The preparation of cobalt oxide nanowires with gold nanoparticle (AuNP) inclusions (Au-Co(3)O(4) nanowires) via colloidal polymerization of dipolar core-shell NPs is reported. Polystyrene-coated ferromagnetic NPs composed of a dipolar metallic cobalt shell and a gold NP core (PS-AuCoNPs) were synthesized by thermolysis of octacarbonyldicobalt [Co(2)(CO)(8)] in the presence of AuNP seeds and polymeric ligands. The colloidal polymerization process of these dipolar PS-AuCoNPs comprises dipolar nanoparticle assembly and solution oxidation of preorganized NPs to form interconnected cobalt oxide nanowires via the nanoscale Kirkendall effect, with AuNP inclusions in every repeating unit of the one-dimensional mesostructure. Calcination of the polymer-coated nanowires afforded polycrystalline Au-Co(3)O(4) nanowires that were determined to be electroactive. Nanocomposite materials were characterized by transmission electron microscopy, field-emission scanning electron microscopy, X-ray diffraction, vibrating sample magnetometry, and cyclic voltammetry. We demonstrate that the optical and electrochemical properties of Au-Co(3)O(4) nanowires are significantly enhanced in comparison with hollow Co(3)O(4) nanowires prepared via colloidal polymerization.

Reversible electron injection into pyridine-capped CdSe nanocrystals (pyr-CdSe NCs), tethered to indium-tin oxide (ITO) substrates using mercaptoalkylcarboxylic acids, is characterized using attenuated total reflectance (ATR) spectroelectrochemistry on a planar waveguide. The sensitivity of this technique provides for characterization of redox processes in submonolayer films of pyr-CdSe NCs. Optically determined onset potentials for electron injection, measured as bleaching/recovery of the exciton absorption band, provide estimates for the conduction band edge (E CB ). Potential-modulated attenuated total reflectance (PM-ATR), in which the in-phase and out-of-phase reflectance response is measured as a function of modulation frequency, provides estimates for rates of electron injection. These apparent rate constants are found to be nearly independent of tether chain length, suggesting that communication between tethered NCs and electrochemically less active (i.e., less conductive) regions on the ITO surface is rate-limiting.