Publications by authors named "Bishnu P Bastakoti"

We report the intercalation of polyacrylonitrile nanoparticles in TiCT 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.

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Lithium-ion batteries (LIBs) serve as the backbone of modern technologies with ongoing efforts to enhance their performance and sustainability driving the exploration of new electrode materials. This study introduces a new type of alloy-conversion-based gallium ferrite (GFO: GaFeO) as a potential anode material for Li-ion battery applications. The GFO was synthesized by a one-step mechanochemistry-assisted solid-state method.

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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.

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Mesoporous honeycomb iron titanate using a sol-gel, evaporation-induced self-assembly method is synthesized. A triblock copolymer, F127, serves as a structure-directing agents, with iron chloride and titanium (IV) isopropoxide as inorganic precursors. The strong intermolecular force of attraction among urea, metal precursors, and polymer led to the formation of the mesoporous honeycomb structure.

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Hydrothermal and photoreduction/deposition methods were used to fabricate Ag nanoparticles (NPs) decorated CoMoO rods. 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.

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A hierarchical nanocomposite of carbon microspheres decorated with tungsten oxide (WO) 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 WO nanocrystals grew via heterogeneous nucleation.

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Zinc (Zn) metal and its alloys have received a lot of interest in biomedical applications due to their biodegradability, biocompatibility, antimicrobial activity, and ability to stimulate tissue regeneration. Bulk Zn has been successfully utilized in a variety of implant applications, most notably as bioabsorbable cardiac stents and orthopedic fixation devices, where it provides adequate mechanical properties while also releasing helpful Zn ions (Zn) during degradation. Such beneficial ions are dose-dependent and, when released in excess, can induce cellular toxicity.

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A laboratory-synthesized triblock copolymer poly(ethylene oxide--acrylic acid--styrene) (PEG-PAA-PS) was used as a template to synthesize hollow BaCO 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.

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Iron oxide nanoparticles (IONPs) were synthesized via a block copolymer-assisted hydrothermal method and the phase purity and the crystal structure were investigated by X-ray diffraction. The Rietveld analysis of X-ray diffractometer spectra shows the hexagonal phase symmetry of α-FeO. Further, the vibrational study suggests Raman active modes: 2A1g + 5Eg associated with α-FeO, which corroborates the Rietveld analysis and orbital analysis of 2PFe.

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Hollow nanostructures of transition metal phosphate are of immense interest in the existing and evolving areas of technology, due to their high surface area, presence of hollow void, and easy tuning of compositions and dimensions. Emerging synthesis methods such as template-free methods, hard-templating, and soft-templating are discussed in this review. Applications of these hollow metal phosphates dominate in energy storage and conversions, with specific advantages as supercapacitor materials.

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Tungsten oxide (WO ) has received ever more attention and has been highly researched over the last decade due to its being a low-cost transition metal semiconductor with tunable, yet widely stable, band gaps. This minireview briefly highlights the challenges in the design and synthesis of porous WO including methods, precursors, solvent effects, crystal phases, and surface activities of the porous WO base material. These topics are explored while also drawing a connection of how the morphology and crystal phase affect the band gap.

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Mesoporous oxides are outstanding metal nanoparticle catalyst supports owing to their well-defined porous structures. Such mesoporous architectures not only prevent the aggregation of metal nanoparticles but also enhance their catalytic performance. Metal/metal oxide heterojunctions exhibit unique chemical and physical properties because of the surface reconstruction around the junction and electron transfer/interaction across the interface.

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The direct synthesis of block copolymer vesicles on the scale of tens to hundreds of nanometers using reversible addition-fragmentation chain transfer (RAFT) dispersion polymerization as an effect of chemical oscillations is reported. RAFT polymerization is successfully accomplished between polyethylene glycol containing a RAFT agent (PEG-CTA) and ethyl acrylate monomer in the presence of the Belousov-Zhabotinsky (B-Z) reaction in oscillatory mode. The self-assembly of poly(ethylene glycol)-b-poly(ethyl acrylate) unimers gives rise to spherical micelles.

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The chemical energy and radicals from an oscillating chemical reaction are used to synthesize a polymer vesicle from a homogeneous solution of monomeric units. Periodically formed radicals from the Belousov-Zhabotinsky (B-Z) reaction initiate radical polymerization between a polyethylene glycol based chain transfer agent (PEG-CTA) and hydrophilic acrylonitrile monomers in water. The growth of a hydrophobic chain on the hydrophilic PEG chain induces self-assembly of polymeric amphiphiles to form micrometer-sized vesicles entrapping an active oscillating B-Z reaction.

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Highly ordered mesoporous resol-type phenolic resin and the corresponding mesoporous carbon materials were synthesized by using poly(ethylene oxide-b-caprolactone) (PEO-b-PCL) diblock copolymer as a soft template. The self-assembled mesoporous phenolic resin was found to form only in a specific resol concentration range of 40-70 wt % due to an intriguing balance of hydrogen-bonding interactions in the resol/PEO-b-PCL mixtures. Furthermore, morphological transitions of the mesostructures from disordered to gyroid to cylindrical and finally to disordered micelle structure were observed with increasing resol concentration.

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We introduce a novel application of an oscillatory chemical reaction to the synthesis of block copolymers. The Belousov-Zhabotinsky (B-Z) reaction is coupled with the polymerization of an amphiphilic block copolymer. Radicals generated in the B-Z reaction initiate the polymerization between a polyethylene glycol (PEG) macroreversible addition-fragmentation chain-transfer agent and butyl acrylate monomers.

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We introduce a simple method to prepare hollow carbon nanospheres (HCNs) by using triblock copolymer poly(styrene-b-2-vinylpyridine-b-ethylene oxide) (PS-b-P2VP-b-PEO) micelles as a new class of soft-templates. Simply by changing the solvent we can prepare ultra-small sized micelles of the triblock copolymer PS-b-P2VP-b-PEO soft template to obtain HCNs with ultra-small diameters (43 nm) and hollow cores (19 nm). Furthermore, we use these HCNs to make electric double-layer capacitors (EDLCs) that exhibit superior performance.

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Mesoporous iron phosphate (FePO4 ) was synthesized through assembly of polymeric micelles made of asymmetric triblock co-polymer (polystyrene-b-poly-2-vinylpyridine-b-ethylene oxide; PS-PVP-PEO). The phosphoric acid solution stimulates the formation of micelles with core-shell-corona architecture. The negatively charged PO4 (3-) ions dissolved in the solution strongly interact with the positively charged PVP(+) units through an electrostatic attraction.

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Herein, we introduce a new polypeptide-functionalized mesoporous silica template fabricated from a biodegradable poly(ethylene oxide-b-ɛ-caprolactone) (PEO-b-PCL) diblock copolymer and a poly(tyrosine) (PTyr) biopolymer. The crystallization behavior of the PEO-b-PCL diblock copolymer changes after blending, but the secondary structure of PTry remains stable. After selective solvent extraction in THF, the PEO-b-PCL is removed, but PTyr remains within the silica matrix due to its different solubility.

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Crystallized anatase TiO2 microflowers with high surface area are synthesized by a simple template-free solvothermal method using N,N-dimethylformamide (DMF). Titanium sources undergo well-organized assembly in DMF to form flower-shaped TiO2 particles. After the calcination, the anatase frameworks are highly crystallized, and the surface area is increased up to 256 m2 x g(-1).

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A facile method for the fabrication of well-dispersed mesoporous Pt nanospheres involves the use of a polymeric micelle assembly. A core-shell-corona type triblock copolymer [poly(styrene-b-2-vinylpyridine-b-ethylene oxide), PS-b-P2VP-b-PEO] is employed as the pore-directing agent. Negatively charged PtCl4 (2-) ions preferably interact with the protonated P2VP(+) blocks while the free PEO chains prevent the aggregation of the Pt nanospheres.

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Large-sized (ca. 40 nm) mesoporous Er2O3 thin films are synthesized by using a triblock copolymer poly(styrene-b-2-vinyl pyridine-b-ethylene oxide) (PS-b-P2VP-b-PEO) as a pore directing agent. Each block makes different contributions and the molar ratio of PVP/Er(3+) is crucial to guide the resultant mesoporous structure.

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A hybrid mesoporous TiO2/Zn2Ti3O8 film with a pore size of around 40 nm is successfully synthesized by the polymeric micelle assembly approach. The chemically distinct units of polymeric micelles of the poly(styrene-2-vinylpyridine-ethylene oxide) triblock copolymer simultaneously contribute to the formation of mesoporous TiO2/Zn2Ti3O8 films with enhanced photocatalytic activity during H2 evolution reaction.

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Stimuli-responsive materials are of immense importance because of their ability to undergo alteration of their properties in response to their environment. The properties of such materials can be tuned by subtle adjustments in temperature, pH, light, and so forth. Among such smart materials, multi-stimuli-responsive polymeric materials are of pronounced significance as they offer a wide range of applications and their properties can be tuned through several mechanisms.

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Hyperthermia is one of the promising treatments for cancer therapy. However, the development of a magnetic fluid agent that can selectively target a tumor and efficiently elevate temperature while exhibiting excellent biocompatibility still remains challenging. Here a new core-shell nanostructure consisting of inorganic iron oxide (Fe3O4) nanoparticles as the core, organic alginate as the shell, and cell-targeting ligands (ie, D-galactosamine) decorated on the outer surface (denoted as Fe3O4@Alg-GA nanoparticles) was prepared using a combination of a pre-gel method and coprecipitation in aqueous solution.

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