Nanotechnology

NiO NPs and Barium doped NiO NPs calcined for different periods of time (3hr, 4hr) at 700?C were synthesized through co-precipitation method. XRD analysis confirmed that all the samples exhibit FCC cubic structure. The doping of barium and also increasing the calcinations time of Ba:NiO increases the crystallite size .Optical absorption spectra reveal that energy gap decreases from 3.75 eV to 3.35 eV due to the increase in crystallite size.PL spectral analysis shows that emission intensity decreases with decreasing grain size. . The morphology of the NiO NPs and Ba:NiO NPs has been analyzed by FESEM and SEM respectively The results of antimicrobial activity of NiO NPs and Ba:NiO (4 hrs) against E-Coli indicated that NiO NPs have excellent inhibitory activity.

In the present work, Y2O3:Eu3+ nanoparticles like-spheres have been synthesized via simple method. Synthesis conditions such as calcination temperature and the additive 2,3-dihyrosybutanedioic acid are played a role for synthesizing Y2O3:Eu3+ nanoparticles with superior optical properties. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) studies have been carried out to understand surface morphological features and the particle size. The as-obtained nanoparticles have average crystallite size ranging between 25 to 45 nm. Crystal structure of the nanoparticles has been investigated by X-ray diffraction (XRD) technique. The incorporation of Eu3+ activator in these nanoparticles has been checked by luminescence characteristics, establishing that the main emission peak located at 613 nm corresponds to the hypersensitive forced electric dipole transition between 5D0 and 7F2 level of Eu3+ ions.

Synthesis of a nanocomposite hydrogel P-PAMPS-PAAm/ZnO, has been made by the polymerization of 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) and acrylamide (AAm) in the presence of pectin (P) and zinc oxide (ZnO) using microwave irradiation technique. FTIR, XRD, SEM and TEM studies indicated the formation of a gel network and incorporation of ZnO particles within gel structure. The system was evaluated for adsorption of Cu (II) and Pb(II) ions from aqueous solutions. About 77 mgg-1 of Cu(II) and 125 mgg-1 of Pb(II) could be adsorbed from aqueous solutions. Different isotherm models have been employed to study the adsorption process and the data is found to fit well with Langmuir isotherm model. The kinetic studies revealed a second-order adsorption process. About 95% of the metal ions adsorbed could be stripped in acidic medium of pH 1.2 indicating the reusability of the gel.

Mechanical properties of seven types of Ag - clay nano films were investigated. Elasticity of Modulus, Tensile Strength, Toughness, Elongation at break, Tear Strength and color of nano films were compared with those of the regular Low Density Poly Ethylene film. Results showed that inclusion of nano particles increased Modulus of Elasticity, Tensile Strength and Tear Strength but Elongation at break point and toughness of the films were decreased. The effect of film type on Modulus of Elasticity, Tensile Stress and Tear Strength, were significant at the 0.01 level and for Elongation at break point and toughness was significant at the 0.05 level. Investigation of film color parameters and ?E showed that the 1000 ppm nano Ag film has more color than other films. The smallest ?E was related to the control film. ?E value of the nano Ag films increased with increasing nano particle content and in nano composite films, decreased with increasing clay content. In sum, the nano film with 1000 ppm nano Ag content was the best film and control film was the worst film. In conclusion, the nano composite film (SC3) with 500 ppm nano Ag- 450 ppm nano clay content was the best film in terms of the mechanical properties.

Zinc oxide nanostructure were successfully synthesized by chemical method and deposited on Al2O3 substrate using PLD. XRD analysis demonstrated that the ZnO nanostructure has a wurtzite structure with orientation of (002). SEM results indicated that by increasing the calcined temperature, the dimension of the ZnO nanostructure increases. The optimum temperature for synthesizing high density ZnO nanostructure was determined to be 1250 K. Room temperature PL spectra of the ZnO nanostructure showed a strong UV emission peak located at around 380 nm and a relatively weak green emission at around 540 nm, confirming that the as-grown nanorods possess good optical properties. The sensitivity of zinc oxide NRs films to 50 ppm vapor NO2 gas as a function of working temperature with different doping.

The thermal evaporation system type (Edwards) has been used to evaporate high purity (99.9 %) silver on glass substrates at room temperature under low pressure (about 10-6 torr) for different thickness (50, 75, 100, 125 and 150) nm. Using a rapid thermal oxidation (RTO) of Ag film at oxidation temperature 350 oC and different oxidation times, Ag2O thin film was prepared. The optical properties of Ag2O film were investigated and compared with other published results. The gas response behaviors of the p-Ag2O/PSi/c-Si – based gas sensor to H2 gas were investigated. The film gas response dependence on the temperature and test gas concentration was tested.

In this paper, we present the concept demonstrating some of the possibilities of nanotechnologies might enable in the future communication devices. Nanotechnology aloows control of physical problem of nanostructures and devices with single molecule precision. The device is build by numerous nano-transistors. This device is used for sensing toxicity of the materials. The devices constructed by nanotechnology can be stretched and folded to desired length since it has the strength of spider silk. As the transistors are temperature dependent, the devices are auto-chargeable when exposed to sunlight (solar energy). Nanoscale electronics are invisible to human eye, the devices are transparent.

Precious metals doped anatase titanium dioxide nanoparticles are used in various applications including environmental photocatalysis and solar cells. In this work we present the synthesis of Au- doped and Pt-doped TiO2 nanoparticles employing sol-gel methodology. The doping procedures based either on UV photodeposition (UV-PD). The morphology, composition, particle size and specific surface area of these synthesized nanoparticles have been characterized using several instrumental techniques namely, Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray Spectroscopy (EDXS), X-Ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and Brunauer–Emmett–Teller (BET) theory. Au impregnated (2%) nano anatase TiO2 powder was examined in photo decolourization of Orange G as dye environmental pollutant under visible light illumination and optimum operational conditions.

The electron density and charge transport studies of organic field effect transistors (OFETs) based 2-phenyl-3Hpyrrole molecule have been calculated from the quantum chemical and DFT methods. Density functional theory calculations with B3LYP/aug-cc-PVDZ basis sets was used to determine ground state gas space molecular geometries (bond lengths and bond angles), electron density and bonding features of this molecule. The electron densities at the bond critical point (BCP) of aromatic Car–Car bonds are much stronger than the other bonds in the molecule. The calculated HOMO and LUMO energies is ~5.50 eV [B3LYP/aug-cc-PVDZ], this shows that charge transfer occurs within the molecule. The HOMO–LUMO gap calculated from quantum chemical calculations has been compared with the value calculated from the density of states. The negative electrostatic potential (ESP) is concentrated solely around the N atoms, whereas in the rest of the region a positive ESP to dominate.

Porous Silicon (PS) layers were prepared by electrochemical etching in a single-tank cell on the surface of single-crystalline p-type (100) silicon wafers, using hydrofluoric acid (HF) and ethanol (C2H5OH) in the volume ratio of 1:2. The surface and cross-section morphologies of the PS were observed from images obtained using Scanning Electron Microscope (SEM). Likewise, the porosity of the PS sample was determined using the parameters obtained from SEM images by geometrical method. SEM images indicated that, the pores were surrounded by a thick columnar network of silicon walls. This porous silicon layer can be considered as a sponge like structure. The X-ray diffraction (XRD) pattern showed the growth of PS layer on silicon wafer and the grain size of the PS layer was found to be around 60.2 nm. The effective refractive index of porous silicon was calculated using Effective Medium Approximation (EMA) analysis. The optical properties of PS were investigated using Fourier Transform Infrared (FTIR) spectroscopy and Photoluminescence (PL). The surface chemical bonds of the PS were observed by FTIR and the band gap of the PS sample was obtained from PL spectra. The efficiency of ethanol gas sensing properties of PS was investigated at room temperature. The sensor was found to operate with maximum efficiency at a concentration of 100 ppm hence, this PS material can be used as an effective sensor element to detect ethanol vapour.