A novel metal-free porous covalent organic polymer for efficient room-temperature photocatalytic CO2 reduction via dry-reforming of methane

Abstract

At room temperature, the conversion of greenhouse gases into valuable chemicals using metal-free catalysts for dry reforming of methane (DRM) is quite promising and challenging. Herein, we developed a novel covalent organic porous polymer (TPE-COP) with rapid charge separation of the electron–hole pairs for DRM driven by visible light at room temperature, which can efficiently generate syngas (CO and H2). Both electron donor (tris(4-aminophenyl)amine, TAPA) and acceptor (4,4′,4″,4‴-((1 E,1′E,1″E, 1‴E)-(ethene-1,1,2,2-tetrayltetrakis (benzene-4,1-diyl))tetrakis (ethene-2,1-diyl))tetrakis (1-(4-formylbenzyl)quinolin-1-ium), TPE-CHO) were existed in TPE-COP, in which the push–pull effect between them promoted the separation of photogenerated electron–hole, thus greatly improving the photocatalytic activity. Density functional theory (DFT) simulation results show that TPE-COP can form charge-separating species under light irradiation, leading to electrons accumulation in TPE-CHO unit and holes in TAPA, and thus efficiently initiating DRM. After 20 h illumination, the photocatalytic results show that the yields reach 1123.6 and 30.8 μmol g−1 for CO and H2, respectively, which are significantly higher than those of TPE-CHO small molecules. This excellent result is mainly due to the increase of specific surface area, the enhancement of light absorption capacity, and the improvement of photoelectron-generating efficiency after the formation of COP. Overall, this work contributes to understanding the advantages of COP materials for photocatalysis and fundamentally pushes metal-free catalysts into the door of DRM field.

Keywords

• Metal-free
• Photocatalytic CO2 reduction
• Covalent organic polymer
• Dry-reforming of methane
• Electron donor and acceptor