期刊
JOURNAL OF MATERIALS CHEMISTRY A
卷 7, 期 11, 页码 6482-6490出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ta00580c
关键词
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资金
- Chinese National Science Foundation [21437003, 21673126, 21761142017, 2162100-3]
- Collaborative Innovation Center for Regional Environmental Quality
Herein, an efficient full-spectrum responsive p-Ag2S/n-PDI (perylenediimide) heterojunction was successfully constructed. The self-assembled PDI nanostructure was formed via hydrogen bonding and pi-pi stacking. Ag2S quantum dots were tightly loaded onto the surface of PDI nanofibers via a two-step electrostatic process. When the mass ratio of Ag2S to PDI was 1 : 0.6, the p-Ag2S/n-PDI heterojunction showed optimum photocatalytic properties. The full-spectrum photocatalytic activity of p-Ag2S/n-PDI was found to be 5.13 and 1.79 times higher than pure PDI for phenol degradation and O-2 evolution, respectively. The results showed that Ag2S quantum dots promoted the well-organized pi-pi stacking degree of the self-assembled PDI, which was helpful for the migration of photo-generated electrons along the quasi-one-dimensional pi-pi stacking of PDI. Simultaneously, Ag2S quantum dots were found to enhance the light absorption of Ag2S/PDI. More interestingly, the p-Ag2S/n-PDI heterojunction exhibited excellent photoelectric properties, indicating more effective separation of carriers, which arose as a result of the built-in electric field between the Ag2S and PDI. Besides this, the p-Ag2S/n-PDI heterojunction produces more active species than pure PDI, resulting in a much stronger oxidation ability. This work details some interesting ideas for designing efficient heterojunction photocatalysts that have a supramolecular organic nanostructure.
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