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Molecularly Engineered Covalent Organic Frameworks for Hydrogen Peroxide Photosynthesis
Synthesizing H(2)O(2) from water and air via a photocatalytic approach is ideal for efficient production of this chemical at small‐scale. However, the poor activity and selectivity of the 2 e(−) water oxidation reaction (WOR) greatly restricts the efficiency of photocatalytic H(2)O(2) production. He...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305556/ https://www.ncbi.nlm.nih.gov/pubmed/35166425 http://dx.doi.org/10.1002/anie.202200413 |
Sumario: | Synthesizing H(2)O(2) from water and air via a photocatalytic approach is ideal for efficient production of this chemical at small‐scale. However, the poor activity and selectivity of the 2 e(−) water oxidation reaction (WOR) greatly restricts the efficiency of photocatalytic H(2)O(2) production. Herein we prepare a bipyridine‐based covalent organic framework photocatalyst (denoted as COF‐TfpBpy) for H(2)O(2) production from water and air. The solar‐to‐chemical conversion (SCC) efficiency at 298 K and 333 K is 0.57 % and 1.08 %, respectively, which are higher than the current reported highest value. The resulting H(2)O(2) solution is capable of degrading pollutants. A mechanistic study revealed that the excellent photocatalytic activity of COF‐TfpBpy is due to the protonation of bipyridine monomer, which promotes the rate‐determining reaction (2 e(−) WOR) and then enhances Yeager‐type oxygen adsorption to accelerate 2 e(−) one‐step oxygen reduction. This work demonstrates, for the first time, the COF‐catalyzed photosynthesis of H(2)O(2) from water and air; and paves the way for wastewater treatment using photocatalytic H(2)O(2) solution. |
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