Abstract
To understand the crystallization (devitrification) kinetics of Al-rich Al–RE–TM (RE=rare earth, TM=transition metal) amorphous alloys, the devitrification of Al 88Gd 6La 2Ni 4 was studied by in situ electrical resistivity and transmission electron microscopy (TEM) investigations. This glass composition was chosen because it shows a well-defined glass transition temperature ( T g) and transforms to α-Al on partial devitrification. Surprisingly, we show that crystallization appears to be preceded by a phase separation into Al-rich and solute-rich amorphous regions, having a typical dimension of 40 nm. TEM studies reveal a preferential rapid nucleation of α-Al at the interface of the phase-separated regions. A Johnson–Mehl–Avrami analysis of crystallization-induced changes in the electrical resistivity shows limited agreement with the theory, with an Avrami exponent n close to unity. This is explained by a simple numerical model that is consistent with the microstructure; i.e., rapid nucleation at the phase boundary followed by diffusion-limited growth.
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