Melamine-based metal-organic frameworks for high-performance supercapacitor applications.

Melamine-based metal-organic frameworks (MOFs) for high-performance supercapacitor applications are described in this paper. Melamine (Me) is employed as an organic linker, and three metal ions cobalt, nickel, and iron (Co, Ni, Fe) are used ascentral metal ions to manufacture the desired MOF materials (Co-Me, Ni-Me, and Fe-Me). While melamine is an inexpensive organic linker for creating MOF materials, homogenous molecular structures can be difficult to produce. The most effective technique for expanding the molecular structures of MOFs through suitable experimental optimization is used in this work. The MOFs materials are characterized using standard techniques. The kinetics of the materials' reactions are investigated using attenuated total reflectance. X-ray photoelectron spectroscopy (XPS), powder X-ray diffraction (P-XRD), Fourier transform infrared (ATR-FT-IR) spectroscopy, and Brunauer-Emmett-Teller (BET) studies verified the development of the MOFs structure. The surface morphology of the produced materials is investigated using field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), and atomic force microscopy (AFM). The elements found in MOFs are studied via XPS analysis, energy dispersive X-ray diffraction (EDX), mapping, and mapping. The materials' absorption characteristics were examined by the use of UV-visible absorption spectroscopy. The thermal stability of the materials is examined by thermogravimetric analysis (TGA); these materials are more stable, according to the findings, even at high temperatures. The electrochemical investigation determines the specific capacitance of the materials. The specific capacitance of Co-Me, Ni-Me, and Fe-Me in 3 M KOH electrolyte is 1267.36, 803.22, and 507.59F/g @ 1 A-1, according to the three-electrode arrangement. The two-electrode device maximizes power and energy density by using an asymmetrical supercapacitor in a 3 M KOH electrolyte. The power and energy densities of Co-Me, Ni-Me, and Fe-Me are 3650.63, 2813.21, and 6210.45 W kg-1, and 68.43, 46.32, and 42.2 Wh kg-1, respectively. According to the materials stability test, the MOFs are highly stable after 10,000 cycles. Preliminary results suggest that the materials are suitable for usage in high-end supercapacitor uses.

Green Synthesis of Metal-Doped ZnO Nanoparticles Using Bauhinia racemosa Lam. Extract and Evaluation of Their Photocatalysis and Biomedical Applications.

A fascinating problem in the fields of nanoscience and nanobiotechnology has recently emerged, and to tackle this, the production of metal oxide nanoparticles using plant extracts offers numerous benefits over traditional physicochemical methods. In the present investigation, ZnO nanoparticles were fabricated from Bauhinia racemosa Lam. (BR) leaves extract with various transition metal (TM) dopants (Ni, Mn, and Co). Plant leaves extract containing metal nitrate solutions were utilized as a precursor to synthesize the pristine and TM-doped ZnO nanoparticles. Structural, functional, optical, and surface properties of the fabricated samples were studied by using physicochemical and photoelectrochemical measurements. The organic pollutants tetracycline (TC), ampicillin (AMP), and amoxicillin (AMX) were used in the photocatalytic degradation assessment of the fabricated samples. Through X-ray diffraction (XRD) and transmission electron microscopy (TEM) investigation, the fabricated nanoparticles wurtzite crystal structure was verified. Moreover, Fourier transform infrared (FT-IR) analysis verified the existence of functional groups in the fabricated nanoparticles. The migration of electrons from the deep donor level and zinc interstitial to the Zn-defect and O-defect is related to the emission peaks seen at 468, 480, 534, and 450 nm in photoluminescence (PL) spectra. Co-ZnO nanoparticles demonstrated potent and excellent photocatalytic degradation performance for TC (91.09%), AMP (87.97%), and AMX (92.42%) antibiotics within 210, 180, and 150 min of visible light irradiation. Co-ZnO nanoparticles also demonstrated strong antimicrobial performance against Escherichia coli, Staphylococcus aureus, Klebsiella pneumoniae, Aspergillus flavus, Aspergillus niger, and Bacillus subtilis. Further investigation of in vitro cytotoxic potential against the A549 cell line (IC50 = 24 ± 0.5 µg/mL) utilizing MTT assay and the free radical scavenging performance of Co-ZnO nanoparticles estimated by DPPH assay utilizing l-ascorbic acid as a reference was also performed. Anti-inflammatory potential is also reviewed by comparing it with the standard drug Diclofenac, and the maximum activity was obtained for Ni-ZnO nanoparticles (IC50 = 72.4 µg/mL).

Boosting Fenton's Oxidation Reaction by a Food Waste-Derived Catalyst for Oxidizing Organic Dyes: Synergistic Effect of Complex Iron Oxides and the Layer Carbon Structure.

The constant increase in the human population drives the demand for food supply and thereby increasing the food wastage dramatically all over the world. Especially, around 60% of banana biomass has been generated as inedible domestic waste. Herein, we successfully employed banana waste as a catalyst for Fenton's oxidation reaction. The biomass-derived catalysts were subjected to various characterization techniques such as XRD, ATR-FTIR, confocal Raman spectroscopy, and XPS, XRF, BET, SEM, and TEM analyses. The XRD results revealed that, after carbonization of the dried banana bract material, a perloffite-like metal oxide phase was formed due to the aerial oxidation reaction. Characterization results of Raman and ATR-FTIR confirm that the carbonized catalyst possesses a layer-like structure with different types of functional groups. The calcium, magnesium, potassium, sodium, and iron are the dominating metal species in the resultant material, which was evident from the XRF and EDAX analyses. The carbonized banana bract catalyst is successfully utilized for the Fenton's oxidation reaction at neutral pH. The experimental results showed that the degradation efficiency of the fresh catalyst was 95% in 4 h of reaction time, and the stability of the catalyst was retained up to nine consecutive cycles. The high activity of MB, methylene blue, is mainly attributed to the strong interaction between oxy functional groups of the catalyst and MB molecule as compared to RhB. Further, the calculated efficiency of the hydrogen peroxide was found to be 99% and the self-decomposition of hydrogen peroxide by the formed metal oxides was highly limited.