Realization of aligned three-dimensional single-crystal chromium nanostructures by thermal evaporation

Aligned three-dimensional single-crystal chromium nanostructures are fabricated onto a silicon substrate by thermal evaporation in a conventional thermal evaporator, where the incident angle of Cr vapor flux with respect to the substrate surface normal is fixed at 88°. The effects of the deposition time and incident angle on the morphology of the resulting nanostructures are investigated. The achieved Cr nanostructures are characterized by scanning electron microscopy, energy dispersive X-ray analysis, X-ray diffraction, transmission electron microscopy, high-resolution transmission electron microscopy, and surface area measurement. This study provides a convenient way to fabricate three-dimensional single-crystal Cr nanostructures, which is suitable for batch fabrication and mass production. Finally, the same technique is employed to fabricate the nanostructures of other metals such as Ag, Au, Pd, and Ni

A general route to the synthesis of surfactant-free, solvent-dispersible ternary and quaternary chalcogenide nanocrystals

A general route to the synthesis of surfactant-free CuInS2 (CIS), Cu2CoSnS4 (CCTS) and Cu2ZnSnS4 (CZTS) nanocrystals dispersible in low boiling point solvents is proposed. These nanocrystal inks should be of great interest to the fabrication of thin film absorbers of chalcogenide solar cells

Highly-crystallized quaternary chalcopyrite nanocrystals via a high-temperature dissolution–reprecipitation route

Quaternary chalcopyrite (Cu2CoSnS4, Cu2ZnSnS4) nanocrystals displaying high crystallization and controlled morphology were synthesized via a high-temperature growth regime achieved by dissolution–reprecipitation of tailored ultrafine precursors in the temperature range 400–500 °C

Synthesis and Optical Properties of Cu2CoSnS4 Colloidal Quantum Dots

Monodisperse quaternary chalcopyrite Cu2CoSnS4 colloidal quantum dots have been synthesized by acid peptization of a tailored Cu2CoSnS4 precursor displaying loosely packed, ultrafine primary crystallites. Well-defined peaks shifted to higher energy compared to the Cu2CoSnS4 bulk band gap value were observed on the UV-Vis absorption curve consistent with a quantum confinement behavior. First investigations by room temperature time resolved photoluminescence (TRPL) spectroscopy suggest that the photoluminescence emission does not arise from a donor–acceptor recombination.

Synthesis of large-area and aligned copper oxide nanowires from copper thin film on silicon substrate

Large-area and aligned copper oxide nanowires have been synthesized by thermal annealing of copper thin films deposited onto silicon substrate. The effects of the film deposition method, annealing temperature, film thickness, annealing gas, and patterning by photolithography are systematically investigated. Long and aligned nanowires can only be formed within a narrow temperature range from 400 to 500°C. Electroplated copper film is favourable for the nanowire growth, compared to that deposited by thermal evaporation. Annealing copper thin film in static air produces large-area, uniform, but not well vertically aligned nanowires along the thin film surface. Annealing copper thin film under a N2/O2 gas flow generates vertically aligned, but not very uniform nanowires on large areas. Patterning copper thin film by photolithography helps to synthesize large-area, uniform, and vertically aligned nanowires along the film surface. The copper thin film is converted into bicrystal CuO nanowires, Cu2O film, and also perhaps some CuO film after the thermal treatment in static air. Only CuO in the form of bicrystal nanowires and thin film is observed after the copper thin film is annealed under a N2/O2 gas flow

Size and morphology control of ultrafine refractory complex oxide crystals

High-temperature complex oxides are of considerable interest as their applications cover a broad spectrum from catalytic to optical technology. Indeed, new exciting opportunities might emerge if these high-temperature complex oxides, in which structure crystallization is achieved at temperatures T > 1000 °C, could be synthesized as nonaggregated, ultrafine building blocks. In general, such refractory complex oxide particles are difficult to synthesize as ultrafine crystals because of the strong driving force available for sintering and coarsening in this high-temperature range. This paper reports a new synthetic process for the preparation of nonaggregated, ultrafine barium hexa-aluminate, BaO, 6Al2O3, (BHA), and Ba0.9Eu0.1MgAl10O17, (BAM) crystals in which structure crystallization occurs around 1300 °C. Our process is based on the Ba2+ and Al3+ ions high-temperature controlled diffusion from carbon−inorganic hybrid compounds prepared from soft chemistry routes. Control of morphology of these refractory complex aluminates displaying nanoplatelets morphology was achieved via the tailoring of high-temperature diffusion lengths of the various cations involved in the formation of these ultrafine refractory crystals

Nanostructured materials with highly dispersed Au–Ce0.5Zr0.5O2 nanodomains: A route to temperature stable Au catalysts?

Our strategy to inhibit Au(0) growth with temperature involves the preparation of ultrafine Au clusters that are highly dispersed and strongly interacting with a thermally stable high-surface-area substrate. Temperature-stable Au-cluster-based catalysts were successfully prepared through the controlled synthesis of 3.5 nm Ce0.5Zr0.5O2 colloidal building blocks containing tailored strongly bound Au-cluster precursors. With the objective of stabilizing these Au clusters with temperature, grain growth of Ce0.5Zr0.5O2 nanodomains was inhibited by their dispersion through Al2O3 nanodomains. High surface area Au–Ce0.5Zr0.5O2–Al2O3 nanostructured composites were thus designed highlighting the drastic effect of Au cluster dispersion on Au(0) cluster growth. High thermal stability of our Au(0)-cluster-based catalysts was shown with the surprising catalytic activity for CO conversion observed on our nanostructured materials heated to temperatures as high as 800 C for 6 h

Surface characterization and properties of ordered arrays of CeO2 nanoparticles embedded in thin layers of SiO2

We demonstrated the surface composite character down to the nanometer scale of SiO2-CeO2 composite high surface area materials, prepared using 5 nm colloidal CeO2 nanoparticle building blocks. These materials are made of a homogeneous distribution of CeO2 nanoparticles in thin layers of SiO2, arranged in a hexagonal symmetry as shown by small-angle X-ray scattering and transmission electron microscopy. Since the preparation route of these composite materials was selected in order to produce SiO2 wall thickness in the range of the CeO2 nanoparticle diameter, these materials display surface nanorugosity as shown by inverse chromatography. Accessibility through the porous volume to the functional CeO2 nanoparticle surfaceswasevidenced throughanorganic acid chemisorption technique allowing quantitative determination of CeO2 surface ratio. This surface composite nanostructure down to the nanometer scale does not affect the fundamental properties of the functional CeO2 nanodomains, such as their oxygen storage capacity, but modifies the acid-base properties of the CeO2 surface nanodomains as evidenced by Fourier transform IR technique. These arrays of accessible CeO2 nanoparticles displaying high surface area and high thermal stability, along with the possibility of tuning their acid base properties, will exhibit potentialities for catalysis, sensors, etc

Colloidal and monocrystalline Ln3+ doped apatite calcium phosphate as biocompatible fluorescent probes

Ultrafine individualised mono crystalline Ca102x(PO4)62x-(HPO4)x(OH)22x deficient calcium hydroxyapatite nanocrystals displaying fluorescence under visible excitation are proposed for utilisation as biocompatible biological probes

Effects of the nature of the doping salt and of the thermal pre-treatment and sintering temperature on spark plasma sintering of transparent alumina

A slurry of a-Al2O3 was doped with Mg, Zr and La nitrates or chlorides, in various amounts in the range 150-500 wt ppm and then freeze-dried to produce nanosized doped powder (~150 nm). The powder was sintered by SPS to yield transparent polycrystalline alpha alumina. The influence of the nature of the doping element and the starting salt, the thermal treatment before sintering and the sintering emperature on the transparency of the ceramics were investigated. The transparency of the ceramics of nanosized Al2O3 was shown to depend mainly on the way the powder was prepared, the nature of the doping salt also had an effect. Finally, a high real inline transmittance, reaching 48.1% was achieved after optimization