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Due to the importance of energy storage systems based on supercapacitors, various studies have been conducted. In this research CuO, NCNO and the flower like CuO/NCNO have been studied as a novel materials in this field. The resulte showed that the synthesized CuO nanostructutes have flower like morphology which studied by FE-SEM analisis. Further, the XRD pattern confirmed the crystalline properties of the CuO/NCNO nanocomposite, and the Raman verified the functional groups and vibrations of the components of CuO/NCNO nanocomposite. In a two-electrode system at a current density of 4 A/g, the capacitance, power density, and energy density were 450 F/g, 3200 W/kg, and 98 Wh/kg, respectively. The charge transfer resistances of CuO and NCNO/CuO electrodes obtained 8 and 2 Ω respectively, which show that the conductivity and supercapacitive properties of nanocomposite are better than pure components. Also, the stability and low charge transfer resistance are other advantages obtained in a two-symmetrical electrode investigation. The stability investigation showed that after 3000 consecutive cycles, only 4% of the initial capacitance of the CuO/NCNO electrode decreased.

Morphine, as one of the most important narcotic drugs, significantly affects the nervous system and increases euphoria, which raises the likelihood of its misuse. Therefore, its measurement is of great importance. In this work, a new electrochemical sensor based on a nanocomposite of CuS/g-C 3 N 5 /AgNPs was developed for modifying Screen printed carbon electrodes (SPCEs) and used for the measurement of morphine through cyclic voltammetry and differential pulse voltammetry. Various analytical methods initially characterized the nanocomposite. The prepared sensor, which also has an extensive surface area, achieved a detection limit of 0.01 µM for morphine in a concentration range of 0.05–100 µM at pH 7. Besides its excellent capability in measuring morphine in real samples, the sensor exhibits good stability, reproducibility, and repeatability. The presence of CuS, due to its excellent high surface area alongside silver nanoparticles, leads to an increase in the conductivity of the g-C 3 N 5 modified electrode, resulting in an increased oxidative current of morphine at the surface of the prepared sensor. Therefore, measuring low concentrations of morphine with this sensor was made possible. Additionally, measuring morphine without interference from various species is a strong point of the electrochemical sensor for morphine detection, and combined with the simplicity and ease of the method, it allows for morphine measurements to be conducted in the shortest possible time.

In this study, green synthesis, characterizations, photocatalytic performance, and antibacterial applications of α-Mn 2 O 3 nanoparticles are reported. The synthesized nanoparticles were characterized by Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), transmission electron microscope (TEM), Scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), Brunauer Emmett Teller (BET), Electrochemical Impedance Spectroscopy (EIS), Photoluminescence (PL), and Differential reflectance spectroscopy (DRS) analysis. The investigation verified that the α-Mn 2 O 3 nanoparticles possessed a cubic structure, with a crystallite size of 23 nm. The SEM and TEM techniques were used to study the nanoscale morphology of α- Mn 2 O 3 nanoparticles, which were found to be spherical with a size of 30 nm. Moreover, the surface area was obtained as 149.9 m 2  g −1 utilizing BET analysis, and the band gap was determined to be 1.98 eV by DRS analysis. The photocatalysis performance of the α-Mn 2 O 3 NPs was evaluated for degrading Eriochrome Black T (EBT) dye under visible light and degradation efficiency was 96% in 90 min. The photodegradation mechanism of EBT dye was clarified with the use of radical scavenger agents, and the degradation pathway was confirmed through Liquid Chromatography–Mass Spectrometry (LC–MS) analysis. Additionally, the produced nanoparticles could be extracted from the solution and continued to exhibit photocatalysis even after five repeated runs under the same optimal conditions. Also, the antibacterial activity of green synthesized α-Mn 2 O 3 nanoparticles was investigated by using the broth microdilution method towards Enterococcus faecalis ATCC 29212 (Gram-positive), Staphylococcus aureus ATCC 29213 (Gram-positive), Salmonella typhimurium ATCC 14028 (Gram-negative), Klebsiella pneumoniae ATCC 7881 (Gram-negative), Escherichia coli ATCC 25922 (Gram-negative), Proteus mirabilis ATCC 7002 (Gram-negative), and Pseudomonas aeruginosa ATCC 27853 (Gram-negative) bacterial strains.

Since viral polymerases are responsible for viral replication, they are a prime target in antiviral drug development. The present study evaluated the antiviral potential of 174 secondary metabolites of the Sordariales order against aspartyl polymerases, including hepatitis C virus nonstructural protein 5B (HCV NS5B) and Severe acute respiratory syndrome coronavirus 2 RNA-dependent RNA polymerase (SARS CoV-2 RdRp). A two-step virtual screening was performed, identifying 76 ligands binding to the active site, while 10 showed binding energies below -7 kcal/mol. Ligands 1–3 exhibited better binding affinities than the Ribavirin. Lig-3 demonstrated the most intense interaction. These interacted through hydrogen bonding and hydrophobic interactions with the key catalytic motifs that may disrupt viral replication by inhibiting polymerase activities. Next, the effects of these ligands induced in polymerase structure and dynamics were analyzed by 300 ns molecular dynamics (MD) simulations, showing that ligand binding altered structural dynamics in critical motifs responsible for NTP and RNA template binding. RMSF and PCA analyses revealed reduced protein mobility and significant structural destabilization, particularly for Lig-1 and Lig-3 in SARS-CoV-2 RdRp and Lig-2 and Lig-3 in HCV NS5B. Additionally, Rg and SASA analyses indicated structural compression in ligand-bound complexes, corroborating the hypothesis of enzymatic inhibition. MM/PBSA analysis highlighted Lig-1 and Lig-3 as having stronger binding energies for SARS-CoV-2 RdRp, while Lig-3 and Lig-2 displayed higher binding energies for HCV NS5B. With promising ADME/T properties, Lig-3 is a promising multi-target antiviral candidate against HCV NS5B and SARS-CoV-2 RdRp, meriting further in vitro and in vivo investigations.

MgFe 2 O 4 @ZnAl 2 O 4 magnetic nanocomposites were synthesized with the easy and green sol–gel method, and their photocatalytic efficiency was followed toward degradation of reactive blue 222 (RB222) dye under visible light irradiation. Prepared nanocomposites were fully characterized. The SEM and TEM images revealed the spherical morphology of the produced nanocomposites, with average size of 20–25 nm. The XRD pattern of sample exhibited the successful synthesis of the MgFe 2 O 4 @ZnAl 2 O 4 MNCs with crystallite size 13 nm. The saturation magnetization (Ms) of the nanocomposites was examined using VSM, indicating a value of 6.59 emu/g. The absence of Hc and Mr values confirms the superparamagnetic nature of the nanoparticles. In addition, the surface area was calculated to be 78.109 m 2 /g utilizing BET analysis, and the band gap was determined to be 1.88 eV by DRS analysis. The photocatalytic, photolysis, and adsorption performance were investigated and result shown photodegradation activity was higher than others. These results confirm the synergetic effect between the MgFe 2 O 4 @ZnAl 2 O 4 MNCs and visible light irradiation to degradation of organic dye. The results indicate that rapid degradation of 96% of RB222 dye occurred in just 10 min, with a TOC removal rate of approximately 59%. Furthermore, radical scavenger agents also clarified photodegradation of RB222 dye.

Over the past decade, CdS QDs have become versatile semiconductors. Surface modification of CdS QDs has become an interesting case study, as it can eliminate surface defects and improve their photochemical properties. In this study, we report a new strategy of using carbon quantum dots containing a large number of thiol groups (CQDs-SH) as a passivating agent for the stabilization of CdS quantum dots (QDs). Various characterization techniques have clearly revealed that the CdS QDs have been successfully passivated by CQDs-SH. The photocatalytic performance of CQDs-SH/CdS QDs was investigated for the degradation of the insecticide imidacloprid from an aqueous solution. Parameters affecting the photodegradation process, including the light source, photocatalyst amount, initial concentration of the pollutant, radiation time, pH, oxidizing agent, and temperature, were investigated. Furthermore, the HPLC technique was applied to quantitatively analyze imidacloprid and its degradation products. The results of the HPLC analysis revealed that under simulated visible light at pH 9, imidacloprid scarcely existed after 90 min of irradiation (90.13% degradation). The LC–MS method was also used to detect the degradation products and investigate the mechanism of photodegradation of the pesticide. The results showed that the CQDs-SH/CdS QDs composite was a promising photocatalyst for the degradation of imidacloprid in wastewater.

The application of metal-matrix composite coatings for protecting and improving the service life of sliding components has demonstrated to have the potential of meeting the requirements of a diverse range of engineering industries. Recently, a significant body of research has been devoted to studying the mechanical and tribological performance of dispersion-strengthened MCrAlY coatings. These coatings belong to a class of emerging wear-resistant materials, offering improved properties and being considered as promising candidates for the protection of engineering structural materials exposed to tribological damage, especially at elevated temperature regimes. This paper attempts to comprehensively review the different reinforcements used in the processing of MCrAlY-based alloys and how they influence the mechanical and tribological properties of the corresponding coatings. Furthermore, the major fabrication techniques together with their benefits and challenges are also reviewed. Discussion on the failure mechanisms of these coatings as well as the main determining factors are also included. In addition, a comprehensive survey of studies and investigations in recent times are summarized and elaborated to further substantiate the review.

Excessive Cu 2+ intake can cause neurological disorders (e.g. Wilson’s disease) and adversely affect the gastrointestinal, liver, and kidney organs. The presence of Cu 2+ is strongly linked to the emergence and progression of Wilson's disease (WD), and accurately measuring the amount of copper is a crucial step in diagnosing WD at an early stage in a clinical setting. In this work, CQDs were fabricated through a facile technique as a novel fluorescence-based sensing platform for detecting Cu(II) in aqueous solutions, and in the serum samples of healthy and affected individuals by WD. The CQDs interact with Cu(II) ions to produce Turn-on and Turn-off states at nano-molar and micro-molar levels, respectively, with LODs of 0.001 µM and 1 µM. In fact, the Cu 2+ ions can act like a bridge between two CQDs by which the charge and electron transfer between the CQDs may increase, possibly can have significant effects on the spectroscopic features of the CQDs. To the best of our knowledge, this is the first reported research that can detect Cu(II) at low levels using two different complexation states, with promising results in testing serum. The potential of the sensor to detect Cu(II) was tested on serum samples from healthy and affected individuals by WD, and compared to results obtained by ICP-OES. Astonishingly, the results showed an excellent correlation between the measured Cu(II) levels using the proposed technique and ICP-OES, indicating the high potential of the fluorimetric CQD-based probe for Cu(II) detection. The accuracy, sensitivity, selectivity, high precision, accuracy, and applicability of the probe toward Cu(II) ions make it a potential diagnostic tool for Wilson's disease in a clinical setting.

This study presents a novel nanocomposite hydrogel film, composed of physically crosslinked polyacrylamide (PAM) and carbon nanotube (CNT) flakes, as a potential drug delivery system. Field emission scanning electron microscopy (FESEM) analysis elucidated the microstructure and interconnected pore network of the hydrogel, highlighting their direct influence on drug loading capacity and release profile. The hydrogel exhibited outstanding swelling behavior and structural stability under physiological conditions. These attributes rendered the hydrogel suitable as an effective drug carrier for release of doxorubicin (DOX), as a model drug. The DOX-loaded hydrogel demonstrated a sustained release profile at pH 5.5. Biocompatibility and cytotoxicity of the hydrogel were assessed through MTT assays using human embryonic kidney 293 (HEK-293) and MCF-7 human breast cancer cell lines over 24- and 48-hour intervals. The results confirmed the biocompatibility of the hydrogel, while the DOX-loaded hydrogel effectively inhibited MCF-7 proliferation cells, validating its therapeutic potential. Moreover, toxicity evaluations, including brine shrimp lethality and hemolysis assays, confirmed the low toxicity and excellent hemocompatibility of the hydrogel. These findings underscore the potential of the PAM/CNT nanocomposite hydrogel as a versatile and safe drug delivery system, with promising applications in advanced therapeutic strategies.