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Rational Design of Self-Supported CuO(x)-Decorated Composite Films as an Efficient and Easy-Recycling Catalyst for Styrene Oxidation

[Image: see text] The applications of graphene-based materials in catalysis are limited by their strong tendency to aggregate, which may lead to a decrease in active sites. Herein, we propose a facile and controllable strategy to fabricate a series of heterogeneous catalysts with a unique nanostruct...

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Detalles Bibliográficos
Autores principales: Du, Bin, Qiu, Lili, Chen, Yuting, Zhang, Ziqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296588/
https://www.ncbi.nlm.nih.gov/pubmed/34308047
http://dx.doi.org/10.1021/acsomega.1c02031
Descripción
Sumario:[Image: see text] The applications of graphene-based materials in catalysis are limited by their strong tendency to aggregate, which may lead to a decrease in active sites. Herein, we propose a facile and controllable strategy to fabricate a series of heterogeneous catalysts with a unique nanostructure wherein CuO(x)-decorated reduced graphene oxide (rGO) sheets are incorporated into a solid matrix composed of poly(vinylpyrrolidone) (PVP) and carboxymethyl cellulose (CMC). The resultant materials are self-supported films and could be directly used as catalysts for the liquid-phase oxidation of styrene without the requirement for extra substrates. The employment of PVP-CMC (PC) as the support for CuO(x)-decorated rGO sheets successfully inhibits their aggregation. Benefiting from the dispersion of copper species, these films exhibit good catalytic activity and recyclability under mild reaction conditions. Especially, they can be conveniently removed from the reaction mixture by tweezers due to their structural stability. For catalyzing multiple reactions with high efficiency and facile recyclability, this study offers a universal strategy to design heterogeneous catalysts based on graphene materials and provides a promising platform.