Pendant Proton‐Relays Systematically Tune the Rate and Selectivity of Electrocatalytic Ammonia Generation in a Fe‐Porphyrin Based Metal–Organic Framework

Abstract Electrocatalytic nitrite reduction (eNO 2 RR) is a promising alternative route to produce ammonia (NH 3 ). Until now, several molecular catalysts have shown capability to homogeneously reduce nitrite to NH 3 , while taking advantage of added secondary‐sphere functionalities to direct catalytic performance. Yet, realizing such control over heterogeneous electrocatalytic surfaces remains a challenge. Herein, we demonstrate that heterogenization of a Fe‐porphyrin molecular catalyst within a 2D Metal–Organic Framework (MOF), allows efficient eNO 2 RR to NH 3 . On top of that, installation of pendant proton relaying moieties proximal to the catalytic site, resulted in significant improvement in catalytic activity and selectivity. Notably, systematic manipulation of NH 3 faradaic efficiency (up to 90 %) and partial current (5‐fold increase) was achieved by varying the proton relay‐to‐catalyst molar ratio. Electrochemical and spectroscopic analysis show that the proton relays simultaneously aid in generating and stabilizing of reactive Fe‐bound NO intermediate. Thus, this concept offers new molecular tools to tune heterogeneous electrocatalytic systems.