Work function regulation of surface-engineered Ti 2 CT 2 MXenes for efficient electrochemical nitrogen reduction reaction

is observed due to the hybridization of frontier orbitals. The symmetry matching rule of the frontier orbitals of π* 2p and the σ 2p orbitals of N with Ti d orbitals further illustrates the "acceptance-donation" interaction. These theoretical insights highlight the underlying mechanism of the synergetic effect of surficial vacancy and exposed transition metal atoms, and provide an alternative view of designing efficient NRR electrocatalysts.