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Shi, D.*; Niu, X.*; Elakneswaran, Y.*; Li, A.*; Kikuchi, Ryosuke*; Hiraki, Yoshihisa; Sato, Junya; Osugi, Takeshi; Walkley, B.*
Journal of Nuclear Materials, 633, p.156997_1 - 156997_12, 2026/11
Times Cited Count：0 Percentile：0.00(Materials Science, Multidisciplinary)Tokunaga, Yo; Ishitobi, Takayuki; Sakai, Hironori; Kambe, Shinsaku*; Harima, Hisatomo*; Nakamura, Ai*; Maurya, A.*; Li, D.*; Homma, Yoshiya*; Honda, Fuminori*; et al.
Physical Review Letters, 137(4), p.046501_1 - 046501_6, 2026/07
Times Cited Count：2 Percentile：73.88(Physics, Multidisciplinary)Huang, D.*; Fu, H.*; Lyu, M.*; Feng, Y.*; Kajimoto, Ryoichi; Nakamura, Mitsutaka; Honda, Takashi*; Liu, E.*; Li, B.*; Li, X.*; et al.
Physical Review Research (Internet), 8(3), p.033017_1 - 033017_7, 2026/07
Kyriakou, I.*; Papadopoulos, A.*; Polopetrakis, I.*; Kotroumbelou, C.*; Plante, I.*; Matsuya, Yusuke; Kai, Takeshi; Qiu, R.*; Li, J.*; Kundr
t, P.*; et al.
Physics in Medicine & Biology, 71(8), p.085009_1 - 085009_25, 2026/04
Times Cited Count：3 Percentile：80.13(Engineering, Biomedical)Several Monte Carlo Track-Structure (MCTS) codes for liquid water have been developed worldwide over the last 40 years; however, use the different interaction cross sections. This study evaluates the uncertainties of physical features (electronic stopping power, pathlength, dose-point-kernel, and microdosimetry) of low-energy electron transport in liquid water by using 6 types of MCTS codes. The intercomparison results reveal significant differences among MCTS codes at low energies, especially below ~100 eV, potentially compromising the accuracy of DNA damage simulations where such electrons play a key role. The present work highlights the need for further development of the physics models used in MCTS codes to reduce the uncertainties associated with low-energy electron transport calculations in liquid water.
Che, G.*; Tang, X.*; Liu, J.*; Lang, P.*; Fei, Y.*; Yang, X.*; Wang, Y.*; Gao, D.*; Wang, X.*; Ju, J.*; et al.
Nano Letters, 25(39), p.14467 - 14472, 2025/09
Times Cited Count：2 Percentile：40.34(Chemistry, Multidisciplinary)Mechanochemical radical polymerization has unique advantages in the synthesis of polymer due to its reduced solvent consumption and adaptability of insoluble monomers. However, it suffers from the uncontrollable degradation of the formed polymers during reaction and new synthetic strategy with precise controllability needs to be developed. Here, by employing high static pressure up to 30 GPa, we found 1,3,5-trifluorobenzene undergoes radical polymerization by breaking the conjugated 
-bonds, and forms a carbon nanothread with high selectivity (Polymer-I polymorph). Based on the crystal structure at the threshold pressure and the calculated energy barriers for the bonding pathway, we concluded that the benzene-rings react via a 1-2 radical polymerization pathway. Our work highlights high pressure is a robust method to initiate the solid-state radical polymerization, even for very stable aromatics, and offers fresh insights for the synthesis of polymeric carbon-based materials with high selectivity.
Go, G.*; Goli, D. P.*; Esaki, Nanse; Tserkovnyak, Y.*; Kim, S. K.*
Physical Review Research (Internet), 7(2), p.L022066_1 - L022066_7, 2025/06
Xu, J.*; Lang, P.*; Liang, S.*; Zhang, J.*; Fei, Y.*; Wang, Y.*; Gao, D.*; Hattori, Takanori; Abe, Jun*; Dong, X.*; et al.
Journal of Physical Chemistry Letters (Internet), 16(10), p.2445 - 2451, 2025/03
Times Cited Count：3 Percentile：64.75(Chemistry, Physical)The Alder-ene reaction is a chemical reaction between an alkene with an allylic hydrogen, and it provides an efficient method to construct the C-C bond. Traditionally, this reaction requires catalysts, high temperatures, or photocatalysis. In this study, we reported a high-pressure-induced solid-state Alder-ene reaction of 1-hexene at room temperature without a catalyst. 1-Hexene crystallizes at 4.3 GPa and polymerizes at 18 GPa, forming olefins. By exploring gas chromatography-mass spectrometry, we discovered that 1-hexene generates dimeric products through the Alder-ene reaction under high pressures. The in situ neutron diffraction shows that the reaction process did not obey the topochemical rule. A six-membered ring transition state including one C-H 
bond and two alkene bonds was evidenced by the theoretical calculation, whose energy obviously decreased when compressed to 20 GPa. Our work offers a novel and promising method to realize the Alder-ene reaction at room temperature without a catalyst, expanding the application of this important reaction.
Papadopoulos, A.*; Kyriakou, I.*; Matsuya, Yusuke; Cort
s-Giraldo, M. A.*; Galocha-Oliva, M.*; Plante, I.*; Steward, R. D.*; Tran, N. H.*; Li, W.*; Daglis, I. A.*; et al.
Radiation and Environmental Biophysics, 64(1), p.117 - 135, 2025/03
Times Cited Count：3 Percentile：70.03(Biology)Radiation quality for determining biological effects is commonly linked to the microdosimetric quantity, especially dose-mean lineal energy y
. Calculations of y can be performed by sophisticated Monte Carlo track structure (MCTS) codes. The y estimate depends on the type of the MCTS code and analysis model. This study focused on proton beams with 1 MeV-1 GeV, which are important in radiation protection, space applications, radiation therapy, etc., and compared the estimates of the y in liquid water by various MCTS codes (PHITS, RITRACK, and Geant4-DNA) and analysis models (refined Xapsos model). The comparison results showed that good agreement with the refined Xapsos model and various MCTS codes can be attained at less than 10-20% level, and Q values by the analytic model are also in better agreement with MCTS simulation data. These findings conclude that the refined analytic model might be used as an alternative to time- and CPU-intensive MCTS simulations and advance practical calculations of radiation qualities and risk assessment.
In
GeYokoyama, Akira*; Nakachi, Ryu*; Homma, Yoshiya*; Nakamura, Ai*; Shimizu, Yusei*; Li, D.*; Miyake, Atsushi*; Honda, Fuminori*; Aoki, Dai*; Onuki, Yoshichika*; et al.
Journal of the Physical Society of Japan, 94(2), p.023701_1 - 023701_4, 2025/02
Times Cited Count：1 Percentile：31.62(Physics, Multidisciplinary)Yang, X.*; Che, G.*; Wang, Y.*; Zhang, P.*; Tang, X.*; Lang, P.*; Gao, D.*; Wang, X.*; Wang, Y.*; Hattori, Takanori; et al.
Nano Letters, 25(3), p.1028 - 1035, 2025/01
Times Cited Count：10 Percentile：86.24(Chemistry, Multidisciplinary)Saturated sp
-carbon nanothreads (CNTh) have garnered significant interest due to their predicted high Young's modulus and thermal conductivity. While the incorporation of heteroatoms into the central ring has been shown to influence the formation of CNTh and yield chemically homogeneous products, the impact of pendant groups on the polymerization process remains underexplored. In this study, we investigate the pressure-induced polymerization of phenol, revealing two phase transitions occurring below 0.5 and 4 GPa. Above 20 GPa, phenol polymerizes into degree-4 CNThs featuring hydroxyl and carbonyl groups. Hydrogen transfer of hydroxyl groups was found to hinder the formation of degree-6 nanothreads. Our findings highlight the crucial role of the hydroxyl group in halting further intracolumn polymerization and offer valuable insights for future mechanism research and nanomaterial synthesis.
Se from combined conversion-electron and 
-ray spectroscopySmallcombe, J.; Garnsworthy, A. B.*; Korten, W.*; Singh, P.*; Muir, D.*; Pr
chniak, L.*; Ali, F. A.*; Andreoiu, C.*; Ansari, S.*; Ball, G. C.*; et al.
Physical Review C, 110(2), p.024318_1 - 024318_16, 2024/08
Times Cited Count：2 Percentile：37.47(Physics, Nuclear)Braby, L. A.*; Conte, V.*; Dingfelder, M.*; Goodhead, D. T.*; Pinsky, L. S.*; Rosenfeld, A. B.*; Sato, Tatsuhiko; Waker, A. J.*; Guatelli, S.*; Magrin, G.*; et al.
Journal of ICRU, 23(1), p.1 - 168, 2023/12
This report provides a comprehensive description of the basic concepts and theories, computational and experimental procedures, and applications of microdosimetry.
states in the electronic structure of the intermediate-valence superconductor CeIr
Fujimori, Shinichi; Kawasaki, Ikuto; Takeda, Yukiharu; Yamagami, Hiroshi; Sasabe, Norimasa*; Sato, Yoshiki*; Shimizu, Yusei*; Nakamura, Ai*; Maruya, A.*; Homma, Yoshiya*; et al.
Electronic Structure (Internet), 5(4), p.045009_1 - 045009_7, 2023/11
Li, S.; Yamaguchi, Yoshihito; Katsuyama, Jinya; Li, Y.; Deng, D.*
Proceedings of the ASME 2023 Pressure Vessels and Piping Conference (PVP 2023) (Internet), 7 Pages, 2023/07
Kinjo, Katsuki*; Fujibayashi, Hiroki*; Matsumura, Hiroki*; Hori, Fumiya*; Kitagawa, Shunsaku*; Ishida, Kenji*; Tokunaga, Yo; Sakai, Hironori; Kambe, Shinsaku; Nakamura, Ai*; et al.
Science Advances (Internet), 9(30), p.2736_1 - 2736_6, 2023/07
Times Cited Count：30 Percentile：91.98(Multidisciplinary Sciences)
X-ray synchrotron diffractionLi, H.*; Liu, Y.*; Zhao, W.*; Liu, B.*; Tominaga, Aki; Shobu, Takahisa; Wei, D.*
International Journal of Plasticity, 165, p.103612_1 - 103612_20, 2023/06
Times Cited Count：51 Percentile：97.13(Engineering, Mechanical)In order to clarify the strength properties of Co-free maraging steel, tensile experiment using high energy synchrotron X-ray diffraction was performed. Diffraction profiles from the martensitic and austenitic phases were obtained, and their strength and width were observed to vary as loading. Analysis of the diffraction profiles showed that the content of martensite in the as-aged material decreased slowly at low stress levels and decreased rapidly at high stress levels. On the other hand, the austenite phase in the as-solution materials was significantly transformed the martensite phase as the stress increased. It was clarified to be responsible for their respective strength properties.
Kodeli, I. A.*; Fleming, M.*; Cabellos, O.*; Leal, L.*; Celik, Y.*; Ding, Y.*; Jansky, B.*; Neudecker, D.*; Novak, E.*; Simakov, S.*; et al.
EPJ Web of Conferences, 284, p.15002_1 - 15002_8, 2023/05
Times Cited Count：3 Percentile：84.66(Nuclear Science & Technology)Working Party on International Nuclear Data Evaluation Co-operation Subgroup 47 (WPEC SG47) entitled "Use of Shielding Integral Benchmark Archive and Database for Nuclear Data Validation" was started in June 2019 with the objectives to promote more systematic and wider use of shielding benchmark experiments in nuclear data and transport code validation and development, to provide feedback on the Shielding Integral Benchmark Archive and Database (SINBAD). Complementing the database with new features was discussed, for example providing the nuclear data sensitivity profiles more systematically would facilitate and better guide the use of data, and the information on the geometry, (radiation source) and materials is expected to allow an easier and less error prone computational model preparation for different transport codes. Examples of the use and some views on future development of the SINBAD benchmark database will be presented in the paper.
-axis knight shift on UTe with 
= 2.1 KMatsumura, Hiroki*; Fujibayashi, Hiroki*; Kinjo, Katsuki*; Kitagawa, Shunsaku*; Ishida, Kenji*; Tokunaga, Yo; Sakai, Hironori; Kambe, Shinsaku; Nakamura, Ai*; Shimizu, Yusei*; et al.
Journal of the Physical Society of Japan, 92(6), p.063701_1 - 063701_5, 2023/05
Times Cited Count：75 Percentile：98.70(Physics, Multidisciplinary)
Te-NMR on the uranium-based superconductor UTeFujibayashi, Hiroki*; Kinjo, Katsuki*; Nakamine, Genki*; Kitagawa, Shunsaku*; Ishida, Kenji*; Tokunaga, Yo; Sakai, Hironori; Kambe, Shinsaku; Nakamura, Ai*; Shimizu, Yusei*; et al.
Journal of the Physical Society of Japan, 92(5), p.053702_1 - 053702_5, 2023/05
Times Cited Count：12 Percentile：75.23(Physics, Multidisciplinary)Tabata, Chihiro; Watanabe, Hirohito*; Shirasaki, Kenji*; Sunaga, Ayaki*; Fukuda, Takamitsu*; Li, D.*; Yamamura, Tomoo*
Journal of Molecular Structure, 1277, p.134870_1 - 134870_8, 2023/04
Times Cited Count：6 Percentile：20.38(Chemistry, Physical)Neutral and cationic U(IV) sandwiched phthalocyanine (Pc) complexes were prepared. The neutral species, UPc
, was obtained by the reaction of UCl
] and phthalonitrile, and the [UPc][BF] crystals were grown by electrolysis. The structures of the complexes were determined crystallographically. A U(IV) ion has two 
electrons, which carry a magnetic moment localized at the U sites, making the complex magnetically active. The magnetic susceptibility measurement of UPc revealed that the system was paramagnetic with local magnetic moments down to 2 K, but these magnetic moments were suppressed, possibly by a ligand field effect. The paramagnetism was also confirmed by the magnetization curve without hysteresis. The cationic complex, [UPc][BF]] crystalized in a tetragonal structure with the space group 
, in which the UPc molecules stacked along the tetragonal 
-axis. The structure was similar to that of [LnPc][BF]], but with distinct disorder in the stacking plane. The stabilities of the crystal and molecular structures and the electronic configurations of UPc and [UPc][BF]] were evaluated via the 
calculations that included the multiconfigurational nature of the actinide element.
