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Mn
Co
Ni
Cu
)VO
Yamamoto, Hajime*; Tsuji, Takuya; Matsumura, Daiju; 16 of others*
Inorganic Chemistry, 64(34), p.17496 - 17502, 2025/08
O
and/or SiO
for methanol synthesis; Deciphering the additive-induced boost in catalytic performance by XAFSIwasaki, Kosei*; Ashida, Yuya*; Matsumura, Daiju; Kawakami, Kotaro*; Shibuya, Kana*; Tazawa, Masaru*; Tsuji, Takuya; Shimizu, Hajime*
Journal of CO
Utilization, 97, p.103111_1 - 103111_9, 2025/07
Tanaka, Hirohisa*; Matsumura, Daiju; 8 of others*
International Journal of Hydrogen Energy, 141, p.1317 - 1327, 2025/06
Tanaka, Hirohisa*; Matsumura, Daiju; 10 of others*
International Journal of Hydrogen Energy, 141, p.1088 - 1097, 2025/06
Tonna, Ryutaro*; Sasaki, Takayuki*; Okamoto, Yoshihiro; Kobayashi, Taishi*
Journal of Nuclear Materials, 612, p.155820_1 - 155820_11, 2025/06
The dissolution behavior of (U,Zr)O
, the primary uranium solid phase in the fuel debris from the Fukushima Daiichi nuclear power plant accidents, was investigated thermodynamically and kinetically under atmospheric conditions. Cubic (U,Zr)O
samples with a uniform solid solution of Zr were prepared using wet chemistry methods, and static batch immersion tests were conducted. In strongly acidic conditions, where the solubility of U and Zr exceeded their concentrations, congruent dissolution of both elements was observed with (U,Zr)O
dissolving at the same rate as UO
. In moderately acidic conditions, where the U solubility was higher than its concentration with Zr reaching a steady state at lower solubility, the U dissolution rate from (U,Zr)O
decreased compared to UO
. In the presence of oxalic acid, with increased Zr solubility due to the formation of complexes, the U dissolution rate from (U,Zr)O
did not decrease. This indicates that Zr in (U,Zr)O
formed a secondary solid phase on the solid surface under conditions of lower Zr solubility, which in turn suppressed the oxidative dissolution of U.
Fablet, L.*; P
drot, M.*; Choueikani, F.*; Kieffer, I.*; Proux, O.*; Pierson-Wickmann, A.-C.*; Cagniart, V.*; Yomogida, Takumi; Marsac, R.*
Environmental Science; Nano, 12(5), p.2815 - 2827, 2025/05
Times Cited Count:2 Percentile:90.52(Chemistry, Multidisciplinary)Nickel is an omnipresent trace element in the environment. Due to its high affinity for iron oxide nanoparticles, its elimination from soils and water by these nanoparticles represents an interesting strategy, specially by magnetites, which is naturally present in the environment. However, the interactions between Ni and magnetite are poorly understood, because of the difficulty to control the stoichiometry (Fe(II)-to-Fe(III) ratio) of magnetite. The behavior of Ni in the presence of magnetite nanoparticles with different stoichiometries, in aqueous solution and inert atmosphere, are probed by adsorption experiments and X-ray Absorption Spectroscopy. This study helps predicting the interactions between Ni and magnetite in environmental conditions, which can be used for the development of efficient remediation strategies.
Ueda, Yuki; Micheau, C.; Motokawa, Ryuhei
Fuain Kemikaru, 54(5), p.53 - 60, 2025/05
no abstracts in English
Pt
Ga
with a honeycomb structure using extended X-ray absorption fine structureMatsumoto, Yuji*; Watabe, Yuki*; Iesari, F.*; Osumi, Masakatsu*; Ota, Kyugo*; Haga, Yoshinori; Hatada, Keisuke*; Okajima, Toshihiko*
Metals, 15(4), p.436_1 - 436_13, 2025/04
Times Cited Count:0 Percentile:0.00(Materials Science, Multidisciplinary)
crystalsTakatori, Sayuri*; Pimon, M.*; Pollitt, S.*; Bartokos, M.*; Beeks, K.*; Gr
neis, A.*; Hiraki, Takahiro*; Homma, Tetsuo*; Hosseini, N.*; Leitner, A.*; et al.
New Journal of Physics (Internet), 27(4), p.043024_1 - 043024_10, 2025/04
Times Cited Count:0 Percentile:0.00(Physics, Multidisciplinary)Recent reports on laser excitation of the low-energy thorium-229 (
Th) nuclear isomeric state in calcium fluoride single crystals render this system a promising candidate for a solid-state nuclear clock. However, experimental characterization of the microscopic ion arrangement around the doped
Th and its electronic charge state, crucial for the precise control of the clock transition and assessing the solid-state clock's performance, remains an unresolved task. This study uses X-ray absorption fine structure spectroscopy of
Th:CaF
to investigate the charge state and coordination environment of doped
Th. The results indicate that
Th is doped with a 4+ valence at the substitutional site of the Ca
ion, with charge compensated provided by two F
ions located at interstitial sites adjacent to
Th.
Yomogida, Takumi; Takahashi, Yoshio*
Chikyu Kagaku, 59(1), p.1 - 10, 2025/03
X-ray absorption fine structure XAFS spectroscopy techniques, which are applicable to almost all elements, provide information on elemental valence and local structure with high elemental selectivity and high sensitivity. It has become an indispensable method in space geochemistry and environmental chemistry. This review presents examples of the application of fluorescence XAFS methods to elements that are difficult to detect by conventional methods, and examples where new chemical species information has been obtained by increasing the energy resolution of the X-ray fluorescence (XRF) detection system to obtain XAFS.
Scaria, J.*; P
drot, M.*; Fablet, L.*; Yomogida, Takumi; Nguyen, T. T.*; Sivry, Y.*; Catrouillet, C.*; Pradas del Real, A. E.*; Choueikani, F.*; Vantelon, D.*; et al.
Environmental Science & Technology, 59(11), p.5747 - 5755, 2025/03
Times Cited Count:3 Percentile:96.35(Engineering, Environmental)Understanding and predicting the interaction mechanisms between chromium and magnetite is of particular interest to elucidate the biogeochemical behavior of Cr in the environment and to develop optimal soil remediation and water treatment strategies. However, while the elimination of the most toxic form of (Cr(VI)) by its reduction to Cr(III) has widely been documented, elucidating the exact mechanism involved in Cr(III) sorption to magnetite has attracted less attention. This study examined the interaction of Cr(III) solution with 10 nm-sized magnetites, whose stoichiometries were carefully defined and preserved in anaerobic conditions. This study reveals the joint effects of pH and magnetite stoichiometry on Cr(III) sorption mechanism, and that Cr(III)-(hydr)oxide precipitation is not necessarily the driving process of Cr(III) elimination from solutions. These results will help predict the fate and transport of chromium, as well as developing magnetite-based chromium remediation processes.
by solvent extraction as a potential method to determine Fe
in glass containing Sn
Kanno, Naoki*; Nakase, Masahiko*; Saijo, Yoshitaka*; Matsumura, Daiju; Tsuji, Takuya; Takeshita, Kenji*; Tsukahara, Takehiko*
Progress in Nuclear Science and Technology (Internet), 7, p.154 - 160, 2025/03
O
, FeUO
, and UO
-Zr-stainless steel system samples generated in an oxidative atmosphere in the presence of malonic acidTonna, Ryutaro*; Sasaki, Takayuki*; Okamoto, Yoshihiro; Kobayashi, Taishi*
Journal of Nuclear Materials, 605, p.155561_1 - 155561_9, 2025/02
Times Cited Count:0 Percentile:0.00(Materials Science, Multidisciplinary)
-orbital transition metal multielemental alloy nanoparticles by atomically dispersed 4
-orbital Pd for a 100-fold extended lifetimeZhu, B.*; Huang, S.*; Seo, O.*; Cao, M.*; Matsumura, Daiju; Gu, H.*; Wu, D.*
Journal of the American Chemical Society, 147(13), p.11250 - 11256, 2025/02
Kato, Yuto*; Sasaki, Takayuki*; Tonna, Ryutaro*; Kobayashi, Taishi*; Okamoto, Yoshihiro
Applied Geochemistry, 175, p.106196_1 - 106196_9, 2024/11
Times Cited Count:2 Percentile:45.35(Geochemistry & Geophysics)Ueda, Yuki; Micheau, C.; Akutsu, Kazuhiro*; Tokunaga, Kohei; Yamada, Masako*; Yamada, Norifumi*; Bourgeois, D.*; Motokawa, Ryuhei
Langmuir, 40(46), p.24257 - 24271, 2024/11
Times Cited Count:1 Percentile:16.77(Chemistry, Multidisciplinary)Microscopic structures in liquid-liquid extraction, such as structuration between extractants or extracted complexes in bulk organic phases and at interfaces, can influence macroscopic phenomena, such as the distribution behavior of solutes, including extraction efficiency, selectivity, and phase separation of the organic phase. In this study, we correlated the macroscopic behavior of the extraction of Zr(IV) ions from nitric acid solutions with microscopic structural information in order to understand at the molecular level the key factors contributing to the higher metal ion extraction performance in the fluorous extraction system comprising fluorous phosphate (TFP) in perfluorohexane as compared to the analogous organic extraction system comprising organic phosphate (THP) in n-hexane. Extended X-ray absorption fine structure, neutron reflectometry, and small-angle neutron scattering revealed the local coordination structure around the Zr(IV) ion, the accumulation of extractant molecules at the interface, and the structuration of extractant molecules in the bulk extraction phase, respectively. In the fluorous extraction system, extractant aggregates with were formed after contact with nitric acid. In contrast, in the organic extraction system, only extractant dimers were formed. We speculate that differences in the local coordination structure around the Zr(IV) ion and the structuration of the extractant molecules in the bulk extraction phase contribute to the high Zr(IV) extraction performance in the fluorous extraction system. In particular, the size of the aggregates hardly changed with increasing Zr(IV) concentration in the fluorous phase, which may be closely related to the absence of phase splitting in the fluorous extraction system.
Tsuji, Takuya; Matsumura, Daiju; Kobayashi, Toru
SPring-8/SACLA Riyo Kenkyu Seikashu (Internet), 12(5), p.259 - 262, 2024/10
no abstracts in English
Krajewska, A.*; Tsuji, Takuya; Matsumura, Daiju; 15 of others*
Science Advances (Internet), 10(41), p.eadn3880_1 - eadn3880_10, 2024/10
Times Cited Count:4 Percentile:70.50(Multidisciplinary Sciences)
Yamamoto, Hajime*; Ikeda, Osamu*; Honda, Takashi*; Kimura, Kenta*; Aoyama, Takuya*; Ogushi, Kenya*; Suzuki, Akio*; Ishii, Kenji*; Matsumura, Daiju; Tsuji, Takuya; et al.
Physical Review Materials (Internet), 8(9), p.094402_1 - 094402_6, 2024/09
Times Cited Count:3 Percentile:43.86(Materials Science, Multidisciplinary)Nankawa, Takuya
Kagaku, 79(8), p.48 - 52, 2024/08
Lacquer is a natural paint with excellent water and chemical resistance. It has long been known that adding a very small amount of iron into raw lacquer produces a very beautiful black color called Shikoku. However, the structure and reactions of lacquer are still largely unknown, and the reason of black color is also unclear. In this study, we analyzed the structure of raw lacquer and black lacquer films by using different kind of quantum beams. As a result, black lacquer has a completely different nanostructure from raw lacquer, and that the color changes depending on the difference in the structure. This result is the first successful analysis of the structure of the lacquer film, which had been a mystery for many years. This commentary describes this research and also explains how this research has been proceeded.