A novel gap-plasmon of Fe3O4@Ag core-shell nanoparticles for surface enhanced fluorescence detection of Rhodamine B（RB） was developed. Fe3O4@Ag core-shell nanostructures with Ag shell and Fe3O4 core were synthetized by self-assembled method with the assistance of 3-mercaptopropyl trimethoxy silane（MPTS）. To study the RB fluorescence enhanced by gap-plasmon, the fluorescence properties of RB on the substrates with different nanogap densities were systematically investigated, and the results showed that the fluorescence intensity of RB on Fe3O4@Ag core-shell NPs substrate was much stronger than that on bare glass substrate, and the fluorescence intensity was further improved by using multilayer Fe3O4@Ag core-shell NPs substrate which had higher nanogap density. Different from the mechanism that is based on the maximum overlap of the surface plasmon resonance（SPR） band and emission band, the mechanism of the fluorescence enhancement in our work is based on the localized surface plasmon（LSP） and the gap plasmon near-field coupling with the Fe3O4@Ag core-shell NPs. Besides, the detection limit obtained was as low as 1×10^（-7） mol/L, and the Fe3O4@Ag core-shell NPs substrate had high selectivity for RB fluorophores. It was demonstrated that the Fe3O4@Ag core-shell NPs substrate had activity, good stability, and selectivity for fluorescence detection of RB. And the detection of RB by the surface plasmon enhanced fluorescence was more convenient and rapid than the traditional detection methods in previous works.
In this paper, microphase behavior of an ABC triblock copolymer, polystyrene-block-poly（2-vinylpyridine）-block- poly（ethylene oxide）, namely PS-b-P2VP-b-PEO, was systematically studied during spin-coating and solvent vapor annealing based on various parameters, including the types of the solvent, spin speed and thickness. The morphological features and the microdomain location of the different blocks were characterized by atomic force microscope （AFM） and high resolution transmission electron microscopy （HRTEM）. With increasing thickness, the order-order transition from nanopores array to the pattern of nanostripes was observed due to microdomain coarsening. These processes of pattern transformation were based on the selectivity of toluene for different blocks and on the contact time between solvent molecules and the three blocks. This work provides different templates for preparation of gold nanoparticle array on silicon wafer, which can be adopted as an active surface-enhanced Raman scattering （SERS） substrate for poly（3-hexylthiophene） （P3HT）.
Hai-liang Huang易国斌Xi-hong ZuBen-bin ZhongHong-sheng Luo
