Nitrogen Speciation Dictates Industrial‐Current Oxygen Reduction in Metal‐Free Macrocycles for H ₂ O ₂ Synthesis

Oxygen activation is a cornerstone of sustainable electrosynthesis, yet controlling reactive intermediates without metallic centers remains challenging at industrial current densities. Here we establish nitrogen speciation as a molecular descriptor for governing oxygen activation in metal‐free macrocycles. Guided by density functional theory, we designed a tetra‐aza macrocycle with nearly exclusive pyridinic nitrogen, distinct from the mixed‐nitrogen environments of conventional porphyrins and phthalocyanines. This configuration uniquely stabilizes the key *OOH intermediate while strengthening interfacial electronic coupling with carbon supports. When integrated into a flow‐cell electrolyzer, the catalyst achieves ∼95% H 2 O 2 Faradaic efficiency and stability for over 800 h at 300 mA cm −2 , continuously generating >3 wt.% H 2 O 2 . Furthermore, in situ generated reactive oxygen species enable selective ambient upgrading of furfural to oxime (>90% yield). Techno‐economic analysis supports the economic viability of the process. By linking well‐defined nitrogen coordination to scalable device performance, this work provides a blueprint for translating molecular precision into practical electrocatalytic manufacturing.