Publications by authors named "Bikash Kumar Jena"

The rational design and synthesis of bifunctionally active and durable oxygen electrocatalysts have garnered significant attention for electrochemical energy conversion and storage. Intermetallic nanostructures are particularly promising for these applications due to their unique catalytic properties and exceptional durability. In this study, we present a fascinating synthetic approach for the direct synthesis of a bifunctional oxygen electrocatalyst based on nitrogen-doped carbon-encapsulated ordered PdFe (o-PdFe@NC) intermetallic, using a cyano-bridged bimetallic single-source precursor tailored for aqueous rechargeable zinc-air batteries (ZABs).

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Herein, a microporous organic-inorganic hybrid, vanadium phosphonate (VPn) material has been developed. With the combined advantages of the periodic organic-inorganic skeleton, a regular microporous channel with a crystalline pore wall, and good surface area, VPn displays electrocatalytic NRR activity with a selective NH yield (11.84 μg h mg), faradaic efficiency of 26.

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Multifunctional devices integrated with electrochromic and supercapacitance properties are fascinating because of their extensive usage in modern electronic applications. In this work, vanadium-doped cobalt chloride carbonate hydroxide hydrate nanostructures (V-CH NSs) are successfully synthesized and show unique electrochromic and supercapacitor properties. The V-CH NSs material exhibits a high specific capacitance of 1219.

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The hydrogen-bonded organic frameworks (HOFs) have gained significant attention due to their various alluring applications in the fascinating field of supramolecular chemistry. Herein, we report the electrocatalytic activity of HOFs toward the hydrogen evolution reaction (HER) by utilizing the molecular adduct of cyanuric and trithiocyanuric acid with various organic substrates (melamine and 4,4'-bipyridine). Both the experimental and theoretical findings provide insights and validate the electrocatalytic activity toward HER applications.

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Herein, a one-step hydrothermal reaction is developed to synthesize a Ni-doped ReS nanostructure with sulphur defects. The material exhibited excellent OER activity with a current density of 10 mA cm at an overpotential of 270 mV, a low Tafel slope of 31 mV dec, and good long-term durability of 10 h in 1 M KOH. It shows high faradaic efficiency of 96%, benefiting from the rapid charge transfer caused by the concerted effect of Ni-in and S-out on the ReS nanostructure.

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Hydrogen evolution reaction (HER) by electrochemical water splitting is one of the most active areas of energy research, yet the benchmark electrocatalysts used for this reaction are based on expensive noble metals. This is a major bottleneck for their large-scale operation. Thus, development of efficient metal-free electrocatalysts is of paramount importance for sustainable and economical production of the renewable fuel hydrogen by water splitting.

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The electrochemical energy conversions play an essential role in the production of sustainable and renewable energy. However, the performance is not up to the mark due to the absence of highly efficient and stable electrocatalysts. Recently, both 2D-matrix and single-atom catalysts (SACs) are two intense research topics in the field of electrocatalysis due to the high activity and stability and to maximize the utilization efficiency.

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In recent years, several novel strategies for speeding up the slow kinetics of the water oxidation reaction have attracted considerable attention for generation of O2. This is particularly important from the environmental perspective. Here we report a SBA-15 type, 2D-hexagonal functionalized mesoporous organosilica material as support for small Ag nanoparticles (NPs) by grafting the silica surface with 3-aminopropyltriethoxysilane, followed by chemical impregnation of Ag NPs at its surface, to obtain a AgNPs@SBA-NH2 material.

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The development of efficient materials for the generation and storage of renewable energy is now an urgent task for future energy demand. In this report, molybdenum disulphide hollow sphere (MoS-HS) and its reduced graphene oxide hybrid (rGO/MoS-S) have been synthesized and explored for energy generation and storage applications. The surface morphology, crystallinity and elemental composition of the as-synthesized materials have been thoroughly analysed.

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Room-temperature stabilization of metastable β-NiMoO is achieved through urea-assisted hydrothermal synthesis technique. Structural and morphological studies provided significant insights for the metastable phase. Furthermore, detailed electrochemical investigations showcased its activity toward energy storage and conversion, yielding intriguing results.

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Here, a facile one-step approach has been developed for the synthesis of carbon quantum dots (CQDs) from Good's buffer. The as-synthesized CQDs emit a bright greenish blue coloured fluorescence after exposure to a 365 nm UV-lamp illumination. The bright fluorescence nature of the CQDs has proven them to be excellent probes for cellular imaging.

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A stripy pattern of continuous epitaxial growth of thin Au nanowires on plasmonic Cu3P platelets is reported. The obtained Au-Cu3P heterostructures retain their wide area interfacial heterojunction, which is typically not observed in metal-semiconductor heterostructures. This is performed by phosphine-mediated in situ reduction of Au ions on specific facets of Cu3P platelets.

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A simple single-step chemical vapor deposition (CVD) method has been used to grow the faceted Au-ZnO hetero-nanostructures (HNs) either with nanowires (NWs) or with triangular nanoflakes (TNFs) on crystalline silicon wafers with varying oxygen defect density in ZnO nanostructures. This work reports on the use of these nanostructures on substrates for photodegradation of rhodamine B (RhB) dyes and phenol under the visible light illumination. The photoluminescence measurements showed a substantial enhancement in the ratio of defect emission to band-edge emission for TNF (ratio ≈ 7) compared to NW structures (ratio ≤ 0.

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A facile and green approach for the synthesis of highly electroactive branched Pt nanostructures well dispersed on graphene has been developed by in situ reduction of graphene oxides and Pt(iv) ions in an aqueous medium. The as-synthesized branched Pt and graphene hybrid nanomaterials (GR-BPtNs) were thoroughly characterized using Transmission Electron Microscope (TEM), UV-Visible spectroscopy, Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA) and Raman spectroscopy. This report clearly exploits the decisive role of the graphene support, the pH of the solution and the stabiliser on shaping the branched morphology of the Pt nanostructures well dispersed on graphene.

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A new approach for shaping Au nanostructures by tuning the molecular structure of biomolecules has been explored. Different molecules, such as catechol, rutin, and quercetin, which have structural similarity to the catechol ring, were used to induce Au nanostructures under similar conditions. The as-synthesized nanostructures are characterized by using TEM, XPS, XRD, and UV/Vis spectral measurements.

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A facile approach has been developed for synthesis of highly-structured, anisotropic Pd nanostructures. The dendritic Pd nanostructures show superior performance toward oxidation of formic acid and methanol for fuel cell application.

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A novel 3-D nanoarchitectured platform based on Pt nanoparticles (nPts) is developed for the sensing of sub-nanomolar levels of hydrogen peroxide and for the fabrication of amperometric biosensor for uric acid, cholesterol and glucose. The nPts have been immobilized on the thiol functional group containing sol-gel silicate 3-D network derived from 3-mercaptopropyltrimethoxysilane (MPTS). The nanoparticles on the 3-D architecture have size distribution between 7 and 10nm.

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Here we report a new type of microelectrode sensor for single-cell exocytotic dopamine release. The new microsensor is built by forming a gold-nanoparticle (AuNP) network on a carbon fiber microelectrode. First a gold surface is obtained on a carbon fiber microdisk electrode by partially etching away the carbon followed by electrochemical deposition of gold into the pore.

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In this technical note, we report a process in scaling down the fabrication of Au disk nanoelectrodes as small as approximately 4 nm in radii. We have developed a bottom-up approach toward the fabrication of individual disk-shape Au nanoelectrodes. This new approach is based upon electrochemical deposition of Au in a silica nanopore electrode and involves the following four steps.

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Au nanoparticle (nAu) based electrochemical platform for the amperometric sensing of isoniazid at sub-nanomolar level is developed. The sol-gel derived 3-dimensional silicate network pre-assembled on a conducting substrate is chemically decorated with nAu of 70-100 nm by seed-mediated growth approach. The Au nanoseeds are first chemisorbed onto the thiol functional groups of the silicate network and their size was enlarged by hydroxylamine seeding.

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Gold nanoparticle based nanostructured electrode has been developed for the amperometric detection of ultratrace amount of toxic Cr(VI). The nano-sized Au particles have been grown on a conducting substrate modified with sol-gel-derived thiol functionalized silicate network and used for the electroanalysis of Cr(VI). The nanostructured interface show well-defined voltammetric peak for the reduction of Cr(VI) at approximately 0.

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Simultaneous electrochemical detection of As(III), Hg(II), and Cu(II) using a highly sensitive platform based on gold nanoelectrode ensembles (GNEEs) is described. GNEEs were grown by colloidal chemical approach on thiol-functionalized solgel derived three-dimensional silicate network preassembled on a polycrystalline gold (Au) electrode. GNEEs on the silicate network have been characterized by field emission scanning electron microscopy, X-ray diffraction, diffuse reflectance spectroscopy, and electrochemical measurements.

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A simple optical method for the sensing of biomedically important polyionic drugs, protamine and heparin based on the reversible aggregation and de-aggregation of gold nanoparticles (AuNPs) is described. The polycationic protamine induces the aggregation of negatively charged citrate-stabilized AuNPs, resulting in a shift in the surface plasmon (SP) band and a consequent color change of the AuNPs from red to blue. Addition of polyanionic heparin dissipates the aggregated AuNPs due to its strong affinity to protamine and the blue color changes to the native color.

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This article describes the synthesis of branched flower-like gold (Au) nanocrystals and their electrocatalytic activity toward the oxidation of methanol and the reduction of oxygen. Gold nanoflowers (GNFs) were obtained by a one-pot synthesis using N-2-hydroxyethylpiperazine-N-2-ethanesulphonic acid (HEPES) as a reducing/stabilizing agent. The GNFs have been characterized by UV-visible spectroscopy, transmission electron microscopy (TEM), X-ray diffraction (XRD), and electrochemical measurements.

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