ZnO hierarchical nanostructures: simple solvothermal synthesis and growth mechanism.

Hierarchical nano/micro structures of ZnO have been fabricated by solvothermal approach on sol-gel derived ZnO thin films. Paintbrush like nano/micro rod assembly, double-sided brush and windmill type architectures of ZnO are obtained when the ZnO thin film coated substrates were treated solvothermally in water at pH 10. Aligned nanorods are obtained at pH approximately 13.

Direct synthesis of ZnS nanoribbons, micro-sheets and tetrapods.

ZnS nano and micro structures such as nanoribbons, large sheets and tetrapod shaped crystals were fabricated by direct thermal evaporation of ZnS powder without using any catalyst. Formation of the one dimensional structures such as nanoribbons and micron order sheets was attributed to the vapor-solid growth mechanism. The formation of octahedron nucleus with cubic crystal structures was proposed as the growth unit of the wurtzite crystal structured tetrapods.

CdS:Mn nanorods: solvothermal synthesis and properties.

Manganese (0.05-9 mol.%) doped CdS nanorods were synthesized via solvothermal route using ethylenediamine (En) and a mixture of En and water as the solvents.

Mn(2+)-induced substitutional structural changes in ZnS nanoparticles as observed from positron annihilation studies.

Zinc sulfide nanoparticles doped with different concentrations of manganese ions (Mn(2+)) were synthesized at various temperatures to investigate the effects of substitution and the associated defect evolution. Positron lifetime and Doppler broadening measurements were used as probes. The initial stage of defect recovery was dominated by the occupation of Zn(2+) vacancies by Mn(2+) ions, bringing in characteristic changes in the positron lifetimes, intensities and Doppler broadened lineshape parameters.

Biomolecule assisted hydrothermal synthesis of chainlike network of silver sulfide nanostructures.

A L-cysteine assisted hydrothermal route has been utilized for the growth of Ag2S nanostructures with chainlike network. It was observed that the experimental parameters such as the synthesis temperature and variation in the molar ratio of the anionic and cationic precursors play critical role in determining the morphology and crystal structure of the products. X-ray diffraction study revealed the formation of monoclinic acanthite Ag2S.

Multicolor luminescence from transition metal ion (Mn2+ and Cu2+) doped ZnS nanoparticles.

Mn and Cu doped ZnS nanoparticles in powder form were prepared by a simple solvothermal route. Particle size and crystal structure of the products were investigated through X-ray diffraction study revealing the formation of cubic ZnS nanoparticles of average diameter 2.5 nm.

Positron annihilation spectroscopic studies of solvothermally synthesized ZnO nanobipyramids and nanoparticles.

Zinc oxide (ZnO) samples in the form of hexagonal-based bipyramids and particles of nanometer dimensions were synthesized through solvothermal route and characterized by x-ray diffraction and transmission electron microscopy. Positron annihilation experiments were performed to study the structural defects such as vacancies and surfaces in these nanosystems. From coincidence Doppler broadening measurements, the positron trapping sites were identified as Zn vacancies or Zn-O-Zn trivacancy clusters.

Fabrication of SnS2 flower like nanoflake assemblies through thermal evaporation.

Uniform as well as flower like patterns of SnS2 nanoflakes were produced by a thermal evaporation process. Interpenetrating phenomenon was observed between the individual nanoflakes during the course of their lateral growth. The interpenetrating growth and controlled vapor concentration as well as the substrate temperature leads to the formation of flower like assemblies of SnS2 nanoflakes.

Silica encapsulated Ni nanoparticles: variation of optical and magnetic properties with particle size.

Ni nanoparticles embedded in SiO2 matrix were prepared by sol-gel process. The molar percentages of Ni were varied from 2 to 20% of total SiO2 present in the matrix. Transmission electron microscope (TEM) images revealed that particle sizes varied from 8.

Direct synthesis of ZnO nanowire arrays on Zn foil by a simple thermal evaporation process.

ZnO nanowire arrays were synthesized on zinc foil by a simple thermal evaporation process at relatively low temperature. Morphology and size controlled synthesis of the ZnO nanostructures was achieved by variation of the synthesis temperature, reaction time and the surface roughness of the substrate. A gas-solid and self-catalytic liquid-solid mechanism is proposed for the growth of nanowires at different temperatures.

Ga2O3 and GaN nanocrystalline film: reverse micelle assisted solvothermal synthesis and characterization.

Gallium oxide (beta-Ga2O3) nanoparticles were successfully deposited on quartz glass substrates using sodium bis(2-ethylhexyl) sulfosuccinate (AOT)/n-hexane/ethylene glycol monomethyl ether (EGME) reverse micelle-mediated solvothermal process with different omega values. The mean diameter of Ga2O3 particles was approximately 2-3 nm and found to be approximately independent of omega values of the reverse micelles. However, when the Ga2O3 nanocrystalline films were nitrided at 900 degrees C under flowing NH3 atmosphere for 1 h, the mean diameter of the resulted gallium nitride (wurtzite-GaN) nanoparticles varied from 3-9 nm.

Growth of ZnO nanocrystals by a solvothermal technique and their photoluminescence properties.

ZnO nanocrystals with various morphologies such as nanorod arrays, flower like assemblies, spherical particles, hexagonal cones, and self assembled microstructures were prepared by a solvothermal approach. It was observed that morphology of the ZnO nanostructures were very much solvent dependent in solvothermal approach. Water, ethylenediamine, and ethylene glycol-water mixture favors the formation of nanorods.

Single layer polycrystalline ZnO-Al2O3 nanocomposite thin films: optical and electrical properties.

Nanometric size dependent optical absorption coefficients, dispersive nature of the dielectric constants and ac conductivity are observed for the single layer ZnOx(Al2O3)1-x (x = 0.20 and 0.50) nanocomposites thin films.

Chelating ligand-mediated synthesis of hollow ZnS microspheres and its optical properties.

Monodispersed hollow ZnS microspheres have been successfully synthesized by a facile ethylenediamine tetraacetic acid (EDTA) mediated hydrothermal route. The sizes of the hollow spheres vary from 1.5 to 3.

Multipod znO nanoforms: low temperature synthesis and characterization.

ZnO nanotetrapods were synthesized by a simple thermal evaporation of Zn powder at a relatively low temperature approximately 600 degrees C. The tetrapods have four legs with hexagonal cross-section. Interpenetrating growth was observed in some of these nanotetrapods.

Solvothermal synthesis of CdS nanorods: role of basic experimental parameters.

CdS nanorods with varying dimensions were synthesized by solvothermal process. It was observed that the anions present with the Cd-salts play an important role in determining the dimensions of the CdS nanorods. The crystalline nature of the sources was found to play a crucial role in determining the phase of the products.

Positron annihilation studies of defects and interfaces in ZnS nanostructures of different crystalline and morphological features.

Nanostructures of ZnS, both particles and rods, were synthesized through solvothermal processes and characterized by x-ray diffraction and high resolution transmission electron microscopy. Positron lifetime and Doppler broadening measurements were made to study the features related to the defect nanostructures present in the samples. The nanocrystalline grain surfaces and interfaces, which trapped significant fractions of positrons, gradually disappeared during grain growth, as indicated by the decreasing fraction of orthopositronium atoms.

Simple solvothermal route to synthesize ZnO nanosheets, nanonails, and well-aligned nanorod arrays.

ZnO nanosheets, nanonails, and well-aligned nanorods were fabricated on Zn foils by a solvothermal approach using ethanol as the solvent. A lower synthesis temperature and a shorter time period favor the formation of nanosheets. By optimizing the synthesis temperature and time period, ZnO nanonails with a hexagonal cap and a long stem could be produced.

Surfactant-assisted route to synthesize well-aligned ZnO nanorod arrays on sol-gel-derived ZnO thin films.

Anisotropic growth of ZnO nanorod arrays on ZnO thin films was achieved at a temperature of 90 degrees C by a surfactant-assisted soft chemical approach with control over size and orientation. ZnO thin films with c-axis preferred orientation had been achieved by the sol-gel technique. Lengths, diameters, and the degree of alignment of the ZnO nanorods were controlled by changing the experimental parameters.

Optical and magnetic properties of manganese-incorporated zinc sulfide nanorods synthesized by a solvothermal process.

Manganese-incorporated ZnS (MnxZn1-xS) nanorods were synthesized by a simple solvothermal process. Synthesized nanorods were single crystalline. Manganese incorporation in the ZnS lattice induces a phase transformation from hexagonal wurtzite to cubic zinc blende structure.

Controlled synthesis and photoluminescence properties of ZnS nanowires and nanoribbons.

Rapid synthesis of wurtzite ZnS nanowires and nanoribbons has been achieved by a simple thermal evaporation of ZnS powder onto Si substrate in the presence of Au catalyst. A vapor-liquid-solid process is proposed for the formation of the ZnS nanostructures. The flow rate of the inert carrier Ar gas along with the temperature play an important role in defining the morphology of the ZnS nanostructures.

Potential of cadmium sulphide nanorods as an optical microscopic probe to the folding state of cytochrome C.

The folding behavior of cytochrome C (Cyt-C) conjugated with CdS nanorods (CdSnr) is amenable to monitoring by bright field microscopy, the porosity and percolating behavior of such protein conjugated nanoclusters depending on the folding history prior to the conjugation. The method has been used to predict the thermal melting behavior as well as guanidine hydrochloride induced unfolding of Cyt-C. Dynamic light scattering studies indicate that the size distribution of the nanoforms widens in presence of the protein.

Synthesis and characterization of one-dimensional MgO nanostructures.

Magnesium oxide (MgO) nanowire arrays, nanoribbons, two- and three-dimensional network like nanostructures were prepared by the simple thermal evaporation of Mg powder with and without using catalyst at a relatively low temperature. The non-catalytic approaches favor the formation of network like nanoforms whereas the catalytic approaches favors the formation of one-dimensional nanowire arrays and quasi one-dimensional nanoribbons depending on the temperature and vapor concentrations of the growth site. The diameter and length of the MgO network like columns varied within 40-50 nm and approximately 200 nm respectively.

One-dimensional ZnO nanostructure arrays: synthesis and characterization.

One-dimensional ZnO nanostructure arrays such as nanowires, nanonails, and nanotrees, have been synthesized by oxygen assisted thermal evaporation of metallic zinc on a quartz substrate over a large area. Morphological evolution of ZnO nanostructures at different time scales and different positions of the substrates have been studied by electron microscopy. A self-catalyzed vapor-liquid-solid (VLS) process is believed to be responsible for the nucleation and subsequently a vapor-solid process is operative for further longitudinal growth.

Shape selective growth of CdS one-dimensional nanostructures by a thermal evaporation process.

CdS one-dimensional nanoforms such as nanowires, nanoribbons, network-like nanowires, pearl necklace type nanowires, helical-like nanowires, and nanowire arrays were formed on Si substrates by a simple thermal evaporation route. The shapes of the one-dimensional CdS nanoforms were controlled by varying the experimental parameters such as temperature and position of the substrates. Formation of the CdS one-dimensional nanoforms was initiated by the Au catalyzed vapor-liquid-solid technique, whereas the vapor-solid process played a crucial role in defining the shapes of the nanoforms.