Sonochemical Reaction of Bifunctional Molecules on Silicon (111) Hydride Surface

While the sonochemical grafting of molecules on silicon hydride surface to form stable Si–C bond via hydrosilylation has been previously described, the susceptibility towards nucleophilic functional groups during the sonochemical reaction process remains unclear. In this work, a competitive study between a well-established thermal reaction and sonochemical reaction of nucleophilic molecules (cyclopropylamine and 3-Butyn-1-ol) was performed on p-type silicon hydride (111) surfaces. The nature of surface grafting from these reactions was examined through contact angle measurements, X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). Cyclopropylamine, being a sensitive radical clock, did not experience any ring-opening events. This suggested that either the Si–H may not have undergone homolysis as reported previously under sonochemical reaction or that the interaction to the surface hydride via a lone-pair electron coordination bond was reversible during the process. On the other hand, silicon back-bond breakage and subsequent surface roughening were observed for 3-Butyn-1-ol at high-temperature grafting (≈150 °C). Interestingly, the sonochemical reaction did not produce appreciable topographical changes to surfaces at the nano scale and the further XPS analysis may suggest Si–C formation. This indicated that while a sonochemical reaction may be indifferent towards nucleophilic groups, the surface was more reactive towards unsaturated carbons. To the best of the author’s knowledge, this is the first attempt at elucidating the underlying reactivity mechanisms of nucleophilic groups and unsaturated carbon bonds during sonochemical reaction of silicon hydride surfaces.

Jean-Louis Luche and the Interpretation of Sonochemical Reaction Mechanisms

Sonochemistry can be broadly defined as the science of chemical and physical transformations produced under the influence of sound. The use of sound energy is rather a young branch of chemistry and does not have the clear definitive rules of other, more established, divisions such as those in cycloaddition reactions or photochemistry. Nevertheless, there are a few guidelines which can help to predict what is going to happen when a reaction mixture is submitted to ultrasonic irradiation. Jean-Louis Luche, formulated some ideas of the mechanistic pathways involved in sonochemistry more than 30 years ago. He introduced the idea of “true” and “false” sonochemical reactions both of which are the result of acoustic cavitation. The difference was that the former involved a free radical component whereas only mechanical effects played a role the latter. The authors of this paper were scientific collaborators and friends of Jean-Louis Luche during those early years and had the chance to discuss and work with him on the mechanisms of sonochemistry. In this paper we will review the original rules (laws) as predicted by Jean-Louis Luche and how they have been further developed and extended in recent years.

Sonochemical reaction to control the near-infrared photoluminescence properties of single-walled carbon nanotubes

A simple one-step operation to control the PL properties of SWNTs by ultrasonic irradiation was developed with an appropriate surfactant under the optimized conditions of the irradiation time, SWNT concentration, and reaction atmosphere.

Phase Transition of La0.62Sr0.38MnO3 Perovskite Manganites

Bulk and nano La0.62Sr0.38MnO3 perovskite manganite samples were prepared using solid state and sonochemical reaction respectively. The ultrasonic velocities measurement was made on prepared samples using ultrasonic through transmission method, at a fundamental frequency of 5 MHz over wide range of temperatures. The temperature dependence of the ultrasonic parameters shows an interesting anomaly in bulk and nano perovskite samples. The observed dramatic softening and hardening in sound velocities are related to phase transitions. Further, a decrease in grain size in the nanostructured sample leads to a shift in the ferromagnetic transition temperature (TC) from 375 to 370 K.

Sonochemically Synthesized ZnO Nanostructured Piezoelectric Layers for Self-Powered Sensor Applications

ABSTRACTIn this paper, we report on the flexible thin film piezoelectric nanogenerators based on two-dimensional ZnO nanoflakes (NFs) directly deposited onto flexible polyethylene terephthalate (PET) using a simple sonochemical reaction in aqueous solution at room temperature. Our sonochemical synthesis method is a rapid, highly stable, low-cost, and reproducible method, which can be performed at ambient conditions. These advantages of the sonochemical method allow the synthesis of many different ZnO nanostructures. The structural investigations using scanning electron microscopy (SEM), atomic force microscopy (AFM), and X-ray diffraction (XRD) indicated that the ZnO NFs grew with high level of crystallinity and without any thermal damage on the substrates. The fabrication of these device provides a promising solution for developing flexible and self-powered electronic devices particularly wearable and implantable sensors. This ZnO-NFs based nanogenerator provides 62 mV of potential and significant reproducibility having with lower p-value (0.0212).

Reaction Parameters for Controlled Sonosynthesis of Gold Nanoparticles

The synthesis of gold nanoparticles by sonochemical technique has been previously performed with excellent results. The synthesis has been carried out in the presence of citric acid, a strong reducing agent, which allows the nucleation and growth of gold nanoparticles, at the same time that controls particle size. In this work, we report the use of sodium tartrate as a mild reducing agent that allows a better understanding of the effect of the reaction parameters during gold nanoparticle synthesis. A conventional sonication bath (37 kHz) was used for the sonochemical synthesis. This work focuses on the reaction temperature effect and the effect of sodium tartrate concentration. It was confirmed that particle size, and particle morphology is dependent of these two reaction parameters. Equally, colloidal stabilization was related to reaction temperature and sodium tartrate concentration. It was also determined that Ostwald ripening takes place during sonochemical reaction under our conditions, allowing us to understand the mechanism that takes place during synthesis. Gold nanoparticles with main particle size of 17 nm were achieved by this method.