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Journal Articles

Dissolution of zirconium-cerium oxide solid solution in an aqueous system

Kobayashi, Taishi*; Sato, Yutaro*; Tonna, Ryutaro*; Matsumura, Daiju; Sasaki, Takayuki*; Ikeda, Atsushi

Dalton Transactions (Internet), 53(46), p.18616 - 18628, 2024/10

https://doi.org/10.1039/D4DT02272F

Journal Articles

Effects of Fe ions, ultraviolet irradiation, and heating on microscopic structures of black lacquer films

Nankawa, Takuya; Sekine, Yurina; Matsumura, Daiju; Hiroi, Kosuke; Takata, Shinichi; Kamiya, Yoshimi*; Honda, Takayuki*

Langmuir, 40(11), p.5725 - 5730, 2024/03

https://doi.org/10.1021/acs.langmuir.3c03412

Times Cited Count：0 Percentile：0.00(Chemistry, Multidisciplinary)

The chemical reaction between Fe and lacquer has been used to create the black color lacquer since ancient times. Here, the chemical state of Fe ions in black lacquer was investigated by using X-ray absorption near edge structure (XANES), extended X-ray absorption fine structure (EXAFS), and Fourier transform-infrared (FT-IR) spectroscopy. Fe(II) or Fe(III) was added to the lacquer paste to prepare black lacquer films by air drying, heating, or UV irradiation. The XANES spectral features of all the film samples were similar, meaning that the Fe ions in the samples existed in the trivalent state regardless of the oxidation state of the initially added Fe. The corresponding Fourier transforms of the EXAFS spectra around the Fe K-edge were used to investigate Fe sites in the lacquer films. The spectra of all the film samples were similar shapes, but the peak intensities decreased in the order air dried heated UV irradiated films. This result indicates that heating and UV irradiation made the coordination structure of Fe in the lacquer non-uniform, and that heating caused the greatest non-uniformity. The complementary use of XANES, XAFS, and FT-IR spectroscopy is highly effective for non-destructive analysis of black lacquer in precious cultural artifacts.

Journal Articles

Local structural changes in V-Ti-Cr alloy hydrides with hydrogen absorption/desorption cycling

Ikeda, Kazutaka*; Sashida, Sho*; Otomo, Toshiya*; Oshita, Hidetoshi*; Honda, Takashi*; Hawai, Takafumi*; Saito, Hiraku*; Ito, Shinichi*; Yokoo, Tetsuya*; Sakaki, Koji*; et al.

International Journal of Hydrogen Energy, 51(Part A), p.79 - 87, 2024/01

https://doi.org/10.1016/j.ijhydene.2023.10.318

Times Cited Count：3 Percentile：43.34(Chemistry, Physical)

Journal Articles

Ga K-edge XANES study of Ga-exchanged zeolites at high temperatures under different atmospheres including vacuum, CO, and pressurized H $_{2}$

Huang, M.*; Kinjo, Tetsuya*; Yasumura, Shunsaku*; Toyao, Takashi*; Matsumura, Daiju; Saito, Hiroyuki*; Shimizu, Kenichi*; Namiki, Norikazu*; Maeno, Zen*

Catalysis Science & Technology, 13(23), p.6832 - 6838, 2023/12

https://doi.org/10.1039/D3CY01250F

Times Cited Count：0 Percentile：0.00(Chemistry, Physical)

Journal Articles

Weakened oxygen adsorbing the Pt-O bond of the Pt catalyst induced by vacancy introduction into carbon support

Okazaki, Hiroyuki*; Idesaki, Akira*; Koshikawa, Hiroshi*; Matsumura, Daiju; Ikeda, Takashi*; Yamamoto, Shunya*; Yamaki, Tetsuya*

Journal of Physical Chemistry C, 127(49), p.23628 - 23633, 2023/12

https://doi.org/10.1021/acs.jpcc.3c04117

Times Cited Count：0 Percentile：0.00(Chemistry, Physical)

Journal Articles

Local structure analysis of Bi $_{0.5}$ Na $_{0.5}$ TiOBaTiO solid solutions

Yoneda, Yasuhiro; Kobayashi, Toru; Tsuji, Takuya; Matsumura, Daiju; Saito, Yuji; Noguchi, Yuji*

Japanese Journal of Applied Physics, 62(SM), p.SM1006_1 - SM1006_8, 2023/11

https://doi.org/10.35848/1347-4065/ace3cd

Times Cited Count：4 Percentile：58.64(Physics, Applied)

Bi $_{0.5}$ Na $_{0.5}$ TiOBaTiO (BNTBT) solid solutions have been extensively studied because they exhibit good piezoelectric properties. In addition, a wide variety of phases are observed depending on the BT composition. Soft X-ray absorption spectroscopy and high-energy X-ray diffraction experiments of BNTBT solid solutions were performed using synchrotron radiation. From the electronic structure and local structure of BNTBT solid solution, the substitution effect of BT occurred mainly at the A site, which is the substitution site of Ba. The rhombohedral strain of the TiO octahedron did not change with the change in BT composition, suggesting that the change in the electronic structure at the O- absorption edge is due to the change in the hybridization state.

Journal Articles

Precise observation of spontaneous oscillation of CO oxidation reaction for Rh metal nanoparticle catalyst by using time-resolved X-ray absorption fine structure technique with dispersive optics

Matsumura, Daiju; Kimura, Yusaku*; Tsuji, Takuya; Mizuki, Junichiro*

SPring-8/SACLA Riyo Kenkyu Seikashu (Internet), 11(5), p.296 - 299, 2023/11

https://doi.org/10.18957/rr.11.5.296

no abstracts in English

Journal Articles

Local atomic displacements and sign of the structural transformation in medium-entropy alloys observed in extended X-ray absorption fine structure spectra

Ikeda, Yoichi*; Umemoto, Yoshihiko*; Matsumura, Daiju; Tsuji, Takuya; Hashimoto, Yuki*; Kitazawa, Takafumi*; Fujita, Masaki*

Materials Transactions, 64(9), p.2254 - 2260, 2023/09

https://doi.org/10.2320/matertrans.MT-M2023043

Times Cited Count：3 Percentile：56.29(Materials Science, Multidisciplinary)

Journal Articles

Local structure analysis of DyN-ZrN solid solutions

Yoneda, Yasuhiro; Tsuji, Takuya; Matsumura, Daiju; Okamoto, Yoshihiro; Takaki, Seiya; Takano, Masahide

Physica B; Condensed Matter, 663, p.414960_1 - 414960_9, 2023/08

https://doi.org/10.1016/j.physb.2023.414960

Times Cited Count：0 Percentile：0.00(Physics, Condensed Matter)

We performed various synchrotron X-ray measurements to extract local and average structures of DyN-ZrN solid solutions. We performed the nanoscale structural analysis by combining X-ray absorption fine structure and high-energy X-ray diffraction. The DyN-ZrN solid solution has a rock-salt type cubic crystal structure, and there are instabilities such as the chemical order of the metal site and the distribution of the bond length of the nitrogen site.

Journal Articles

Sorption structure of cesium in various clay minerals by Cs ${it L$_{1}$}$ -edge XAFS measurement

Tsuji, Takuya; Matsumura, Daiju; Kobayashi, Toru

SPring-8/SACLA Riyo Kenkyu Seikashu (Internet), 11(4), p.214 - 217, 2023/08

https://doi.org/10.18957/rr.11.4.214

no abstracts in English

Journal Articles

Development of hydrogen oxidation reaction catalysts to overcome CO poisoning and elucidation of reaction mechanism

Inagawa, Kohei*; Matsumura, Daiju; Taniguchi, Masashi*; Uegaki, Shinya*; Nakayama, Tomohito*; Urano, Junnosuke*; Aotani, Takuro*; Tanaka, Hirohisa*

Journal of Physical Chemistry C, 127(24), p.11542 - 11549, 2023/06

https://doi.org/10.1021/acs.jpcc.3c02237

Times Cited Count：0 Percentile：0.00(Chemistry, Physical)

Journal Articles

Cu -edge X-ray absorption fine structure study of -type $_{2}$ CuO $_{4+alpha-delta}$ ( = Rare Earth); Toward unified understanding of electronic state of -type cuprate

Chen, Y.*; Asano, Shun*; Wang, T.*; Xie, P.*; Kitayama, Shinnosuke*; Ishii, Kenji*; Matsumura, Daiju; Tsuji, Takuya; Taniguchi, Takanori*; Fujita, Masaki*

JPS Conference Proceedings (Internet), 38, p.011050_1 - 011050_6, 2023/05

https://doi.org/10.7566/JPSCP.38.011050

Journal Articles

Uranium hydroxide/oxide deposits on uranyl reduction

Ouchi, Kazuki; Matsumura, Daiju; Tsuji, Takuya; Kobayashi, Toru; Otobe, Haruyoshi; Kitatsuji, Yoshihiro

RSC Advances (Internet), 13(24), p.16321 - 16326, 2023/05

https://doi.org/10.1039/D3RA02899B

Times Cited Count：1 Percentile：20.85(Chemistry, Multidisciplinary)

We clarified the chemical state transformation of deposits following the reduction of uranyl ion (U $^{rm VI}$ O $_{2}$ $^{2+}$ ) from the results of electrochemical quartz crystal microbalance, impedance spectra and X-ray absorption fine structure measurements. We propose the following deposition mechanism: (1) U $^{rm IV}$ is formed by the disproportionation of U $^{rm V}$ . (2) U $^{rm IV}$ forms U $^{rm IV}$ hydroxide deposits, and (3) finally, the hydroxide deposits transform into U $^{rm IV}$ oxide, generally having a larger electrical resistance than the former.