Equivalent relative biological effectiveness for cell survival and micronuclei formation; Insights from a biophysical approach

Matsuya, Yusuke; Saga, Ryo*; Wang, Y.*; Sato, Tatsuhiko

Medical Physics, 52(10), p.e70040_1 - e70040_14, 2025/09

https://doi.org/10.1002/mp.70040

Radiation-induced micronuclei (MN), which are chromosome fragments, are currently used as a quantitative indicator of the chromosomal aberrations detectable at a relatively early phase. The technique to assay the MN formation has been followed with increasing interest. However, the meaning of MN and the corresponding cellular responses remains uncertain. This study presents a biophysical model for estimating MN frequency by the extension of an integrated microdosimetric-kinetic (IMK) model that allows the prediction of cell survival after exposure, and theoretically explores the cellular responses associated with MN formation. By introducing a probability of MN formation from lethal lesions due to misrepair, our developed model enables the prediction of MN formation frequency depending on linear energy transfer and dose rate. Our model analyses confirmed that the relative biological effectiveness for cell survival and MN frequency are equivalent under the same irradiation conditions, indicating that MN is useful in both radiation therapy and radiation protection to quantitatively evaluate curative effects and histological damage at early stages after exposure.

All-temperature barocaloric effects at pressure-induced phase transitions

Zhao, X.*; Zhang, Z.*; Hattori, Takanori; Wang, J.*; Li, L.*; Jia, Y.*; Li, W.*; Xue, J.*; Fan, X.*; Song, R.*; et al.

Nature Communications (Internet), 16, p.7713_1 - 7713_8, 2025/08

https://doi.org/10.1038/s41467-025-63068-z

Caloric effects usually occur in the vicinity of solid-state phase transitions with a limited refrigeration temperature span. Here, we introduce and realize an unprecedented concept -all temperature barocaloric effect, i.e., a remarkable barocaloric effect in KPF across an exceptionally wide temperature span, from 77.5 to 300 K and potentially down to 4 K, covering typical room temperature, liquid nitrogen, liquid hydrogen, and liquid helium refrigeration regions. The directly measured barocaloric adiabatic temperature change reaches 12 K at room temperature and 2.5 K at 77.5 K upon the release of a 250 MPa pressure. This effect is attributed to a persistent phase transition to a rhombohedral high pressure phases. We depict the thermodynamic energy landscape to account for the structural instability. This unique all-temperature barocaloric effect presents a novel approach to highly applicable solid-state refrigeration technology, transcending the conventional multi-stage scenario.

in a hadronic molecule and a triangle singularity approach at finite temperature

Zhang, Y.*; Hosaka, Atsushi; Wang, Q.*; Yasui, Shigehiro*

Physical Review D, 112(1), p.016014_1 - 016014_14, 2025/07

https://doi.org/10.1103/5nlp-vwrc

no abstracts in English

On the role of austenite stability in yielding behavior of a medium Mn steel with a duplex austenite-martensite microstructure

Wang, Y.*; Gong, W.; Harjo, S.; 7 of others*

Acta Materialia, 288, p.120840_1 - 120840_14, 2025/04

https://doi.org/10.1016/j.actamat.2025.120840

Solid-state Alder-ene reaction of 1-hexene under high pressure

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

https://doi.org/10.1021/acs.jpclett.4c03696

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.

High-pressure polymerization of phenol toward degree-4 carbon nanothread

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

https://doi.org/10.1021/acs.nanolett.4c04895

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.

Strong low-energy rattling modes enabled liquid-like ultralow thermal conductivity in a well-ordered solid

Liu, P.-F.*; Li, X.*; Li, J.*; Zhu, J.*; Tong, Z.*; Kofu, Maiko*; Nirei, Masami; Xu, J.*; Yin, W.*; Wang, F.*; et al.

National Science Review, 11(12), p.nwae216_1 - nwae216_10, 2024/12

https://doi.org/10.1093/nsr/nwae216

Brightening triplet excitons enable high-performance white-light emission in organic small molecules via integrating n-- transitions

Yang, 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

https://doi.org/10.1038/s41467-024-52196-7

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.

Application of neutron characterization techniques to metallic structural materials

Wang, Y.*; Gong, W.; Su, Y. H.; Li, B.*

Acta Metallurgica Sinica, 60(8), p.1001 - 1016, 2024/08

https://doi.org/10.11900/0412.1961.2024.00063

Dual nanoprecipitation and nanoscale chemical heterogeneity in a secondary hardening steel for ultrahigh strength and large uniform elongation

Wang, S.*; Wang, J.*; Zhang, S.*; Wei, D.*; Chen, Y.*; Rong, X.*; Gong, W.; Harjo, S.; Liu, X.*; Jiao, Z.*; et al.

Journal of Materials Science & Technology, 185, p.245 - 258, 2024/06

https://doi.org/10.1016/j.jmst.2023.10.048