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首页> 外文期刊>Science and technology of advanced materials >Crystal structure of η″-Fesub3/subAlsub7+ x /sub determined by single-crystal synchrotron X-ray diffraction combined with scanning transmission electron microscopy
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Crystal structure of η″-Fesub3/subAlsub7+ x /sub determined by single-crystal synchrotron X-ray diffraction combined with scanning transmission electron microscopy

机译:η“-fe 3 Al 7+ x 通过单晶同步X射线衍射和扫描透射电子显微镜确定确定的晶体结构

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The crystal structure of η″-Fesub3/subAlsub7+x/sub , the low-temperature phase of η-Fesub2/subAlsub5/sub with a composition on the Fe-rich side of the solid solubility range, has been determined by synchrotron X-ray single-crystal diffraction combined with scanning transmission electron microscopy. The η″ phase possesses commensurate long-period-ordered superlattice structures (space group Pmcn) based on the parent orthorhombic unit cell of η-Fesub2/subAlsub5/sub, consisting of twin domains (orientation variants) alternately stacked along the long-periodicity axis. Each of the twin domains possesses a motif structure belonging to the base-centered monoclinic space group C2/m, with a cell volume twice that of the parent orthorhombic unit cell (space group Cmcm). One-fourth of the c-axis chain sites corresponding to Al2- and Al3-sites in the η phase are respectively occupied by both Fe and Al atoms and exclusively by Al atoms in a regular manner. This regularity is disturbed in the twin-boundary region, giving rise to structural/compositional modulation. Because of the different chemical compositions between the motif structure and twin-boundary region, the η″ phase with various compositions can be constructed only by changing the number of the parent orthorhombic unit cells to be stacked along the orthorhombic c-axis, without changing the atomic arrangements for the motif structure or the twin boundary to account for the observed solid solubility range. The chemical formula of the η″ phase can thus be expressed as Fesub3/subAlsub7+x/sub under a simple assumption on the occupancies for Al/Fe atoms in the c-axis chain sites.
机译:η“-fe 3 Al 7 + x ,η-fe 2 Al 5的低温相位的晶体结构在固体溶解度范围的Fe的含量上的组合物中,通过同步X射线单晶衍射与扫描透射电子显微镜联合确定。 η“相具有基于η-fe 2 Al 5 的母体正交单位单元的长期有序的超晶格结构(空间组pmcn),由双胞胎组成域(定向变型)沿长周期轴交替堆叠。每个双结构域具有属于基居中心单斜视组C2 / m的基序结构,细胞体积是母体正交单元细胞(空间组CMCM)的两倍。对应于η相中的Al 2和Al3-位点的C轴链位点的四分之一分别由Fe和Al原子分别由Al Atoms以规则方式占据。在双边界区域中,这种规律性受到干扰,产生了结构/组成调节。由于基序结构和双边界区域之间的不同化学组成,η“相对于各种组合物的相位可以仅通过改变沿邻骨C轴堆叠的母体正极单元单元的数量来构造,而不改变主题结构或双边界的原子布置,以考虑观察到的固体溶解度范围。因此,η“相的化学式可以在C轴上的Al / Fe原子占用的简单假设下表示为Fe 3 Al 7 + x / sub>连锁网站。

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