Hiroya SAKURAI

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Organization: NIMS , Japan
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Title: (PhD)

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Co-reporter:Ting-Hui Kao, Hiroya Sakurai, Taras Kolodiazhnyi, Yutaro Suzuki, Momoko Okabe, Toru Asaka, Koichiro Fukuda, Susumu Okubo, Shohei Ikeda, Shigeo Hara, Takahiro Sakurai, Hitoshi Ohta and Hung-Duen Yang  
Journal of Materials Chemistry A 2015 vol. 3(Issue 14) pp:3452-3459
Publication Date(Web):05 Feb 2015
DOI:10.1039/C4TC02458C
YSrCrO4 is first synthesized and found to be a hettotype of the K2NiF4 structure, although the combination of Y and Sr ions in K2NiF4-type oxides is very rare. The space group of the compound is determined to be orthorhombic Pccn by the electron diffraction and the powder X-ray diffraction. Magnetic and dielectric properties of the compound, together with LaSrCrO4, YCaCrO4 and A2MnO4 (A = Sr and Ca), are investigated. YSrCrO4 shows two-dimensional (2D) spin correlations and a canted antiferromagnetic (AF) ordering. With increasing distortion of the crystal structure, 2D spin correlations and the AF transition temperature decrease, while spontaneous magnetization increases. From the multi-frequency electron spin resonance (ESR) measurements, the g-values of the paramagnetic state are estimated to be 1.976, 1.978 and 1.976 for YSrCrO4, LaSrCrO4 and YCaCrO4, respectively. Evidence of AF ordering of the Cr oxides is obtained microscopically from ESR. The dielectric measurements suggest the existence of in-gap states, while no magneto-dielectric coupling was observed in the above compounds.
Co-reporter:Dr. Hiroya Sakurai;Dr. Taras Kolodiazhnyi;Dr. Yuichi Michiue;Dr. Eiji Takayama-Muromachi;Yuichi Tanabe;Dr. Hikomitsu Kikuchi
Angewandte Chemie International Edition 2012 Volume 51( Issue 27) pp:6653-6656
Publication Date(Web):
DOI:10.1002/anie.201201884
Co-reporter:Dr. Hiroya Sakurai;Dr. Taras Kolodiazhnyi;Dr. Yuichi Michiue;Dr. Eiji Takayama-Muromachi;Yuichi Tanabe;Dr. Hikomitsu Kikuchi
Angewandte Chemie 2012 Volume 124( Issue 27) pp:6757-6760
Publication Date(Web):
DOI:10.1002/ange.201201884
Co-reporter:Hiroya Sakurai, Minoru Osada and Eiji Takayama-Muromachi
Chemistry of Materials 2007 Volume 19(Issue 25) pp:6073
Publication Date(Web):November 14, 2007
DOI:10.1021/cm0714786
It was found that Na+ ions in NaxCoO2 can be partially substituted by H3O+ ions while maintaining a constant Co valence simply by immersion in water. The magnetic susceptibility of Nax(H3O)zCoO2 (x + z = 0.70) changed drastically from Curie–Weiss type to Pauli paramagnetic type, indicating that the electronic band structure was modified by the isovalent ion substitution of Na+/H3O+. Two possible origins of the change in the electronic structure are discussed.
Co-reporter:Ting-Hui Kao, Hiroya Sakurai, Taras Kolodiazhnyi, Yutaro Suzuki, Momoko Okabe, Toru Asaka, Koichiro Fukuda, Susumu Okubo, Shohei Ikeda, Shigeo Hara, Takahiro Sakurai, Hitoshi Ohta and Hung-Duen Yang
Journal of Materials Chemistry A 2015 - vol. 3(Issue 14) pp:NaN3459-3459
Publication Date(Web):2015/02/05
DOI:10.1039/C4TC02458C
YSrCrO4 is first synthesized and found to be a hettotype of the K2NiF4 structure, although the combination of Y and Sr ions in K2NiF4-type oxides is very rare. The space group of the compound is determined to be orthorhombic Pccn by the electron diffraction and the powder X-ray diffraction. Magnetic and dielectric properties of the compound, together with LaSrCrO4, YCaCrO4 and A2MnO4 (A = Sr and Ca), are investigated. YSrCrO4 shows two-dimensional (2D) spin correlations and a canted antiferromagnetic (AF) ordering. With increasing distortion of the crystal structure, 2D spin correlations and the AF transition temperature decrease, while spontaneous magnetization increases. From the multi-frequency electron spin resonance (ESR) measurements, the g-values of the paramagnetic state are estimated to be 1.976, 1.978 and 1.976 for YSrCrO4, LaSrCrO4 and YCaCrO4, respectively. Evidence of AF ordering of the Cr oxides is obtained microscopically from ESR. The dielectric measurements suggest the existence of in-gap states, while no magneto-dielectric coupling was observed in the above compounds.
calcium dichromium tetraoxide
Cobalt oxide, hydrate