Electrophoretic Fabrication of ZnO/CuO and ZnO/CuO/rGO Heterostructures-based Thin Films as Environmental Benign Flexible Electrode for Supercapacitor.

Sustainable fabrication of flexible hybrid supercapacitor electrodes is extensively investigated during the current era to solve global energy problems. Herein, we used a cost-effective and efficient electrophoretic deposition (EPD) approach to fabricate a hybrid supercapacitor electrode. ZnO/CuO and ZnO/CuO/rGO heterostructure were prepared by sol-gel synthesis route and were electrophoretically deposited on indium tin oxide (ITO) substrate as a thin uniform layer using 1 V for 20 min at 50 mV/s. ZnO/CuO and ZnO/CuO/rGO heterostructure coated ITOs were then employed as the working electrode in a three-electrode setup for supercapacitor measurements. The fabricated electrodes have been investigated by Galvanostatic charge-discharge (GCD), electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV) to study their charge storage properties. ZnO/CuO revealed a specific capacitance of 1945 F g-1 at 2 mV/s and 999 F g-1 at 5 A g-1. However, an increased specific capacitance of 2305 F g-1 was measured for ZnO/CuO/rGO heterostructure at 2 mV/s and 1235 F g-1 at 5 A g-1. The lower internal resistance was observed for ZnO/CuO/rGO heterostructure, indicating good conductivity of the electrode material. Thus, the overall results of the current study suggest that EPD-assisted ZnO/CuO/rGO heterostructure hybrid electrode possess a substantial potential for energy storage as a supercapacitor.

Ecospheric Decontamination Attained via Green Nanobiotechnological NiO-Based Nanocatalyst Derived from Nature's Biofactories.

INTRODUCTION: Water contamination from dye effluents from various industrial sources has become a major challenge of the scientific community that is difficult to remediate using orthodox chemical and biological procedures. As such, there is a need for more suitable and cost-effective ways to treat such effluents. The present work describes a green-synthesis approach for preparation of three types of Ni-based oxides as effective catalytic materials to remove environmental pollutants. Metal oxide nanomaterials are cheap, abundant, and ecofriendly earth metals, and thus are promising materials for catalytic applications for environmental detoxification. METHODS: An aqueous leaf extract of Prunus persica was used as a reducing agent for the synthesis of NiO, NiO-PdO, and NiO-ZnO nanoparticles (NPs). The leaf extract was treated with each metal-salt precursor based on sol-gel synthesis, and then the final procured NPs were analyzed by spectroscopic techniques for structural and morphological makeup. The pure NPs were further explored for catalytic degradation of hazardous aqueous dye at ambient conditions, instead of following any sophisticated experimental conditions. RESULTS AND DISCUSSION: Morphological features revealed the pure formation of NiO, NiO-ZnO, and NiO-PdO NPs of size <100nm, characterized by X-ray diffraction spectroscopy and scanning electron microscopy. Catalytic tests with methyl orange revealed the remediation potential of synthesized material, showing the pseudo-first order kinetics (R 2<1) for NiO, NiO-PdO, and NiO-ZnO. NiO-ZnO gave outstanding results both in dark (R 2=0.88) and light (R 2=0.82) with degradation percentage of 99% (dark) in comparison with the other two catalysts. Moreover, excellent catalyst stability for NiO-ZnO) was observed, even after the fourth cycle, under both light and dark conditions and was separated easily during centrifugation. CONCLUSION: Although all three materials depicted the degradation potential with good stability, but the NiO-ZnO catalyst was the best catalytic material in the present investigation, with prominent degradation percentage, and can be considered as an efficient catalytic material. Thus, we conclude that P. persica-inspired catalytic material could pave the path toward environmental remediation, alternative clean energy, and other biological applications.

Organic template-based ZnO embedded Mn3O4 nanoparticles: synthesis and evaluation of their electrochemical properties towards clean energy generation.

To deal with fossil fuel depletion and the rise in global temperatures caused by fossil fuels, cheap and abundant materials are required, in order to fulfill energy demand by developing high-performance fuel cells and electrocatalysts. In this work, a natural organic agent has been used to synthesize nano-structured ZnO/Mn3O4 with high surface area and enhanced electrocatalytic performance. Upon pre-annealing treatment, mixed metal oxide precipitates are formed due to the complex formation between a metal oxide and organic extract. The thermally annealed mixed oxide ZnO/Mn3O4 was characterized by XRD diffractometer, Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDX). Gas chromatography-mass spectrometry (GC-MS) identified methyldecylamine as a major stabilizing agent of the synthesized nanomaterial. Using a Tauc plot, the calculated band energy for the synthesized ZnO/Mn3O4 mixed metal oxide was 1.65 eV. Moreover, we have demonstrated the effects of incorporated organic compounds on the surface chemistry, morphology and electrochemical behavior of ZnO/Mn3O4. The phyto-functionalized ZnO/Mn3O4 was deposited on Ni-foam for electrocatalytic studies. The fabricated electrode revealed good performance with low over-potential and Tafel slope, suggesting it to be suitable as a potential catalyst for water splitting application, in particular for the oxygen evolution reaction (OER). The overall findings of the current study provide a cost-effective and efficient organic template for functionalization and sustainable fabrication of ZnO/Mn3O4 nanomaterial for application as an electrocatalyst.

Phyto-inspired and scalable approach for the synthesis of PdO-2Mn2O3: a nano-material for application in water splitting electro-catalysis.

A modified co-precipitation method has been used for the synthesis of a PdO-2Mn2O3 nanocomposite as an efficient electrode material for the electro-catalytic oxygen evolution (OER) and hydrogen evolution reaction (HER). Palladium acetate and manganese acetate in molar ratio 1 : 4 were dissolved in water, and 10 ml of an aqueous solution of phyto-compounds was slowly added until completion of precipitation. The filtered and dried precipitates were then calcined at 450 °C to obtain a blackish brown colored mixture of PdO-2Mn2O3 nanocomposite. These particles were analyzed by ultra violet visible spectrophotometry (UV-vis), infrared spectroscopy (FTIR), powder X-ray diffractometry (XRD), scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS) for crystallinity, optical properties, and compositional and morphological makeup. Using Tauc's plot, the direct band gap (3.18 eV) was calculated from the absorption spectra. The average crystallite sizes, as calculated from the XRD, were found to be 15 and 14.55 nm for PdO and Mn2O3, respectively. A slurry of the phyto-fabricated PdO-2Mn2O3 powder was deposited on Ni-foam and tested for electro-catalytic water splitting studies in 1 M KOH solution. The electrode showed excellent OER and HER performance with low over-potential (0.35 V and 121 mV) and Tafel slopes of 115 mV dec-1 and 219 mV dec-1, respectively. The outcomes obtained from this study provide a direction for the fabrication of a cost-effective mixed metal oxide based electro-catalyst via an environmentally benign synthesis approach for the generation of clean energy.