Competing Effects of pH, Cation Identity, H2O Saturation, and N2 Concentration on the Activity and Selectivity of Electrochemical Reduction of N2 to NH3 on Electrodeposited Cu at Ambient Conditions

The electrochemical reduction of N 2 to produce NH 3 at ambient conditions is an effective and sustainable route to store and carry hydrogen, balance the nitrogen cycle, and provide means to produce on-demand fertilizers. The efficient electrosynthesis of NH 3 is challenging because of the lower activation of N 2 and higher activity toward the hydrogen evolution reaction (HER). Here, we propose theory-guided activity descriptors to identify an efficient N 2 reduction reaction (NRR) catalyst, followed by its implementation in a flow-through gas diffusion electrode (GDE) to quantify the effects of pH, cation identity, H 2 O saturation, and N 2 concentration on the kinetics of the NRR. The identified Cu catalyst with dominant (111) facets electrodeposited on a carbon paper provides optimal active sites to obtain maximum NH 3 faradaic efficiency (FE) of 18 ± 3% at −0.3 V vs RHE and the maximum NH 3 current density of 0.25 ± 0.03 mA cm –2 (0.86 nmol·cm –2 ·s –1 ) at −0.5 V vs RHE in alkaline medium. The electrolyte pH mostly affects the HER by pH-induced binding of *H and reorganization of H 2 O, which favor the NRR at an optimal pH of 13.5. Increasing the size of monovalent cations stabilizes NRR intermediates and increases the NH 3 current density from Li + to K + . However, increasing the size of the cation from K + to Rb + reduces the FE of NRR, which is due to a direct reduction of H 2 O in the solvation shell of larger cations to produce H 2 . Another strategy to improve NH 3 FE is to reduce the H 2 O saturation on the catalyst, which can be achieved by sparging the reactant gas directly through the GDE. Increasing the N 2(g) flow rate not only increases the gas–liquid mass transfer coefficient but also reduces the H 2 O saturation in the pores of the GDE, which primarily suppresses the HER. The fixed potential DFT calculations reveal an associative distal mechanism for the NRR over Cu(111), where the hydrogenation of *N 2 is the rate-limiting step. This finding also corroborates with the measured reaction order with respect to N 2 .