Abstract:In this study, the influence of metals (Mg, Al, and Ca) and reaction conditions (time, temperature, and metal grain size) on the metallothermic reduction of Stöber silica nanoparticles (NPs) to form porous Si was explored. Mg metal was found to be an effective reducing agent even at temperatures below its melting point; however, it also induced a high degree of structural damage and morphology change. Al was effective at reducing silica NPs only at its melting point and higher temperatures, but the resulting particles retained a higher degree of structural morphology as compared to those reduced using Mg. Ca was found to be ineffective in reducing silica. A new reductant, a mixture of 70% Mg and 30% Al, was found to induce the least amount of morphology change, and the reactions proceeded at temperatures (450 °C) lower than those required by Mg or Al individually. Furthermore, porous Si-NPs obtained using Mg, Al, and the mixture of 70% Mg and 30% Al as reductants were investigated as carriers for ibuprofen loading and release. Porous Si obtained from Mg and Mg/Al mixture reductions showed higher drug loading and a sustained drug release profile whereas porous Si obtained from Al reduction had lower loading and showed a conventional release profile over 24 hours.

Magnesiothermic reduction of silicon oxide can result in the formation of nanostructured, mesoporous elemental silicon (mp-Si), which has been explored in a variety of energy applications such as Li-ion battery anodes, photocatalytic water splitting, CO 2 reduction, drug delivery vehicles, and sensors as well as for gas storage. The physical properties of the resultant mp-Si generated via magnesiothermic reduction, and thus the potential utility, are highly dependent on the specific reduction conditions utilized. Herein, we report a modified magnesiothermic reduction method which allows for the synthesis of high surface area mp-Si nanoparticles. The reaction was initiated at 650 °C and then cooled to a lower temperature to minimize heat-induced morphological damage. The nanoparticles were characterized by using powder X-ray diffraction, scanning and transmission electron microscopies, and N 2 adsorption isotherm measurements. Particles prepared by using two-step annealing with the initial processing condition of 650 °C for 30 min followed by 300 °C for 4 h resulted in crystalline and completely reduced mp-Si with a high specific surface area of 542 ± 18 m 2 /g. mp-Si nanoparticles generated by using these specific parameters were further used for stoichiometric CO 2 conversion to CH 3 OH, and the reaction yields were 2.5 times higher than prior reports, demonstrating usefulness in effecting an important chemical transformation.

No abstract

No abstract

No abstract