Reversing the size-dependence of surface plasmon resonances

• Published in: Proceedings of the National Academy of Sciences - PNAS 2010-08, Vol.107 (33), p.14530-14534
• Main Authors: Peng, Sheng, McMahon, Jeffrey M., Schatz, George C., Gray, Stephen K., Sun, Yugang
• Format: Article
• Language: English
• Subjects: Absorption spectra; Algorithms; Amines - chemistry; Chemical reactions; Chemicals; Conductivity; Damping; Electrons; Hexanes; Metal Nanoparticles - chemistry; Metal Nanoparticles - ultrastructure; Microscopy, Electron, Transmission; Models, Theoretical; Molecular chemistry; Molecules; Nanoparticles; Nanotechnology - instrumentation; Nanotechnology - methods; Optical properties; Particle Size; Physical Sciences; Silver; Silver - chemistry; Silver Nitrate - chemistry; Spectrophotometry - methods; Surface Plasmon Resonance - methods; Surfactants
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1007524107

The size-dependence of surface plasmon resonances (SPRs) is poorly understood in the small particle limit due to complex physical/chemical effects and uncertainties in experimental samples. In this article, we report an approach for synthesizing an ideal class of colloidal Ag nanoparticles with highly uniform morphologies and narrow size distributions. Optical measurements and theoretical analyses for particle diameters in the d ≈ 2–20 nm range are presented. The SPR absorption band exhibits an exceptional behavior: As size decreases from d ≈ 20 nm it blue-shifts but then turns over near d ≈ 12 nm and strongly red-shifts. A multilayer Mie theory model agrees well with the observations, indicating that lowered electron conductivity in the outermost atomic layer, due to chemical interactions, is the cause of the red-shift. We corroborate this picture by experimentally demonstrating precise chemical control of the SPR peak positions via ligand exchange.