Electron microscopy studies on interfacial solid-state reactions induced by electronic excitation.

Kazuhisa Sato
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Abstract

We have studied the effects of electron irradiation on Pt/a-SiOx thin films by transmission electron microscopy and electron diffraction. Pt2Si was formed by 75 keV electron irradiation at 298 K and 90 K. Such a low temperature synthesis of Pt2Si can be attributed to the dissociation of a-SiOx induced by electronic excitation; Si-O bonds dissociate through Auger decay of core-holes generated by electronic excitation, and then, dissociated Si atoms form Pt-Si bonds. The morphology of Pt islands extensively changed during Pt2Si formation even at 90 K. Coalescence and growth of metallic particles are not due to thermal effects during electron irradiation but to athermal processes accompanied by silicide formation. To maintain the reaction interface between metallic particles and the dissociated Si atoms by electronic excitation, a considerable concomitant morphology change occurs. Similarly, Fe2Si was synthesized by using the same technique. In this way, we have demonstrated a versatile method for selectively forming nanoscale metal silicides in electron irradiated areas at room temperature. We also propose a new mechanism for crystallization of amorphous alloys which is mediated by additional solute atoms produced by electronic excitation. Crystallization of amorphous Pd-Si alloy thin films can be realized by 75 keV electron irradiation at 90 K via the electronic excitation, where both knock-on damage and a possible thermal crystallization can be excluded. Supply of dissociated Si to the Pd-Si layer may cause instability of the amorphous phase, which serves as the trigger for the remarkable structural change; ie, additional solute atom mediated crystallization.

电子激发诱导界面固相反应的电镜研究。
通过透射电镜和电子衍射研究了电子辐照对Pt/a-SiOx薄膜的影响。在298k和90k的温度下,通过75kev的电子辐照形成Pt2Si。Pt2Si的低温合成可归因于电子激发引起的a- siox解离;Si- o键通过电子激发产生的核心空穴的俄歇衰变解离,然后,解离的Si原子形成Pt-Si键。即使在90k时,Pt2Si的形成过程中,Pt岛的形态也发生了很大的变化。金属颗粒的聚结和生长不是由于电子辐照的热效应,而是由于伴随着硅化物形成的非热过程。为了通过电子激发维持金属颗粒和离解Si原子之间的反应界面,发生了相当大的伴随形态变化。同样,用同样的方法合成了Fe2Si。通过这种方式,我们展示了一种在室温下在电子辐照区选择性形成纳米级金属硅化物的通用方法。我们还提出了一种由电子激发产生的附加溶质原子介导的非晶合金结晶新机制。在90 K的温度下,通过75 keV的电子激发,可以实现非晶Pd-Si合金薄膜的结晶,同时可以排除碰撞损伤和可能的热结晶。向Pd-Si层提供解离的Si可能会导致非晶相的不稳定,从而引发显着的结构变化;即附加溶质原子介导结晶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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