Renewable energy-driven, electrocatalytic nitrogen reduction
reaction
(NRR) is a promising strategy for ammonia synthesis. However, improving
catalyst activity and selectivity under ambient conditions has long
been challenging. In this work, we obtained the potential active V–N
center through theoretical prediction and successfully constructed
the associated V–N2/N3 structure on N-doped
carbon materials. Surprisingly, such a catalyst exhibits excellent
electrocatalytic NRR performance. The V–N2 catalyst
affords a remarkably high faradaic efficiency of 76.53% and an NH3 yield rate of 31.41 μgNH3
h–1 mgCat.
–1 at −0.3 V vs RHE. The structural characterization
and density functional theory (DFT) calculations verified that the
high performance of the catalyst originates from the tuned d-band
upon coordination with nitrogen, in line with the original design
intention as derived theoretically. Indeed, the V–N2 center with carbon defects enhances dinitrogen adsorption and charge
transfer, thereby lowering the energy barriers to form the *NNH intermediates.
Such a strategy as a rational designcontrollable synthesistheoretical
verification may prove effective as well for other chemical processes.