RESUMO
The present study demonstrates the crucial role of agave americana extract in enhancing the optical properties of zinc oxide (ZnO) through thermal treatment method. Various analytical and surface science techniques have been used to identify the morphology, crystalline structure, chemical composition, and optical properties, including scanning electron microscopy, x-ray diffraction, high resolution transmission electron microscopy (HRTEM), x-ray spectroscopy (EDS) and UV-visible spectroscopy techniques. The physical studies revealed the transformation of ZnO nanorods into nanosheets upon addition of an optimized amount of agave americana extract, which induced large amount of amorphous carbon deposited onto ZnO nanostructures as confirmed by HRTEM analysis. The use of increasing amount of americana extract has significantly reduced the average crystallite size of ZnO nanostructures. The resultant hybrid system of C@ZnO has produced a significant effect on the ultraviolet light-assisted photodegradation of malachite green (MG) dye. The photocatalyst dose was fixed at 10 mg for each study whereas the amount of agave americana extract and MG dye concentration are varied. The functionality of hybrid system was greatly enhanced when the amount of agave americana extract increased while dye concentration kept at lower level. Ultimately, almost 100% degradation efficiency was achieved via the prepared hybrid material, revealing combined contribution from synergy, stabilization of ZnO due to excess of carbon together with the high charge separation rate. The obtained results suggest that the driving role of agave americana extract for surface modification of photocatalyst can be considered for other nanostructured photocatalysts.
Assuntos
Agave , Nanocompostos , Óxido de Zinco , Carbono , Catálise , Fotólise , Extratos Vegetais/química , Corantes de Rosanilina , Óxido de Zinco/químicaRESUMO
Recently, the nanostructured nickel-cobalt bimetallic oxide (NiCo2O4) material with high electrochemical activity has received intensive attention. Beside this, the biomass assisted synthesis of NiCo2O4 is gaining popularity due to its advantageous features such as being low cost, simplicity, minimal use of toxic chemicals, and environment-friendly and ecofriendly nature. The electrochemical activity of spinel NiCo2O4 is associated with its mixed metal oxidation states. Therefore, much attention has been paid to the crystal quality, morphology and tunable surface chemistry of NiCo2O4 nanostructures. In this study, we have used citrus lemon juice consisting of a variety of chemical compounds having the properties of a stabilizing agent, capping agent and chelating agent. Moreover, the presence of several acidic chemical compounds in citrus lemon juice changed the pH of the growth solution and consequently we observed surface modified and structural changes that were found to be very effective for the development of energy conversion and energy storage systems. These naturally occurring compounds in citrus lemon juice played a dynamic role in transforming the nanorod morphology of NiCo2O4 into small and well-packed nanoparticles. Hence, the prepared NiCo2O4 nanostructures exhibited a new surface-oriented nanoparticle morphology, high concentration of defects on the surface (especially oxygen vacancies), sufficient ionic diffusion and reaction of electrolytic ions, enhanced electrical conductivity, and favorable reaction kinetics at the interface. The electrocatalytic properties of the NiCo2O4 nanostructures were studied in oxygen evolution reaction (OER) at a low overpotential of 250 mV for 10 mA cm-2, Tafel slope of 98 mV dec-1, and durability of 40 h. Moreover, an asymmetric supercapacitor was produced and the obtained results indicated a high specific capacitance of (Cs) of 1519.19 F g-1, and energy density of 33.08 W h kg-1 at 0.8 A g-1. The enhanced electrochemical performance could be attributed to the favorable structural changes, surface modification, and surface crystal facet exposure due to the use of citrus lemon juice. The proposed method of transformation of nanorod to nanoparticles could be used for the design of a new generation of efficient electrocatalyst materials for energy storage and conversion uses.
RESUMO
The design of efficient, stable, durable and noble metal free electro catalysts for oxygen evolution reaction (OER) are of immediate need, but very challenging task. In this study, iron induction into cobalt oxide (Co3O4) has resulted composite structure by wet chemical method. The iron impurity has brought an electronic disorder into Fe3O4/cobalt oxide composite thereby efficient oxygen evolution reaction is demonstrated. An addition of iron content into composite resulted the alternation of morphology from Nano rods to clusters of nanoparticles. The successive addition of iron into composite system reduced the onset potential of OER as compared to the pristine cobalt oxide. A Tafel slope of 80 mVdec-1 indicates the favorable oxygen evolution reaction kinetics on the sample 4. An over-potential of 370 mV is required to reach a 10 mAcm-2 current density which is acceptable for a nonprecious catalyst. The catalyst is highly durable and stable for 30 hours. Electrochemical impedance spectroscopy further provided a deeper insight on charge transfer resistance and sample 4 has low charge transfer resistance that supported the OER polarization curves. The sample 4 has more electrochemical active surface area of 393.5 cm². These obtained results are exciting and highlighting the importance of composite structure and leave a huge space for the future investigations on composite materials for energy related applications.