Herein, a facile green synthesis route was reported for the synthesis of Ag–ZnO nanocomposites using potato residue by simple and cost effective combustion route and investigated the photocatalytic degradation of methylene blue (MB) dye. In the preparation potato extract functioned as a biogenic reducing as well as stabilizing agent for the reduction of Ag + , thus eliminating the need for conventional reducing/stabilizing agents. Ag–ZnO nanocomposites with different Ag mass fractions ranging from 2 to 10% were characterized by using XRD, FT-IR, XPS, SEM, TEM, and UV–Vis spectroscopy. XRD analysis revealed that the as prepared Ag–ZnO nanocomposites possessed high crystallinity with hexagonal wurtzite structure. TEM and SEM images showed that the Ag–ZnO nanocomposites in size ranging from 15 to 25 nm have been obtained, and the particle size was found to increase with the increase in percentage of Ag. FTIR results confirmed the characteristics band of ZnO along with the Ag bands. XPS analysis revealed a pair of doublet with peaks corresponding to Ag and a singlet with peaks corresponding to ZnO. With the increase of concentration of Ag in ZnO, the intensity of NBE emission in the PL spectra was observed to be decrease, resulted to the high photocatalytic activity. Photocatalytic properties of Ag–ZnO nanocomposites evaluated against the MB dye under visible-light irradiation showed superior photodegradation of ~ 96% within 80 min for 2% Ag–ZnO nanocomposites. The apparent reaction rate constant for 2% Ag–ZnO nanocomposites was higher than that of other nanocomposites, which proved to be the best photocatalyst for the maximum degradation of MB. Furthermore, various functional parameters such as dosing, reaction medium, concentration variation were performed on it for better understanding. The enhancement in photocatalytic degradation might be due to the presence of Ag nanoparticles on the surface of ZnO by minimizing the recombination of photo induced charge carriers in the nanocomposites.

In this study, we report the fabrication of graphitic carbon nitride doped zinc oxide nanocomposites, g-C3N4/ZnO, (Zn-Us) by using different amount of urea. They were further characterized by X-ray Diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), Raman, UV-vis, Scanning electron microscopy (SEM), and Transmission electron microscopy (TEM) techniques. The prepared nanocomposites were used as photocatalysts for the mineralization of the light sensitive dyes Methylene Blue (MB) and Rose Bengal (RB) under UV light irradiation, and corresponding photo-mechanism was proposed. Benefiting from these photocatalytic characteristics, urea derived g-C3N4/ZnO photocatalysts have been found to have excellent photodegradation activity against the MB and RB for 6 h and 4 h, respectively. Under the given experimental conditions, the degradation percentage of fabricated Zn-Us were shown ~90% for both model dyes. Compared to cationic MB dye, anionic RB dye is more actively degraded on the surface of prepared photocatalysts. The results obtained can be effectively used for future practical applications in wastewater treatment

In the present work, the aim is to synthesize reduced graphene oxide (rGO) and zinc:reduced graphene oxide composite catalysts (ZnO:rGO) for esterification of acetic acid with n-heptanol. The physical and chemical characteristics of the rGO and rGO-metal oxide composite catalysts such as textural surface characteristics, surface morphology, thermal stability, functional groups, and elemental analysis were studied. The surface areas of rGO, ZnO(0.5 M), and ZnO(1 M) were recorded, respectively, at 31.72, 27.65, and 36.19 m2 g–1. Furthermore, esterification reaction parameters such as the reaction time, catalyst dosage, and reaction temperature for acetic acid were optimized to check the feasibility of rGO-metal oxide composites for a better conversion percentage of acetic acid. The optimized catalyst was selected for further optimization, and the optimum reaction parameters found were 0.1 wt % of catalyst, 160 min reaction duration, and 100 °C reaction temperature with a maximal yield of 100%. At 110 °C, the reaction conducted in the presence of 0.1 g of catalyst displayed more yield than the uncatalyzed reaction.

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A new double-open-cubane core Cd(II)-O-Cu(II) bimetallic ligand mixed cluster of type [Cl2Cu4Cd2(NNO)6(NN)2(NO3)2].CH3CN was made available in EtOH/CH3CN solution. The 1-hydroxymethyl-3,5-dimethylpyrazole (NNOH) and 3,5-dimethylpyrazole (NNH) act as N,O-polydentate anion ligands in coordinating the Cu(II) and Cd(II) centers. The structure of the cluster in the solid state was proved by XRD study and confirmed in the liquid state by UV-vis analysis. The XRD result supported the construction of two octahedral and one square pyramid geometries types around the four Cu(II) centers and only octahedral geometry around Cd(II) two centers. Interestingly, NNOH ligand acts as a tetra-µ3-oxo and tri-µ2-oxo ligand; meanwhile, the N-N in NNH acts as classical bidentate anion/neutral ligands. The interactions in the lattice were detected experimentally by the XRD-packing result and computed via Hirschfeld surface analysis (HSA). The UV-vis., FT-IR and Energy Dispersive X-ray (EDX), supported the desired double-open cubane cluster composition. The oxidation potential of the desired cluster was evaluated using a 3,5-DTB-catechol 3,5-DTB-quinone as a catecholase model reaction.