Size-dependent diffusion controls natural aging in aluminium alloys

A key question in materials science is how fast properties evolve, which relates to the kinetics of phase transformations. In metals, kinetics is primarily connected to diffusion, which for substitutional elements is enabled via mobile atomic-lattice vacancies. In fact, non-equilibrium vacancies are...

Full description

Saved in:
Bibliographic Details
Published inNature communications Vol. 10; no. 1; pp. 4746 - 6
Main Authors Dumitraschkewitz, Phillip, Uggowitzer, Peter J., Gerstl, Stephan S. A., Löffler, Jörg F., Pogatscher, Stefan
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 18.10.2019
Nature Publishing Group
Nature Portfolio
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:A key question in materials science is how fast properties evolve, which relates to the kinetics of phase transformations. In metals, kinetics is primarily connected to diffusion, which for substitutional elements is enabled via mobile atomic-lattice vacancies. In fact, non-equilibrium vacancies are often required for structural changes. Rapid quenching of various important alloys, such as Al- or Mg-alloys, results for example in natural aging, i.e. slight movements of solute atoms in the material, which significantly alter the material properties. In this study we demonstrate a size effect of natural aging in an AlMgSi alloy via atom probe tomography with near-atomic image resolution. We show that non-equilibrium vacancy diffusional processes are generally stopped when the sample size reaches the nanometer scale. This precludes clustering and natural aging in samples below a certain size and has implications towards the study of non-equilibrium diffusion and microstructural changes via microscopy techniques. Aluminium alloys can naturally age and form microstructural clusters that affect their mechanical properties. Here, the authors show that nanosized samples do not under undergo natural aging because diffusion-controlled clustering processes are inhibited.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-019-12762-w