A Scalable General Synthetic Approach toward Ultrathin Imine-Linked Two-Dimensional Covalent Organic Framework Nanosheets for Photocatalytic CO2 Reduction

Fabricating ultrathin two-dimensional (2D) covalent organic framework (COF) nanosheets (NSs) in large scale and high yield still remains a great challenge. This limits the exploration of the unique functionalities and wide range of application potentials of such materials. Herein, we develop a scalable general bottom-up approach to facilely synthesize ultrathin (<2.1 nm) imine-based 2D COF NSs (including COF-366 NSs, COF-367 NSs, COF-367-Co NSs, TAPB-PDA COF NSs, and TAPB-BPDA COF NSs) in large scale (>100 mg) and high yield (>55%), via an imine-exchange synthesis strategy through adding large excess amounts of 2,4,6-trimethylbenzaldehyde into the reaction system under solvothermal conditions. Impressively, visualization of the periodic pore lattice for COF-367 NSs by a scanning tunneling microscope (STM) clearly discloses the ultrathin 2D COF nature. In particular, the ultrathin COF-367-Co NSs isolated are subject to the heterogeneous photocatalyst for CO2-to-CO conversion, showing excellent efficiency with a CO production rate as high as 10 162 mu mol g(-1) h(-1) and a selectivity of ca. 78% in aqueous media under visible-light irradiation, far superior to corresponding bulk materials and comparable with the thus far reported state-of-the-art visible-light driven heterocatalysts.