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Abstract This research aims to develop chitosan-zein protein films supplemented withBergenia ciliata(Bc) extract, a traditionally important medical herb of Himalayan origin. The film’s physicochemical, mechanical, antioxidant, and antimicrobial properties were systematically explored. The opacity of chitosan film increased from 2.42 ± 0.97 to 10.32 ± 1.44 upon introducing zein (Z) protein in chitosan (Cs) in a 1:2 ratio (w/w); conferring enhanced UV-blocking attributes. IncorporatingB. ciliataextracts in the chitosan-zein film (Cs-Z-Bc) under optimized conditions further increased the opacity to 16.27 ± 1.03 without compromising the tensile strength. The α-diphenyl-β-picrylhydrazyl scavenging activity of the Cs-Z-Bc film was found to be 97.07 ± 1.09%. Additionally, these optimized films displayed significant antimicrobial efficacy, with zones of inhibition of 11.4 mm measured for gram-positive strains likeC. subtilisandS. aureusand 11.2 mm and 11.1 mm forE. coliandK. pneumoniae(gram-negative) bacterial strains. The film also showed excellent biodegradable properties. The shelf life study of Himalayan cheese was significantly increased when wrapped with the film. These findings suggested thatB. ciliataextract-fortified chitosan-zein films can be an excellent food packaging material. 

Hydrothermal and photoreduction/deposition methods were used to fabricate Ag nanoparticles (NPs) decorated CoMoO₄rods. Improvement of charge transfer and transportation of ions by making heterostructure was proved by cyclic voltammetry and electrochemical impedance spectroscopy measurements. Linear sweep voltammetry results revealed a fivefold enhancement of current density by fabricating heterostructure. The lowest Tafel slope (112 mV/dec) for heterostructure compared with CoMoO₄(273 mV/dec) suggested the improvement of electrocatalytic performance. The electrochemical CO₂reduction reaction was performed on an H-type cell. The CoMoO₄electrocatalyst possessed the Faraday efficiencies (FEs) of CO and CH₄up to 56.80% and 19.80%, respectively at  − 1.3 V versus RHE. In addition, Ag NPs decorated CoMoO₄electrocatalyst showed FEs for CO, CH₄, and C₂H₆were 35.30%, 11.40%, and 44.20%, respectively, at the same potential. It is found that CO₂reduction products shifted from CO/CH₄to C₂H₆when the Ag NPs deposited on the CoMoO₄electrocatalyst. In addition, it demonstrated excellent electrocatalytic stability after a prolonged 25 h amperometric test at  − 1.3 V versus RHE. It can be attributed to a synergistic effect between the Ag NPs and CoMoO₄rods. This study highlights the cooperation between Ag NPs on CoMoO₄components and provides new insight into the design of heterostructure as an efficient, stable catalyst towards electrocatalytic reduction of CO₂to CO, CH₄, and C₂H₆products. 

We report the intercalation of polyacrylonitrile nanoparticles in Ti3C2Tx MXene layers through simple sonication. The use of polyacrylonitrile, which was synthesized via radical polymerization, offered dual benefits: (1) It increased the interlayer spacing of MXene, thereby exposing more surface area and enhancing ion transport channels during charge and discharge cycles, and (2) Integrating MXene with polyacrylonitrile enables the creation of a composite with conductive properties, following percolation principle. X-ray diffraction analysis showed an increase in the c-lattice parameter, indicative of the interlayer spacing, from 22.31 Å for the pristine MXene to 37.73 Å for the MXene−polyacrylonitrile composite. The intercalated polyacrylonitrile nanoparticles facilitated the delamination by weakening the interlayer interactions, especially during sonication. Electrochemical assessments revealed significant improvement in the properties of the MXene−polyacrylonitrile composite compared to the pristine MXene. The assembled asymmetric device achieved a good specific capacitance of 32.1 F/g, an energy density of 11.42 W h/kg, and 82.2% capacitance retention after 10,000 cycles, highlighting the practical potential of the MXene−polyacrylonitrile composite. 

Abstract An amphiphilic block copolymer, poly (styrene-2-polyvinyl pyridine-ethylene oxide), was used as a structure-directing and stabilizing agent to synthesize TiO₂/RuO₂nanocomposite. The strong interaction of polymers with metal precursors led to formation of a porous heterointerface of TiO₂/RuO₂. It acted as a bridge for electron transport, which can accelerate the water splitting reaction. Scanning electron microscopy, energy-dispersiveX-ray spectroscopy, transmission electron microscopy, andX-ray diffraction analysis of TiO₂/RuO₂samples revealed successful fabrication of TiO₂/RuO₂nanocomposites. The TiO₂/RuO₂nanocomposites were used to measure electrochemical water splitting in three-electrode systems in 0.1-M KOH. Electrochemical activities unveil that TiO₂/RuO₂-150 nanocomposites displayed superior oxygen evolution reaction activity, having a low overpotential of 260 mV with a Tafel slope of 80 mVdec⁻¹. Graphical abstract 

Abstract Hydrogen gas is a prominent focus in pursuing renewable and clean alternative energy sources. The quest for maximizing hydrogen production yield involves the exploration of an ideal photocatalyst and the development of a simple, cost‐effective technique for its generation. Iron titanate has garnered attention in this context due to its photocatalytic properties, affordability, and non‐toxic nature. Over the years, different synthesis routes, different morphologies, and some modifications of iron titanate have been carried out to improve its photocatalytic performance by enhancing light absorption in the visible region, boosting charge carrier transfer, and decreasing recombination of electrons and holes. The use of iron titanate photocatalyst for hydrogen evolution reaction has seen an upward trend in recent times, and based on available findings, more can be done to improve the performance. This review paper provides a comprehensive overview of the fundamental principles of photocatalysis for hydrogen generation, encompassing the synthesis, morphology, and application of iron titanate‐based photocatalysts. The discussion delves into the limitations of current methodologies and present and future perspectives for advancing iron titanate photocatalysts. By addressing these limitations and contemplating future directions, the aim is to enhance the properties of materials fabricated for photocatalytic water splitting. 

A chemical reaction network has been utilized as an energy and radical source to synthesize porous carbon nitride for energy storage applications. 

Abstract A hierarchical nanocomposite of carbon microspheres decorated with tungsten oxide (WO₃) nanocrystals resulted from the hydrothermal treatment of a precursor solution containing glucose and tungstic acid. The dehydration of glucose molecules formed oligosaccharides, which consequently carbonized, turning into carbon microspheres. The carbon microspheres then acted as a spherical nucleus onto which WO₃nanocrystals grew via heterogeneous nucleation. The reaction product showed a phase junction of orthorhombic and monoclinic WO_3,which transitioned to mix-phase of tetragonal and monoclinic WO₃after a subsequent heat treatment at 600 °C in an inert condition. The electrochemical tests showed that incorporating WO₃onto the carbon (WO₃/C) resulted in a three-fold increase in the specific capacitance compared to WO₃alone and a high coulombic and energy efficiencies of 98.2% and 92.8%, respectively. The nanocomposite exhibited supercapacitance with both Faradaic and non-Faradaic charge storage mechanisms. Electrochemical impedance spectroscopy showed a lower charge transfer resistance for the composite at R_ct = 11.7Ω. 

Metal indium sulfides (ZnIn₂S₄, NiIn₂S₄, and CuInS₂) were synthesized using a hydrothermal method for electrochemical reduction of CO₂in to methane. 

A laboratory-synthesized triblock copolymer poly(ethylene oxide-b-acrylic acid-b-styrene) (PEG-PAA-PS) was used as a template to synthesize hollow BaCO3 nanoparticles (BC-NPs). The triblock copolymer was synthesized using reversible addition–fragmentation chain transfer radical polymerization. The triblock copolymer has a molecular weight of 1.88 × 104 g/mol. Transmission electron microscopy measurements confirm the formation of spherical micelles with a PEG corona, PAA shell, and PS core in an aqueous solution. Furthermore, the dynamic light scattering experiment revealed the electrostatic interaction of Ba2+ ions with an anionic poly(acrylic acid) block of the micelles. The controlled precipitation of BaCO3 around spherical polymeric micelles followed by calcination allows for the synthesis of hollow BC-NPs with cavity diameters of 15 nm and a shell thickness of 5 nm. The encapsulation and release of methotrexate from hollow BC-NPs at pH 7.4 was studied. The cell viability experiments indicate the possibility of BC-NPs maintaining biocompatibility for a prolonged time.