Enhancing the Photocatalytic Activity via Direct CovalentFunctionalization in Single-Walled Carbon Nanotubes
[EN] Herein, the direct covalent functionalization of single-walled carbon nanotubes (SWNT) is presented with an amino-decorated phenyl-phenothiazine (PTH-NH2) organophotocatalyst through the diazonium chemistry protocol. Three different SWNT-PTH hybrids are prepared by varying the amount of PTH-NH2...
| Autores: | , , , , , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2024 |
| País: | España |
| Institución: | Universitat Politècnica de València (UPV) |
| Repositorio: | RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia |
| Idioma: | inglés |
| OAI Identifier: | oai:riunet.upv.es:10251/205723 |
| Acceso en línea: | https://riunet.upv.es/handle/10251/205723 |
| Access Level: | acceso abierto |
| Palabra clave: | Carbon nanotubes Covalent functionalization Electronic communication Phenothiazines Photocatalysis QUIMICA ORGANICA |
| Sumario: | [EN] Herein, the direct covalent functionalization of single-walled carbon nanotubes (SWNT) is presented with an amino-decorated phenyl-phenothiazine (PTH-NH2) organophotocatalyst through the diazonium chemistry protocol. Three different SWNT-PTH hybrids are prepared by varying the amount of PTH-NH2 and diazonium agent and are fully characterized. These hybrids differ not only in the degree of functionalization, but also in the chemical structure and the photophysical properties. The study shows that these features affect the photoredox activity of the materials in the photo-debromination of aromatic halides. Thus, sample SWNT-PTH-5, a functionalized nanotube with a 5% wt loading of PTH, surpasses the catalytic performance of homogeneous PTH in 11 different substrates, finishing the reaction in shorter times, in a recyclable manner and without catalyst leaching. This study demonstrates the importance of controlling the functionalization degree of SWNT with photocatalysts to prepare photocatalytic materials with even higher catalytic activity than that presented by the homogeneous PTH catalyst. |
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