3D hierarchical Ag nanostructures formed on poly(acrylic acid) brushes grafted graphene oxide as promising SERS substrates.

In this study, in situ generation of Ag nanostructures with various morphology on poly(acrylic acid) (PAA) brushes grafted onto graphene oxide (GO), for use as substrates for surface-enhanced Raman scattering (SERS), is demonstrated. The overall synthetic strategy involves the loading of Ag precursor ions ((Ag+ and [Ag(NH3)2]+) onto PAA brush-grafted GO, followed by their in situ reduction to Ag nanostructures of various morphology using a reducing agent (NaBH4 or ascorbic acid). Novel 3D hierarchical flowerlike Ag nanostructures were obtained by using AgNO3 as precursor and ascorbic acid as reducing agent. Using 4-aminothiophenol as probe molecules, the as-prepared hierarchical Ag nanostructures exhibited excellent SERS performance, providing enhancement factors of ∼107.

Shape-Controlled Synthesis of Au-Polypyrrole Composites Using Poly(4-vinylpyridine) Brush Grafted on Graphene Oxide as a Reaction Chamber.

Controlling the shape of the conducting polymer-noble metal composites is a key factor in determining their properties and applications. In this paper, we demonstrate a novel strategy to fabricate Au-polypyrrole (PPy) composites with unusual morphology using poly(4-vinylpyridine) (P4VP) brush grafted on graphene oxide (GO) as a reaction chamber. When the GO/P4VP brush bearing AuCl4- ions is exposed to pyrrole vapor or directly immersed into pyrrole solution, novel Au-PPy nanotubules and flower-like Au mesoparticles-PPy composites are formed on the surface of GO/P4VP brush, respectively. The application of the as-prepared GO/P4VP/Au-PPy composites in catalysis and surface-enhanced Raman scattering (SERS) are investigated. The relevant results exhibit that the GO/P4VP/Au-PPy nanotubules can act as an efficient catalyst for reduction of 4-nitrophenol, and the GO/P4VP/flower-like Au mesoparticles-PPy composites can be used as a sensor platform for the detection of organic molecules by SERS.