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Encapsulated CdSe/CdS nanorods in double-shelled porous nanocomposites for efficient photocatalytic CO(2) reduction

Colloidal quantum dots have been emerging as promising photocatalysts to convert CO(2) into fuels by using solar energy. However, the above photocatalysts usually suffer from low CO(2) adsorption capacity because of their nonporous structures, which principally reduces their catalytic efficiency. He...

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Detalles Bibliográficos
Autores principales: Li, Hui, Cheng, Caikun, Yang, Zhijie, Wei, Jingjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617972/
https://www.ncbi.nlm.nih.gov/pubmed/36309504
http://dx.doi.org/10.1038/s41467-022-34263-z
Descripción
Sumario:Colloidal quantum dots have been emerging as promising photocatalysts to convert CO(2) into fuels by using solar energy. However, the above photocatalysts usually suffer from low CO(2) adsorption capacity because of their nonporous structures, which principally reduces their catalytic efficiency. Here, we show that synchronizing imine polycondensation reaction to self-assembly of colloidal CdSe/CdS nanorods can produce micro-meso hierarchically porous nanocomposites with double-shelled nanocomposites. Owing to their hierarchical pores and the ability to separate photoexcited electrons, the self-assembled porous nanocomposites exhibit remarkably higher activity (≈ 64.6 μmol g(−1) h(−1)) toward CO(2) to CO in solid-gas regime than that of nonporous solids from self-assembled CdSe/CdS nanorods under identical conditions. Importantly, the length of the nanorods is demonstrated to be crucial to correlate their ability to long-distance separation of photogenerated electrons and holes along their axial direction. Overall, this approach provides a rational strategy to optimize the CO(2) adsorption and conversion by integrating the inorganic and organic semiconductors.