Sono-Chemical Synthesis of Silver Quantum Dots Immobilized on Exfoliated Graphitic Carbon Nitride Nanostructures Using Ginseng Extract for Photocatalytic Hydrogen Evolution, Dye Degradation, and Antimicrobial Studies.

Due to modernization and the scarcity of fossil fuel resources, energy demand is continuously increasing. In this regard, it is essential and necessary to create a renewable energy source that can meet future energy demands. Recently, the production of H2 by water splitting and removing pollutants from the water has been essential for issues of energy and environmental demands. Herein, g-C3N4 and Ag-g-C3N4 composite structures have been successfully fabricated by the ultrasonication method. The physio/photochemical properties of prepared g-C3N4 and Ag-g-C3N4 were examined with different analytical techniques such as FTIR, XRD, UV-DRS, SEM, TEM, PL, and XPS analyses. The silver quantum dots (QDS) anchored to g-C3N4 structures performed the profound photocatalytic activities of H2 production, dye degradation, and antimicrobial activity under visible-light irradiation. The Ag/g-C3N4 composite with an Ag loading of 0.02 mole has an optimum photoactivity at 335.40 µmol g-1 h-1, which is superior to other Ag loading g-C3N4 composites. The synthesized Ag/g-C3N4 nanoparticles showed potential microbial inhibition activity during the preliminary screening, and the inhibition zones were comparable to the commercial antibiotic chloramphenicol. The loading of Ag into g-C3N4 paves the suppression, recombination and transfer of photo-generated electron-hole pairs, leading to the enhancement of hydrogen production, the diminishment of pollutants in water under visible light irradiation, and antimicrobial activity against multidrug-resistant pathogens.

Synthesis and luminescence properties of Pr3+ ion-doped Ba3 Y(PO4 )3 phosphors.

Barium yttrium phosphate (BYP) phosphor doped with trivalent praseodymium ions (BaY(1-x) (PO4 )3 :Pr3+ (x = 0, 0.01, 0.05, 0.1, 0.15, and 0.2 wt%) was synthesized using a high temperature solid-state reaction method. Structural properties were analyzed through X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. XRD patterns confirmed the structure of the synthesized phosphor and average crystalline size was estimated (approximately 63.8 Å). Vibrational functional groups were identified using FTIR spectroscopy. The emission spectrum was recorded under an 444 nm excitation wavelength, which showed various emission transitions of Pr3+ ions. Commission Internationale de l'éclairage coordinates, colour purity, and colour correlated temperature values were calculated for the BYP:Pr3+ phosphors and these coordinate values fell in the yellow region of the visible spectrum.

Enhanced solar-driven photocatalytic performance of a ternary composite of SnO2 quantum dots//AgVO3 nanoribbons//g-C3N4 nanosheets (0D/1D/2D) structures for hydrogen production and dye degradation.

Herein, we report the synthesis of between SnO2 QDs /AgVO3 nanoribbons/g-C3N4 nanosheets of ternary photocatalytic systems for the production of H2 through light irradiation. The SnO2/AgVO3/g-C3N4 photocatalyst was successfully produced by using the hydrothermal process. The structural characterizations of the samples revealed the successful formation of ternary heterostructures where SnO2, AgVO3 and g-C3N4 (quantum dots/nanoribbons/nanosheets) 0D/1D/2D structures make a good interface with each other. The fabricated heterostructures of AgVO3/g-C3N4 and SnO2/AgVO3/g-C3N4 photocatalytic structures performed enriched photocatalytic performance for H2 production over that of the pristine g-C3N4, AgVO3 and SnO2 photocatalysts. The AgVO3/g-C3N4 and SnO2 /AgVO3/g-C3N4 of photocatalysts were found to produce H2 of around 17,000 µmol g-1 and 77,000 µmol g-1, respectively, which is much 4.5 times greater than that of AgVO3/g-C3N4 photocatalyst. Moreover, the photodegradation behaviours of prepared catalysts were studied with the dye (rhodamine B, RhB) under light irradiation. The ternary composite SnO2/AgVO3/g-C3N4 performed photodegradation of RhB in 50 min. The higher photocatalytic activity for the ternary photocatalysts is predominantly due to the effective charge separation at the perfect interface formation amid SnO2 and AgVO3/g-C3N4.

Phytogenic Synthesis of Pd-Ag/rGO Nanostructures Using Stevia Leaf Extract for Photocatalytic H2 Production and Antibacterial Studies.

Continuously increasing energy demand and growing concern about energy resources has attracted much research in the field of clean and sustainable energy sources. In this context, zero-emission fuels are required for energy production to reduce the usage of fossil fuel resources. Here, we present the synthesis of Pd-Ag-decorated reduced graphene oxide (rGO) nanostructures using a green chemical approach with stevia extract for hydrogen production and antibacterial studies under light irradiation. Moreover, bimetallic nanostructures are potentially lime lighted due to their synergetic effect in both scientific and technical aspects. Structural characteristics such as crystal structure and morphological features of the synthesized nanostructures were analyzed using X-ray diffraction and transmission electron microscopy. Analysis of elemental composition and oxidation states was carried out by X-ray photoelectron spectroscopy. Optical characteristics of the biosynthesized nanostructures were obtained by UV-Vis absorption spectroscopy, and Fourier transform infrared spectroscopy was used to investigate possible functional groups that act as reducing and capping agents. The antimicrobial activity of the biosynthesized Pd-Ag-decorated rGO nanostructures was excellent, inactivating 96% of Escherichia coli cells during experiments over 150 min under visible light irradiation. Hence, these biosynthesized Pd-Ag-decorated rGO nanostructures can be utilized for alternative nanomaterial-based drug development in the future.

In situ microwave-assisted solvothermal synthesis via morphological transformation of ZnCo2O4 3D nanoflowers and nanopetals to 1D nanowires for hybrid supercapacitors.

Over recent decades, the conversion of energy and its storage have been in the lime light due to the depletion of fossil resources. The electrochemical energy storage devices like supercapacitors and batteries, and their materials and fabrication methods have been extensively evaluated, which is the best solution for the energy crisis. Herein, zinc cobaltite (ZnCo2O4; ZCO) nanostructures grown on nickel (Ni) foam by microwave-assisted solvothermal fabrication for hybrid supercapacitors are reported. Two different structures/samples, ZCO-15/Ni (nanoflowers) and ZCO-30/Ni (nanowires), were obtained by simply adjusting the reaction time. The electrochemical and physicochemical properties of the as-prepared samples were systematically determined. Particularly, ZCO-15/Ni exhibits excellent structural stability due to its dual morphologies: nanoflowers and nanopetals, and exhibits a large electroactive surface area (25.61 m2 g-1), pore diameter (48.38 nm), and robust adhesion to Ni foam, enabling ion and electron transport. ZCO-15/Ni foam electrode delivers an excellent specific capacity of 650.27 C g-1 at 0.5 A g-1 and admirable cyclic performance of 91% capacitance retention after 5000 cycles compared to ZCO-30/Ni electrode. The excellent electrochemical performance of ZCO makes them promising electrode materials for batteries, hybrid supercapacitors, and other alternative energy storage applications.

Highly Transparent Conductive Reduced Graphene Oxide/Silver Nanowires/Silver Grid Electrodes for Low-Voltage Electrochromic Smart Windows.

Transparent conductive electrodes (TCEs) based on hybrid structures (silver nanowires) have been compressively reconnoitered in next-generation electronics such as flexible displays, artificial skins, smart windows, and sensors because of their admirable conductivity as well as flexibility, which make them favorable substitutes to replace ITO (indium tin oxide) as a transparent conductor. Nevertheless, silver-based TCEs grieve from poor stability because of the corrosion and oxidation of silver in electrolytes. To overcome these issues, a RGO (reduced graphene oxide) layer on silver was promoted to resolve the difficulties of corrosion and oxidation in the electrolyte. Moreover, we successfully designed and demonstrated low-voltage WO3-based electrochromic devices (ECDs) with fabricated hybrid TCEs. The hybrid electrodes with RGO/silver nanowires/metal grid/PET (RAM) electrode exhibited improvements in the switching stability and optoelectronic properties, such as the sheet resistance (0.714 ohm/sq) as well as optical transparency of 90.9%. The coloration and bleaching behavior of the ECD was observed in an applied low-voltage range of -1.0 to 0.0 V with a maximum optical difference of 72% at 700 nm, which yielded a coloration efficiency (η) of ∼33.4 cm2/C. The highly conductive hybrid TCEs exhibit favorable features for numerous embryonic flexible electronics and optoelectronic devices.