Koustav Banerjee, Duong T. H. Truong, Darcy Simondson, Ngoc Trung Nguyen, Cuong K. Nguyen, Cameron L. Bentley, Rebecca Y. Hodgetts, Douglas R. Macfarlane, Hoang‐Long Du, Alexandr N. Simonov
Protonation of the lithium nitride intermediate is a critical step of the lithium redox-mediated nitrogen reduction reaction (Li-NRR), which is commonly provided by the ethanol proton carrier. While the field explores alternative, more stable H + shuttles, the capability of NH 3 to deliver protons for the conversion of Li 3 N into NH 3 and Li + has been majorly overlooked. Herein, we demonstrate a high ammonia yield rate of 350 ± 40 nmol s –1 cm –2 and faradaic efficiency of 93 ± 6% under 15 bar nitrogen in 6 h Li-NRR experiments when 0.08 M NH 3 is added to ethanol-free tetrahydrofuran solutions of 2 M lithium bis(trifluoromethylsulfonyl)imide electrolyte. Extended two-day-long experiments demonstrated the stability of the NH 3 -promoted Li-NRR, with only slightly decreased performance. In contrast, the introduction of NH 4 + suppresses the Li-NRR under these conditions. These results suggest that the proton shuttling during the Li-NRR might be provided by the reaction product, potentially enabling an important technological simplification.