Iron oxide nanoparticles (α- Fe₂O₃) were synthesized using an unconventional, eco-friendly technique utilizing a Hibiscus rosa sinensis flower (common name, China rose) extract as a reducer and stabilizer agent. The microwave method was successfully used for the synthesis of iron oxide nanoparticles. Various volume ratios of iron chloride tetrahydrate to the extract were taken and heated by the microwave oven for different periods to optimize iron oxide nanoparticle production. The synthesized iron oxide nanoparticles were characterized using the ultraviolet-visible spectrometer (UV-Vis), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and X-ray diffraction (XRD). X-ray diffraction confirmed the formation of α- Fe₂O₃ nanoparticles (hematite). The average size of iron oxide nanoparticles was found to be 51nm. The antibacterial activity of the synthesized iron nanoparticles was investigated against different bacteria such as Staphylococcus aureus, Pseudomonas aeruginosa, Klebsiella pneumonia, and Escherichia coli. The results showed that the synthesized iron nanoparticles exhibited an inhabitation effect on all studied bacteria.

This study reports the synthesis of gold nanoparticles (AuNPs) using an unconventional, eco-friendly method that utilizes cinnamon bark extract as a reducing agent and stabilizer. The synthesized AuNPs were characterized using UV–Vis spectroscopy and transmission electron microscopy (TEM). UV–Vis spectrum shows the surface plasmon resonance (SPR) peak around 535 nm. TEM shows the spherical shape of AuNPs and the particle size distribution at around 35 nm. The ability of the synthesized AuNPs as a quencher of eosin Y dye was monitored using a fluorometer. It was found that in the presence of AuNPs, the fluorescence peak of eosin is quenched. The fluorescence of the mixture of eosin and AuNPs is enhanced in the presence of bovine serum albumin (BSA) protein. TEM shows that the average size of the AuNPs is reduced from 35 to 5 nm with the addition of eosin, and the size of AuNPs then increased to 26 nm upon adding BSA to the mixture of ANPs and eosin. These fluorescence fluctuations may be used for trace identification and biosensing.

Nanoparticles of gold and silver were prepared by a reduction method and by employing green chemistry principles such as using curcumin as a reducing and a stabilizing agent. The formation of nanoparticles was confirmed by UV-Vis absorption spectra and TEM. Mie theory was used to determine the particle sizes. The nonlinear refraction and absorption properties of the particles were measured using the z-scan technique. A large value of third-order nonlinearities was obtained using the nanoparticles produced.

In this work, stable and spherical silver nanoparticles (AgNPs) were synthesized in situ from silver salt (silver nitrate) using the aqueous extract of the okra plant (Abelmoschus esculentus) at room temperature and ambient pH conditions. The influences of different parts of the plant (such as the leaves, stems, and pods) on the chemical-reducing effectiveness of silver nitrate to silver nanoparticles were investigated. The aqueous extract of the leaves was found to be more effective in the chemical reduction of silver nanoparticles and in stabilizing them at the same time. The silver nanoparticles produced were stable and did not precipitate even after storage for 1 month. The extract of the stem was less effective in the reduction capacity followed by the extract of the pods. The results indicate that the different amounts of phytochemicals present in the leaves, stems, and pods of the okra plant are responsible for the chemical reduction and stabilizing effect. The silver nanoparticles were characterized by UV-Vis spectroscopy, Fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDX). The surface plasmon resonance (SPR) peak at 460 nm confirmed the formation of silver nanoparticles. The nanoparticles were spherical with an average size of 16 nm and polycrystalline with face-centered cubic (fcc) structures. The z-scan technique was used to study the nonlinear refraction and absorption coefficients of AgNPs at wavelengths of 488 and 514 nm under C.W. mode excitation. The nonlinear refraction index and nonlinear absorption coefficients were calculated in the theoretical equations in the experimental data. The antibacterial properties of the nanoparticles were evaluated against Gram-positive and Gram-negative bacteria.

We report on single pass optical gain and lasing measurements on a blue-emitting copolymer, poly(m-phenylene vinylene-co-2,5-dioctyloxy-p-phenylene vinylene) under 0.5 ns pulsed photoexcitation. This soluble copolymer is designed and synthesized for light amplification and lasing applications. Blue photoluminescence is achieved by introduction of the meta linkage of the phenylene rings in the polymer backbone, which reduces the extent of delocalization of π electrons. The large Stokes shift of about 70 nm implies a low reabsorption rate, and leads to easier creation of population inversion and hence to efficient light amplification. A solution of the polymer exhibits amplified spontaneous emission evidenced by spectral narrowing and a superlinear increase of output intensity when it is photoexcited at 337 nm. By means of the variable excitation stripe length method, net gains of 18 and 24 cm⁻¹ are deduced for different pump energies of 71 and 113 μJ, respectively. Moreover, laser emission from the polymer solution is obtained in a simple cavity formed by Fresnel reflections at the cuvette–solution interfaces. A conversion efficiency as high as 27% and a wide tuning range between 470 and 492 nm in solutions are demonstrated.