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Dei, Shuntaro; Shibata, Masahito*; Negishi, Kumi*; Sugiura, Yuki; Amano, Yuki; Bateman, K.*; Wilson, J.*; Yokoyama, Tatsunori; Kagami, Saya; Takeda, Masaki; et al.
Results in Earth Sciences (Internet), 3, p.100097_1 - 100097_16, 2025/12
Interactions between cement and host rock in geological repositories for radioactive waste will result in a chemically disturbed zone, which may potentially affect the long-term safety. This paper investigates the chemical evolution at the interface between cement (Ordinary Portland Cement: OPC and Low Alkaline Cement: LAC) and mudstone after 11 years of in situ reactions at the Horonobe Underground Research Laboratory. The study combines various analytical techniques to identify the key reactions at the cement-rock interface, including cement dissolution, precipitation of secondary minerals such as calcite and C-(A-)S-H phases, cation exchange in montmorillonite and reduced porosity in mudstone. The study also highlights the effects of cement-mudstone interactions on radionuclide migration, such as reduction of diffusivity due to reduced porosity and enhancement of sorption due to incorporation into secondary minerals in the altered mudstone.
Reiser, J. T.*; Neeway, J. J.*; Cooley, S. K.*; Parruzot, B.*; Heredia-Langner, A.*; Gin, S.*; Thomas, M.*; Smith, N. J.*; Icenhower, J. P.*; Stone-Weiss, N.*; et al.
International Journal of Applied Glass Science, 16(4), p.e16707_1 - e16707_16, 2025/10
Times Cited Count:0 Percentile:0.00(Materials Science, Ceramics)
Shamoto, Shinichi; Shin, K.*; Akatsu, Mitsuhiro*; Imai, Masaki; Ueta, Daichi*; Yokoo, Tetsuya*; Nemoto, Yuichi*; Hassan, A. M. A.*; Chang, L.-J.*; Ieda, Junichi; et al.
Applied Physics Letters, 127(13), p.132403_1 - 132403_5, 2025/09
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
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.
Takeuchi, Yutaro*; Sato, Yuma*; Yamane, Yuta*; Yoon, J.-Y.*; Kanno, Yukinori*; Uchimura, Tomohiro*; De Zoysa, K. V.*; Han, J.*; Kanai, Shun*; Ieda, Junichi; et al.
Science, 389(6762), p.830 - 834, 2025/08
Times Cited Count:0 Percentile:80.70Chauvin, N.*; Martin, P.*; Ogata, Takanari*; Calabrese, R.*; Janney, D.*; Hirooka, Shun; Kato, Masato; Staicu, D.*; McClellan, K.*; White, J.*; et al.
NEA/NSC/R(2024)1 (Internet), 289 Pages, 2025/07
no abstracts in English
Birkholzer, J. T.*; Graupner, B. J.*; Harrington, J.*; Jayne, R.*; Kolditz, O.*; Kuhlman, K. L.*; LaForce, T.*; Leone, R. C.*; Mariner, P. E.*; McDermott, C.*; et al.
Geomechanics for Energy and the Environment, 42, p.100685_1 - 100685_17, 2025/06
Times Cited Count:1 Percentile:65.19(Energy & Fuels)Hartzell, S.*; Furutani, K. M.*; Parisi, A.*; Sato, Tatsuhiko; Kase, Yuki*; Deglow, C.*; Friedrich, T.*; Beltran, C. J.*
Radiation (Internet), 5(2), p.21_1 - 21_24, 2025/06
Hartzell, S.*; Parisi, A.*; Sato, Tatsuhiko; Beltran, C. J.*; Furutani, K. M.*
Physics in Medicine & Biology, 70(10), p.105010_1 - 105010_19, 2025/05
Times Cited Count:0 Percentile:72.00(Engineering, Biomedical)
hydridosilicate at high pressures; A Bridge to BaSiH
polyhydrideBeyer, D. C.*; Spektor, K.*; Vekilova, O. Y.*; Grins, J.*; Barros Brant Carvalho, P. H.*; Leinbach, L. J.*; Sannemo-Targama, M.*; Bhat, S.*; Baran, V.*; Etter, M.*; et al.
ACS Omega (Internet), 10(15), p.15029 - 15035, 2025/04
Times Cited Count:0 Percentile:59.84(Chemistry, Multidisciplinary)Hydridosilicates featuring SiH
octahedral moieties represent a rather new class of compounds with potential properties relating to hydrogen storage and hydride ion conductivity. Here, we report on the new representative BaSiH
obtained from reacting the Zintl phase hydride BaSiH
with H
fluid at pressures above 4 GPa and subsequent decompression to ambient pressure. It consists of complex SiH
ions, which are octahedrally coordinated by Ba
counterions. The arrangement of Ba and Si atoms deviates only slightly from an ideal fcc NaCl structure. IR and Raman spectroscopy showed SiH
bending and stretching modes in the ranges 800-1200 and 1400-1800 cm
, respectively. BaSiH
is thermally stable up to 95
C above which decomposition into BaH
and Si takes place. DFT calculations indicated a direct band gap of 2.5 eV. The discovery of BaSiH
consolidates the compound class of hydridosilicates, accessible from hydrogenations of silicides at gigapascal pressures (
10 GPa). The structural properties of BaSiH
suggest that it presents an intermediate (or precursor) for further hydrogenation at considerably higher pressures to the predicted superconducting polyhydride BaSiH
.
Pandian, K.*; Neikter, M.*; Ekh, M.*; Harjo, S.; Kawasaki, Takuro; Woracek, R.*; Hansson, T.*; Pederson, R.*
JOM, 77(4), p.1803 - 1815, 2025/04
Times Cited Count:1 Percentile:69.96(Materials Science, Multidisciplinary)
Md produced in the
He +
Es reactionNishio, Katsuhisa; Hirose, Kentaro; Makii, Hiroyuki; Orlandi, R.; Kean, K. R.*; Tsukada, Kazuaki; Toyoshima, Atsushi*; Asai, Masato; Sato, Tetsuya; Chiera, N. M.*; et al.
Physical Review C, 111(4), p.044609_1 - 044609_12, 2025/04
Times Cited Count:0 Percentile:74.26(Physics, Nuclear)Sari, A.*; Meleshenkovskii, I.*; Ogawa, Tatsuhiko; Tran, K.-T.*; Jinaphanh, A.*; Jouanne, C.*; Zoia, A.*
Nuclear Instruments and Methods in Physics Research A, 1072, p.170168_1 - 170168_17, 2025/03
Electron accelerators cover a wide range of applications, from nuclear waste package assay and security-related tasks to radiation therapy. High-energy photons produced by electron Bremsstrahlung radiation might induce photonuclear reactions emitting secondary neutrons. In this paper, we perform a two-stage benchmark for Monte Carlo simulation of photoneutron fields from electron accelerators operating in the 4-20 MeV range. On the one hand, we benchmark three independently developed Monte Carlo codes, i.e., MCNP, TRIPOLI-4; and PHITS, using ENDF7u photonuclear data from the ENDF/B-VII.1 library. On the other hand, we benchmark two photonuclear data sub-libraries, i.e., ENDF7u and JENDL-5, as well as nuclear reaction models, using the PHITS code. Errors in ENDF7u for W-184 and Ta-181 cause unphysical shapes of the photoneutron energy spectra with the three codes. Questionable behaviors are also found with JENDL-5, which calls for further examinations in this recently released library. For the cases of heavy water and beryllium, the photoneutron energy spectra obtained with MCNP6 is invalidated. We identified that the problem stems from wrong treatment of the reference frame in using the ACE data files by MCNP and previous versions of PHITS. Results obtained for tungsten and tantalum show that photoneutrons are overall emitted in an isotropic manner. However, results obtained for heavy water and beryllium display different tendencies. This investigation should help Monte Carlo code users to refine the current validity domain of the latest releases of MCNP6, PHITS and TRIPOLI-4 for the simulation of photoneutrons.
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:2 Percentile:88.66(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.
Amano, Yuki; Sachdeva, R.*; Gittins, D.*; Anantharaman, K.*; Lei, S.*; Valentin-Alvarado, L. E.*; Diamond, S.*; Beppu, Hikari*; Iwatsuki, Teruki; Mochizuki, Akihito; et al.
Environmental Microbiome (Internet), 19, p.105_1 - 105_17, 2024/12
Times Cited Count:0 Percentile:0.00(Genetics & Heredity)Zhu, M.*; Romerio, V.*; Steiger, N.*; Nabi, S. D.*; Murai, Naoki; Kawamura, Seiko; Povarov, K. Y.*; Skourski, Y.*; Sibille, R.*; Keller, L.*; et al.
Physical Review Letters, 133(18), p.186704_1 - 186704_6, 2024/11
Times Cited Count:12 Percentile:92.96(Physics, Multidisciplinary)Parisi, A.*; Furutani, K. M.*; Sato, Tatsuhiko; Beltran, C. J.*
Medical Physics, 51(10), p.7589 - 7605, 2024/10
Times Cited Count:4 Percentile:85.64(Radiology, Nuclear Medicine & Medical Imaging)In this study, we have developed an approximate MKM (microdosimetric kinetic model) based on LET (dose-averaged linear energy transfer) to address the challenges of biological relative effectiveness (RBE) models for proton therapy. This is an attempt to apply the mechanism-based approach used in carbon ion therapy to proton beams. This LET-based MKM establishes a correlation between dose-averaged LET and microbiological indices and successfully models survival rates for multiple cell lines. This has resulted in a mathematical description of RBE based on physical quantities that can be readily used in proton therapy planning systems.
Mo,
Mo, and
MoKumar, V.*; Chapman, R.*; Ollier, J.*; Orlandi, R.; Smith, J. F.*; Spohr, K.-M.*; Torres, D. A.*; Wady, P.*; 10 of others*
Physical Review C, 110(4), p.044308_1 - 044308_18, 2024/10
Times Cited Count:2 Percentile:57.54(Physics, Nuclear)
-
transitionsYang, Q.*; Yang, X.*; Wang, Y.*; Fei, Y.*; Li, F.*; Zheng, H.*; Li, K.*; Han, Y.*; Hattori, Takanori; Zhu, P.*; et al.
Nature Communications (Internet), 15, p.7778_1 - 7778_9, 2024/09
Times Cited Count:16 Percentile:92.39(Multidisciplinary Sciences)Luminescent materials that simultaneously embody bright singlet and triplet excitons hold great potential in optoelectronics, signage, and information encryption. However, achieving high-performance white-light emission is severely hampered by their inherent unbalanced contribution of fluorescence and phosphorescence. Herein, we address this challenge by pressure treatment engineering via hydrogen bonding cooperativity effect to realize the mixture of n-
-
transitions, where the triplet state emission was boosted from 7% to 40% in isophthalic acid (IPA). A superior white-light emission based on hybrid fluorescence and phosphorescence was harvested in pressure-treated IPA, and the photoluminescence quantum yield was increased to 75% from the initial 19% (blue-light emission). In-situ high-pressure IR spectra, X ray diffraction, and neutron diffraction reveal continuous strengthening of the hydrogen bonds with the increase of pressure. Furthermore, this enhanced hydrogen bond is retained down to the ambient conditions after pressure treatment, awarding the targeted IPA efficient intersystem crossing for balanced singlet/triplet excitons population and resulting in efficient white-light emission. This work not only proposes a route for brightening triplet states in organic small molecule, but also regulates the ratio of singlet and triplet excitons to construct high-performance white-light emission.
HfAlayed, B.*; Page, R. D.*; Joss, D. T.*; Uusitalo, J.*; Qi, C.*; Briscoe, A. D.*; AlAqeel, M. A. M.*; Andel, B.*; Antalic, S.*; Auranen, K.*; et al.
Physical Review C, 110(3), p.034303_1 - 034303_9, 2024/09