The energy relaxation of the electrons in the conduction band of 12 and 30 nm diameter copper nanoparticles in colloidal solution was investigated using femtosecond time-resolved transient spectroscopy. Experimental results show that the hot electron energy relaxation is faster in 12 nm copper nanoparticles (0.37 ps) than that in 30 nm copper nanoparticles (0.51 ps), which is explained by the size-dependent electron-surface phonon coupling. Additional mechanisms involving trapping or energy transfer processes to the denser surface states (imperfection) in the smaller nanoparticles are needed to explain the relaxation rate in the 12 nm nanoparticles. The observed fluorescence quantum yield from these nanoparticles is found to be enhanced by roughly 5 orders of magnitude for the 30 nm nanoparticles and 4 orders of magnitude for the 12 nm nanoparticles (relative to bulk copper metal). The increase in the fluorescence quantum yield is attributed to the electromagnetic enhancement of the radiative recombination of the electrons in the s-p conduction band below the Fermi level with the holes in the d bands due to the strong surface plasmon oscillation in these nanoparticles.

Diffusive transport within complex environments is a critical piece of the chemistry occurring in such diverse membrane systems as proton exchange and bilayer lipid membranes. In the present study, fluorescence correlation spectroscopy was used to evaluate diffusive charge transport within a strong polyelectrolyte polymer brush. The fluorescent cation rhodamine-6G was used as a counterion probe molecule, and the strong polyelectrolyte poly(styrene sulfonate) was the polymer brush. Such strong polyelectrolyte brushes show promise for charge storage applications, and thus it is important to understand and tune their transport efficiencies. The polymer brush demonstrated preferential solvation of the probe counterion as compared to solvation by the aqueous solvent phase. Additionally, diffusion within the polymer brush was strongly inhibited, as evidenced by a decrease in diffusion constant of 4 orders of magnitude. It also proved possible to tune the transport characteristics by controlling the solvent pH, and thus the ionic strength of the solvent. The diffusion characteristics within the charged brush system depend on the brush density as well as the effective interaction potential between the probe ions and the brush. In response to changes in ionic strength of the solution, it was found that these two properties act in opposition to each other within this strong polyelectrolyte polymer brush environment. A stochastic random walk model was developed to simulate interaction of a diffusing charged particle with a periodic potential, to show the response of characteristic diffusion times to electrostatic field strengths. The combined results of the experiments and simulations demonstrate that responsive diffusion characteristics in this brush system are dominated by changes in Coulombic interactions rather than changes in brush density. More generally, these results support the use of FCS to evaluate local charge transport properties within polyelectrolyte brush systems, and demonstrate that the technique shows promise in the development of novel polyelectrolyte films for charge storage/transport materials.

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