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Fujiwara, Hidenori*; Nakatani, Yasuhiro*; Aratani, Hidekazu*; Kanai, Yuina*; Yamagami, Kohei*; Hamamoto, Satoru*; Kiss, Takayuki*; Yamasaki, Atsushi*; Higashiya, Atsushi*; Imada, Shin*; et al.
Physical Review B, 108(16), p.165121_1 - 165121_10, 2023/10
Times Cited Count:0 Percentile:0.00(Materials Science, Multidisciplinary)Davies, S. J. C.*; Bolea-Alamanac, B.*; Endo, Kaori*; Yamamoto, Yu*; Yamasaki, Shudo*; Malins, A.; Evans, J.*; Sullivan, S.*; Ando, Shuntaro*; Nishida, Atsushi*; et al.
Journal of Transport & Health, 28, p.101564_1 - 101564_11, 2023/01
Saito, Yuji; Fujiwara, Hidenori*; Yasui, Akira*; Kadono, Toshiharu*; Sugawara, Hitoshi*; Kikuchi, Daisuke*; Sato, Hideyuki*; Suga, Shigemasa*; Yamasaki, Atsushi*; Sekiyama, Akira*; et al.
Physical Review B, 102(16), p.165152_1 - 165152_8, 2020/10
Times Cited Count:1 Percentile:4.84(Materials Science, Multidisciplinary)Muramatsu, Haruka*; Hayashi, Tasuku*; Yuasa, Naoki*; Konno, Ryohei*; Yamaguchi, Atsushi*; Mitsuda, Kazuhisa*; Yamasaki, Noriko*; Maehata, Keisuke*; Kikunaga, Hidetoshi*; Takimoto, Misaki; et al.
Journal of Low Temperature Physics, 200(5-6), p.452 - 460, 2020/09
Times Cited Count:2 Percentile:10.49(Physics, Applied)Yamaguchi, Atsushi*; Muramatsu, Haruka*; Hayashi, Tasuku*; Yuasa, Naoki*; Nakamura, Keisuke; Takimoto, Misaki; Haba, Hiromitsu*; Konashi, Kenji*; Watanabe, Makoto*; Kikunaga, Hidetoshi*; et al.
Physical Review Letters, 123(22), p.222501_1 - 222501_6, 2019/11
Times Cited Count:43 Percentile:89.99(Physics, Multidisciplinary)Aratani, Hidekazu*; Nakatani, Yasuhiro*; Fujiwara, Hidenori*; Kawada, Moeki*; Kanai, Yuina*; Yamagami, Kohei*; Fujioka, Shuhei*; Hamamoto, Satoru*; Kuga, Kentaro*; Kiss, Takayuki*; et al.
Physical Review B, 98(12), p.121113_1 - 121113_6, 2018/09
Times Cited Count:5 Percentile:23.50(Materials Science, Multidisciplinary)Nakatani, Yasuhiro*; Aratani, Hidekazu*; Fujiwara, Hidenori*; Mori, Takeo*; Tsuruta, Atsushi*; Tachibana, Shoichi*; Yamaguchi, Takashi*; Kiss, Takayuki*; Yamasaki, Atsushi*; Yasui, Akira*; et al.
Physical Review B, 97(11), p.115160_1 - 115160_7, 2018/03
Times Cited Count:5 Percentile:23.50(Materials Science, Multidisciplinary)Nakatani, Yasuhiro*; Fujiwara, Hidenori*; Aratani, Hidekazu*; Mori, Takeo*; Tachibana, Shoichi*; Yamaguchi, Takashi*; Kiss, Takayuki*; Yamasaki, Atsushi*; Yasui, Akira*; Yamagami, Hiroshi*; et al.
Journal of Electron Spectroscopy and Related Phenomena, 220, p.50 - 53, 2017/01
Times Cited Count:2 Percentile:15.91(Spectroscopy)We report the soft X-ray angle-resolved photoemission study for LaNiGe to reveal the electronic structures derived from non-4 bands of the heavy fermion compound CeNiGe. The photoemission spectra recorded at the La M absorption edges clearly show the enhancement of the La 5 components in the valence band spectra. The circular dichroism of photoemission spectra reveals the band-dependent dichroic response due to the orbital symmetry.
Yamasaki, Atsushi*; Fujiwara, Hidenori*; Tachibana, Shoichi*; Iwasaki, Daisuke*; Higashino, Yuji*; Yoshimi, Chiaki*; Nakagawa, Koya*; Nakatani, Yasuhiro*; Yamagami, Kohei*; Aratani, Hidekazu*; et al.
Physical Review B, 94(11), p.115103_1 - 115103_10, 2016/11
Times Cited Count:17 Percentile:59.01(Materials Science, Multidisciplinary)In this study, we systematically investigate three-dimensional(3D) momentum-resolved electronic structures of Ruddlesden-Popper-type iridium oxides SrIrO using soft-X-ray angle-resolved photoemission spectroscopy (SX-ARPES). Our results provide direct evidence of an insulator-to-metal transition that occurs upon increasing the dimensionality of the IrO-plane structure. This transition occurs when the spin-orbit-coupled = 1/2 band changes its behavior in the dispersion relation and moves across the Fermi energy. By scanning the photon energy over 350 eV, we reveal the 3D Fermi surface in SrIrO and -dependent oscillations of photoelectron intensity in SrIrO. To corroborate the physics deduced using low-energy ARPES studies, we propose to utilize SX-ARPES as a powerful complementary technique, as this method surveys more than one whole Brillouin zone and provides a panoramic view of electronic structures.
Berner, G.*; Sing, M.*; Fujiwara, Hidenori*; Yasui, Akira*; Saito, Yuji; Yamasaki, Atsushi*; Nishitani, Yoshihito*; Sekiyama, Akira*; Pavlenko, N.*; Kopp, T.*; et al.
Physical Review Letters, 110(24), p.247601_1 - 247601_5, 2013/06
Times Cited Count:135 Percentile:96.30(Physics, Multidisciplinary)The interface between LaAlO and SrTiO hosts a two-dimensional electron system of itinerant carriers, although both oxides are band insulators. Interface ferromagnetism coexisting with superconductivity has been found and attributed to local moments. Experimentally, it has been established that Ti 3 electrons are confined to the interface. Using soft X-ray angle-resolved resonant photoelectron spectroscopy we have directly mapped the interface states in space. Our data demonstrate a charge dichotomy. A mobile fraction contributes to Fermi surface sheets, whereas a localized portion at higher binding energies is tentatively attributed to electrons trapped by O vacancies in the SrTiO.
Nagata, Hidezumi*; Hirao, Norie*; Onoki, Takamasa*; Baba, Yuji; Yamasaki, Yuki*; Nakahira, Atsushi*
Journal of the Ceramic Society of Japan, 116(1350), p.216 - 219, 2008/02
Times Cited Count:10 Percentile:51.78(Materials Science, Ceramics)Bulky palladium catalyst supported on mesoporous silica (Pd-MCM-41) was successfully synthesized by hydrothermal hot-pressing method. The structure of the palladium species in Pd-MCM-41 bulk before and after heat-treatment process was investigated by X-ray diffraction (XRD), X-ray absorption near edge structure (XANES) and transmission electron microscopy (TEM). On the basis of these results, the microstructures and mesoporous properties of Pd-MCM-41 were discussed. As a result, it was revealed that the obtained Pd-MCM-41 bulks possessed a high area of over 1000 m/g and the electronic state of palladium in Pd-MCM-41 bulk is almost equal to palladium (0) metal.
Wada, Atsushi*; Watanabe, Masayuki; Yamanoi, Yoshinori*; Nankawa, Takuya; Namiki, Kosuke*; Yamasaki, Mikio*; Murata, Masaki*; Nishihara, Hiroshi*
Bulletin of the Chemical Society of Japan, 80(2), p.335 - 345, 2007/02
Times Cited Count:22 Percentile:56.90(Chemistry, Multidisciplinary)Lanthanide complexes with linear and cyclic octadentate oligopyridine-amine ligands were synthesized, and their molecular structures were determined by single-crystal X-ray crystallography. All of the complexes had a distorted capped square antiprism (CSAP) geometry, and the coordination environments of lanthanide complexes were more distortedfor the complexes with the linear ligand than those with the cyclic ligand. The Eu complexes with the linear ligand showed more intense emissions, which were attributed to the D F transition, than the complex withthe cyclic ligand in acetonitrile, which can be attributed to the distortion in the coordination environments. These results indicate that the coordination environments of lanthanide complexes, and thus the luminescence properties, can be controlled by tuning the geometrical structures of polydentate ligands.
Mo, S.-K.*; Kim, H.-D.*; Denlinger, J. D.*; Allen, J. W.*; Park, J.-H.*; Sekiyama, Akira*; Yamasaki, Atsushi*; Suga, Shigemasa*; Saito, Yuji; Muro, Takayuki*; et al.
Physical Review B, 74(16), p.165101_1 - 165101_12, 2006/10
Times Cited Count:49 Percentile:84.47(Materials Science, Multidisciplinary)We present high-resolution bulk-sensitive photoemission spectra of (V)O (=Cr,Ti). The measurements were made for the paramagnetic metal (PM), paramagnetic insulator (PI), and antiferromagnetic insulator (AFI) phases of (V)O. In the PM phase, we observe a prominent quasiparticle peak in general agreement with theory, which combines dynamical mean-field theory with the local density approximation. For both the PI and AFI phases, the vanadium 3 parts of the valence spectra are not simple one peak structures. For the PI phase, there is not yet a good theoretical understanding of these structures. Spectra taken in the same phases with different compositions show interesting monotonic changes as the dopant concentration increases, regardless of the dopant species. With increased Cr-doping, the AFI phase gap decreases and the PI phase gap increases.
Mo, S.-K.*; Denlinger, J. D.*; Kim, H.-D.*; Park, J.-H.*; Allen, J. W.*; Sekiyama, Akira*; Yamasaki, Atsushi*; Kadono, Koji*; Suga, Shigemasa*; Saito, Yuji; et al.
Physical Review Letters, 90(18), p.186403_1 - 186403_4, 2003/05
Times Cited Count:143 Percentile:95.37(Physics, Multidisciplinary)no abstracts in English
Iwasaki, T.*; Sekiyama, Akira*; Yamasaki, Atsushi*; Okazaki, Makoto*; Kadono, Koji*; Utsunomiya, Hiroshi*; Imada, Shin*; Saito, Yuji; Muro, Takayuki*; Matsushita, Tomohiro*; et al.
Physical Review B, 65(19), p.195109_1 - 195109_9, 2002/05
Times Cited Count:24 Percentile:71.27(Materials Science, Multidisciplinary)no abstracts in English
Yamasaki, Atsushi*; Imada, Shin*; Arai, Ryuji*; Utsunomiya, Hiroshi*; Suga, Shigemasa*; Muro, Takayuki*; Saito, Yuji; Kanomata, Takeshi*; Ishida, Shoji*
Physical Review B, 65(10), p.104410_1 - 104410_6, 2002/03
Times Cited Count:61 Percentile:89.14(Materials Science, Multidisciplinary)The magnetic circular dichroism (MCD) of core-level absorption [x-ray absorption spectroscopy (XAS)] spectra in the soft x-ray region has been measured for the ferromagnetic Heusler alloys CoTiSn, CoZrSn, and CoNbSn. The many-peak structures which are clearly observed in the Co 2p-3d XAS-MCD spectra cannot be well explained by atomic multiplet calculations but are better explained by the Co 3d unoccupied states predicted by linear muffin-tin orbital atomic sphere approximation band structure calculations. The MCD spectra show an obvious contribution of the orbital angular momentum component to the magnetic moment in these alloys. The ratio between the orbital angular momentum and spin derived from the MCD spectra varies by more than a factor of 2 within these alloys. The mechanism of this variation is discussed in comparison with the band structure calculations.
Yamasaki, Atsushi*; Imada, Shin*; Utsunomiya, Hiroshi*; Muro, Takayuki*; Saito, Yuji; Negishi, H.*; Sasaki, M.*; Inoue, M.*; Suga, Shigemasa*
Physica E, 10(1-3), p.387 - 390, 2001/05
Times Cited Count:5 Percentile:32.03(Nanoscience & Nanotechnology)no abstracts in English
Kato, Junya; Miyauchi, Atsushi; Yamasaki, Akito*
no journal, ,
no abstracts in English
Kato, Junya; Miyauchi, Atsushi; Aoshima, Atsushi; Shiotsuki, Masao; Yamashita, Teruo; Nakajima, Masayoshi; Morikawa, Yo; Miura, Akihiko; Fukui, Toshiki*; Yamasaki, Akito*; et al.
no journal, ,
no abstracts in English
Tanaka, Keita*; Hirano, Kosuke*; Yamaguchi, Atsushi*; Muramatsu, Haruka*; Hayashi, Tasuku*; Yuasa, Naoki*; Nakamura, Keisuke; Takimoto, Misaki; Haba, Hiromitsu*; Shirasaki, Kenji*; et al.
no journal, ,
Muramatsu, Haruka*; Yuasa, Naoki*; Hayashi, Tasuku*; Konno, Ryohei*; Yamaguchi, Atsushi*; Mitsuda, Kazuhisa*; Yamasaki, Noriko*; Kikunaga, Hidetoshi*; Nakamura, Keisuke; Takimoto, Misaki; et al.
no journal, ,
no abstracts in English