PHSF) has a key role because it can polarize from cold to epithermal neutrons, and flip neutron spins by flipping the $$^{3}$$He nuclear spin direction. We have developed the portable PHSF consisting of a cylindrical glass cell filled with $$^{3}$$He gas which is installed a solenoid coil of 20 cm in diameter and 30 cm long. After polarizing the $$^{3}$$He gas by irradiating a laser light based on a SEOP technique, the PHSF is brought by hands to experimental areas with kept its polarization. We carried out the feasibility test on our portable PHSF in the MLF of J-PARC and demonstrated it worked well by evaluating flipping ratios of polarized neutrons and attempting to visualize magnetic fields generated by sample coils.

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:13 Percentile:29.85(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

Probing the Ba 5d states in BaTiO$$_{3}$$ and BaSO$$_{4}$$; A Resonant X-ray emission study at the Ba-L$$_{3}$$ edge

Yoshii, Kenji; Jarrige, I.; Suzuki, Chikashi; Matsumura, Daiju; Nishihata, Yasuo; Yoneda, Yasuhiro; Fukuda, Tatsuo; Tamura, Kazuhisa; Ito, Yoshiaki*; Mukoyama, Takeshi*; et al.

Journal of Physics and Chemistry of Solids, 73(9), p.1106 - 1110, 2012/09

 Times Cited Count:11 Percentile:43.91(Chemistry, Multidisciplinary)

We have directly probed the Ba 5d states in the ferroelectric barium titanate BaTiO$$_{3}$$ using resonant X-ray emission spectroscopy (RXES) and X-ray absorption spectroscopy in the partial fluorescence mode (PFY-XAS) at the Ba-L$$_{3}$$ edge. The results are compared with those of the non-ferroelectric BaSO$$_{4}$$. While the RXES spectra point to a localized character for the Ba 5d states in both compounds, the main peak of the PFY-XAS spectrum, corresponding to the dipolar transitions from 2p to 5d, is found to be significantly broader for BaTiO$$_{3}$$ than for BaSO$$_{4}$$. On the basis of band structure calculations, this broadening is ascribed to strong hybridization between the unoccupied Ba 5d and O 2p states in the ferroelectric. This suggests that the hybridization between the conduction states of the Ba$$^{2+}$$ and O$$^{2-}$$ ions, and not only Ti$$^{4+}$$ and O$$^{2-}$$, plays a central role in determining the electronic structure of BaTiO$$_{4}$$.

Journal Articles

Development of polarized Xe gas target for neutron experiment at J-PARC

Sakai, Kenji; Oku, Takayuki; Shinohara, Takenao; Kira, Hiroshi; Oi, Motoki; Maekawa, Fujio; Kakurai, Kazuhisa; Ino, Takashi*; Arimoto, Yasushi*; Shimizu, Hirohiko*; et al.

Journal of Physics; Conference Series, 340, p.012037_1 - 012037_7, 2012/02

 Times Cited Count:2 Percentile:62.44(Physics, Condensed Matter)

At the Materials and Life science experimental Facility (MLF) in J-PARC, an experiment of detecting a neutron polarizing ability caused by a neutron-nuclear (n-N) spin correlation term at a resonant peak of $$^{129}$$Xe is planned. The Xe gas having a high polarization under low magnetic field and room temperature by a spin exchange optical pumping (SEOP) technique is expected to become a suitable target for verification of the neutron optical theorem (NOPT). We evaluated measurable quantities based on the NOPT, developed a polarized Xe gas system, and carried out a feasibility test of our apparatus. This paper reports on the present status of the experiment.

Journal Articles

Developments of in-situ SEOP polarized $$^{3}$$He neutron spin filter in Japan

Kira, Hiroshi; Sakaguchi, Yoshifumi; Oku, Takayuki; Suzuki, Junichi; Nakamura, Mitsutaka; Arai, Masatoshi; Endo, Yasuo; Chang, L.-J.; Kakurai, Kazuhisa; Arimoto, Yasushi*; et al.

Journal of Physics; Conference Series, 294, p.012014_1 - 012014_5, 2011/06

 Times Cited Count:11 Percentile:94.49(Physics, Applied)

Journal Articles

Applications of $$^{3}$$He neutron spin filters on the small-angle neutron scattering spectrometer SANS-J-II

Sakaguchi, Yoshifumi; Kira, Hiroshi; Oku, Takayuki; Shinohara, Takenao; Suzuki, Junichi; Sakai, Kenji; Nakamura, Mitsutaka; Aizawa, Kazuya; Arai, Masatoshi; Noda, Yohei; et al.

Journal of Physics; Conference Series, 294(1), p.012017_1 - 012017_7, 2011/06

 Times Cited Count:2 Percentile:65.41(Physics, Applied)

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