Hydrogen absorption by Zircaloy-2 has been studied in neutral sodium sulfate solutions using steady-state polarization measurements, electrochemical impedance spectroscopy (EIS), and scanning electrochemical microscopy (SECM). For applied potentials < −1 V (vs. saturated calomel electrode, SCE), water reduction occurs in faults in the passive oxide covering the alloy. For potentials ≤−1.3 V SCE , SECM detects a distribution of reactive locations on the electrode surface. Matched SECM and SEM images of the same electrode surface show more reactive sites to be located in the β-phase grain boundaries than on the α-grains. The reactivity of surface locations was determined using SECM probe approach curves. Secondary phase particles incorporating impurities such as Fe, Ni, and Cr as Zr(Fe, Cr) 2 and Zr 2 (Fe, Ni) are particularly reactive spots, which may act as "windows" for hydrogen absorption into the alloy. This claim is supported by the observation that the surface of the α-grains remains passive even at potentials as low as −2.0 V SCE . The need to include a Warburg impedance element in modeling EIS recorded at potentials ≥−1.3 V SCE suggests that H 2 O reduction is confined to tight flaws in the oxide at grain boundary locations.