A Promoted Charge Separation/Transfer System from Cu Single Atoms and C3N4 Layers for Efficient Photocatalysis

Abstract Establishing highly effective charge transfer channels in carbon nitride (C 3 N 4 ) for enhancing its photocatalytic activity is still a challenging issue. Herein, for the first time, the engineering of C 3 N 4 layers with single‐atom Cu bonded with compositional N (CuN x ) is demonstrated to address this challenge. The CuN x is formed by intercalation of chlorophyll sodium copper salt into a melamine‐based supramolecular precursor followed by controlled pyrolysis. Two groups of CuN x are identified: in one group each of Cu atoms is bonded with three in‐plane N atoms, while in the other group each of Cu atoms is bonded with four N atoms of two neighboring C 3 N 4 layers, thus forming both in‐plane and interlayer charge transfer channels. Importantly, ultrafast spectroscopy has further proved that CuN x can greatly improve in‐plane and interlayer separation/transfer of charge carriers and in turn boost the photocatalytic efficiency. Consequently, the catalyst exhibits a superior visible‐light photocatalytic hydrogen production rate (≈212 µmol h −1 /0.02 g catalyst), 30 times higher than that of bulk C 3 N 4 . Moreover, it leads to an outstanding conversion rate (92.3%) and selectivity (99.9%) for the oxidation of benzene under visible light.