Electrochemical Reduction of N 2 to Ammonia Promoted by Hydrated Cation Ions: Mechanistic Insights from a Combined Computational and Experimental Study.

Alkali ions, major components at the electrode-electrolyte interface, are crucial to modulating reaction activity and selectivity of catalyst materials. However, the underlying mechanism of how the alkali ions catalyze the N 2 reduction reaction (NRR) into ammonia remains elusive, posing challenges for experimentalists to select appropriate electrolyte solutions. In this work, by employing a combined experimental and computational approach, we proposed four essential roles of cation ions at Fe electrodes for N 2 fixation: (i) promoting NN bond cleavage; (ii) stabilizing NRR intermediates; (iii) suppressing the competing hydrogen evolution reaction (HER); and (iv) modulating the interfacial charge distribution at the electrode-electrolyte interface. For N 2 adsorption on an Fe electrode with cation ions, our constrained ab initio molecular dynamic (c-AIMD) results demonstrate a barrierless process, while an extra 0.52 eV barrier requires to be overcome to adsorb N 2 for the pure Fe-water interface. For the formation of *NNH species within the N 2 reduction process, the calculated free energy barrier is 0.50 eV at the Li + -Fe-water interface. However, the calculated barrier reaches 0.81 eV in pure Fe-water interface. Furthermore, experiments demonstrate a high Faradaic efficiency for ammonia synthesis on a Li + -Fe-water interface, reaching 27.93% at a working potential of -0.3 V vs RHE and pH = 6.8. These results emphasize how alkali metal cations and local reaction environments on the electrode surface play crucial roles in influencing the kinetics of interfacial reactions.