Elucidation of solid particle interfacial phenomena in liquid sodium; Magnetic interactions on liquid metal and solid atoms at the solid interface

Tei, C.; Otaka, Masahiko; Kuwahara, Daisuke*

Chemical Physics Letters, 829, p.140755_1 - 140755_6, 2023/10

https://doi.org/10.1016/j.cplett.2023.140755

We were able to detect the nuclear magnetic resonance (NMR) signal of a liquid sodium clinging to the interface of solid metal particles for the first time. In this study, we confirmed the difference in the relaxation times due to the difference in the interactions between liquid sodium and metal particles suspended in the liquid sodium. It was found that the surface of the micro titanium particles and liquid metallic sodium interact physically, not chemically.

Observation of proton-transfer-coupled spin transition by single-crystal neutron-diffraction measurement

Nakanishi, Takumi*; Hori, Yuta*; Shigeta, Yasuteru*; Sato, Hiroyasu*; Wu, S.-Q.*; Kiyanagi, Ryoji; Munakata, Koji*; Ohara, Takashi; Sato, Osamu*

Physical Chemistry Chemical Physics, 25(17), p.12394 - 12400, 2023/05

https://doi.org/10.1039/D3CP00527E

Roles of excess minority carrier recombination and chemisorbed O species at SiO/Si interfaces in Si dry oxidation; Comparison between p-Si(001) and n-Si(001) surfaces

Tsuda, Yasutaka; Yoshigoe, Akitaka; Ogawa, Shuichi*; Sakamoto, Tetsuya*; Yamamoto, Yoshiki*; Yamamoto, Yukio*; Takakuwa, Yuji*

Journal of Chemical Physics, 157(23), p.234705_1 - 234705_21, 2022/12

https://doi.org/10.1063/5.0109558

Kinetics of the interfacial curing reaction for an epoxy-amine mixture

Yamaguchi, Ko*; Kawaguchi, Daisuke*; Miyata, Noboru*; Miyazaki, Tsukasa*; Aoki, Hiroyuki; Yamamoto, Satoru*; Tanaka, Keiji*

Physical Chemistry Chemical Physics, 24(36), p.21578 - 21582, 2022/09

https://doi.org/10.1039/D2CP03394A

Structures of liquid and aqueous water isotopologues at ambient temperature from path integral simulations

Thomsen, B.; Shiga, Motoyuki

Physical Chemistry Chemical Physics, 24(18), p.10851 - 10859, 2022/05

https://doi.org/10.1039/D2CP00499B

study of nuclear quantum effects on sub- and supercritical water

Thomsen, B.; Shiga, Motoyuki

Journal of Chemical Physics, 155(19), p.194107_1 - 194107_11, 2021/11

https://doi.org/10.1063/5.0071857

Effect of resonant core-level excitation in an atom on photoemission from the neighboring atoms

Baba, Yuji*; Shimoyama, Iwao

Chemical Physics, 550, p.111302_1 - 111302_5, 2021/10

https://doi.org/10.1016/j.chemphys.2021.111302

The effect of a core-to-valence resonant photoexcitation in an atom on photoemission from the neighboring atoms has been experimentally investigated. For SiO fine powder mixed with boron nitride matrix, it was found that the intensity of the O photoelectrons was reduced around the Si resonant photoexcitation. On the other hand, the intensity of the B or N photoelectrons from the matrix material did not change regardless of the photon energy. Similar phenomenon was also observed for SiN powder mixed with cellulose as a matrix material. The results demonstrated that photoemission from the nearest-neighbor atoms that are directly bound to silicon is perturbated by the core-to-valence resonant photoexcitation in silicon. Using the phenomenon, it is expected that species of the nearest neighbor atom can be identified by a resonant core-level excitation in a target atom.

Phase transition and chemical reactivity of 1H-tetrazole under high pressure up to 100 GPa

Gao, D.*; Tang, X.*; Wang, X.*; Yang, X.*; Zhang, P.*; Che, G.*; Han, J.*; Hattori, Takanori; Wang, Y.*; Dong, X.*; et al.

Physical Chemistry Chemical Physics, 23(35), p.19503 - 19510, 2021/09

https://doi.org/10.1039/D1CP02913D

Pressure-induced phase transition and polymerization of nitrogen-rich molecules are widely focused due to its extreme importance for the development of green high energy density materials. Here, we present a study of the phase transition and chemical reaction of 1H-tetrazole up to 100 GPa by using Raman, IR, X-ray diffraction, neutron diffraction techniques and theoretical calculation. A phase transition above 2.6 GPa was identified and the high-pressure structure was determined with one molecule in a unit cell. The 1H-tetrazole polymerizes reversibly below 100 GPa, probably through a carbon-nitrogen bonding instead of nitrogen-nitrogen bonding. Our studies updated the structure model of the high pressure phase of 1H-tetrazole, and presented the possible intermolecular bonding route for the first time, which gives new insights to understand the phase transition and chemical reaction of nitrogen-rich compounds, and benefit for designing new high energy density materials.

Relevance of hydrogen bonded associates to the transport properties and nanoscale dynamics of liquid and supercooled 2-propanol

Zhai, Y.*; Luo, P.*; Nagao, Michihiro*; Nakajima, Kenji; Kikuchi, Tatsuya*; Kawakita, Yukinobu; Kienzle, P. A.*; Z, Y.*; Faraone, A.*

Physical Chemistry Chemical Physics, 23(12), p.7220 - 7232, 2021/03

https://doi.org/10.1039/d0cp05481j

Radiation-induced effects on the extraction properties of hexa--octylnitrilo-triacetamide (HONTA) complexes of americium and europium

Toigawa, Tomohiro; Peterman, D. R.*; Meeker, D. S.*; Grimes, T. S.*; Zalupski, P. R.*; Mezyk, S. P.*; Cook, A. R.*; Yamashita, Shinichi*; Kumagai, Yuta; Matsumura, Tatsuro; et al.

Physical Chemistry Chemical Physics, 23(2), p.1343 - 1351, 2021/01

https://doi.org/10.1039/D0CP05720G

The candidate An(III)/Ln(III) separation ligand hexa--octylnitrilo-triacetamide (HONTA) was irradiated under envisioned SELECT (Solvent Extraction from Liquid waste using Extractants of CHON-type for Transmutation) process conditions using a solvent test loop in conjunction with cobalt-60 gamma irradiation. We demonstrate that HONTA undergoes exponential decay with increasing gamma dose to produce a range of degradation products which have been identified and quantified by HPLC-ESI-MS/MS techniques. The combination of HONTA destruction and degradation product ingrowth, particularly dioctylamine, negatively impacts the extraction and back-extraction of both americium and europium ions. The loss of HONTA was attributed to its reaction with the solvent (-dodecane) radical cation of (HONTA + R) = (7.61 0.82) 10 M s obtained by pulse radiolysis techniques. However, when this ligand is bound to either americium or europium ions, the observed -dodecane radical cation kinetics increase by over an order of magnitude. This large reactivity increase to additional reaction pathways occurring upon metal-ion binding. Lastly nanosecond time-resolved measurements showed that both direct and indirect HONTA radiolysis yielded the short-lived (100 ns) HONTA radical cation as well as a longer-lived (s) HONTA triplet excited state. These HONTA species are important precursors to the suite of HONTA degradation products observed.