“…During the past few years, aqueous-based electrochemical reduction of N 2 to NH 3 (nitrogen reduction reaction, NRR) has received some attention, but the highly stable and apolar NN bond (bond energy of 941 kJ mol −1 ), as well as the competing hydrogen evolution reaction (HER) and limited N 2 solubility result in ultra-low reactive rates (<10 mmol g cat −1 h −1 ), selectivity and faradaic efficiency. 6,7,10,11 In contrast, the electrochemical reduction of nitrate to NH 3 (nitrate reduction reaction, NO 3 − RR, NO 3 − + 6H 2 O + 8e − → NH 3 + 9OH − ) is an alternative and attractive route for low-temperature ammonia synthesis due to the following advantages: (1) deoxygenation of NO 3 − requires a much lower energy of 204 kJ mol −1 , 12 thus the NO 3 − RR is energy-efficient compared to the Haber–Bosch process and NRR; (2) the source of nitrate is widespread. Nitrate-rich wastewater streams are available for the NO 3 − RR since nitrate is extensively found in industrial and agricultural runoff.…”