Browsing by Author "Averitt, Richard Douglas"

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    Buckminsterfullerene purification and buckminsterfullerene film characterization
    (1994) Averitt, Richard Douglas; Halas, Naomi J.
    A method is described which utilizes the difference in vapor pressure between C$\sb{60}$ and heavier fullerenes to produce C$\sb{60}$ powder with a purity of 99.97%. Using the material from this process allows for the growth of high purity polycrystalline C$\sb{60}$ thin films. These films are characterized using Raman spectroscopy and temperature dependent photoluminescence. The temperature dependence of the photoluminescence spectra indicates that both intermolecular and intramolecular processes are involved in the radiative recombination of the excited states. A model is proposed to describe the temperature dependence of the photoluminescence. A possible interpretation of this model is that there is a barrier to the formation of self trapped excitons.
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    Gold nanoshells: Optical properties and femtosecond electron dynamics
    (1998) Averitt, Richard Douglas; Halas, Naomi J.
    The chemistry, optical properties, and femtosecond electron dynamics of gold nanoshells are described. The gold nanoshells consist of Au-coated Au$\sb2$S nanoparticles prepared via aqueous phase chemistry using HAuCl$\sb4$ and Na$\sb2$S. During the course of the reaction, the plasmon-related absorption peak first shifts from $\sim$650 nm out to $\sim$900 nm, then shifts back to $\sim$650 nm. It is shown, using generalized Mie scattering theory, that this plasmon peak shift is determined by the relative thickness of the Au shell and the Au$\sb2$S core diameter. This understanding of the optical properties of these nanoparticles is used to elucidate the nanoparticle growth kinetics. The dynamics of the electrons in the Au shell are studied with femtosecond pump-probe spectroscopy using a cavity-dumped Ti:sapphire laser. The induced change in the transmission of the gold nanoshell films studied has a lifetime of $\sim$1.6 ps. The origin of the measured signal is shown to be due to the creation of a hot electron distribution that returns to equilibrium via electron-dissipative interactions with the nanoparticle core and the embedding medium.