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Electronic structure of Fe-based amorphous alloys studied using electron-energy-loss spectroscopy

机译:铁基非晶态合金的电子结构,利用电子能量损失谱研究

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The local atomic electronic structures of Fe-Mo-C-B metallic glasses are investigated using electron energy-loss spectroscopy (EELS). The fracture behavior of this Fe-based amorphous alloy system undergoes the transition from being ductile to exhibiting brittleness when alloyed with Cr or Er atoms. In addition, the glass-forming ability is also enhanced. This plastic-to-brittle transition is suggested to correlate with the change of local atomic short-range order or bonding configurations. Therefore, the bonding configuration of Fe-Mo-C-B-Er(Cr) amorphous alloys is investigated by studying the electronic structure of Fe and C atoms using electron energy-loss spectroscopy. It is shown that the normalized EELS white line intensities of Fe-L_(2,3) edges decrease slightly with an increasing amount of Er additions, while no noticeable difference is obtained with Cr additions. As for the C K edge, a prominent change of edge shape is observed for both alloy systems, where the first peak corresponding to a ls→ 1 π* transition increases with increasing Er and Cr additions. Accordingly, it is concluded that changes in the local atomic and electronic structure occur around Fe and C atoms when Er and Cr are introduced into the alloys. Furthermore, it is pointed out that the formation of Er-C and Cr-C carbide like local order inferred from the observed C K edge spectra can provide a plausible explanation for the plastic-to-brittle transition observed in these Fe-based amorphous alloys. In spite of the complexity of electronic and atomic structure in this multicomponent Fe-based metallic glass system, this study could serve as a starting point for providing a qualitative interpretation between electronic structure and plasticity in the Fe-Mo-C-B amorphous alloy system. Complimentary techniques, such as x-ray diffraction and high-resolution transmission electron microscope are also employed, providing a more complete structural characterization.
机译:使用电子能量损失谱(EELS)研究了Fe-Mo-C-B金属玻璃的局部原子电子结构。当与Cr或Er原子合金化时,该Fe基非晶态合金体系的断裂行为经历了从延性转变为表现出脆性的转变。另外,玻璃形成能力也得到增强。建议这种由塑性到脆性的转变与局部原子短程顺序或键构型的变化相关。因此,通过使用电子能量损失谱研究Fe和C原子的电子结构,研究了Fe-Mo-C-B-Er(Cr)非晶态合金的键合构型。结果表明,随着Er的添加量的增加,Fe-L_(2,3)边的归一化EELS白线强度略有降低,而Cr的添加量没有明显的差异。至于C K边缘,在两种合金体系中均观察到边缘形状的显着变化,其中对应于ls→1π*跃迁的第一个峰随Er和Cr添加量的增加而增加。因此,可以得出结论,当将Er和Cr引入合金中时,在Fe和C原子周围发生局部原子和电子结构的变化。此外,要指出的是,从观察到的C K边缘光谱推断出的类似Er-C和Cr-C碳化物的局部顺序的形成,可以为在这些铁基非晶态合金中观察到的塑性到脆性转变提供合理的解释。尽管在这种多成分的铁基金属玻璃系统中电子和原子结构很复杂,但这项研究仍可作为在Fe-Mo-C-B非晶态合金系统中对电子结构和塑性之间进行定性解释的起点。还使用了补充技术,例如X射线衍射和高分辨率透射电子显微镜,可提供更完整的结构表征。

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