A new Ni–diaminoglyoxime–g-C3N4 complex towards efficient photocatalytic ethanol splitting via a ligand-to-metal charge transfer (LMCT) mechanism

Abstract

We report a novel Ni–diaminoglyoxime–g-C₃N₄ (Ni–DAG–CN) complex for H₂ evolution through photocatalytic ethanol splitting. Compared to that of pristine g-C₃N₄, Ni–DAG–CN exhibits a 21-fold enhancement of photocatalytic activity (296.1 μmol h⁻¹ g⁻¹) under irradiation with excellent stability. The enhanced photocatalytic activity can be attributed to a proposed ligand-to-metal charge transfer (LMCT) mechanism, which is illustrated both experimentally and theoretically. This work provides great potential in the future design of low-cost, high-performance photocatalysts for H₂ evolution from alcohol splitting.