The formation of precipitates in metallic alloys is determined by a two-way chemomechanical coupling. While the dependence on solute diffusion is apparent, the opposite effect, namely the impact of nanoprecipitates on the diffusion, is highlighted in the present paper. Using severe plastic deformation and post-deformation annealing of an Al-based alloy, different microstructures and sizes of Al 3 Sc-based nanoprecipitates are produced. The enhanced diffusion along grain boundaries in the so-called C-type kinetic regime is used as a probe to ensure a well-defined distance of the diffusion path from the precipitates and to prohibit their evolution during measurements. Tracer measurements with the radioisotope 57 Co reveal a remarkable nonmonotonic dependence of the diffusion rates on the annealing temperature. It has been fully explained by an ab initio informed phenomenological model that considers the elastic stress around the coherent and noncoherent precipitates.

Grain boundary diffusion in severely deformed Al-based AA5024 alloy is investigated. Different states are prepared by combination of equal channel angular processing and heat treatments, with the radioisotope 57 Co being employed as a sensitive probe of a given grain boundary state. Its diffusion rates near room temperature (320 K) are utilized to quantify the effects of severe plastic deformation and a presumed formation of a previously reported deformation-modified state of grain boundaries, solute segregation at the interfaces, increased dislocation content after deformation and of the precipitation behavior on the transport phenomena along grain boundaries. The dominant effect of nano-sized Al3Sc-based precipitates is evaluated using density functional theory and the Eshelby model for the determination of elastic stresses around the precipitates.