Coordination Engineering in Zirconium-Nitrogen-Functionalized Materials for N2 Reduction: A First-Principles Simulation

Abstract

Coordination engineering was employed to optimize the coordination environment of the Zr atom anchored on the porphyrins (PP). Five promising ZrPP-A candidates as electrocatalysts for nitrogen reduction reaction (NRR) were identified through a four-step screening strategy. First-principles calculations were utilized to evaluate the performance of the candidate electrocatalysts for NRR. A comprehensive search for reaction pathways revealed that NRR reactions with these selected catalysts tend to follow a hybrid pathway. It is found that orbital hybridization and charge transfer between Zr and its coordination atoms, as well as between ZrPP-A and the adsorbed N2 ensured the stability and high catalytic activity of these selected ZrPP-A. Zr plays a crucial role in coordinating charge transfer during the NRR process. Simultaneously, the coordinating atoms and the PP moiety jointly provide additional charge transfers to or from the adsorbate. An asymmetric coordination environment results in an asymmetric charge distribution of the substrate, causing the adsorbed polarized N2 molecule oriented toward the asymmetric charge aggregation region. Our work underscores the importance of considering not only the single-atom catalyst itself but also its coordination environment for the rational design of efficient catalysts.