Browsing by Author "Azuma, M"

Now showing 1 - 2 of 2
  • No Thumbnail Available
    Item
    Hydrothermal synthesis, crystal structure, and superconductivity of a double-perovskite Bi oxide
    (American Chemical Society, 2015-12-23) Rubel, MHK; Takei, T; Kumada, N; Ali, MM; Miura, A; Tadanaga, K; Oka, K; Azuma, M; Yashima, M; Fujii, K; Magome, E; Moriyoshi, C; Kuroiwa, Y; Hester, JR; Avdeev, M
    Double-perovskite Bi oxides are a new series of superconducting materials, and their crystal structure and superconducting properties are under investigation. In this paper, we describe the synthesis and characterization of a new double-perovskite material that has an increased superconductive transition temperature of 31.5 K. The structure of the material was examined using powder neutron diffraction (ND), synchrotron X-ray diffraction (SXRD), and transmission electron microscopy (TEM). Rietveld refinement of the sample based on ND and SXRD data confirmed an A-site-ordered (K1.00)(Ba1.00)3(Bi0.89Na0.11)4O12 double-perovskite-type structure with the space group Im3̅m (No. 229). This structural analysis revealed the incorporation of Na with Bi in the structure and a bent bond between (Na, Bi)–O–(Na, Bi). TEM analyses also confirmed a cubic double-perovskite structure. This hydrothermally synthesized compound exhibited a large shielding volume fraction, exceeding 100%, with onset of superconductivity at ∼31.5 K. Its electrical resistivity dropped near onset at ∼28 K, and zero resistivity was confirmed below 13 K. The calculated band structure revealed that the metallicity of the compound and the flatness of the conduction bands near the Fermi level (EF) are important for the appearance of superconductivity. © 2015 American Chemical Society
  • No Thumbnail Available
    Item
    Pressure-modulated magnetism and negative thermal expansion in the Ho2Fe17 intermetallic compound
    (American Chemical Society, 2023-05-25) Cao, YL; Zhou, H; Khmelevskyi, S; Lin, K; Avdeev, M; Wang, CW; Wang, B; Hu, F; Kato,; Hattori, T; Abe, J; Ohara, K; Kawaguchi, S; Li, Q; Fukuda, M; Nishikubo, T; Lee, K; Koike, T; Liu, Q; Miao, J; Deng, JX; Shen, B; Azuma, M; Xing, X
    Hydrostatic and chemical pressure are efficient stimuli to alter the crystal structure and are commonly used for tuning electronic and magnetic properties in materials science. However, chemical pressure is difficult to quantify and a clear correspondence between these two types of pressure is still lacking. Here, we study intermetallic candidates for a permanent magnet with a negative thermal expansion (NTE). Based on in situ synchrotron X-ray diffraction, negative chemical pressure is revealed in Ho2Fe17 on Al doping and quantitatively evaluated by using temperature and pressure dependence of unit cell volume. A combination of magnetization and neutron diffraction measurements also allowed one to compare the effect of chemical pressure on magnetic ordering with that of hydrostatic pressure. Intriguingly, pressure can be used to control suppression and enhancement of NTE. Electronic structure calculations indicate that pressure affected the top of the majority band with respect to the Fermi level (EF), which has implications for the magnetic stability, which in turn plays a critical role in modulating magnetism and NTE. This work presents a good example of understanding the effect of pressure and utilizing it to control properties of functional materials. © 2024 American Chemical Society