B. R. Mehta

Rapid synthesis of silver nanoparticles using dried medicinal plant of basil

Plants respond to heavy metal stress by metal complexation process like production of phytochelations or by other metal chelating peptides. In this paper we report the synthesis of silver nanoparticles (AgNPs) from the room dried stem and root of Ocimum sanctum. The broth of the plant is used as a reducing agent for the synthesis of Ag nanoparticles at room temperature. The reaction process was simple and was monitored by ultraviolet-visible spectroscopy (UV-vis). There was formation of highly stable silver nanoparticles in the solution. The morphology and crystalline phase of the NPs were determined from transmission electron microscopy (TEM), selected area electron diffraction (SAED) and X-ray diffraction (XRD) spectra. Transmission Electron Microscopy studies showed that the silver nanoparticles obtained from roots and stem were of sizes 10+/-2 and 5+/-1.5 nm, respectively. The various phytochemicals present within the ocimum plant result in effective reduction of silver salts to nanoparticles but their chemical framework is also effective at wrapping around the nanoparticles to provide excellent robustness against agglomeration.

Optical and structural properties of nanocrystalline copper oxide thin films prepared by activated reactive evaporation

Abstract Nanocrystalline Cu 2 O thin films have been synthesized using an activated reactive evaporation technique. Structural and optical characterizations of these films have been carried out using: glancing angle X-ray diffractometer; Fourier transform infrared spectrometer; transmission electron microscope; and UV-VIS-NIR spectrophotometer. The nanocrystallite size in these films was varied by varying deposition parameters. Optical studies show a direct allowed transition and a shift in the optical absorption edge from the bulk value with nanocrystallite size and stoichiometry of these films. These results show that single phase nanocrystalline Cu 2 O thin films can be synthesized at a relatively low substrate temperature using the activated reactive evaporation technique. These studies indicate that nanocrystallinity results in the stability of cubic Cu 2 O phase in these films.

Biosynthesis of Silver Nanoparticles from Desmodium triflorum: A Novel Approach Towards Weed Utilization

A single-step environmental friendly approach is employed to synthesize silver nanoparticles. The biomolecules found in plants induce the reduction of Ag+ ions from silver nitrate to silver nanoparticles (AgNPs). UV-visible spectrum of the aqueous medium containing silver ions demonstrated a peak at 425 nm corresponding to the plasmon absorbance of silver nanoparticles. Transmission electron microscopy (TEM) showed the formation of well-dispersed silver nanoparticles in the range of 5–20 nm. X-ray diffraction (XRD) spectrum of the AgNPs exhibited 2θ values corresponding to the silver nanocrystal. The process of reduction is extracellular and fast which may lead to the development of easy biosynthesis of silver nanoparticles. Plants during glycolysis produce a large amount of H+ ions along with NAD which acts as a strong redoxing agent; this seems to be responsible for the formation of AgNPs. Water-soluble antioxidative agents like ascorbic acids further seem to be responsible for the reduction of AgNPs. These AgNPs produced show good antimicrobial activity against common pathogens.

Structure and photoluminescence studies on ZnS:Mn nanoparticles

ZnS:Mn was produced in nanocrystalline form by a chemical method using polyvinylpyroledone as a chemical capping agent. Mn was stoichiometrically substituted for Zn in ZnS. The manganese (Mn) concentration was varied over its whole solid solution limit in ZnS, i.e., from 0 to 40%. In the high concentration regime this material formed may be thus written as nanocrystalline (Zn, Mn)S. The material formed is thus a wide gap diluted magnetic semiconductor. The characterized material was in powder form. X-ray diffraction was used to estimate the crystallite size and to confirm formation of the material in single phase. The average crystallite size obtained was about 2 nm. The material remained cubic over the whole Mn solid solution range. The room temperature photoluminescence (PL) when deconvoluted using a Gaussian fit showed two extra peaks in nanocrystalline ZnS:Mn when compared to pure nanocrystalline ZnS, which had only two peaks. Mn incorporation significantly enhanced the PL intensity in nanocrystalline...

Tailored nanoparticle films from monosized tin oxide nanocrystals: Particle synthesis, film formation, and size-dependent gas-sensing properties

In order to investigate the change of gas-sensitive properties of undoped tin oxide nanoparticle films depending on particle size, a thin film synthesis technique has been developed. Well-defined tin oxide nanoparticles have been prepared using a gas-phase condensation method. Pure SnO was used as starting material and was evaporated at T=820 °C. The resulting particles were sintered and crystallized in-flight at T=650 °C. Size-selected nanoparticles ranging from 10 to 35 nm were produced to form a nanoparticle film by means of electrostatic precipitation or low pressure impaction. The effect of in-flight oxidation, sintering, and crystallization on the structure, size, and size distribution of nanoparticles have been studied in detail. The samples show n-type semiconductors’ behavior like bulk SnO2. The influence of particle size on gas sensitivity and response behavior is investigated for C2H5OH at operating temperatures 200–300 °C using silicon substrates having an interdigitated contact pattern and an...

Surface-modified CuO layer in size-stabilized single-phase Cu2O nanoparticles

Activated reactive evaporation has been used to grow copper oxide nanoparticles in the size range of 8–100 nm. X-ray diffraction spectra clearly show the presence of a single Cu2O phase. Detailed x-ray photoelectron spectroscopy studies show an increase in the ionicity of the Cu2O system with decreasing particle size. Depth profiling and finger printing of x-ray photoelectron spectra reveal that the Cu2O nanoparticles are capped with a CuO surface layer of thickness ≈1.6 nm. This study strongly suggests that the stabilization of the cubic Cu2O nanophase is enhanced by the formation of a CuO surface layer.

Modifying the nanocrystalline characteristics—structure, size, and surface states of copper oxide thin films by high-energy heavy-ion irradiation

In the present study, x-ray diffraction, Raman spectroscopy, spectroscopic ellipsometry, photoluminescence, and x-ray photoelectron spectroscopy techniques were used to study the effect of 120 MeV 107Ag9+ ion irradiation on nanocrystalline Cu2O thin films grown by the activated reactive evaporation technique. The influence of dense electronic excitations during ion irradiation on the structural and optical properties of the Cu2O thin films was studied. Experimental results demonstrate that the phase and the size of nanocrystallites in the Cu2O thin films as well as associated surface states can be tailored by controlling ion fluence. The Cu2O higher symmetry cubic phase is observed to be quite stable under a higher temperature and irradiation-induced thermal spikes, which accompanies ion irradiation.

On the origin of photoluminescence in indium oxide octahedron structures

A sixfold decrease in photoluminescence signal intensity at 590nm with increase in deposition time from 3to12h has been observed in single crystalline indium oxide octahedron structures grown by vapor-phase evaporation method. Electron paramagnetic resonance and energy dispersive x-ray analysis confirm that the concentration of oxygen vacancies increases with deposition time. These results are contrary to the previous reports where oxygen vacancies were shown to be responsible for photoluminescence in indium oxide structures. Our results indicate that indium interstitials and their associated complex defects other than oxygen vacancies are responsible for the photoluminescence in In2O3 microstructures.

Fast response and recovery of hydrogen sensing in Pd–Pt nanoparticle–graphene composite layers

This study reports the fast response and recovery of hydrogen sensing in nanoparticle-graphene composite layers fabricated using chemical methods and comprising of isolated Pd alloy nanoparticles dispersed onto graphene layers. For 2% hydrogen at 40 °C and 1 atm pressure, a response time of <2 s and a recovery time of 18 s are observed. The fast response and recovery observed during sensing are due to hydrogen-induced changes in the work function of the Pd alloy and modification in the distribution of defect states in the graphene band gap due to gas adsorption. The results of hydrogen sensing in the new class of Pd-Pt nanoparticle-graphene composite material are important for understanding the effect of gas adsorption on electronic conduction in graphene layers and for developing a new type of gas sensor based on changes in the electronic properties of the interface.

Size dependence of core and valence binding energies in Pd nanoparticles: Interplay of quantum confinement and coordination reduction

An analysis is given of the electronic structure of Pd nanoparticles synthesized by inert gas evaporation technique. A study of the effect of size on various core and valence electrons in Pd nanoparticles reveals a varied dependence of binding energy of electrons in different electronic levels. The shift in the Pd x-ray photoelectron spectroscopy 4d valence band centroid is more than the core level shift. The results of the present study provide a direct evidence of interplay of quantum confinement (a size effect) and coordination reduction (a surface effect).