We present a simple, novel procedure to selectively deposit gold nanoparticles using pure water. It enables patterning of nanoparticle monolayers with a remarkably high degree of selectivity on flat as well as microstructured oxide surfaces. We demonstrate that water molecules form a thin ‘capping’ layer on exposed thiol molecules within the mercaptan self-assembled layer. This reversible capping of water molecules locally ‘deactivates’ the thiol groups, therewith inhibiting the binding of metallic gold nanoparticles to these specific areas. In addition, we show that this amazing role of water molecules can be used to selectively metalize the patterned gold nanoparticle arrays. Employing an electroless seeded growth process, the isolated seeds are enlarged past the percolation threshold to deposit conducting metal layers.

Iron oxide microspheres possess a wide range of applications in lithium storage batteries, sensors, photocatalysis, environmental remediation, magnetic resonance imaging and drug delivery. The most commonly used method for the preparation of iron oxide microspheres is hydrothermal synthesis. Besides this, other synthetic methods such as co-precipitation, electrostatic self- assembly, microwave and sol-gel have been reported. The reported synthetic methods usually require longer time (2 to 48 hours) and expensive experimental set up. In the present study, a novel low temperature thermal decomposition approach for the synthesis of iron oxide microspheres has been reported. Thermal decomposition of an iron-urea complex ([Fe(CON2H4)6](NO3)3) in a mixture of diphenyl ether and dimethyl formamide at 200 °C for 35 minutes leads to the formation of iron oxide microspheres. The microspheres were characterized using a variety of analytical techniques such as X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), diffuse reflectance spectroscopy (DRS) and magnetometry. The XRD results indicated amorphous nature for the as prepared iron oxide, whereas after calcination at 500 °C, crystalline α-Fe2O3 phase is obtained. The SEM images indicated uniform spheres with an average diameter of 1.2 ± 0.3 μm. The DRS results too gave evidence for the formation of α-Fe2O3 on calcination of the microspheres at 500 oC.The field and temperature dependent magnetic measurement results indicated superparamagnetic behavior for the as prepared iron oxide microspheres indicating that the microspheres consist of iron oxide nanoparticles. On the other hand, an antiferromagnetic behavior was observed for the microspheres calcined at 500 °C. The present synthetic method is a novel method to produce magnetic materials with controlled morphologies.

The addition of high refractive index (RI) inorganic nanoparticles (NPs) to LED encapsulation materials can lead to higher light extraction efficiency. In addition, the NPs can be carriers for additional functionality such as color conversion. Using a simple “grafting-to” approach, bimodal polydimethylsiloxane (PDMS) brushes were grafted onto high-RI ZrO2 NPs. Subsequently, an organic phosphor, 6-[fluorescein-5(6)-carboxamido]hexanoic acid (FCHA), was attached onto the PDMS-grafted ZrO2 NPs via a facile ligand exchange process. The bimodal polymer brush design enables homogenous dispersion of the surface functionalized NPs within the silicone matrix. The functionalized NPs with ∼53 wt% ZrO2 core have a ∼0.08 higher RI than neat silicone, and the NP-filled silicone nanocomposites exhibit a transparency of ∼ 90% in the 550-800 nm wavelength range. In addition, the nanocomposites could be excited at a wavelength around 455 nm by a blue LED and undergo secondary yellow emission at around 571 nm. It is expected that the prepared nanocomposites can be used as high-efficiency, non-scattering, color-tuned materials for advanced LED encapsulation.

The aim of this study was to investigate the application of modified clay as a support in the synthesis of silver nanoparticles. Silver nitrate (AgNO3) was used as the silver precursor in several concentrations (0.005 M, 0.01 M, 0.02 M, 0.05 M, and 0.1 M) to obtain Ag-MMT purified and modified clay nanocomposites. The properties of nanocomposites were also studied as a function of the concentration of the reducing agent, sodium borohydride (NaBH4). It was observed through X-ray Diffraction that the MMT purified structure was gradually exfoliated with increased concentrations of AgNO3, while the modified clay structure remained intact. As observed through UV-vis spectra, samples of Ag+-MMT were reduced with NaBH4 to produce Ago and its particle diameter is dependent on the concentration of NaBH4.

The mechanism for the gelation reaction of colloidal silica, Si(OH)4 +Si(OH)3 (O)- ----> Si2O8H5- + H2O, by an anionic pathway was investigated using density functional theory(DFT). Using transition state theory, the rate constants were obtained by analyzing the potential energy surface at the reactants, saddle point, and the products. In addition, reaction rate constants were investigated in the presence of ammonium chloride (NH4Cl) and sodium chloride (NaCl). These salts act as catalysts to induce gelation by destabilizing the double layer of colloidal silica to allow for Van der Waal interactions. Furthermore, it was observed that ammonium chloride plays an important role by initiating a hydride transfer allowing the reaction to proceed from the second transition state to the final product.