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On the Dimensional Control of 2 D Hybrid Nanomaterials

Thermotropic smectic liquid crystalline polymers were used as a scaffold to create organic/inorganic hybrid layered nanomaterials. Different polymers were prepared by photopolymerizing blends of a hydrogen bonded carboxylic acid derivative and a 10 % cross‐linker of variable length in their liquid c...

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Detalles Bibliográficos
Autores principales: Longo, Alessandro, Mulder, Dirk‐Jan, van Kuringen, Huub P. C., Hermida‐Merino, Daniel, Banerjee, Dipanjan, Dasgupta, Debarshi, Shishmanova, Irina K., Spoelstra, Anne B., Broer, Dirk J., Schenning, Albert P. H. J., Portale, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601213/
https://www.ncbi.nlm.nih.gov/pubmed/28707452
http://dx.doi.org/10.1002/chem.201701493
Descripción
Sumario:Thermotropic smectic liquid crystalline polymers were used as a scaffold to create organic/inorganic hybrid layered nanomaterials. Different polymers were prepared by photopolymerizing blends of a hydrogen bonded carboxylic acid derivative and a 10 % cross‐linker of variable length in their liquid crystalline phase. Nanopores with dimensions close to 1 nm were generated by breaking the hydrogen bonded dimers in a high pH solution. The pores were filled with positively charged silver (Ag) ions, resulting in a layered silver(I)‐polymeric hybrid material. Subsequent exposure to a NaBH(4) reducing solution allowed for the formation of supported hybrid metal/organic films. In the bulk of the film the dimension of the Ag nanoparticles (NPs) was regulated with subnanometer precision by the cross‐linker length. Ag nanoparticles with an average size of 0.9, 1.3, and 1.8 nm were produced inside the nanopores thanks to the combined effect of spatially confined reduction and stabilization of the nanoparticles by the polymer carboxylic groups. At the same time, strong Ag migration occurred in the surface region, resulting in the formation of a nanostructured metallic top layer composed of large (10–20 nm) NPs.