In-situ formation of silver nanoparticles stabilized by amphiphilic star-shaped copolymer and their catalytic application

[Display omitted] ► Silver nanoparticles were in situ synthesized by a “green” route. ► Polymeric micelles were utilized as nanoreactors for silver nanoparticles formation. ► PDMAEMA segments served as a reducing agent and a stabilizer. Silver nanoparticles (Ag NPs) were prepared via in situ reducti...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Applied surface science 2012-01, Vol.258 (7), p.2655-2660
Hauptverfasser: Huang, Xiujuan, Xiao, Yan, Zhang, Wei, Lang, Meidong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:[Display omitted] ► Silver nanoparticles were in situ synthesized by a “green” route. ► Polymeric micelles were utilized as nanoreactors for silver nanoparticles formation. ► PDMAEMA segments served as a reducing agent and a stabilizer. Silver nanoparticles (Ag NPs) were prepared via in situ reduction of silver nitrate (AgNO3) using polymeric micelles as nanoreactors without any additional reductant. The micelles were constructed from the amphiphilic star-shaped copolymer composed of poly(ɛ-caprolactone) (PCL) segment, 2-(dimethylamino)ethyl methacrylate (DMAEMA or DMA) units and oligo(ethylene glycol)monomethyl ether methacrylate (OEGMA or OEG) units. The Ag NPs stabilized by those star-shaped copolymers were characterized using UV–vis spectrum, DLS, TEM and FTIR. It confirmed that PDMAEMA exhibited the reducing property unless pH was above 7. The Ag NPs were sphere-like with a diameter of 10–20nm, which was independent of the architecture of the copolymer and AgNO3 concentration. Furthermore, the catalytic activity of these Ag NPs was investigated by monitoring the reduction of p-nitrophenol (4-NP) by NaBH4. The result showed that the Ag NPs formed by coordination reduction can be effectively applied in catalytic reaction.
ISSN:0169-4332
1873-5584
DOI:10.1016/j.apsusc.2011.10.113