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At present, there is considerable interest in polymer-metal chalcogenides/oxides based nano-composites on account of their tunable optical, magnetic, electronic and catalytic properties. Here in, we report a simple single step approach for the in-situ synthesis of combined cobalt sulphide/cobalt oxide in polyphenylenesulphide (PPS) polymer matrix. We have illustrated the suitability of this methodology by reacting commonly available cobalt precursors with engineering thermoplastic, PPS. The cobalt precursor was homogeneously mixed with PPS in the molar ratios of 1:1, 1:5, 1:10, 1:15, respectively, followed by heating the mixtures obtained at the melting temperature of the polymer (285?C) for six hours. The resultant products were characterized by X-ray Diffractometry (XRD), Field-Emission Scanning Electron Microscopy (FESEM), High Resolution Transmission Electron Microscope (HRTEM), Diffuse Reflectance Spectroscopy (DRS) technique and Fourier Transformation Infra red Spectroscopy (FTIR). Formation of mixed phases viz., sulphide and oxide of cobalt within modified PPS matrix was confirmed by XRD. The resultant nanoparticles of cobalt sulphide and cobalt oxide embedded in the PPS matrix showed crooked and chunk morphology. The optical properties of the resultant nanocomposites indicate the shift in the absorption hump due to nanoscale size effect.

In our contemporary endeavor, metallic molybdenum (Mo) and semiconducting molybdenum trioxide (MoO3) nanostructures have been simultaneously generated via solid state reaction between molybdenum (III) chloride (MoCl3) and polyphenylene sulfide (PPS) at 285 (°)C in unimolar ratio for different time durations, namely, 6 h, 24 h, and 48 h. The resultant nanocomposites (NCs) revealed formation of predominantly metallic Mo for all the samples. However, MoO3 gradually gained prominent position as secondary phase with rise in reaction time. The present study was intended to investigate the antibacterial potential of metal-metal oxide-polymer NCs, i.e., Mo- MoO3-PPS against microorganisms, viz., Pseudomonas aeruginosa, Staphylococcus aureus, Klebsiella pneumoniae, and Aspergillus fumigatus. The antibacterial activity of the NCs was evaluated by agar well diffusion investigation. Maximum sensitivity concentrations of NCs were determined by finding out minimum inhibitory concentration (MIC) and minimum bactericidal/fungicidal concentration (MBC/MFC). Moreover, the NCs prepared at reaction time of 48 h exhibited best MBC values and were tested with time kill assay which revealed that the growth of S. aureus was substantially inhibited by Mo- MoO3-PPS NCs. This synchronized formation of Mo- MoO3 nanostructures in an engineering thermoplastic may have potential antimicrobial applications in biomedical devices and components. Prima facie results on antifungal activity are indicative of the fact that these materials can show anti-cancer behavior.

We, herein, report the antimicrobial properties of uncapped silver nanoparticles for a Gram positive model organism, Bacillus subtilis. Uncapped silver nanoparticles have been prepared using less-explored DC arc thermal plasma technique by considering its large scale generation capability. It is observed that the resultant nanoparticles show size as well as optical property dependent antimicrobial effect.

We herein report the feasibility of polymer-inorganic solid-state reaction route for simultaneous in situ generation of Ag & Ag2S nanostructures in polymer network wherein an engineering thermoplastic, polyphenylene sulphide (PPS), itself acts as a chalcogen source as well as a stabilizing matrix for the resultant nanoproducts. Typical solid-state reaction was accomplished by simply heating the physical admixture of the two reactants i.e. AgNO3 and PPS by varying molar ratios mainly 1:1, 1:5, 1:15, 1:20, at the crystalline melting temperature (285 °C) of PPS. The synthesized nanoparticles were characterized by various physico-chemical techniques like X-ray Diffractometry, Scanning Electron Microscopy equipped with EDAX, Transmission Electron Microscopy and UV-Visible spectroscopy. The prima facie observations suggest the effective formation and subsequent entrapment of mainly nanocrystalline metallic silver (fcc) in PPS matrix for all the molar ratios chosen for the reaction. Additionally, simultaneous occurrence of nanocrystalline Ag2S (monoclinic phase) is also noticed in case of heated admixture of AgNO3: PPS with equimolar ratio. The TEM analysis reveals nanoscale polydispersity (5nm to 70nm) and prevalence of mainly spherical morphological features in all the cases with occasional indications of triangular and hexagonal morphological features depending upon the reaction molar ratio.

The paper reports the deterministic effects of a focusing electric field in improving the purity and yield of the arc-generated carbon nanotubes (CNTs). The method utilizes a focusing electrostatic field, which was superimposed on the arc symmetrically. The focusing voltage was varied from 0 to 1200 V at steps of 200 V and a number of cathode deposits, thus generated, were collected and thoroughly analysed in their totality with the help of weight balance, Raman spectroscopy, transmission electron microscopy and thermogravimetry. With the optimally configured focusing electric field, the arc generator is found to utilize nearly 85% of the consumed anode material, for converting into cathode deposit consisting of CNTs, as compared with about 35% in the conventional arc plasma method. The sample prepared under optimized conditions exhibited high oxidation temperature (851 °C) in the thermogravimetric analysis, negligible D band intensity along with a reduced G band line-width (14 cm−1) in the Raman spectrum, confirming the presence of high purity CNTs with a high relative yield.

An efficient modified arc plasma method, where a focusing electric field is superimposed on the arc electric field, is optimized for the bulk generation of highly pure multi-walled carbon nanotubes. Raman spectroscopy and thermogravimetric measurements have been used to optimize the process.

Thin films of CdS have been prepared by chemical spray pyrolysis by spraying precursor solution directly onto soda lime glass (SLG) substrates. Influence of substrate temperature on structural, optical, morphological and electrical properties have been investigated by using various techniques such as low angle X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), transmission electron microscopy (TEM), UV–visible spectroscopy photoluminescence (PL) spectroscopy etc. Formation of CdS has been confirmed by low angle XRD, Raman spectroscopy and XPS analysis. XRD pattern showed that CdS films are polycrystalline, have hexagonal structure and prefer orientation of crystallites shifts from (101) to (002) with increase in substrate temperature. Raman spectroscopy revealed that exciton-phonon coupling depends on substrate temperature and hence on crystallite size. Optical band gap increased from 2.43 to 2.99 eV when substrate temperature increased from 325 to $475\,^\circ {\rm{C}}$. Transmittance of the film also showed an increasing trend from $\sim 52 \% $ to $\sim 80 \% $ with increase in substrate temperature. Such high band gap and transmittance values of CdS films prepared at $475\,^\circ {\rm{C}}$ make it a useful window material in CdS/CdTe and CdS/Cu2S heterojunction solar cells.

The incessant use of antibiotics against infectious diseases has translated into a vicious circle of developing new antibiotic drug and its resistant strains in short period of time due to inherent nature of micro-organisms to alter their genes. Many researchers have been trying to formulate inorganic nanoparticles-based antiseptics that may be linked to broad-spectrum activity and far lower propensity to induce microbial resistance than antibiotics. The way-out approaches in this direction are nanomaterials based (1) bactericidal and (2) bacteriostatic activities. We, herein, present hitherto unreported observations on microbial abatement using non-cytotoxic molybdenum disulfide nanostructures (MSNs) which are synthesized using microwave assisted solvothermal route. Inhibition of biofilm formation using MSNs is a unique feature of our study. Furthermore, this study evinces antimicrobial mechanism of MSNs by reactive oxygen species (ROS) dependent generation of superoxide anion radical via disruption of cellular functions.

Herein we report an extremely simple one-pot synthesis of lead sulphide nanorods inside the engineering thermoplastic (i.e. polyphenylene sulphide) which plays a dual role of stabilizing matrix as well as a chalcogen source. The effect of molar ratios of the reactants on the morphology of the samples was studied. The prima facie observations suggest the effective formation of 1-D PbS nanorods along with cubic lead as an impurity phase. The average aspect ratio is found to be approximately 4 to 42 depending upon the reactant molar ratio.

We herein propose a facile single-step approach involving solid-state reaction between silver salt and engineering thermoplastic polyphenylene sulfide for simultaneous in situ generation of nanosca...

The present work describes the preliminary results on large-scale synthesis and characterisation of copper (Cu) and aluminium nitride (AlN) nano powders by transferred arc thermal plasma technique. The transferred arc was used to vaporise the precursor materials (Cu, Al metal 99.9% pure). Nano particles are formed in the gas phase as a result of homogeneous nucleation. The vapours of Al were allowed to react with NH3 gas for the synthesis of AlN. Rapid quenching using Ar/N2 then produced the desired nano powders. For the generation of Cu nano powders, argon was used as a quench gas. The resultant nano-powders of Cu, AlN were collected under the controlled atmosphere. TEM and AFM results show the particle size ranging between 70 nm and 100 nm. These particles possess exotic applications in defence systems, armour for aircraft and vehicles, aeronautical systems, power electronics, microelectronics etc.

Uncapped silver nanoparticles were synthesised using hitherto unexplored DC arc thermal plasma technique using Ar, He and mixture of Ar and He as plasma gases. Effect of change in plasma gases on the morphological properties of synthesised nanoparticles has been studied. XRD revealed formation of phase pure cubic silver. TEM study disclosed formation of nanoparticles with size in the range of 20-50 nm and 5-30 nm for silver nanopowders synthesised with He and Ar as plasma gases, respectively while a bimodal size distribution with sizes ranging from ∼20 nm to 150 nm is observed for silver nanopowders synthesised with mixture of He and Ar as plasma gases in 2 : 3 ratio. UV-visible spectroscopy results also support the wide particle size distribution. Demixing effect is presumably responsible for increase in particle size and wide variation in particle size distribution in case of nanoparticles synthesised using mixed gas plasmas.

1-D nanorod bundles as well as sea urchin and starfish like hierarchical morphological nanoarchitectures of CdS have been synthesised using a facile microwave assisted hydrothermal/semi-solvothermal technique. Observation of interesting regular/irregular pine-tree like secondary growth over these hierarchical nanoarchitectures is an important aspect of this work. Cadmium acetate and thiourea were used as precursor materials and were dissolved in solution containing mixture of diethylene triamine (DETA) and deionised water (DIW) in different volume ratios prior to subjecting the resultant solution to microwave radiation of 300 W at a reaction time of 10 min and temperature of 140°C. XRD revealed formation of hexagonal CdS with strong (002) preferred orientation (c-axis orientation). Morphology dependent optical properties are studied using room temperature photoluminescence spectroscopy. We feel such secondary growth will be highly favourable in determining the non-linear properties of optoelectronic devices fabricated using such novel hierarchical nanoarchitectures.