ZnS and CdS nanoparticles were prepared by a simple microwave irradiation method under mild conditions. The obtained nanoparticles were characterized by XRD, TEM and EDX. The results indicated that high purity of nanosized ZnS and CdS was successfully obtained with cubic and hexagonal crystalline structures, respectively. The band gap energies of ZnS and CdS nanoparticles were estimated using UV-visible absorption spectra to be about 4.22 and 2.64 eV, respectively. Photocatalytic degradation of methylene blue was carried out using physical mixtures of ZnS and CdS nanoparticles under a 500-W halogen lamp of visible light irradiation. The residual concentration of methylene blue solution was monitored using UV-visible absorption spectrometry. From the study of the variation in composition of ZnS:CdS, a composition of 1:4 (by weight) was found to be very efficient for degradation of methylene blue. In this case the degradation efficiency of the photocatalyst nanoparticles after 6 h irradiation time was about 73% with a reaction rate of 3.61 × 10−3 min−1. Higher degradation efficiency and reaction rate were achieved by increasing the amount of photocatalyst and initial pH of the solution.
Photocatalysis based on semiconductor quantum dots which utilize the solar energy can be used for the elimination of pollutants from aqueous media and applied for water purification. Degradation of dyes is a standard method to check the photocatalytic activity of any type of photocatalyst. In this paper polyvinyl pyrrolidone (PVP)-capped ZnS and CdS nanoparticles were prepared by a simple microwave irradiation method and studied in detail for their photocatalytic activity in visible range. The obtained nanoparticles were characterized by XRD, TEM, UV-Vis and EDX. The prepared PVP-capped ZnS and CdS nanoparticles have average sizes of $5.1 and 18.3 nm with cubic and hexagonal crystalline structures, respectively. PVP capped CdS nanoparticles exhibited a unique property of optical absorption in visible region with a wave length below than 460 nm followed by a clear long tail up to 700 nm and showed excellent activity toward degradation of dye under visible light illumination. The photocatalytic activity of PVP-capped CdS nanoparticles was found to be improved by mixing with appropriate amount of PVP-capped ZnS nanoprticles. From the study of variation in weight percentages of PVP-capped ZnS nanoparticles, the physical mixture with 20% of PVP-capped ZnS nanoparticles was found to be very efficient for degradation of methylene blue. In this case the degradation efficiency after 6 h illumination was about 81%.
Coating of ZnS and CdS nanoparticles with organic and inorganic materials can extend their light absorption in the visible region and their stability against photo-corrosion. Such materials could emerge as excellent photocatalysts for the elimination of pollutants from aqueous media using solar energy. In this study, PVP (polyvinyl pyrrolidone)-capped ZnS and CdS nanoparticles, ZnS/CdS and CdS/ZnS core shell nanoparticles were synthesized by microwave irradiation method and characterized using different techniques. The XRD patterns exhibited cubic and hexagonal structures for coated ZnS and CdS nanoparticles, respectively. Morphological evaluation of TEM images showed that the nanoparticles are generally spherical in shape. The UV-visible spectra confirmed a shift in the band gap of coated nanoparticles to longer or shorter wavelengths due to size and potential-well effects. The photocatalytic activity of nanoparticles toward dye degradation under visible light was found to be improved after coating. PVP-capped ZnS and CdS exhibited an enhancement in the initial methylene blue degradation efficiency by a factor of about 1.3. ZnS nanoparticles coated by CdS displayed the initial efficiency 3.2 times higher than bare ZnS. The maximum dye removal was obtained in presence of CdS/ZnS core shells which is 1.4 times more efficient than bare CdS.
In this letter, we investigate the fabrication of Silicon nanostructure patterned on lightly doped (1015 cm−3) p-type silicon-on-insulator by atomic force microscope nanolithography technique. The local anodic oxidation followed by two wet etching steps, potassium hydroxide etching for silicon removal and hydrofluoric etching for oxide removal, are implemented to reach the structures. The impact of contributing parameters in oxidation such as tip materials, applying voltage on the tip, relative humidity and exposure time are studied. The effect of the etchant concentration (10% to 30% wt) of potassium hydroxide and its mixture with isopropyl alcohol (10%vol. IPA ) at different temperatures on silicon surface are expressed. For different KOH concentrations, the effect of etching with the IPA admixture and the effect of the immersing time in the etching process on the structure are investigated. The etching processes are accurately optimized by 30%wt. KOH +10%vol. IPA in appropriate time, temperature, and humidity.
Calcium borate nanoparticles have been synthesized by a thermal treatment method via facile co-precipitation. Differences of annealing temperature and annealing time and their effects on crystal structure, particle size, size distribution and thermal stability of nanoparticles were investigated. The formation of calcium borate compound was characterized by X-ray diffraction (XRD) and Fourier Transform Infrared spectroscopy (FTIR), Transmission electron microscopy (TEM), and Thermogravimetry (TGA). The XRD patterns revealed that the co-precipitated samples annealed at 700 °C for 3 h annealing time formed an amorphous structure and the transformation into a crystalline structure only occurred after 5 h annealing time. It was found that the samples annealed at 900 °C are mostly metaborate (CaB2O4) nanoparticles and tetraborate (CaB4O7) nanoparticles only observed at 970 °C, which was confirmed by FTIR. The TEM images indicated that with increasing the annealing time and temperature, the average particle size increases. TGA analysis confirmed the thermal stability of the annealed samples at higher temperatures.
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