Modulating the Site Density of Mo Single Atoms to Catch Adventitious O Atoms for Efficient H<sub>2</sub>O<sub>2</sub> Oxidation with Light
Congmin Zhang, Lichen Bai, Min Chen, Xuejiao Sun, Mengzhao Zhu, Qinglong Wu, Xiaoping Gao, Qun Zhang, Xusheng Zheng, Zhen‐Qiang Yu, Yuen Wu
Abstract
Abstract Coordination environment and site density have great impacts on the catalytic performance for single atoms (SAs). Herein, the site density of Mo‐SAs on red polymeric carbon nitrides (RPCN) is modulated via a local carbonization strategy to controllably catch adventitious O atoms from open environment. The addition of melamine derivants with hydrocarbyl chains induces local carbonization during RPCN pyrolysis. These local carbonization regions bring abundant graphitic N 3C to anchor Mo‐SAs, and most of Mo‐SAs catch the O atoms in air, forming the O 2 ‐covered Mo‐N 3 coordination. The dopants of carbon source with different structures and amounts can modulate the site density of Mo‐SAs, therefore controlling the amounts of coordinated O atoms. Furthermore, coordinated O atoms around Mo‐SAs construct the catalytic environment with Lewis base and gather photo‐generated electrons under light. Such O‐covered Mo‐SAs endow RPCN materials (Mo‐RPCN) with a strong ability for hydrogen abstraction, leading to the 99.51% ratio (28.8 mmol min −1 g −1 ) rate for thioanisole conversion with H 2 O 2 assisted advance oxidation technology. This work brings a new sight on the coordinated atoms dominant oxidation process.