Integrating Multifunctionalities into a 3D Covalent Organic Framework for Efficient CO <sub>2</sub> Photoreduction
Ke Cheng, Shuo Kong, Jungeng Wang, Qiurong Wang, Shiling Yuan, Pei‐Zhou Li, Yanli Zhao
Abstract
Abstract Fabrication of highly efficient photocatalysts for CO 2 conversion is still challenging. Herein, integrating nitrogen‐rich organic cages and the photoactive porphyrin moieties together, a 3D covalent organic framework (COF), Cage‐PorCOF, is successfully synthesized. After incorporating metal ions (Co 2+ and Ni 2+ ) into the cage‐based COF, Cage‐PorCOF(Co) and Cage‐PorCOF(Ni) are subsequently constructed for the CO 2 photoreduction. Catalytic experiments show impressive performance in CO 2 photoreduction with CO generation rates of up to 48 748 and 28 446 µmol g −1 h −1 in the first initiating hour for Cage‐PorCOF(Co) and Cage‐PorCOF(Ni), respectively, which is attributed to the synergistic effects from CO 2 ‐affinity of the porous frameworks and incorporated metal atoms, the light‐absorption and charge separation ability of metalloporphyrin groups as well as the fully exposed single‐atomic catalytic sites confirmed by both experimental and theoretical analyses. This study demonstrates that by the integration of multiple functionalities into 3D porous solids, highly effective photocatalysts for CO 2 conversion can be achieved.