Quasi‐“In Situ” Analysis of the Reactive Liquid‐Solid Interface during Magnesium Corrosion Using Cryo‐Atom Probe Tomography

Abstract

The early stages of corrosion occurring at liquid‐solid interfaces controls the evolution of the material's degradation process, yet due to their transient state, their analysis remains a formidable challenge. Here we perform corrosion tests on a MgCa alloy, a candidate material for biodegradable implants using pure water as a model system. The corrosion reaction was suspended by plunge freezing into liquid nitrogen. We studied the evolution of the early‐stage corrosion process on the nanoscale by correlating cryo‐atom probe tomography with transmission‐electron microscopy and spectroscopy. We observed the outward growth of Mg hydroxide and the inward growth of an intermediate corrosion layer consisting of hydroxides of different compositions, mostly monohydroxide Mg(OH) instead of the expected MgO layer. In addition, Ca partitions to these newly formed hydroxides and oxides. Density‐functional theory calculations suggest a domain of stability for this previously experimental unreported Mg(OH) phase. These new approach and findings advance the understanding of the early stages of magnesium corrosion, and in general reactions and processes at liquid‐solid interfaces, which can further facilitate the development of corrosion‐resistant materials or better control of the biodegradation rate of future implants.This article is protected by copyright. All rights reserved