Abstract
Conjugated polymers are promising light harvesters for water reduction/oxidation due to their simple synthesis and adjustable bandgap. Herein, both cyanamide and triazole functional groups are first incorporated into a heptazine-based carbon nitride (CN) polymer, resulting in a mesoporous conjugated cyanamide-triazole-heptazine polymer (CTHP) with different compositions by increasing the quantity of cyanamide/triazole units in the CN backbone. Varying the compositions of CTHP modulates its electronic structures, mesoporous morphologies, and redox energies, resulting in a significantly improved photocatalytic performance for both H2 and O2 evolution under visible light irradiation. A remarkable H2 evolution rate of 12723 µmol h−1 g−1 is observed, resulting in a high apparent quantum yield of 11.97% at 400 nm. In parallel, the optimized photocatalyst also exhibits an O2 evolution rate of 221 µmol h−1 g−1, 9.6 times higher than the CN counterpart, with the value being the highest among the reported CN-based bifunctional photocatalysts. This work provides an efficient molecular engineering approach for the rational design of functional polymeric photocatalysts.
| Original language | English |
|---|---|
| Article number | 2003162 |
| Journal | Small |
| Volume | 16 |
| Issue number | 37 |
| DOIs | |
| Publication status | Published - 1 Sept 2020 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- conjugated polymers
- hydrogen evolution reaction
- oxygen evolution reaction
- photocatalysts
- water splitting
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