Electrodeposited Copper Tin Sulfide/Reduced Graphene Oxide Nanospikes for a High-Performance Supercapacitor Electrode.

Copper tin sulfide, Cu4SnS4 (CTS), a ternary transition-metal chalcogenide with unique properties, including superior electrical conductivity, distinct crystal structure, and high theoretical capacity, is a potential candidate for supercapacitor (SC) electrode materials. However, there are few studies reporting the application of Cu4SnS4 or its composites as electrode materials for SCs. The reported performance of the Cu4SnS4 electrode is insufficient regarding cycle stability, rate capability, and specific capacity; probably resulting from poor electrical conductivity, restacking, and agglomeration of the active material during continued charge-discharge cycles. Such limitations can be overcome by incorporating graphene as a support material and employing a binder-free, facile, electrodeposition technique. This work reports the fabrication of a copper tin sulfide-reduced graphene oxide/nickel foam composite electrode (CTS-rGO/NF) through stepwise, facile electrodeposition of rGO and CTS on a NF substrate. Electrochemical evaluations confirmed the enhanced supercapacitive performance of the CTS-rGO/NF electrode compared to that of CTS/NF. A remarkably improved specific capacitance of 820.83 F g-1 was achieved for the CTS-rGO/NF composite electrode at a current density of 5 mA cm-2, which is higher than that of CTS/NF (516.67 F g-1). The CTS-rGO/NF composite electrode also exhibited a high-rate capability of 73.1% for galvanostatic charge-discharge (GCD) current densities, ranging from 5 to 12 mA cm-2, and improved cycling stability with over a 92% capacitance retention after 1000 continuous GCD cycles; demonstrating its excellent performance as an electrode material for energy storage applications, encompassing SCs. The enhanced performance of the CTS-rGO/NF electrode could be attributed to the synergetic effect of the enhanced conductivity and surface area introduced by the inclusion of rGO in the composite.

Ce4+-Substituted Ni-Al mixed oxide: fluoride adsorption performance and reusability.

In this study, Ce4+-doped Ni-Al mixed oxides (NACO) were synthesized and comprehensively characterized for their potential application in fluoride adsorption. NACOs were examined using Transmission Electron Microscopy (TEM) and Scanning Electron Microscopy (SEM), revealing a sheet-like morphology with a nodular appearance. X-ray diffraction (XRD) analysis confirmed the formation of mixed oxides of cubic crystal structure, with characteristic planes (111), (200), and (220) at 2θ values of 37.63°, 43.61°, and 63.64°, respectively. Further investigations using X-ray Photoelectron Spectroscopy (XPS) identified the presence of elements such as Ni, Al, Ce, and O with oxidation states +2, +3, +4, and -2, respectively. The Brunauer-Emmett-Teller (BET) analysis indicated that NACO followed a type IV physisorption isotherm, suggesting favorable surface adsorption characteristics. The adsorption kinetics was studied, and the experimental data exhibited a good suit to both pseudo-first order and pseudo-second order, as indicated by high R2 values. Moreover, the Freundlich isotherm model demonstrated a good fit to the experimental data. The result also revealed that NACO has a maximum capacity for adsorption (qmax) of 132 mg g-1. Thermodynamic studies showed that fluoride adsorption onto NACO was feasible and spontaneous. Additionally, NACO exhibited excellent regeneration capabilities, as evidenced by a remarkable 75.71% removal efficiency at the sixth regeneration stage, indicating sustained adsorption capacity even after multiple regeneration cycles. Overall, NACOs displayed promising characteristics for fluoride adsorption, making them potential candidates for efficient and sustainable water treatment technologies.

Biosynthesis of Artemisia abyssinica Leaf Extract-Mediated Bimetallic ZnO-CuO Nanoparticles: Antioxidant, Anticancer, and Molecular Docking Studies.

Currently, plant extract-mediated synthesized metal oxide nanoparticles (MO NPs) have played a substantial role in biological applications. Hence, this study focused on the eco-benign one-pot synthesis of bimetallic ZnO-CuO nanoparticles (ZC NPs) using the leaf extract of Artemisia abyssinica (LEAA) and evaluations of their anticancer, antioxidant, and molecular binding efficacy. The optical absorption peak at 380 nm from UV-visible (UV-vis) analysis revealed the formation of ZC NPs. X-ray diffraction (XRD) results revealed the fabrication of mixed-phase crystals with hexagonal and monoclinic structures of ZC NPs with an average crystallite size of 14 nm. Moreover, the biosynthesis of ZC NPs with a spherical morphology and an average particle size of 13.09 nm was confirmed by scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), and transmission electron microscopy (TEM) results. Fourier transform infrared (FTIR) and thermogravimetric analysis (TGA/DTA) spectroscopy confirmed the involvement of functional groups from LEAA during the synthesis of ZC NPs. ZC NPs have exhibited the ferric ion reducing power (FRAP) with an absorbance of 1.826 ± 0.00 at 200 µg/mL and DPPH (2,2-diphenyl-1-picryl-hydrazyl-hydrate) radical scavenging activity of 95.71 ± 0.02% at 200 µg/mL with an IC50 value of 3.28 µg/mL. Moreover, ZC NPs had shown a promising in vitro anticancer activity of 89.20 ± 0.038 at 500 µg/mL with an IC50 value of 33.12 µg/mL against breast cancer (MCF-7) cell lines. Likewise, ZC NPs have shown strong binding affinity (-8.50 kcal/mol) against estrogen receptor α (ERα) in molecular docking simulations. These findings suggested that the biosynthesized ZC NPs could be used as promising antioxidant and anticancer drug candidates, particularly for breast cancer ailments. However, the in vivo cytotoxicity test will be recommended to ensure further use of ZC NPs.

Kinetics, isotherm, mechanism, and recyclability of novel nano-sized Ce4+-doped Ni-Al layered double hydroxide for defluoridation of aqueous solutions.

Excessive fluoride removal from aqueous solutions is of utmost importance as it has an adverse impact on human health. This study investigates the defluoridation efficiency of a novel nano-sized Ce+4-doped Ni/Al layered double hydroxide (Ni-Al-Ce LDH) for aqueous solutions. The synthesized Ni-Al-Ce LDH exhibited a well-defined nanoscale plate-like morphology and a high surface area with an average size of 11.51 nm, which contributed to its enhanced fluoride adsorption capacity. XRD, SEM, HRTEM, and BET studies confirmed these characteristics. XPS analysis confirmed the presence of Ce4+ ions within the Ni-Al LDH. The experimental results indicated that the process of defluoridation followed a pseudo-second-order model of kinetics, suggesting a chemisorption mechanism. The fluoride adsorption isotherms demonstrated well fits to the Freundlich, Langmuir, and Jovanovic models, indicating both monolayer and multilayer fluoride adsorption on the Ce-doped Ni-Al LDH. The maximum adsorption capacity was found to be 238.27 mg/g (Langmuir) and 130.73 mg/g (Jovanovic) at pH 6.0 and 25 °C. The proposed mechanisms for fluoride adsorption on the LDH include ion exchange, surface complexation, hydrogen bonding, and ligand exchange. The Ni-Al-Ce LDH nanomaterial exhibited good recyclability, maintaining 71% of the fluoride adsorption efficiency even after four consecutive cycles. This study highlights the significant role of Ce doping in improving the performance of Ni-Al LDH as a defluoridation adsorbent.

Multifunctional application of PVA-aided Zn-Fe-Mn coupled oxide nanocomposite.

Zinc oxide (ZnO) is a fascinating semiconductor material with many applications such as adsorption, photocatalysis, sensor, and antibacterial activities. By using a poly (vinyl alcohol) (PVA) polymer as a capping agent and metal oxides (iron and manganese) as a couple, the porous PVA-aided Zn/Fe/Mn ternary oxide nanocomposite material (PTMO-NCM) was synthesized. The thermal, optical, crystallinity, chemical bonding, porosity, morphological, charge transfer properties of the synthesized materials were confirmed by DTG/DSC, UV-Vis-DRS, XRD, FT-IR, BET, SEM-EDAX/TEM-HRTEM-SAED, and CV/EIS/amperometric analytical techniques, respectively. The PTMO-NCM showed an enhanced surface area and charge transfer capability, compared to ZnO. Using the XRD pattern and TEM image analysis, the crystalline size of the materials was confirmed to be in the nanometer range. The porosity and superior charge transfer capabilities of the PTMO-NCM were confirmed from the BET, HRTEM (IFFT)/SAED, and CV/EIS analysis. The adsorption kinetics (adsorption reaction/adsorption diffusion) and adsorption isotherm test confirmed the presence of a chemisorption type of adsorbate/methylene blue dye-adsorbent/PTMO-NCM interaction. The photocatalytic performance was tested on the Congo red and Acid Orange-8 dyes. The superior ascorbic acid sensing capability of the material was understood from CV and amperometric analysis. The noble antibacterial activities of the material were also confirmed on both gram-negative and gram-positive bacteria.

A Review on Enhancing the Antibacterial Activity of ZnO: Mechanisms and Microscopic Investigation.

Metal oxide nanomaterials are one of the preferences as antibacterial active materials. Due to its distinctive electronic configuration and suitable properties, ZnO is one of the novel antibacterial active materials. Nowadays, researchers are making a serious effort to improve the antibacterial activities of ZnO by forming a composite with the same/different bandgap semiconductor materials and doping of ions. Applying capping agents such as polymers and plant extract that control the morphology and size of the nanomaterials and optimizing different conditions also enhance the antibacterial activity. Forming a nanocomposite and doping reduces the electron/hole recombination, increases the surface area to volume ratio, and also improves the stability towards dissolution and corrosion. The release of antimicrobial ions, electrostatic interaction, reactive oxygen species (ROS) generations are the crucial antibacterial activity mechanism. This review also presents a detailed discussion of the antibacterial activity improvement of ZnO by forming a composite, doping, and optimizing different conditions. The morphological analysis using scanning electron microscopy, field emission-scanning electron microscopy, field-emission transmission electron microscopy, fluorescence microscopy, and confocal microscopy can confirm the antibacterial activity and also supports for developing a satisfactory mechanism. Graphical abstract showing the metal oxides antibacterial mechanism and the fluorescence and scanning electron microscopic images.

Synthesis of Silica-Coated Fe3O4 Nanoparticles by Microemulsion Method: Characterization and Evaluation of Antimicrobial Activity.

Magnetite and silica-coated magnetite (Fe3O4) nanoparticles (NPs) were synthesized by water-in-oil (W/O) microemulsion method from hydrated ferric nitrate, ferrous sulfate precursors and ammonia a precipitating agent with the assistance of Tween-80 and SDS surfactants. The synthesized materials were characterized by X-ray diffraction, scanning electron microscopy, thermal analyzer, and infrared spectroscopy. X-ray diffraction pattern of Fe3O4 showed that particles were phase pure with a cubic inverse spinel structure and FT-infrared spectra confirmed the presence of Fe-O bond in tetrahedral and octahedral interstitial sites. The crystallite size determined from powder XRD data with Scherer's equation was in the range of 7.3 ± 0.05 nm-10.83 ± 0.02 nm for uncoated Fe3O4 and 16 ± 0.14 nm for silica-coated Fe3O4 NPs. The SEM micrographs of the uncoated Fe3O4 oxide revealed the agglomeration of the magnetite (Fe3O4) particles. But the silica-coated Fe3O4 oxide exhibited homogeneous distribution of particles with relatively less agglomerate of the particles. The particle size of Fe3O4 NPs slightly increased with the temperature and precursor concentration. The antimicrobial activities of Fe3O4 and silica-coated Fe3O4 nanoparticles were tested against Gram-negative (Escherichia coli and Pseudomonas aeruginosa) and Gram-positive (Staphylococcus aureus and Bacillus subtilis) bacteria. Both Fe3O4 and silica-coated Fe3O4 NPs demonstrated better antimicrobial activities.