In this paper, we describe the formation of Au nanoparticle-graphene oxide (Au-GO) and -reduced GO (Au-rGO) composites by noncovalent attachment of Au nanoparticles premodified with 2-mercaptopyridine to GO and rGO sheets, respectively, viaπ-π stacking and other molecular interactions. Compared with in situ reduction of HAuCl4 on the surface of graphene sheets that are widely used to prepare Au-GO composites, the approach developed by us offers well controlled size, size distribution, and morphology of the metal nanoparticles in the metal-GO nanohybrids. Moreover, we investigated surface enhanced Raman scattering (SERS) and catalysis properties of the Au-graphene composites. We have demonstrated that the Au-GO composites are superior SERS substrates to the Au NPs. Similarly, a comparative study on the catalytic activities of the Au, Au-GO, and Au-rGO composites in the reduction of o-nitroaniline to 1,2-benzenediamine by NaBH4 indicates that both Au-GO and Au-rGO composites exhibit significantly higher catalytic activities than the corresponding Au nanoparticles.

We have fabricated a charge-transfer system using the self-assembly method. We find the nontotally symmetric b(2) modes are selectively enhanced in SERS spectroscopy and represent a laser wavelength-dependent property.

In this paper, a simple method to fabricate a three-dimensional (3D) nanostructure decorated with Ag nanoparticles for surface-enhanced Raman scattering (SERS) is demonstrated. Highly ordered porous anodic aluminum oxide (AAO) templates were employed to construct these compound nanostructures. First, the AAO templates were fabricated using a two-step anodization approach. Second, an alternating current (AC) electrochemical deposition was used to fill AAO templates with Ag nanoparticles. Taking 4-mercaptopyridine (4-MPy) as the probing molecule, high-quality SERS spectra were observed. The UV-vis mirror reflection spectra were measured to investigate the surface plasma resonance (SPR) absorbance. An interesting phenomenon of SPR-affected thin film interference was observed. SERS mapping was performed to characterize the homogeneity of as-prepared substrates. Good homogeneity and stability make these substrates good candidates for SERS spectroscopy.

Nanoscale Ag semishell arrays with controlled size and tunable interparticle distance were prepared by combining nanosphere lithography with reactive ion etching. First, a large-area ordered monolayer of polystyrene (PS) nanospheres was deposited on glass substrates using the Langmuir−Blodgett (LB) technique. The PS spheres with different diameters were employed in LB procedures. Second, the monolayers of PS spheres were etched to control the diameter and tune the interparticle distance. Finally, a Ag layer was evaporated on the etched PS templates. Ag films with periodical nanostructures were obtained and can be used as surface-enhanced Raman scattering (SERS) substrates. These substrates exhibited homogeneity and good enhancement ability. SERS enhancement factor (EF) was represented on the order of 104−105. The correlation between nanoscale morphology and SERS activity of the substrates was investigated. When the size of Ag-semishell was fixed, the EF value decreased with the increase of interparitcle distance. Both local surface plasmon mode and delocalized surface plasmon mode contributed to the total enhancement. The controlled size, tunable interparticle distance, and large-area ordered arrays of these substrates suggest their promising applications as functional components in spectroscopy, immunoassay, biosensors, and biochips.