Polydopamine protected hollow nanosphere with AuAg-nanoframe-core@Carbon@AuAg-nanocrystals-satellite hybrid nanostructure (AuAg@C@AuAg/PDA) for enhancing nanocatalysis
A novel multi-layered AuAg@C@AuAg/PDA core/shell nanosphere with a uniform nanoframe-core and nanocrystals-satellites nanostructure was developed. Owing to the well distributed AuAg nanocrystals and inner AuAg nanoframes protected by PDA, the AuAg@C@AuAg/PDA shows high catalytic activity and the rat...
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Veröffentlicht in: | Journal of hazardous materials 2020-02, Vol.384, p.121276-121276, Article 121276 |
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Sprache: | eng |
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Zusammenfassung: | A novel multi-layered AuAg@C@AuAg/PDA core/shell nanosphere with a uniform nanoframe-core and nanocrystals-satellites nanostructure was developed. Owing to the well distributed AuAg nanocrystals and inner AuAg nanoframes protected by PDA, the AuAg@C@AuAg/PDA shows high catalytic activity and the rate constant (K) to catalyst weight ratio reaches as high as 3.63 min−1 mg-1.
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•AuAg@C@AuAg/PDA core/shell nanosphere with a hollow interior is prepared by a facile method.•AuAg@C@AuAg/PDA shows a unique nanostructure with an inner AuAg nanoframe core and external AuAg-nanocrystals satellites.•This method can be applied in preparing AuAg@C@AuAg/PDA core/shell particles with different morphologies.•AuAg@C@AuAg/PDA shows excellent performance in catalyzing the reduction of 4-nitrophenol.
This work reported a facile method for fabricating multi-layered polydopamine (PDA) encapsulated AuAg@C@AuAg core/shell nanosphere with a hollow interior. During the synthetic process, the preliminary Ag@C nanosphere is easily covered by an AuAg/PDA hybrid layer through the in situ redox-oxidized polymerization to form the Ag-AuAg@C@AuAg/PDA precursor, in which the AuAg bimetallic nanocrystals are simultaneously obtained via the electrochemical substitution reaction. After etching the residue Ag core, the final AuAg@C@AuAg/PDA hybrid nanosphere is achieved and the inner AuAg shows a unique nanoframe-like nanostructure. The carbon shell plays an important role for the formation and structure evolution of the AuAg@C@AuAg/PDA, and the composition can be modulated by varying the polymerization process. Owing to the well distributed AuAg nanocrystals and inner AuAg nanoframes, the AuAg@C@AuAg/PDA shows better performance than Ag-AuAg@C@AuAg/PDA precursor in catalyzing 4-nitrophenol, and the rate constant (K) to catalyst weight ratio reaches as high as 3.63 min−1 •mg-1. As a result, this work not only offers a hybrid bi-metallic nanocatalyst with excellent performance, but also has valuable implications for compositional modulation of hollow interior multi-layered nanostructure in adsorption, drug delivery, and nanocatalysis. |
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ISSN: | 0304-3894 1873-3336 |
DOI: | 10.1016/j.jhazmat.2019.121276 |