Photoluminescence Stokes shift and exciton fine structure in CdTe nanocrystals

The photoluminescence spectra of spherical CdTe nanocrystals with zincblende structure are studied by size-selective spectroscopic techniques. We observe a resonant Stokes shift of 15 meV when the excitation laser energy is tuned to the red side of the absorption band at 2.236 eV. The experimental data are analyzed within a symmetry-based tight-binding theory of the exciton spectrum, which is first shown to account for the size dependence of the fundamental gap reported previously in the literature. The theoretical Stokes shift presented as a function of the gap shows a good agreement with the experimental data, indicating that the measured Stokes shift indeed arises from the electron-hole exchange interaction.Comment: 8 pages, 4 figures, LaTe

Combined photooxidation/photoreduction using TiO{sub 2} photocatalysts to treat organic/inorganic metal-laden wastewaters

Titanium dioxide (TiO{sub 2}) colloids prepared from titanium chloride (TiCl{sub 4}) were used as photocatalysts in the experiments. Cysteine was selected as the model derivative for the surface modification of the TiO{sub 2} nanoparticles. Testing of TiO{sub 2} photocatalysts conducted in the absence of organic compounds demonstrated that adsorption of lead ions occurred in the system with either untreated (virgin) or treated (modified using cysteine) TiO{sub 2} photocatalysts. Adsorption rates of the metal ions in the systems that used treated TiO{sub 2} photocatalysts were about three times faster than those where untreated TiO{sub 2} photocatalysts were used. Lead ion concentrations in the irradiated solutions decreased as the UV irradiation time increased; greater metal removals were achieved at longer irradiation times. The rate of decreasing lead ion concentrations in the system that used treated TiO{sub 2} photocatalysts was about two to three times faster than that in the system using untreated TiO{sub 2} photocatalysts. Experiments were also performed in which organic compounds (naphthalene or phenol) and heavy metals (Pb{sup 2+}) were simultaneously treated with TiO{sub 2} photocatalysts. The presence of lead ions did not interfere with the photo-degradation of the selected organic compounds from solution. The presence of phenol compound appeared not to affect the photoreduction of lead ions, while addition of naphthalene compound resulted in a lag-time effect on the photoreduction of lead ions from solution. All of the experimental results showed that the cysteine-modified TiO{sub 2} resulted in faster and more effective removal than that for the untreated TiO{sub 2} system. This technique has resulted in the simultaneous photocatalytic removal/recovery of organic and inorganic compounds in the system

Nanoparticles for Applications in Cellular Imaging

In the following review we discuss several types of nanoparticles (such as TiO2, quantum dots, and gold nanoparticles) and their impact on the ability to image biological components in fixed cells. The review also discusses factors influencing nanoparticle imaging and uptake in live cells in vitro. Due to their unique size-dependent properties nanoparticles offer numerous advantages over traditional dyes and proteins. For example, the photostability, narrow emission peak, and ability to rationally modify both the size and surface chemistry of Quantum Dots allow for simultaneous analyses of multiple targets within the same cell. On the other hand, the surface characteristics of nanometer sized TiO2allow efficient conjugation to nucleic acids which enables their retention in specific subcellular compartments. We discuss cellular uptake mechanisms for the internalization of nanoparticles and studies showing the influence of nanoparticle size and charge and the cell type targeted on nanoparticle uptake. The predominant nanoparticle uptake mechanisms include clathrin-dependent mechanisms, macropinocytosis, and phagocytosis

Probing the Surface of Transition-Metal Nanocrystals by Chemiluminesence

We propose a simple chemiluminescence (CL) method for investigation of the surface of Co-based nanocrystals (NCs). Using a combination of CL and spin-trap electron paramagnetic resonance techniques, we systematically studied the generation of reactive oxygen species (ROS) at the surface of differently sized CoPt(3) spherical NCs and CoPt(3)/Au nanodumbbells. We have shown that differently sized CoPt(3) NCs can promote the formation of ROS and as a result can lead to the oxidation of luminol accompanied by the emission of the light. CL allows monitoring the stability of transition-metal-based NCs against oxidation and dissolution. We found by CL that cobalt ions slowly leach from the surface of CoPt(3) NCs even under very mild conditions; however, the amount of the leached cobalt ions does not exceed the maximal concentration of cobalt at the NC surface indicating that only surface atoms can go into solution