Ultra-fast green microwave assisted synthesis of NaFePO4-C nanocomposites for sodium ion batteries and supercapacitors.

Sodium ion batteries are favored in stationary and large scale power storage due to their low cost and nontoxicity. As the lithium is replaced with sodium due to the cost motive, a cheap processing method is needed to maintain the cell price as low as possible. We report an ultra-fast synthesis method that utilizes the high microwave absorbance of silicon carbide content in rice straw ash. Amorphous/maricite mixtures of sodium iron phosphates-carbon composites (NaFePO4-C) are synthesized, crystallized, and carbon coated using one-step microwave heating. The sodium ion electroactive composites are prepared using different microwave heating durations ranging from 30 to 100 s. High purity inert gases are not needed during synthesis, processing, and even at cell assembly. The materials are characterized by elemental analysis techniques, X-ray diffraction (XRD), scanning/transmission electron microscope (SEM/TEM), and Raman spectroscopy. The electrochemical performance of the synthesized nanocomposites is examined as sodium ion battery cathode and as symmetric supercapacitors. The optimum synthesis time is 60 s for the application as sodium ion batteries and as a supercapacitor. The maximum specific capacity is 108.4 mA h g-1 at 0.2 C in the case of using it as a battery cathode. While the capacitance is 86 F g-1 at 0.5 A g-1 as a supercapacitor. The capacity retention is 92.85% after 40 cycles at 0.2 C as sodium ion battery electrode. For supercapacitor, the capacity retention is 81.7% after 1000 cycles.

One-pot fabrication of Ag @Ag2O core-shell nanostructures for biosafe antimicrobial and antibiofilm applications.

Microbial contamination is one of the major dreadful problems that raises hospitalization, morbidity and mortality rates globally, which subsequently obstructs socio-economic progress. The continuous misuse and overutilization of antibiotics participate mainly in the emergence of microbial resistance. To circumvent such a multidrug-resistance phenomenon, well-defined nanocomposite structures have recently been employed. In the current study, a facile, novel and cost-effective approach was applied to synthesize Ag@Ag2O core-shell nanocomposites (NCs) via chemical method. Several techniques were used to determine the structural, morphological, and optical characteristics of the as-prepared NCs. XRD, Raman, FTIR, XPS and SAED analysis revealed a crystalline hybrid structure of Ag core and Ag2O shell. Besides, SEM and HRTEM micrographs depicted spherical nanoparticles with size range of 19-60 nm. Additionally, zeta potential and fluorescence spectra illustrated aggregated nature of Ag@Ag2O NCs by - 5.34 mV with fluorescence emission peak at 498 nm. Ag@Ag2O NCs exhibited higher antimicrobial, antibiofilm, and algicidal activity in dose-dependent behavior. Interestingly, a remarkable mycocidal potency by 50 µg of Ag@Ag2O NCs against Candida albican; implying promising activity against COVID-19 white fungal post-infections. Through assessing cytotoxicity, Ag@Ag2O NCs exhibited higher safety against Vero cells than bulk silver nitrate by more than 100-fold.