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A very cheap solvent, ethanol, was successfully applied to control ZnO crystal growth for fabricating a series of ZnO composite nanostructures. During the experimental process, a two-step chemical route was adopted. In step-one, ZnO nanowire arrays were grown on fluorine-doped tin oxide coated glass substrate. In step-two, the step-one prepared samples were used as substrates for composite nanostructure deposition. The morphologies of the obtained products were characterized by field emission scanning electron microscopy. The results indicate that the morphologies of the final products can be effectively controlled by changing the water/ethanol ratios in the chemical solution. The obtained ZnO composite nanostructures with various morphologies were successfully employed in dye-sensitized solar cells. The light-to-electricity conversion results show that the composite nanostructures consisting of nanowires and pseudospherical nanostructures enable 80% improvement in solar energy conversion efficiency as compared with the nanowire arrays. These results indicate that the synthesized ZnO composite nanostructures are more suitable for application as photoelectrodes in solar cells.

The strategy to manipulate nanoscale building blocks into well-organized heterostructures is very important to both material synthesis and nanodevice applications. In this work, highly-ordered ZnO/PbS core/shell nanowire arrays were fabricated by a facile and low temperature chemical route. Large area and well-aligned ZnO nanowire arrays were firstly fabricated on conductive glass substrates, and then the synthesis of ZnO/ZnS and ZnO/PbS core/shell nanowire arrays were realized by a chemical conversion method. The morphology, structure, and composition of the obtained nanostructures were confirmed by field-emission scanning electron microscopy, energy-dispersive X-ray analysis, and X-ray diffraction measurements. The optical properties of the synthesized nanostructures were investigated by micro-Raman and photoluminescence spectroscopy. In the synthesized ZnO/PbS core/shell nanowire arrays, the ZnO cores can provide direct conduction pathways for electron transport and PbS shells possess superior photoelectric performance. Therefore, the obtained ZnO/PbS core/shell nanostructures may have potential application in photovoltaic devices.

Water-soluble CdSe nanoparticles have been synthesized from aqueous solution of selenosulfate by using mercaptocarboxylic acid as stabilizer. A comprehensive investigation is presented on the growth mechanism of CdSe nanoparticles and the factors determining the size. The growth mechanism of CdSe nanoparticles composed two kinds of growth mode, aggregation and Ostwald ripening. The growth rate and product properties can be controlled by changing the reaction conditions. The best conditions, for synthesis of CdSe nanoparticles in the current system, are the pH value in the range of 9-10 and a large excess of the cadmium precursor. The structure of CdSe nanoparticles has been studied by using XRD, TEM, and HRTEM.

The attraction force between the AFM tip and the surface of sputtered dielectric thin films (SiO2 and ZrO2) was measured with atomic force microscope (AFM) by applying DC-bias between the AFM tip and the n-Si substrate. Under 0 electric field, there exists van der Waals interaction between the AFM tip and the surface of dielectric films. When DC voltages are applied, the attraction force increases obviously for thin SiO2 (5.2 nm) and ZrO2 (6.8 nm) films due to the columbic interaction between them. A parallel-plate model has been developed to evaluate the ideal columbic tip-surface force for SiO2 and ZrO2 films. Contrary to the calculation result, the columbic force for ZrO2 film (6.8 nm) is lower than that for SiO2 film (5.2 nm), indicating the poor dielectric properties of the ZrO2 film. The poor dielectric properties of ZrO2 film should be due to the interfacial SiOx-containing layer formed between ZrO2 and Si, supporting the conclusion reached in the literature that the interfacial SiOx-containing layer can deleteriously influence the dielectric properties of high-k films.

One of the most important findings in the recent study of deformation and fracture in ordered intermetallics is that many intermetallic alloys with high crystal symmetries (such as L1{sub 2} and B2) are intrinsically quite ductile at ambient temperatures, and that their commonly observed low ductility and brittle fracture are caused mainly by extrinsic factors. Environmental embrittlement has been identified as a major extrinsic factor that embrittles many intermetallic alloys. In this case, the alloys showed brittle fracture and low ductilities when tested in moist air, but they exhibited distinctly high ductilities when tested in high-vacuum or dry-oxygen environments. In order to have a mechanistic understanding of moisture-induced hydrogen embrittlement, it is essential to have a direct measurement of trapped hydrogen atoms with position resolution. In this study, the authors try to develop a laser desorption mass spectrometric method to measure hydrogen atoms in a position-sensitive way. They also compare the amount of trapped hydrogen, with and without exposure to water, for FeAl containing 35.8 at. % Al.