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The asymmetrical-structure of supramolecular precursor to improve internal electric field for simultaneously enhancing contaminant degradation and H2O2 production performance
Asymmetric-structure perylene diimide (PDI) supramolecular photocatalysts were successfully constructed to induce robust internal electric field for efficient photocatalytic activity. Benefitting from the large dipole moment of the asymmetric-structure PDI, the internal electric field has been signi...
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Published in: | Journal of environmental chemical engineering 2022-02, Vol.10 (1), p.107123, Article 107123 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Asymmetric-structure perylene diimide (PDI) supramolecular photocatalysts were successfully constructed to induce robust internal electric field for efficient photocatalytic activity. Benefitting from the large dipole moment of the asymmetric-structure PDI, the internal electric field has been significantly enhanced by 8.4 times. And then the charge separation efficiency of the asymmetric-structure PDI has been dramatically improved by 2.4 times from 4.60% up to 11.22%. Thus, the asymmetric-structure PDI supramolecular presents evidently enhanced photocatalytic degradation performance, up to 4.8 times, even surpassing many reported high-activity organic photocatalysts. Meanwhile, they also exhibited a maximum 9.5-fold increase in photocatalytic hydrogen peroxide production activity. Briefly, this work throws light on enhancing the internal electric field via molecular structure modification to dramatically improve the photocatalytic performance.
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•Asymmetric-structure PDI supramolecular photocatalysts were constructed.•The internal electric field has been significantly enhanced by 8.4 times.•The charge separation efficiency were further improved from 4.60% up to 11.22%.•The asymmetrical PDI exhibited excellent photocatalytic performance. |
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ISSN: | 2213-3437 2213-3437 |
DOI: | 10.1016/j.jece.2021.107123 |