Using cyclic voltammetry, for both p-and n-type GaAs, an anodic peak is observed just before an unlimited anodic current, in acidic, neutral, or basic media in liquid ammonia. This anodic peak is due to an adsorption/precipitation phenomenon. It led to the passivation of the SC surface regardless of pH. After passivation of the electrode, a reduction wave appeared in acidic medium as well in unbuffered neutral medium, but in this last case only for high scan rates. In basic medium, no reduction wave appeared. The initial electrochemical state of GaAs, corresponding to the presence of the anodic peak, is recovered by reduction of the adsorbed film in acidic media, in unbuffered neutral medium, or in buffered neutral medium. No recovery is observed in basic media. These last results show that this recovery occurred only when protons came from the medium ͑acidic medium͒ or protons came from the anodic reaction associated to the anodic peak, or if a proton donor was present. Quantitative analysis of gallium and arsenic elements released in solution showed clearly that a dissolution happened without limitation as soon as the unlimited anodic current was reached. Coulometric measurements point out that the efficiency of dissolution increased with current density in the anodic unlimited current, showing that ammonia oxidation and material oxidation were concomitant reactions. The anodic wave may be considered as the result of the precipitation of a nitrogenous-based complex ͑i.e., amide complex͒ which implies the superficial lattice contribution. The passivation film may be initiated by the formation of strongly adsorbed atoms of nitrogen, intermediaries arising from ammonia oxidation, which can behave as site poison at the interface during nitrogen evolution.In aqueous media, the anodic behavior of narrow bandgap (E G Ͻ 2 eV͒ semiconductors ͑SC͒ is limited by the anodic decomposition of the SC. 1 The use of nonaqueous solvent provides a larger potential window to the electrochemical response of the SC. In recent years, works have been performed in nonaqueous solvents 2-4 in order to study the corrosion of SC. Abshere et al. [3][4] had clearly demonstrated that the photocorrosion of GaAs is governed by traces of water in methanol. For this study, the use of nonaqueous solvents such as acetonitrile, dimethyl formamide and dimethyl sulfoxide brings up a new problem resulting from that these solvents are not water-free and some of them can involve the formation of surface oxides by their decomposition. 5-7 According to the difficulty in obtaining these nonaqueous solvents in water-free conditions, they cannot be used easily for this study because the anodic behavior of SC can be governed by traces of water.Compared to other nonaqueous solvents, liquid ammonia provides a better control of water traces. At room temperature, liquid ammonia is a very strongly basic solvent 8-9 (10 11 times stronger than water͒, and is a very weak acid (10 29 times weaker than water͒. The strong basicity of liquid ammonia allows study of electr...