ABSTRACT Electrochemical nitrate (NO 3 − ) reduction presents a multifunctional strategy to remediate NO 3 − contamination while enabling ammonia (NH 3 ) synthesis. However, it is still a challenge to achieve satisfied performance due to the multiple rate‐limiting steps and competitive hydrogen evolution, particularly under neutral conditions and low concentrations. Herein, a set of single‐atom catalysts (SACs) featuring high loading of multiple metal sites was synthesized as tandem catalysts for NO 3 − to NH 3 . Fe/Cu/Pd−N−C SACs exhibit a superior performance with the high NH 3 Faradaic efficiency of 98%, 95%, and 82% at the NO 3 − concentration of 0.5, 0.1, and 0.01 M , respectively, which are much higher than these of other SACs. Moreover, it also performed very well in the stability and anti‐interference measurements. The exceptional performance is proved to be attributable to the tandem interplay among Fe, Cu, and Pd sites. Specifically, NO 3 − undergoes reduction to NO 2 − over Cu single atoms, and NO 2 − then migrates to Fe single atoms for the subsequent conversion, benefiting from the high adsorption energy. Meanwhile, Pd sites can regulate the generation rate and consumption pathway of active hydrogen. This work offers a viable solution for the recycling and utilization of nitrate pollutants and provides a flexible design strategy for multifunctional electrocatalysts.
Gan et al. (Thu,) studied this question.