The localized corrosion properties of Al 87 Ni 8.7 Y 4.3 and Al 90 Fe 5 Gd 5 , were investigated in the amorphous, high strength partially nanocrystalline, and fully crystalline states. The critical pitting potentials and pit growth behaviors of amorphous and nanocrystalline alloys were improved compared to high purity, polycrystalline Al in 0.6 M NaCl solution. Transition metal (TM) and rare earth additions (RE) were retained in solid solution in amorphous alloys and the remaining amorphous matrix of partially nanocrystalline alloys. Substantial TM and RE solute rejection occurred from nano-and microcrystals. Notably, the improved resistance to pitting was retained in the partially nanocrystalline condition, but was completely lost in the fully crystalline alloys. The opportunity exists to create partially nanocrystalline Al-TM-RE alloys of great strength with corrosion resistance equal to their amorphous counterparts. © 1999 The Electrochemical Society. S1099-0062(99)02-016-7. All rights reserved.Manuscript received February 2, 1999. Available electronically March 18, 1999. It is well established in the literature that glassy alloys and alloys with a low degree of crystallinity offer superior resistance to corrosion and vastly improved mechanical properties over their conventional counterparts. 1,2 Amorphous alloys often have corrosion resistance one to two orders of magnitude greater than polycrystalline alloys with the same alloy composition. 1,2 One theory links the improved resistance of amorphous alloys to their ability to promote amorphous oxide formation. In high temperature gas, vitreous or amorphous oxides offer improved oxidation resistance due to the absence of oxide grain boundaries which provide a rapid diffusion path for concentration gradient driven ion movement. 3,4 In the case of metal passivity in aqueous solutions, ion transport is mostly driven by the electric field across the oxide film. The lack of oxide grain boundaries may lower ion migration rates, rendering the passive film more protective. [3][4][5] The rapid transport and accumulation of cation vacancies at the oxide/metal interface is one theory accounting for oxide breakdown. 6 Moreover, vitreous oxides on amorphous alloys perform well due to enhanced bond flexibility since the vitreous or amorphous material can rearrange to accommodate lattice mismatch and strain between the oxide and the metal. 5,7 As a result of this flexibility, almost all surface atoms can bond with oxygen or OH -without requiring an optimal epitaxial relationship between an ordered metal substrate and oxide. 5 Intolerable changes in oxide/metal misfit strain with halide incorporation is another theory accounting for the rupture of protective oxide films on metals. 8 The improved corrosion resistance associated with the addition of 18% Cr to Fe is attributed, in part, to a change in the protective oxide structure from a well oriented spinel structure at 0-12% Cr to a noncrystalline structure at 18% Cr. 5 This disordering has been shown by low energy electr...