Termination effects of single-atom decorated v-Mo2CTx MXene for the electrochemical nitrogen reduction reaction

The lack of the green, economical and high-efficient catalysts restrict the development of electrochemical nitrogen reduction reaction (NRR). By means of density functional theory (DFT) calculations, we have systematically investigated the NRR catalytic performance of single atoms decorated v-Mo2CT2 (T = O, F, OH, Cl, and Li) MXene (TM@v-Mo2CT2). Our calculation results reveal the introduction of single atom can significantly improve the NRR activity and selectivity on v-Mo2CO2, and Ir@v-Mo2CO2 system possesses the lowest limiting potential of only-0.33 V among all studied systems. The termination effects of TM@v-Mo2CT2 are further discussed and a descriptor of the adsorption energy of *NNH species (Delta E(*NNH)) is proposed to establish the relationship with NRR limiting potential (U-L(NRR)), in which a moderate (Delta E(*NNH)) is required for high NRR activity. Moreover, a good linear relationship between the Delta E(*NNH) and the excess electrons on Ir atom shows that different Delta E(*NNH) originates from the difference of valence state of Ir atom, which is due to the change of coordination environment. Importantly, the synergistic effects of Ir atom and the surface O-terminations during the first hydrogenation step lead to a promoted NRR performance. Our study might provide new possibilities for rational design of costeffective MXene-based NRR electrocatalysts. (C) 2021 Elsevier Inc. All rights reserved.

Automated summary

This study investigates the NRR catalytic performance of single atoms decorated v-Mo2CT2 MXene using DFT calculations. Results show that single atom introduction improves NRR activity and selectivity, with Ir@v-Mo2CO2 having the lowest limiting potential. A relationship between the adsorption energy of *NNH species and NRR activity is proposed.