Using a simple approach, silver nanoparticles (Ag NPs) were synthesized from green coffee bean extract. The optical color change from yellowish to reddish-brown of the green-produced Ag NPs was initially observed, which was confirmed by the UV-Visible spectrophotometer’s surface plasmonic resonance (SPR) bands at 329 and 425 nm. The functional groups of green coffee-capped Ag NPs (GC-capped Ag NPs) were studied using a Fourier transform infrared spectrometer, revealing that Ag NPs had been capped by phytochemicals, resulting in excellent stability, and preventing nanoparticle aggregation. The presence of elemental silver is confirmed by energy dispersive X-ray analysis. In addition to the measurement of the zeta potential of the prepared GC-capped Ag NPs, the size distribution is evaluated by the dynamic light scattering. Depending on the nano-morphological study, the particle diameter of Ag NPs is 8.6 ± 3.5 nm, while the particle size of GC-capped Ag NPs is 29.9 ± 4.3 nm, implying the presence of well-dispersed nanospheres with an average capsulation layer of thickness 10.7 nm. The phyto-capped Ag NPs were found to be crystalline, having a face-centered cubic (FCC) lattice structure and Ag crystallite size of ~7.2 nm, according to the XRD crystallographic analysis. The catalytic performance of phyto-capped Ag NPs in the removal of methylene blue dye by sodium borohydride (NaBH₄) was investigated for 12 min to reach a degradation efficiency of approximately 96%. The scavenging activities of 2,2-Diphenyl-1-picrylhydrazyl (DPPH) free radicals are also examined in comparison to previously reported Ag-based nano-catalysts, demonstrating a remarkable IC₅₀ of 26.88 µg/mL, which is the first time it has been recorded.

In this work, a polyaniline/lead sulfide (PANI/PbS) nanocomposite was prepared by combining the in situ oxidation polymerization method and the surface adsorption process. This nanocomposite was applied as a supercapacitor electrode. The crystal structure, nanomorphology, and optical analysis of PANI and PANI/PbS were investigated. The electrochemical performance of the designed PANI/PbS electrode-based supercapacitor was tested by using cyclic voltammetry (CV), chronopotentiometry (CP), and AC impedance techniques in HCl and Na₂SO₄ electrolytes. The average crystallite size of the PANI/PbS nanocomposite is about 43 nm. PANI/PbS possesses an agglomerated network related to PANI with additional spherical shapes from PbS nanoparticles. After the PANI/PbS nanocomposite formation, there are enhancements in their absorption intensities. At a current density of 0.4 A g⁻¹, the specific capacitance of PANI/PbS in Na₂SO₄ and HCl was found to be 303 and 625 F g⁻¹, respectively. In HCl (625 F g⁻¹ and 1500 mF cm⁻²), the gravimetric and areal capacitances of the PANI/PbS electrode are nearly double those of the Na₂SO₄ electrolyte. Also, the average specific energy and specific power density values for the PANI/PbS electrode in HCl are 4.168 Wh kg⁻¹ and 196.03 W kg⁻¹, respectively. After 5000 cycles, the capacitance loses only 4.5% of its initial value. The results refer to the high stability and good performance of the designed PANI/PbS as a supercapacitor electrode.

Thin films of ZnO and ZnO/carbon nanotubes (CNTs) are prepared and used as CO₂ gas sensors. The spray pyrolysis method was used to prepare both ZnO and ZnO/CNTs films, with CNTs first prepared using the chemical vapor deposition method (CVD). The chemical structure and optical analyses for all the prepared nanomaterials were performed using X-ray diffraction (XRD), Fourier transformer infrared spectroscopy (FTIR), and UV/Vis spectrophotometer devices, respectively. According to the XRD analysis, the crystal sizes of ZnO and ZnO/CNTs were approximately 50.4 and 65.2 nm, respectively. CNTs have average inner and outer diameters of about 3 and 13 nm respectively, according to the transmitted electron microscope (TEM), and a wall thickness of about 5 nm. The detection of CO₂ is accomplished by passing varying rates of the gas from 30 to 150 sccm over the prepared thin-film electrodes. At 150 sccm, the sensitivities of ZnO and ZnO/CNTs sensors are 6.8% and 22.4%, respectively. The ZnO/CNTs sensor has a very stable sensitivity to CO₂ gas for 21 days. Moreover, this sensor has a high selectivity to CO₂ in comparison with other gases, in which the ZnO/CNTs sensor has a higher sensitivity to CO₂ compared to H₂ and C₂H₂.

The development of a non-malignant and sustainable treatment approach for eradicating mephitic organic dyes from freshwater resources is a daunting task. In a similar vein, the current work investigates the mitigation of methylene blue (MB) dye utilizing titanium dioxide nanoparticles (CS-TiO₂ NPs) synthesized using cannabis sativa (bhang) leaf extract via a greener approach. The CS-TiO₂ NPs are well characterized through XRD, FE-SEM, HR-TEM, UV-Vis spectroscopy, FTIR spectroscopy, and EDS spectroscopy. Microscopic studies confirm that the average particle size distribution of the individual particles was found to be in the range of 12.5 ± 1.5 nm, whereas the average size of the CS-TiO₂ NPs aggregates is 24.5 ± 11.5 nm. Additionally, the synthesized CS-TiO₂ NPs manifested remarkable photocatalytic degradation potential against methylene blue dye with a degradation efficiency of 98.2% and an apparent rate constant of 0.0398 min⁻¹. As a result, this research offers a green/sustainable alternative for water purification.

TiO₂ is one of the most investigated materials due to its abundance, lack of toxicity, high faradaic capacitance, and high chemical and physical stability; however, its potential use in energy storage devices is constrained by its high internal resistance and weak van der Waals interaction between the particles. Carbon nanotubes are especially well suited for solving these issues due to their strong mechanical strength, superior electrical conductivity, high electron mobilities, excellent chemical and thermal stability, and enormous specific nanoporous surface. The hydrothermal approach was followed by chemical vapor deposition to produce a network composite of titanium dioxide nanoribbons (TNRs) and multi-walled carbon nanotubes (MWCNTs). The nanocomposite was characterized using a variety of methods. One phase of TiO₂-B nanoribbons has porous pits on its surface, and MWCNTs are grown in these pits to produce a network-like structure in the nanocomposite. With a two-electrode supercapacitor configuration, the TNR/CNT gave a gravimetric capacitance of 33.33 F g⁻¹, which was enhanced to 68.18 F g⁻¹ in a redox-active electrolyte containing hydroquinone (HQ). Additionally, the areal capacitance per footprint was increased from 80 mF cm⁻² in H₂SO₄ to 163.63 mF cm⁻² in H₂SO₄/HQ. The TNR/CNT supercapacitor has superior cyclic stability than the previously reported TiO₂-based electrodes, with 97.5% capacitance retention after 5000 cycles. Based on these results, it looks like the TNR/CNT supercapacitor could provide portable electronic power supplies with new ways to work in the future.

Losses from corrosion contribute roughly 3-5% of the gross domestic product of developed nations, and among the many methods used to avoid corrosion, using silane-based coatings is seen to be of the biggest importance due to their low toxicity and superior adhesive qualities. It is essential to develop an anti-corrosion coating that is efficient, economical, and eco-friendly. The corrosion resistance and durability of various silane-based coatings such as 1,2-bis(triethoxysilyl)ethane (BTSE), bis[3-(triethoxysilyl)propyl]tetrasulfide (TESPT), and vinyltrimethylsilane (VTES) for carbon steel 1018 substrates were investigated in a high-salinity environment (4.5 wt % NaCl). The corrosion resistance performance was evaluated via potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS) techniques. Results revealed that the TESPT film (pH ≈ 7) has the best corrosion resistance performance on the carbon steel surface in the aggressive chloride environment, that is, 99.6%. The high corrosion resistance of the TESPT film is due to the hydrophobic nature of this silane, which leads to the formation of a stable and dense film. These results were supported by X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX) analyses.