Molecular catalysts can promote ammonia oxidation, providing mechanistic insights into the electrochemical N₂ cycle for a carbon-free fuel economy. We report the ammonia oxidation activity of carbon anodes functionalized with the oligomer {[Ru^II(bda-κ-N²O²)(4,4′-bpy)]₁₀(4,4′-bpy)}, Rubda-10, where bda is [2,2′-bipyridine]-6,6′-dicarboxylate and 4,4′-bpy is 4,4′-bipyridine. Electrocatalytic studies in propylene carbonate demonstrate that the Ru-based hybrid anode used in a 3-electrode configuration transforms NH₃ to N₂ and H₂ in a 1:3 ratio with near-unity faradaic efficiency at an applied potential of 0.1 V vs Fc^+/0, reaching turnover numbers of 7500. X-ray absorption spectroscopic analysis after bulk electrolysis confirms the molecular integrity of the catalyst. Based on computational studies together with electrochemical evidence, ammonia nucleophilic attack is proposed as the primary pathway that leads to critical N–N bond formation.