Photoinduced electron transfers with carbon dots.

The photoluminescence in carbon dots (surface-passivated small carbon nanoparticles) could be quenched efficiently by electron acceptor or donor molecules in solution, namely that photoexcited carbon dots are both excellent electron donors and excellent electron acceptors, thus offering new opportunities for their potential uses in light energy conversion and related applications.

Efficient quenching of photoluminescence from functionalized single-walled carbon nanotubes by nitroaromatic molecules.

The photoluminescence from functionalized single-walled carbon nanotubes was found to be highly sensitive to the presence of nitroaromatic compounds such as nitrobenzene, 4-nitrotoluene, and 2,4-dinitrotoluene. The strong luminescence quenching in solution was at the upper limit of diffusion-control and also showed significant static quenching contributions. Mechanistic implication of the results and potential applications are discussed.

Luminescence polarization spectroscopy study of functionalized carbon nanotubes in a polymeric matrix.

Single-walled carbon nanotubes (SWNTs) were well-functionalized for a study of their defect-derived luminescence properties. The soluble nanotube sample was homogeneously dispersed in poly(vinyl alcohol) (PVA) films via solution-phase mixing and then wet-casting. The PVA films embedded with the functionalized SWNTs were strongly luminescent according to spectroscopic and confocal microscopic results. The luminescence from the films was highly polarized, with the observed anisotropy value approaching the limit for collinear absorption and emission dipole moments. The films were mechanically stretched to align the embedded nanotubes, and results from luminescence measurements of the stretched films suggested that the excitation was strongly in favor of the direction along the nanotube axis. Mechanistic implications of the polarization spectroscopy results for the luminescent functionalized nanotubes in the polymeric matrix with and without the mechanic alignment are discussed.

Visible luminescence of carbon nanotubes and dependence on functionalization.

Strong luminescence emissions over a broad wavelength region were detected from well-dispersed carbon nanotubes in most functionalized samples, even with excitation wavelengths into the near-IR. Apparently, the better dispersion and functionalization of the nanotubes resulted in more intense luminescence emissions. These emissions may logically be attributed to the trapping of excitation energy by defect sites in the nanotube structure, which are passivated upon the appropriate functionalization of the nanotubes. Better functionalization improves not only the nanotube dispersion (thus diminishing the quenching due to intertube interactions) but also the surface passivation to make the energy trapping sites more emissive, leading to stronger luminescence emissions. Because of such high sensitivity, the visible luminescence emissions may prove valuable in the evaluation of dispersion in functionalized carbon nanotube samples and related nanocomposite materials.

Spontaneous hydrogen generation from organic-capped Al nanoparticles and water.

The development of technologies that would lead toward the adoption of a hydrogen economy requires readily available, safe, and environmentally friendly access to hydrogen. This can be achieved using the aluminum-water reaction; however, the protective nature and stability of aluminum oxide is a clear detriment to its application. Here, we demonstrate the spontaneous generation of hydrogen gas from ordinary room-temperature tap water when combined with aluminum-oleic acid core-shell nanoparticles obtained via sonochemistry. The reaction is found to be near-complete (>95% yield hydrogen) with a tunable rate from 6.4x10(-4) to 0.01 g of H2/s/g of Al and to yield an environmentally benign byproduct. The potential of these nanoparticles as a source of hydrogen gas for power generation is demonstrated using a simple fuel cell with an applied load.

Formation of protein-metal oxide nanostructures by the sonochemical method: observation of nanofibers and nanoneedles.

The sonochemical reaction of iron pentacarbonyl is explored in water and in water with the protein BSA (bovine serum albumen). In water, the reaction is found to produce spherical nanoparticles of magnetite (Fe3O4) with a particle size distribution of <10 to approximately 60 nm. In water with BSA, the reaction produces either nanofibers or nanoneedles, depending on the concentration of BSA. The nanofiber and nanoneedle samples are found to be mixtures of goethite, lepidocrocite, and hematite (alpha-FeOOH, gamma-FeOOH, and alpha-Fe2O3, respectively). The sonochemical reaction of iron pentacarbonyl with BSA in water is thought to proceed through the thermal decomposition mechanism for iron pentacarbonyl with BSA acting as a templating agent.

Quantum-sized carbon dots for bright and colorful photoluminescence.

We report that nanoscale carbon particles (carbon dots) upon simple surface passivation are strongly photoluminescent in both solution and the solid state. The luminescence emission of the carbon dots is stable against photobleaching, and there is no blinking effect. These strongly emissive carbon dots may find applications similar to or beyond those of their widely pursued silicon counterparts.

Direct conjugation of semiconductor nanoparticles with proteins.

Nanocrystalline CdS particles directly conjugated with bovine serum albumin (BSA) protein were prepared by applying the supercritical fluid processing technique, rapid expansion of a supercritical solution into a liquid solvent. The direct conjugation takes advantage of the unique features of the process for nanoparticle formation. The BSA-conjugated CdS nanoparticles in stable aqueous suspension or in the solid state were characterized by using microscopy, X-ray diffraction, and optical spectroscopy methods. The results show that well-dispersed CdS nanoparticles are coated with BSA in a core-shell-like arrangement and that the protein species associated with the nanoparticles remain functional according to the modified Lowry assay. These BSA-conjugated CdS nanoparticles are also strongly luminescent, with the luminescence spectrum contributed to primarily by the exciton emission.