CdSe;
patterning of metal on GaAs;
metal nanoparticle enhanced fluorescence;
fluorescence resonance energy transfer (FRET);
nanosurface energy transfer (NSET);
N-ALKANOIC ACIDS;
GOLD NANOPARTICLES;
RAMAN-SPECTROSCOPY;
FLUORESCENCE;
SILVER;
NANOCRYSTALS;
PHOTOLUMINESCENCE;
MONOLAYERS;
SIZE;
DEPENDENCE;
D O I:
10.1021/nn900317n
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Here we present a simple platform for probing plasmon enhanced photoluminescence (PL) of quantum dots by confocal microscopy. In this study, self-assembled monolayers of silane-derivative molecules were patterned onto the oxidized GaAs surfaces to direct the attachment of All or Ag nanoparticles onto the surface. Following the directed binding of metal nanoparticles (MNPs), a layer-by-layer deposition of oppositely charged polymers was used to create films with varying thickness by controlling the numbers of deposited layers. CdSe quantum dots (QDs) of similar to 4 and 5.5 nm in diameter with 16-mercaptohexadecanoic acid as a surfactant were then adsorbed onto the outermost polymer layer via electrostatic interactions. Using confocal fluorescence microscopy, the enhanced PL from the CdSe over the Au or Ag nanoparticle patterns could be imaged directly and scaled against the regions with no Au or Ag nanoparticles, and the luminescence of the GaAs (as an internal standard) for different CdSe-metal separations. By using a pattern, PL enhancement as a function of particle-CdSe spacing can be readily probed all on a single platform, where the QDs over MNPs and not over MNPs can be directly compared In the same dielectric environment. The observed luminescence as a function of metal-QD separation can be readily fit to a combined model of metal-fluorophore fluorescence quenching and local electric field enhancement.