Photoluminescence and cathodoluminescence ͑CL͒ spectra of stoichiometric and oxygen-deficient ZnO films grown on sapphire were examined. It was found that the intensities of the green and yellow emissions depend on the width of the free-carrier depletion region at the particle surface; the thinner the width, the larger the intensity. Experimental results and spectral analyses suggest that the mechanism responsible for the green ͑yellow͒ emission is the recombination of a delocalized electron close to the conduction band with a deeply trapped hole in the single ionized oxygen vacancy V o ϩ ͑the single negatively charged interstitial oxygen ion O i Ϫ) center in the particle.

A semiconductor laser whose cavities are “self-formed” due to strong optical scattering in highly disordered gain media is demonstrated. The lasers are made of zinc oxide polycrystalline films grown on amorphous fused silica substrates. Lasing occurs at an ultraviolet wavelength of ∼380 nm under optical pumping. Actual images of the microscopic laser cavities formed by multiple scattering have been captured. These results suggest the possibility of using disordered semiconductor microstructures as alternative sources of coherent light emission.

Visible-light-driven plasmonic photocatalyst Ag-TiO(2) nanocomposite hollow spheres are prepared by a template-free chemically-induced self-transformation strategy under microwave-hydrothermal conditions, followed by a photochemical reduction process under xenon lamp irradiation. The prepared samples are characterized by using scanning electron microscopy, transmission electron microscopy, X-ray diffraction, N(2) adsorption-desorption isotherms, X-ray photoelectron spectroscopy, UV/Vis and Raman spectroscopy. Production of .OH radicals on the surface of visible-light illuminated TiO(2) was detected by using a photoluminescence method with terephthalic acid as the probe molecule. The photocatalytic activity of as-prepared samples was evaluated by photocatalytic decolorization of Rhodamine B (RhB) aqueous solution at ambient temperature under visible-light irradiation. The results show that the surface plasmon absorption band of the silver nanoparticles supported on the TiO(2) hollow spheres was red shifted, and a strong surface enhanced Raman scattering effect for the Ag-TiO(2) nanocomposite sample was observed. The prepared nanocomposite hollow spheres exhibits a highly visible-light photocatalytic activity for photocatalytic degradation of RhB in water, and their photocatalytic activity is higher than that of pure TiO(2) and commercial Degussa P25 (P25) powders. Especially, the as-prepared Ag-TiO(2) nanocomposite hollow spheres at the nominal atomic ratio of silver to titanium (R) of 2 showed the highest photocatalytic activity, which exceeds that of P25 by a factor of more than 2.

Gold nanorods (Au-NRs) have attracted enormous interest due to their size and unique optical properties. Many studies have demonstrated their use in biomedical systems. However, their potential toxicity is not fully understood. This study evaluated the effects of the Au-NRs (15 nM × 64 nM) coated with CTAB (cetyltrimethylammonium bromide) or PEG (polyethylene glycol) in human erythrocytes on the induction of haemolysis and erythroptosis. In our study, erythroptosis (also known as eryptosis) was determined systematically through the measurement of feature events of apoptosis by flow cytometry. We found that the CTAB- and PEG-coated Au-NRs up to 0.5 nM did not cause severe haemolysis. However, the CTAB-Au-NRs were more toxic than the PEG-Au-NRs. The toxicity of the CTAB-Au-NRs was largely due to the CTAB residues from desorption or incomplete purification. Mechanistically, cytosolic Ca(2+) ions seem to be the key mediator in the eryptosis/erythroptosis mediated by the CTAB or CTAB-Au-NRs while caspase-3 and reactive oxygen species did not contribute much to the process.

The effects of metal coating on the near-band-edge emission of ZnO thin films have been studied by photoluminescence and atomic force microscopy. Large enhancement in emission intensity has been observed from ZnO films when they are capped by Ag while negligible effect is seen on Au-coated films. In addition, the enhancement is found to increase with Ag thickness and the intensity eventually saturates at thickness of 200nm. By introducing MgO as a spacer between the metal coating and ZnO, the enhancement is shown to decrease with increasing the spacer thickness, which suggests the presence of the local fields induced by surface plasmons. As the emission energy of ZnO matches closely with the surface plasmon of Ag, it is speculated that the resonant coupling of the spontaneous emission in ZnO into the surface plasmons enhances the emission efficiency.