Bandgap engineering of covalent organic frameworks for boosting photocatalytic hydrogen evolution from water

Solar light-promoted hydrogen production from water using covalent organic frameworks (COFs) as a photocatalyst is an attractive technique for clean energy sources. To boost the photocatalytic performance of COFs, it is necessary to narrow their bandgap. However, the bandgap engineering of COFs at the molecular level is less explored. Here, we synthesized four COFs using 2,4,6-tris(4-aminophenyl)-1,3,5-triazine with 1,3,5-triformylbenzene, 2,4,6-triformylphloroglucinol, 2,4,6-triformylphenol, and 2,4,6-triformylresorcinol, respectively, denoted as COF-OH-n (n = 0-3, representing the number of -OH groups). The different degrees of proton tautomerism in COF-OH-n arise from the different numbers of beta-ketoenamine linkages in their skeletons, leading to the regulation of the visible light absorbing ability, bandgap, and band edge positions of COF-OH-n. Due to irreversible proton tautomerism in COF-OH-3, it exhibited the most suitable band structures with a bandgap of 2.28 eV and a flat band of -0.62 eV among COF-OH-n, resulting in the highest photocatalytic hydrogen production rate from water (i.e., 9.89 mmol g(-1) h(-1)), while the other COFs delivered significantly low photocatalytic performances (e.g., similar to 0, 0.11, and 2.91 mmol g(-1) h(-1) for COF-OH-1, COF-OH-0 and COF-OH-2, respectively).

Automated summary

The study demonstrates that by manipulating the molecular structure of covalent organic frameworks (COFs), it is possible to enhance their photocatalytic performance, leading to improved efficiency in solar light-promoted hydrogen production from water.