Rapid charge transfer in covalent organic framework via through-bond for enhanced photocatalytic CO2 reduction

Abstract

Charge transfer efficiency between discrete photosensitizers and catalytic sites is a key limiting factor in artificial photosynthesis. It is highly desirable but challenging to efficiently combine the two sections into an integration system and get insight into the kinetics and mechanisms. Here in, the photosensitizer [Ru(bpy)3]2+ (bpy = 2,2′-bipyridine) and active cobalt porphyrin (Co-Por) sites were integrated into a covalent organic framework (COF), named COF-RuBpy-Co, for efficient charge transfer and photocatalytic CO2 reduction. The catalyst COF-RuBpy-Co exhibited excellent CO2 photoreduction activity towards CO production with a rate of 547 μmol g−1h−1, which is 1.4-fold enhancement over the physical mixture of Ru(bpy)3Cl2 and COF-Bpy-Co. In situ X-ray photoelectron spectroscopy combined with theoretical calculation results revealed that COF-RuBpy-Co achieved efficient photoelectron transfer from [Ru(bpy)3]2+ to cobalt porphyrin. More importantly, transient absorption spectroscopy indicated that the covalent linking [Ru(bpy)3]2+and Co-Por units realized a faster charge transfer (44.2 ps) over the large π-conjugated system. This work provides vital insights into the charge carrier transfer process and demonstrates the potential of COFs as a platform in artificial photosynthesis.