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The present study explores the influence of Cobalt oxide nanoparticles(Co3O4 NPs) on the physicochemical characteristics of Poly(vinylalcohol)/ Chitosan (PVA/Cs) blend. Using a variety of techniques, the pure blend and the nanocomposites’ composition, structure, optical, thermal, and mechanical properties, and antibacterial activity were characterized. The Co3O4 NPs were produced by precipitation method utilizing cobalt salt as the raw material. The crystalline nature of the nanoparticles and semi-crystalline behavior of the PVA/Cs are demonstrated by the XRD data. Adding nanoparticles to the pure blend reduced the intensity of the semi-crystalline. The rise in absorption intensity observed in UV-visible spectra upon the incorporation of Co3O4 NPs into the PVA/Cs blend indicates an improved dispersion of the nanoparticles within the blend. When Co3O4 NPs are added, the energy band-gap Egdir and Egind of PVA/Cs–Co3O4 samples greatly decrease. According to TGA data, the thermal stability of nanocomposites was significantly higher than that of the PVA/Cs blend, and it rose as the concentration of nanoparticles increased. When compared to neat PVA/Cs film, mechanical property investigation of PVA/Cs–Co3O4 nanocomposites films revealed enhanced features. The effectiveness of the PVA/Cs–Co3O4 nanocomposite films in inhibiting the growth of microorganisms was assessed by evaluating their antimicrobial activity (ANMAC) against a range of bacteria and fungi. The inclusion of Co3O4 NPs led to an increase in activity against Gram-positive Staphylococcus aureus (S. aureus) and Gram-negative Escherichia coli (E. coli) bacteria as well as fungi Candida albicans and Aspergillus niger (C. albicans and A. niger). The addition of Co3O4 NPs to the PVA/Cs blend effectively improved the material’s optical, thermal, mechanical, and antibacterial properties. This remarkable improvement stems from the Co3O4 NPs, which were introduced into the PVA/Cs blend in different amounts, leading to the development of novel nanocomposites. The outstanding properties of Co3O4/PVA/Cs nanocomposite films suggest their potential for applications in optoelectronics and food packaging.

Several fungal endophytes were isolated and screened for their ability to biosynthesize a variety of nanoparticles (NPs), as a potentially simple and eco-friendly method with low cost. Among these fungi, a promising isolate named ORG-1 was found able to synthesize five different NPs types: Co3O4NPs, CuONPs, Fe3O4NPs, NiONPs, and ZnONPs. The ORG-1 strain was identified as Aspergillus terreus according to the morphological and molecular studies. Synthesis of these NPs was initially monitored by UV–Vis spectroscopy and further characterized by Fourier transform infrared spectroscopy. X-ray diffraction patterns revealed their crystalline structure. Dynamic light scattering analysis was applied to study the particle size distribution and stability. Transmission electron microscope studies indicated the morphology of the synthesized NPs. Additionally, the biological activities of the in vitro antioxidant and antimicrobial potentials were evaluated. Co3O4NPs, CuONPs, Fe3O4NPs, NiONPs, and ZnONPs showed promising antioxidant activity with 50% inhibitory concentrations of 85.44, 96.74, 102.41, 87.41, and 108.67 μg mL−1, respectively. The synthesized NPs exhibited potent antimicrobial activities against several plant and human pathogens. To our knowledge, this is the first report on the use of one microbial strain for the synthesis of a variety of NPs. This study suggests endophytic fungi as new and alternate platforms with an exceptional potentiality for the synthesis of NPs with promising activities.Key points• Discovery of a promising endophytic fungus for synthesis of five different types of NPs.• Mycosynthesis and characterization of all the synthesized NPs were investigated.• The synthesized NPs showed promising antioxidant and antimicrobial activities.

Electric vehicles based on lithium-ion batteries (LIB) have seen rapid growth over the past decade as they are viewed as a cleaner alternative to conventional fossil-fuel burning vehicles, especially for local pollutant (nitrogen oxides [NOx], sulfur oxides [SOx], and particulate matter with diameters less than 2.5 and 10 μm [PM2.5 and PM10]) and CO2 emissions. However, LIBs are known to have their own energy and environmental challenges. This study focuses on LIBs made of lithium nickel manganese cobalt oxide (NMC), since they currently dominate the United States (US) and global automotive markets and will continue to do so into the foreseeable future. The effects of globalized production of NMC, especially LiNi1/3Mn1/3Co1/3O2 (NMC111), are examined, considering the potential regional variability at several important stages of production. This study explores regional effects of alumina reduction and nickel refining, along with the production of NMC cathode, battery cells, and battery management systems. Of primary concern is how production of these battery materials and components in different parts of the world may impact the battery’s life cycle pollutant emissions and total energy and water consumption. Since energy sources for heat and electricity generation are subject to great regional variation, we anticipated significant variability in the energy and emissions associated with LIB production. We configured Argonne National Laboratory’s Greenhouse gases, Regulated Emissions, and Energy use in Transportation (GREET®) model as the basis for this study with key input data from several world regions. In particular, the study examined LIB production in the US, China, Japan, South Korea, and Europe, with details of supply chains and the electrical grid in these regions. Results indicate that 27-kWh automotive NMC111 LIBs produced via a European-dominant supply chain generate 65 kg CO2e/kWh, while those produced via a Chinese-dominant supply chain generate 100 kg CO2e/kWh. Further, there are significant regional differences for local pollutants associated with LIB, especially SOx emissions related to nickel production. We find that no single regional supply chain outperforms all others in every evaluation metric, but the data indicate that supply chains powered by renewable electricity provide the greatest emission reduction potential.

The effect of the applied potential on the crystallography, morphology, optical, and electrical properties of copper–cobalt oxide (Cu 2 CoO 3 ) co-electrodeposited on ITO (Indium Tin Oxide) substrate has been studied. The electrochemical behavior of Cu 2 CoO 3 using cyclic voltammetry showed that the co-electrodeposition of Cu 2 CoO 3 occurred at a negative potential of − 0.70 V versus SCE, following a quasi-reversible reaction controlled by the diffusion process. Chronoamperometry (CA) revealed that the nucleation and growth mechanism of Cu 2 CoO 3 follows the instantaneous three-dimensional process according to Scharifker and Hill model. X-ray diffraction (XRD) analysis indicated that the resulting layers at different applied potentials exhibited an orthorhombic structure with a preferred orientation of the crystallites (011) plan. The morphology of the surface changes with potential applied. Furthermore, the optical properties of the copper and cobalt oxide films were investigated using UV-visible spectroscopy; showing that the band gap energy for all the materials increases when the applied potential decreases. The Cu 2 CoO 3 layers obtained are p-type semiconductors. The acceptor density ( N A ) increases with decreasing applied potential.

Cobalt oxide nanoparticles were prepared via green chemistry route and fully characterized by Field Emission Scanning Electron Microscope (FESEM), Energy-dispersive X-ray spectroscopy (EDAX), X-ray diffraction (XRD), High-resolution transmission electron microscopy (HRTEM) and Transmission electron microscopy (TEM) analyses; the CoO and Co3O4 nanoparticles, in sheet-shaped cobalt oxide form, ensued simultaneously in one step. The varying concentrations of NPs were analyzed via 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) test on the cancer cell line (U87) which revealed that with increasing concentration of cobalt oxide nanoparticles, the survival rate of U87 tumor cells decreases; IC50 of nanoparticles being ~ 55 µg/ml−1.Graphic abstract

The rational design of effective bifunctional electrocatalysts is of paramount importance for overall water-splitting technology in sustainable energy conversion. Herein, bimetallic oxide catalysts (RuO 2 -Co 3 O 4 ) derived from Ru combined MOF-derivatives (MOF = metal-organic framework) were demonstrated effective for overall water splitting in an alkaline solution, owing to the combined merits such as the two-dimensional interconnected network structure, the synergetic coupling effects and increased chemical stability. The as-prepared RuO 2 -Co 3 O 4 only requires an overpotential of 260 mV for oxygen evolution and 75 mV for hydrogen evolution at 10 mA/cm 2 in 1 M KOH solution; a low cell voltage of 1.54 V was required to reach the kinetic current density of 10 mA/cm 2 for the water electrolysis when supporting on glass carbon electrode, and very good stability for 40 h was observed. Experimental and theoretical results demonstrated the electronic structure optimization of bimetallic RuO 2 -Co 3 O 4 compared to the individual metal oxide, which promoted interface charges redistribution and the d-band center downshift, resulting in increased activity and stability for water-splitting reactions. This work provides a feasible approach for developing bimetallic oxides for application in energy-relevant electrocatalysis reactions.

Cobalt Oxide (Co 3 O 4 ) nanoparticles were synthesized with an aid of urea by sol–gel method. The results of X-ray diffraction revealed that the formation of face-centered cubic (Fd3m) structure and the average crystallite size of the product were found to be 13.76 nm. The formation of cobalt oxide is confirmed by FT-IR analysis. The results of HR-TEM images reveal that Co 3 O 4 nanoparticles were found to have within the range of 13–15 nm. At 3 M KOH, electrochemical analyses were investigated with impedance spectroscopy and an intrinsic pseudo capacitance and the results were reported. The results of Galvanostatic charge-discharge (GCD) tests revealed the capacitive properties of Co 3 O 4 with the highest specific capacitance of 761.25 F g −1 . Highlights The specific capacitance of Co 3 O 4 nanoparticles was found to be 761.25 F g −1 at 11 mA/cm 2 current density. The Co 3 O 4 nanoparticles were synthesized by a simple sol–gel method. The crystallite size of Co 3 O 4 nanoparticles was found to be 13.76 nm.

Unparalleled in the breadth and depth of its coverage of all important aspects, this book systematically treats the electronic and magnetic properties of stoichiometric and non-stoichiometric cobaltites in both ordered and disordered phases.

Cobalt oxides have been considered as a kind of highly efficient catalyst for the oxidation of volatile organic compounds (VOCs). In this work, lanthanum-cobalt composite oxides were prepared by using the co-precipitation method, and toluene was used as the model compound. Diversified techniques including XRD, SEM, Raman spectra, XPS, H 2 -TPR, and N 2 adsorption-desorption were applied to investigate the physicochemical properties of as-prepared materials. The composite catalysts showed different morphology including larger specific surface area and higher pore volume which would accelerate the adsorption of toluene and improve the amount of active sites on surface. Moreover, the addition of lanthanum could enhance the low-temperature reducibility, and it could be also beneficial to expose more Co 3+ and adsorbed oxygen species on the surface of catalysts which could accelerate the oxidation of toluene and lower onset oxidation temperature. 0.05La-Co (with a molar ratio of lanthanum against cobalt is 0.05) showed the best catalytic performance. The complete conversion of toluene was achieved at 225 °C under the condition of toluene concentration = 1000 ppm and SV = 20,000 ml·g −1 ·h −1 . Stability test over 0.05La-Co was conducted at 225 °C and it could maintain the 100% conversion of toluene for 720 min, indicating the excellent stability of as-prepared catalysts. Undoubtedly, lanthanum-cobalt composite oxide is a kind of promising material for the catalytic oxidation of VOCs.

Metal-doped (Mn, Cu, Ni, and Fe) cobalt oxides were prepared by a coprecipitation method and were used as catalysts for the total oxidation of toluene and propane. The metal-doped catalysts displayed the same cubic spinel Co3O4 structure as the pure cobalt oxide did; the variation of cell parameter demonstrated the incorporation of dopants into the cobalt oxide lattice. FTIR spectra revealed the segregation of manganese oxide and iron oxide. The addition of dopant greatly influenced the crystallite size, strain, specific surface area, reducibility, and subsequently the catalytic performance of cobalt oxides. The catalytic activity of new materials was closely related to the nature of the dopant and the type of hydrocarbons. The doping of Mn, Ni, and Cu favored the combustion of toluene, with the Mn-doped one being the most active (14.6 × 10−8 mol gCo−1 s−1 at 210 °C; T50 = 224 °C), while the presence of Fe in Co3O4 inhibited its toluene activity. Regarding the combustion of propane, the introduction of Cu, Ni, and Fe had a negative effect on propane oxidation, while the presence of Mn in Co3O4 maintained its propane activity (6.1 × 10−8 mol gCo−1 s−1 at 160 °C; T50 = 201 °C). The excellent performance of Mn-doped Co3O4 could be attributed to the small grain size, high degree of strain, high surface area, and strong interaction between Mn and Co. Moreover, the presence of 4.4 vol.% H2O badly suppressed the activity of metal-doped catalysts for propane oxidation, among them, Fe-doped Co3O4 showed the best durability for wet propane combustion.