New nanostructured phases with reversible hydrogen storage capability in immiscible magnesium-zirconium system produced by high-pressure torsion

被引:79
作者
Edalati, Kaveh [1 ,2 ]
Emami, Hoda [1 ]
Ikeda, Yuji [3 ]
Iwaoka, Hideaki [2 ]
Tanaka, Isao [3 ,4 ]
Akiba, Etsuo [1 ,5 ]
Horita, Zenji [1 ,2 ]
机构
[1] Kyushu Univ, WPI, I2CNER, Fukuoka 8190395, Japan
[2] Kyushu Univ, Fac Engn, Dept Mat Sci & Engn, Fukuoka 8190395, Japan
[3] Kyoto Univ, Ctr Elements Strategy Initiat Struct Mat ESISM, Sakyo Ku, Kyoto 6068501, Japan
[4] Kyoto Univ, Dept Mat Sci & Engn, Kyoto 6068501, Japan
[5] Kyushu Univ, Fac Engn, Dept Mech Engn, Fukuoka 8190395, Japan
关键词
Mg-Zr phase diagram; Phase transformations; Metal hydrides; Mechanical alloying; Density functional theory (DFT); MG-ZR; PLASTIC-DEFORMATION; TETRAHEDRON METHOD; HYDRIDES; ALLOYS; INTERMETALLICS; REFINEMENT; ACTIVATION; MECHANISM; METALS;
D O I
10.1016/j.actamat.2016.02.026
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Mg and Zr are immiscible in the solid and liquid states and do not form any binary phases. In this study, Mg and Zr were significantly dissolved in each other by severe plastic deformation (SPD) through the high-pressure torsion (HPT) method and several new metastable phases were formed: nanostructured hcp, nano-twinned fcc, bcc or ordered bcc-based phases. These supersaturated Mg-Zr phases, which did not decompose up to 773 K, exhibited reversible hydrogen storage capability at room temperature. They absorbed similar to 1 wt.% of hydrogen under 9 MPa in similar to 20 s and fully desorbed the hydrogen in the air. First-principles phonon calculations revealed that the disordered hcp and fcc solid solutions were dynamically stable in the whole composition range of the Mg-Zr system. The bcc or bcc-based ordered phases, which were formed only as intermediate phases during the phase transformation to the hcp solid solution alloy, were energetically higher and were dynamically stable only under limited conditions in the Mg-rich compositions. (C) 2016 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:293 / 303
页数:11
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