Orientation relationship between TiFeH and TiFe phases in AB-type Ti-Fe-V-Ce hydrogen storage alloy

被引:3
|
作者
Lee, Seung-Yong [1 ]
Ha, Taejun [1 ,2 ]
Suh, Jin-Yoo [1 ]
Kim, Dong-Ik [1 ]
Lee, Young-Su [1 ]
Shim, Jae-Hyeok [1 ,3 ]
机构
[1] Korea Inst Sci & Technol KIST, Energy Mat Res Ctr, Seoul 02792, South Korea
[2] Korea Inst Ind Technol KITECH, Funct Mat & Components R&D Grp, Kangnung 25440, Gangwon, South Korea
[3] Sungkyunkwan Univ SKKU, KIST SKKU Carbon Neutral Res Ctr, Suwon 16419, Gyeonggi, South Korea
关键词
Hydride; Hydrogen storage alloy; Scanning electron microscopy; Electron backscatter diffraction; Orientation relationship; Habit plane; HYDRIDE; DIFFRACTION; DIFFUSION; ENERGY; SYSTEM;
D O I
10.1016/j.jallcom.2024.173943
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The partially hydrogenated microstructure of an AB-type Ti-Fe-V-Ce hydrogen storage alloy was investigated using scanning electron microscopy (SEM) with electron backscatter diffraction (EBSD). For the first time, the formation of the orthorhombic beta-TiFeH phase was directly observed by using SEM-EBSD. Lamellar structures consisting of TiFeH and body-centered cubic TiFe phases with a (100)TiFeH||(100)TiFe habit-plane pair were observed. Pole figure analysis was performed to confirm the orientation relationship between the TiFeH and TiFe phases to be [011](100)TiFeH||[010](100)TiFe. The formation of TiFeH was characterized by simple lattice expansion with a short-range arrangement of H atoms and surface relief. In addition, unidirectional microcracks along the (100)TiFe planes were observed, presumably owing to the dehydrogenation of the TiFeH phase.
引用
收藏
页数:7
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