LAUSR

In a solid-state diffusional phase transformation involving nucleation and growth, the size of the critical nucleus for a homogeneous process (r*homo=r* ) has been assumed to be a time invariant constant of the transformation. The strain associated with the process has a positive energy contribution and leads to an increase in the value of r*, with respect to that for nucleation from a liquid. With the progress of such a transformation, the strain energy stored in the matrix increases and nuclei forming at a later stage encounter a strained matrix. Using devitrification of a bulk metallic glass as a model system, we demonstrate that r* is not a cardinal time invariant constant for homogeneous nucleation and can increase or decrease depending on the strain energy penalty. We show that the assumption regarding the constancy of r* is true only in the early stages of the transformation and establish that the progress of the transformation leads to an altered magnitude of r*, which is a function of the microstructural details, geometrical variables and physical parameters. With the aid of high-resolution lattice fringe imaging and computations of r*, we further argue that, 'liquid-like' homogeneous nucleation can occur and that the conclusions are applicable to a broad set of solid-state diffusional transformations. The above effect 'opens up' a lower barrier transformation pathway arising purely from the internal variables of the system.