Mass-resolved momentum imaging of three dichloroethylene isomers by femtosecond laser-induced coulomb explosion

Wada, Yoriko*; Akagi, Hiroshi*; Kumada, Takayuki; Itakura, Ryuji*; Wakabayashi, Tomonari*

Photochem (Internet), 2(3), p.798 - 809, 2022/09

https://doi.org/10.3390/photochem2030051

Coulomb explosion experiments using 60 fs laser pulses were conducted for structural characterization of three dichloroethylene isomers. Under laser intensity at 1.8 10 W/cm, mass-resolved momentum imaging (MRMI) for selected fragment ions of Cl and C revealed different patterns for the three isomers. The C ion fragmented from multiply charged trans-1,2-DCE was forced to leave perpendicularly to the direction of the laser polarization, due to recoil forces from adjacent cations. In contrast, the fast ions of C from cis-1,2-DCE exhibited an isotropic distribution, whereas the fast ions of C from 1,1-DCE recoiled along the laser polarization together with the slow C ions, and thereby distinction of the three isomers was demonstrated. Coulomb explosion occurs predominantly at specific orientation, which is useful for potential applications of MRMI analysis to molecular structure assays.

Production of Bh in the Cm(Na,5)Bh reaction and its decay properties

Haba, Hiromitsu*; Fan, F.*; Kaji, Daiya*; Kasamatsu, Yoshitaka*; Kikunaga, Hidetoshi*; Komori, Yukiko*; Kondo, Narumi*; Kudo, Hisaaki*; Morimoto, Koji*; Morita, Kosuke*; et al.

Physical Review C, 102(2), p.024625_1 - 024625_12, 2020/08

https://doi.org/10.1103/PhysRevC.102.024625

Electronic structure of the high- ferromagnetic semiconductor (Ga,Fe)Sb; X-ray magnetic circular dichroism and resonance photoemission spectroscopy studies

Sakamoto, Shoya*; Tu, N. T.*; Takeda, Yukiharu; Fujimori, Shinichi; Hai, P. N.*; Anh, L. D.*; Wakabayashi, Yuki*; Shibata, Goro*; Horio, Masafumi*; Ikeda, Keisuke*; et al.

Physical Review B, 100(3), p.035204_1 - 035204_8, 2019/07

https://doi.org/10.1103/PhysRevB.100.035204

Cation distribution and magnetic properties in ultrathin (NiCo)FeO (x=0-1) layers on Si(111) studied by soft X-ray magnetic circular dichroism

Wakabayashi, Yuki*; Nonaka, Yosuke*; Takeda, Yukiharu; Sakamoto, Shoya*; Ikeda, Keisuke*; Chi, Z.*; Shibata, Goro*; Tanaka, Arata*; Saito, Yuji; Yamagami, Hiroshi; et al.

Physical Review Materials (Internet), 2(10), p.104416_1 - 104416_12, 2018/10

https://doi.org/10.1103/PhysRevMaterials.2.104416

Method to reduce long-lived fission products by nuclear transmutations with fast spectrum reactors

Chiba, Satoshi*; Wakabayashi, Toshio*; Tachi, Yoshiaki; Takaki, Naoyuki*; Terashima, Atsunori*; Okumura, Shin*; Yoshida, Tadashi*

Scientific Reports (Internet), 7(1), p.13961_1 - 13961_10, 2017/10

https://doi.org/10.1038/s41598-017-14319-7

Transmutation of long-lived fission products (LLFPs: Se, Zr, Tc, Pd, I, and Cs) into short-lived or non-radioactive nuclides by fast neutron spectrum reactors without isotope separation has been proposed as a solution to the problem of radioactive wastes disposal. Despite investigation of many methods, such transmutation remains technologically difficult. To establish an effective and efficient transmutation system, we propose a novel neutron moderator material, yttrium deuteride (YD), to soften the neutron spectrum leaking from the reactor core. Neutron energy spectra and effective half-lives of LLFPs, transmutation rates, and support ratios were evaluated with the continuous-energy Monte Carlo code MVP-II/MVP-BURN and the JENDL-4.0 cross section library. With the YD moderator in the radial blanket and shield regions, effective half-lives drastically decreased from 10 to 10 years and the support ratios reached 1.0 for all six LLFPs. This successful development and implementation of a transmutation system for LLFPs without isotope separation contribute to developing a self-consuming cycle of LLFPs using fast spectrum reactors to reduce radioactive waste.

Origin of robust nanoscale ferromagnetism in Fe-doped Ge revealed by angle-resolved photoemission spectroscopy and first-principles calculation

Sakamoto, Shoya*; Wakabayashi, Yuki*; Takeda, Yukiharu; Fujimori, Shinichi; Suzuki, Hakuto*; Ban, Yoshisuke*; Yamagami, Hiroshi; Tanaka, Masaaki*; Oya, Shinobu*; Fujimori, Atsushi*

Physical Review B, 95(7), p.075203_1 - 075203_5, 2017/02

https://doi.org/10.1103/PhysRevB.95.075203

Complex chemistry with complex compounds

Eichler, R.*; Asai, Masato; Brand, H.*; Chiera, N. M.*; Di Nitto, A.*; Dressler, R.*; Dllmann, Ch. E.*; Even, J.*; Fangli, F.*; Goetz, M.*; et al.

EPJ Web of Conferences, 131, p.07005_1 - 07005_7, 2016/12

https://doi.org/10.1051/epjconf/201613107005

In recent years gas-phase chemical studies assisted by physical pre-separation allowed for the productions and investigations of fragile single molecular species of superheavy elements. The latest highlight is the formation of very volatile hexacarbonyl compound of element 106, Sg(CO). Following this success, second-generation experiments were performed to measure the first bond dissociation energy between the central metal atom and the surrounding ligand. The method using a tubular decomposition reactor was developed and successfully applied to short-lived Mo(CO), W(CO), and Sg(CO).

Decomposition studies of group 6 hexacarbonyl complexes, 1; Production and decomposition of Mo(CO) and W(CO)

Usoltsev, I.*; Eichler, R.*; Wang, Y.*; Even, J.*; Yakushev, A.*; Haba, Hiromitsu*; Asai, Masato; Brand, H.*; Di Nitto, A.*; Dllmann, Ch. E.*; et al.

Radiochimica Acta, 104(3), p.141 - 151, 2016/03

https://doi.org/10.1515/ract-2015-2445

Conditions of the production and decomposition of hexacarbonyl complexes of short-lived Mo and W isotopes were investigated to study thermal stability of the heaviest group 6 hexacarbonyl complex Sg(CO). A tubular flow reactor was tested to decompose the hexacarbonyl complexes and to extract the first bond dissociation energies. A silver was found to be the most appropriate reaction surface to study the decomposition of the group 6 hexacarbonyl. It was found that the surface temperature at which the decomposition occurred was correlated to the first bond dissociation energy of Mo(CO) and W(CO), indicating that the first bond dissociation energy of Sg(CO) could be determined with this technique.

Development of a measurement system for the determination of () cross-sections using multi-nucleon transfer reactions

Makii, Hiroyuki; Ota, Shuya*; Ishii, Tetsuro; Wakabayashi, Yasuo*; Furutaka, Kazuyoshi; Nishio, Katsuhisa; Nishinaka, Ichiro; Chiba, Satoshi; Igashira, Masayuki*; Czeszumska, A.*

Nuclear Instruments and Methods in Physics Research A, 797, p.83 - 93, 2015/10

https://doi.org/10.1016/j.nima.2015.05.005

We have installed new experimental apparatus to measure rays from highly excited states populated by the multi-nucleon transfer reactions with heavy-ion projectiles to determine the () cross sections by means of the surrogate reaction method. Apparatus consists of two anti-Compton LaBr(Ce) spectrometers to measure the rays and a Si - detector system to detect outgoing projectile-like particles. Reactions of 153-MeV O beams with Gd and Gd targets were used to study the performance of apparatus. By using the LaBr(Ce) scintillators with relatively large volume (101.6 mm in diameter and 127 mm in length), we have successfully measured rays from the compound nuclei, which have excitation energy above neutron separation energy, populated by Gd(O, O)Gd and Gd(O, O)Gd two-neutron transfer reactions. The present study has demonstrated high capability of apparatus to measure the de-excitation rays in the compound nuclei produced by the multi-nucleon transfer reactions for determination of the () cross sections by using the surrogate reaction method.

Performance of new gas-filled recoil ion separator GARIS-II for asymmetric fusion reaction

Kaji, Daiya*; Morimoto, Koji*; Wakabayashi, Yasuo*; Takeyama, Mirei*; Yamaki, Sayaka*; Tanaka, Kengo*; Haba, Hiromitsu*; Huang, M.*; Murakami, Masashi*; Kanaya, Jumpei*; et al.

JPS Conference Proceedings (Internet), 6, p.030107_1 - 030107_4, 2015/06

https://doi.org/10.7566/JPSCP.6.030107

Performance of the new gas-filled recoil ion separator GARIS-II was investigated using asymmetric Ne-induced fusion reactions. The use of He-H mixture gas for the gas-filled magnet significantly reduced background scattered particles detected at the focal-plane Si detector, and increased a transmission of the asymmetric reaction products. A target-identification system was newly installed for efficient measurements of excitation functions without changing beam energy nor target.