Au Sub‐Nanoclusters on TiO2 toward Highly Efficient and Selective Electrocatalyst for N2 Conversion to NH3 at Ambient Conditions

Abstract

As the NN bond in N₂ is one of the strongest bonds in chemistry, the fixation of N₂ to ammonia is a kinetically complex and energetically challenging reaction and, up to now, its synthesis is still heavily relying on energy and capital intensive Haber–Bosch process (150–350 atm, 350–550 °C), wherein the input of H₂ and energy are largely derived from fossil fuels and thus result in large amount of CO₂ emission. In this paper, it is demonstrated that by using Au sub-nanoclusters (≈0.5 nm ) embedded on TiO₂ (Au loading is 1.542 wt%), the electrocatalytic N₂ reduction reaction (NRR) is indeed possible at ambient condition. Unexpectedly, NRR with very high and stable production yield (NH₃: 21.4 µg h⁻¹ mg⁻¹_cat., Faradaic efficiency: 8.11%) and good selectivity is achieved at −0.2 V versus RHE, which is much higher than that of the best results for N₂ fixation under ambient conditions, and even comparable to the yield and activation energy under high temperatures and/or pressures. As isolated precious metal active centers dispersed onto oxide supports provide a well-defined system, the special structure of atomic Au cluster would promote other important reactions besides NRR for water splitting, fuel cells, and other electrochemical devices.