Nitrobacter sp. extract mediated biosynthesis of Ag2O NPs with excellent antioxidant and antibacterial potential for biomedical application.

In this study, extracellular extract of plant growth promoting bacterium, Nitrobacter sp. is used for the bioconversion of AgNO3 (silver nitrate) into Ag2O (silver oxide nanoparticles). It is an easy, ecofriendly and single step method for Ag2O NPs synthesis. The bio-synthesized nanoparticles were characterized using different techniques. UV-Vis results showed the maximum absorbance around 450 nm. XRD result shows the particles to have faced centered cubic (fcc) crystalline nature. FTIR analysis reveals the functional groups that are involved in bioconversion such as C-N, N-H and C=O. Energy-dispersive X-ray spectroscopy (EDAX) spectrum confirms that the prepared nanoparticle is Ag2O NPs. Particle size distribution result reveals that the average particle size is around 40 nm. The synthesized Ag2O NPs found to be almost spherical in shape. Biosynthesized Ag2O NPs possess good antibacterial activity against selected Gram positive and Gram negative bacterial strains namely Salmonella typhimurium, Staphylococcus aureus, Escherichia coli and Klebsiella pneumoniae when compared to standard antibiotic. In addition, Ag2O NPs exhibits excellent free radical scavenging activity with respect to dosage. Thus, this study is a new approach to use soil bacterial extract for the production of Ag2O NPs for biomedical application.

High ferromagnetic transition temperature in PbS and PbS:Mn nanowires.

Spontaneous magnetization measured in the temperature range 5-300 K with high ferromagnetic transition temperature (T(c)) has been observed in both undoped and Mn doped (2-8 mol %) PbS nanowires (diameter 30 nm) in polymer. For undoped sample, we find T(c) ~ 290 K while for doped samples T(c) varies between 310-340 K depending on Mn concentrations. Both T(c) and coercive fields are critically dependent on Mn concentrations. Coercive fields show a T(0.5) dependence with temperature for a moderate concentration of Mn (4 mol %) in PbS while it deviates from T(0.5) behavior for higher Mn concentrations. Anionic defects arising out of nonstoichiometric growth is solely responsible for the observed magnetism in undoped PbS nanowires. The role of intrinsic strain along with reduced dimensionality in determining such high T(c) and overall magnetizations has been discussed.

Fabrication of luminescent silver doped PbS nanowires in polymer.

We report here fabrication of silver (0 to 1.76 mol%) doped PbS nanowires (radius r approximately 1.75 nm) in polymer by a simple wet chemical process. An X-ray photoelectron spectroscopy study clearly confirms the possibility of silver (Ag) doping in PbS nanowires. Both absorption and photoluminescence spectra reveal very strong quantum confinement effect in PbS nanowires as expected for a r/Bohr radius ratio approximately 0.0972 nm. Visible excitonic emission is observed at room temperature in the photoluminescence spectra of undoped and silver doped PbS nanowires in polymer. The excitonic emission is appreciably blue-shifted when doped by silver (1.76 mol%) indicating strong modification of the electronic states by magnetic silver ions. While Ag2+ centers at the substitutional lattice site show an emission band around 525 nm, Ag0 at the interstitial site act as nonradiative recombination centers. Effect of silver doping on the luminescence intensity is also discussed.