A High-Performance Supercapacitor Based on Hierarchical Template-Free Ni/SnO2 Nanostructures via Hydrothermal Method.

Novel flake-like Ni1-xSnxO2 particles were successfully prepared by template-free hydrothermal synthesis. The prepared samples were investigated for their properties by different characterization techniques. Scanning micrographs showed that the obtained particles consisted of nanoflakes. The X-ray diffraction results of the Ni1-xSnxO2 revealed the formation of mixed-phase Ni/SnO2 having the typical tetragonal structure of SnO2, and the cubic structure of Ni in a nanocrystalline nature. The doping with Ni had a certain influence on the host's lattice structure of SnO2 at different doping concentrations. Confirmation of the functional groups and the elements in the nanomaterials was accomplished using FTIR and EDS analyses. The electrochemical performance analysis of the prepared nanomaterials were carried out with the help of the CV, GCD, and EIS techniques. The specific capacitance of the synthesized nanomaterials with different concentrations of Ni dopant in SnO2 was analyzed at different scanning rates. Interestingly, a 5% Ni-doped SnO2 nanocomposite exhibited a maximum specific capacitance of 841.85 F g-1 at 5 mV s-1 in a 6 M KOH electrolyte. Further, to boost the electrochemical performance, a redox additive electrolyte was utilized, which exhibited a maximum specific capacitance of 2130.33 at 5 mV s-1 and an excellent capacitance retention of 93.22% after 10,000 GCD cycles. These excellent electrochemical characteristics suggest that the Ni/SnO2 nanocomposite could be utilized as an electrode material for high-performance supercapacitors.

Silver-decorated SrTiO3 nanoparticles for high-performance supercapacitors and effective remediation of hazardous pollutants.

SrTiO3/Ag nanocomposites were synthesized using a facile wet impregnation method, employing rigorous experimental techniques for comprehensive characterization. XRD, FTIR, UV, PL, FESEM, and HRTEM were meticulously utilized to elucidate their structural, functional, morphological, and optical properties. The electrochemical performance of the SrTiO3/Ag nanocomposite was rigorously assessed, revealing an impressive specific capacitance of 850 F/g at a current density of 1 A. Furthermore, the photocatalytic activity of the SrTiO3/Ag nanocomposite was rigorously examined using methylene blue (MB) dye, and the results were outstanding. After 120 min of UV irradiation, the nanocomposite exhibited an exceptional MB dye degradation efficiency exceeding 88%. The SrTiO3/Ag nanocomposite represents an exemplary catalyst in terms of efficiency, cost-effectiveness, environmental compatibility, and reusability. The electron and superoxide radicals play a chief role in the MB dye degradation process. The inclusion of Ag within the SrTiO3 matrix facilitated the formation of a conductive nano-network, ultimately resulting in superior capacitive and photocatalytic performance.

Highly Efficient Solar-Light-Active Ag-Decorated g-C3N4 Composite Photocatalysts for the Degradation of Methyl Orange Dye.

In this study, we utilized calcination and simple impregnation methods to successfully fabricate bare g-C3N4 (GCN) and x% Ag/g-C3N4 (x% AgGCN) composite photocatalysts with various weight percentages (x = 1, 3, 5, and 7 wt.%). The synthesized bare and composite photocatalysts were analyzed to illustrate their phase formation, functional group, morphology, and optical properties utilizing XRD, FT-IR, UV-Vis DRS, PL, FE-SEM, and the EDS. The photodegradation rate of MO under solar light irradiation was measured, and the 5% AgGCN composite photocatalyst showed higher photocatalytic activity (99%), which is very high compared to other bare and composite photocatalysts. The MO dye degradation rate constant with the 5% AgGCN photocatalyst exhibits 14.83 times better photocatalytic activity compared to the bare GCN catalyst. This photocatalyst showed good efficiency in the degradation of MO dye and demonstrated cycling stability even in the 5th successive photocatalytic reaction cycle. The higher photocatalytic activity of the 5% AgGCN composite catalyst for the degradation of MO dye is due to the interaction of Ag with GCN and the localized surface plasmon resonance (SPR) effect of Ag. The scavenger study results indicate that O2●- radicals play a major role in MO dye degradation. A possible charge-transfer mechanism is proposed to explain the solar-light-driven photocatalyst of GCN.

Synthesis and characterization of Hypsizygus ulmarius extract mediated silver nanoparticles (AgNPs) and test their potentiality on antimicrobial and anticancer effects.

The prime aim of this research is to discover new, eco-friendly approaches to reducing agents for manufacturing silver nanoparticles (AgNPs) from fresh fruiting bodies of the edible mushroom Hypsizygus ulmarius (Hu). The confirmation of Hu-mediated AgNPs has been characterized by UV visible spectroscopy, XRD, FTIR, SEM with EDX, HRTEM, AFM, PSA, Zeta poetical and GCMS analysis. The absorption peak of Hu-AgNPs at 430 nm has been confirmed by UV-visible spectroscopy analysis. The findings of the particle size study show that AgNPs have a size distribution with an average of 20 nm. The Zeta potential of NPs reveals a significant build-up of negative charges on their surface. The additional hydrate layers that occurred at the surface of AgNPs are shown in the HR-TEM morphology images. The antibacterial activity results showed that Hu-AgNPs were highly effective against both bacterial pathogens, with gram-positive (+) and gram-negative (-) pathogens having a moderate inhibition effect on K. pneumoniae (5.3 ± 0.3 mm), E. coli (5.3 ± 0.1), and S. aureus (5.2 ± 0.3 mm). Hu-AgNPs (IC50 of 50.78 µg/mL) were found to have dose-dependent cytotoxic action against human lung cancer cell lines (A549). Inhibited cell viability by up to 64.31% after 24 h of treatment. To the best of our knowledge, this is the hand information on the myco-synthesis of AgNPs from the H. ulmarius mushroom extract and the results suggest that it can an excellent source for developing a multipurpose and eco-friendly nano product in future.

Photocatalytic degradation of organic pollutants and inactivation of pathogens under visible light via SnO2/rGO composites.

The domains of environmental cleanup and pathogen inactivation are particularly interesting in nanocomposites (NCs) due to their exceptional physicochemical properties. Tin oxide/reduced graphene oxide nanocomposites (SnO2/rGO NCs) have potential uses in the biological and environmental fields, but little is known about them. This study aimed to investigate the photocatalytic activity and antibacterial efficiency of the nanocomposites. The co-precipitation technique was used to prepare all the samples. XRD, SEM, EDS, TEM, and XPS analyses were employed to characterize the physicochemical properties of SnO2/rGO NCs for structural analysis. The rGO loading sample resulted in a decrease in the crystallite size of SnO2 nanoparticles. TEM and SEM images demonstrate the firm adherence of SnO2 nanoparticles to the rGO sheets. The chemical state and elemental composition of the nanocomposites were validated by the XPS and EDS data. Additionally, the visible-light active photocatalytic and antibacterial capabilities of the synthesized nanocomposites were assessed for the degradation of Orange II and methylene blue, as well as the suppression of the growth of S. aureus and E. coli. As a result, the synthesized SnO2/rGO NCs are improved photocatalysts and antibacterial agents, expanding their potential in the fields of environmental remediation and water disinfection.

Development of silver oxide-loaded reduced graphene oxide nanohybrids for enhanced photocatalytic activity under visible light in aqueous solutions.

We report on the synthesis of silver oxide/reduced graphene oxide nanocomposites (Ag/rGO NCs) using a hydrothermal technique. This paper presents a simple method for synthesizing Ag/rGO hybrid nanocomposites, which can be used for environmentally treating hazardous organic pollutants. The photocatalytic degradation of model artificial Rhodamine B dye and bisphenol A was assessed under visible light illumination. The crystallinity, binding energy, and surface morphologies of the synthesized samples were determined. The silver oxide loading sample resulted in a decrease in the rGO crystallite size. SEM and TEM images demonstrate strong adhesion of the Ag NPs to the rGO sheets. XPS analysis validated the binding energy and elemental composition of the Ag/rGO hybrid nanocomposites. The objective of the experiment was to enhance the photocatalytic efficiency of rGO in the visible region using Ag nanoparticles. The synthesized nanocomposites in the visible region exhibited good photodegradation percentages of approximately 97.5% and 98.6% after 120 min of irradiation for pure rGO, Ag NPs, and Ag/rGO nanohybrid, respectively. Furthermore, the Ag/rGO nanohybrid maintained their degradation ability for up to three cycles. The synthesized Ag/rGO nanohybrid demonstrated enhanced photocatalytic activity, expanding their potential for environmental remediation. Based on the investigations, Ag/rGO nanohybrid proved to be an effective photocatalyst and holds promise as an ideal material for future applications in preventing water pollution.

Chitosan functionalized bismuth oxychloride/zinc oxide nanocomposite for enhanced photocatalytic degradation of Congo red.

The industrial discharge of dye pollutant contaminated wastewater is the major cause of water and soil pollution. Photocatalysis is a promising and green remediation technology, which has received widespread attention in the remediation of hazardous dyes from aqueous environment and convert them into harmless compounds. Herein, we report the synthesis of chitosan (CS) functionalized bismuth oxychloride/zinc oxide (BiOCl/ZnO) nanocomposite by a modified hydrothermal route. The physiochemical characterization revealed that the synthesized nanocomposite have crystalline, agglomerated spherical along with rod shaped morphology and size range from 35 to 160 nm. FTIR peaks at 825, 727, 662 and 622 cm-1 specified the presence of BiO and ZnO bonds, whereas peak at 1635 cm-1 revealed the existence of amine groups which confirms the presence of CS in the synthesized CS-BiOCl/ZnO nanocomposite. Catalytic property of synthesized nanocomposite was evaluated by the degradation of Congo red (CR) under UV-light irradiation. CR dye degradation percentage was found to be 93 % within a short period of 40 min by utilizing UV-light. Furthermore, reusability of CS-BiOCl/ZnO photocatalyst was also investigated, and it remained significant photocatalytic activity after three consecutive cycles. Hence, the results obtained in this study revealed that CS-BiOCl/ZnO nanocomposite can be used as a potential photocatalyst to remediate organic pollutants in various industries.