Abstract
The electrocatalytic nitrate reduction reaction (NitRR) is a promising alternative to the traditional Haber-Bosch process. However, the competitive hydrogen evolution reaction results in poor NH(3) selectivity (S (NH3)). Here, a Cu-Co bimetallic catalyst supported on biomass-derived porous carbon (Cu-Co/BPC) is designed and synthesized. Interestingly, the catalyst presents a high NH(3) yield rate of 9114.1 ± 244.8 μg h(-1) cm(-2) at -1.4 V (vs. RHE) and a high faradaic efficiency (FE) of 84.5 ± 1.6% at -1.0 V (vs. RHE). Notably, the S (NH(3)) of Cu-Co/BPC catalyst is kept above 94.2% under a broad range from -1.0 to -1.4 V (vs. RHE), indicating the high NitRR-to-NH(3) selectivity of Cu-Co/BPC. The combination of in situ characterization and experimental results indicates that the electron transfer occurs between Cu and Co, and many active sites are generated for adsorption and activation of N[double bond, length as m-dash]O double bonds, and hydrogenation reactions occur with adjacent H protons to improve the selectivity of NH(3).