Dual enhancement of carrier generation and migration on Au/g-C 3 N 4 photocatalysts for highly-efficient broadband PET-RAFT polymerization
Photoinduced electron/energy transfer RAFT (PET-RAFT) polymerization can produce well-defined polymers with spatiotemporal control. Semiconducting graphitic carbon nitride (g-C 3 N 4 ), as a thermally and chemically stable photocatalyst, has accomplished the PET-RAFT method under UV-irradiation and...
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Veröffentlicht in: | Polymer chemistry 2022-02, Vol.13 (8), p.1022-1030 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Photoinduced electron/energy transfer RAFT (PET-RAFT) polymerization can produce well-defined polymers with spatiotemporal control. Semiconducting graphitic carbon nitride (g-C
3
N
4
), as a thermally and chemically stable photocatalyst, has accomplished the PET-RAFT method under UV-irradiation and blue-light. However, its catalytic efficiency was decreased by the high recombination rate of photogenerated electron–hole pairs, while the control over polymerization was weakened by the ultraviolet-decomposition of RAFT reagents. Herein, a series of Au/g-C
3
N
4
composite photocatalysts were facilely prepared by the deposition–precipitation method. Arrangement of Au nanoparticles (NPs) on g-C
3
N
4
displayed hot electron injection or plasmon-induced resonance energy transfer, which boosts the generation of active electrons for a broadband PET-RAFT process (460–740 nm). The formation of a Schottky barrier enhanced the carrier migration, as it lowered the charge recombination rate. Such a synergistic effect made Au/g-C
3
N
4
outperform Au NPs, g-C
3
N
4
and their physical blend. Furthermore, the effects of the Au content, hole scavenger, chain transfer agent, monomer, solvent, and light-source on the highly efficient PET-RAFT polymerization were studied. |
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ISSN: | 1759-9954 1759-9962 |
DOI: | 10.1039/D1PY01590G |