Abstract
The collaborative interaction between the diatoms can enhance the catalytic activity of the transition metal atoms and facilitate the activation of nitrogen molecules. Based on first-principles calculations, the feasibility of electrocatalytic nitrogen fixation as a diatomic catalyst (TMs@MoSSe) formed by transition metal dimers (V, Cr, Mn, Fe, Co, and Ni) dispersed on a two-dimensional Janus MoSSe monolayer is systematically investigated. The results demonstrate that the MoSSe monolayer loaded with double chromium atoms (Cr2@MoSSe) exhibits exceptional catalytic activity, showcasing an extremely low overpotential of 0.17 V in the enzymatic mechanism. Specifically, this research elucidates the nitrogen reduction capacity of the electrocatalyst by considering its magnetic moment and work function, concluding that a lower work function corresponds to enhanced catalytic activity. Additionally, the product of the magnetic moment and valence electron numbers of the transition metal atoms (μTM⋅dTM) exhibits an inverted volcano relationship with the overpotential. These findings can provide valuable insights for the design of diatomic catalysts.
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