Successful in situ spatiotemporal tracking of corrosion processes occurring at heterogeneous Mg alloy microstructures was achieved through tandem analyses involving electron and electrochemical microscopies. Through cross-correlation of scanning electron microscopy and scanning electrochemical microscopy images and subsequent analytical transmission electron microscopy, the morphology and chemical composition of microstructural components on the surface of a sand-cast AM50 Mg alloy were related to their respective local evolution of H 2 with micron scale resolution prior to, during and post corrosion. The results confirm that the preferential water reduction sites in the initial stages of corrosion are the Al 8 Mn 5 intermetallics while a β-Mg 17 Al 12 precipitate contaminated with Ni becomes cathodically active at a later stage of corrosion. This approach demonstrates the power of correlative approaches to probe and understand local electrochemical phenomena. Owing to their light weight, high strength-to-weight ratio, good castability and high damping capacity, Mg alloys are ideal candidates for automotive structural components.1-5 The compromise of formability, room temperature ductility and price represent major challenges in commercializing these materials. Importantly, Mg alloys also suffer from poor corrosion resistance in aqueous environments 6-8 and due to their positions in the electrochemical activity series, are highly susceptible to accelerated corrosion rates when in galvanic contact with a more noble material.9 At open circuit, the overall galvanic current is null due to a balance between the anodic and cathodic current densities, while on a microscopic scale, a difference in electrochemical potential is obtained. In Mg alloys, galvanic coupling between microstructural components of the alloy (commonly referred to as microgalvanic coupling) stems from an inherent electrochemical potential difference between the Mg matrix and its secondary phases, [10][11][12] and can be tracked using local scanning probe methods.Local scanning probe techniques such as several modes of scanning electrochemical microscopy (SECM), [13][14][15][16][17][18][19] scanning Kelvin probe force microscopy (SKPFM), 20-22 the scanning vibrating electrode technique (SVET) [23][24][25] and local electrochemical impedance spectroscopy (LEIS) 26 have been used to probe the heterogeneous surfaces of Mg alloys and to assess the electrochemical behavior of the different microstructural constituents responsible for microgalvanic corrosion. Among these techniques, SECM has the ability to quantify electrochemical fluxes in situ with high lateral resolution using a microelectrode (ME). 27 This technique has been successfully applied in corrosion research to provide in situ analyses of pitting corrosion at oxide films, [28][29][30] to assess lateral variations in corrosion kinetics, 31 and to detect defects within coated metal samples.
32The feedback mode of SECM has been employed to probe corroding AM60 15 and AZ31 17 Mg alloys. The incre...