Reaction mechanism and kinetics for N₂ reduction to ammonia on the Fe-Ru based dual-atom catalyst

Abstract

Environmental and energy considerations demand that the Haber-Bosch process for reducing N₂ to NH₃ be replaced with electrochemical ammonia synthesis where the H atoms come from water instead of from H₂. But a practical realization of electrochemical N₂ reduction reaction (NRR) requires the development of new generation electrocatalysts with low overpotential and high Faraday efficiency (FE). A major problem here is that the hydrogen evolution reaction (HER) competes with NRR. Herein, we consider new generation dual-site catalysts involving two different metals incorporated into a novel two-dimensional C₃N–C₂N heterostructure that provides a high concentration of well-defined but isolated active sites that bind two distinct metal atoms in a framework that facilitates electron transfer. We report here the mechanism and predicted kinetics as a function of applied potential for both NRR and HER for the (Fe–Ru)/C₃N–C₂N dual atom catalyst. These calculations employ the grand canonical potential kinetics (GCP-K) methodology to predict reaction free energies and reaction barriers as a function of applied potential. The rates are then used in a microkinetic model to predict the turn-over-frequencies (TOF) as a function of applied potential. At U = 0 V, the FE for NRR is 93%, but the current is only 2.0 mA cm⁻². The onset potential (at 10 mA cm⁻²) for ammonia on Fe–Ru/C₃N–C₂N is −0.22 V_(RHE). This leads to a calculated TOF of 434 h⁻¹ per Fe–Ru site. We expect that the mechanisms for NRR and HER developed here will help lead to new generations of NRR with high TOF and FE.

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