Faculty Publications
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Item Polyoxomolybdate-Polypyrrole-Graphene Oxide Nanohybrid Electrode for High-Power Symmetric Supercapacitors(American Chemical Society, 2021) Maity, S.; Je, M.; Biradar, B.R.; Chandewar, P.R.; Shee, D.; Das, P.P.; Mal, S.Supercapacitors have emerged as one of the most promising candidates for high-performance, safe, clean, and economical routes to store and release of nonfossil energy. Designing hybrid materials by integrating double-layer and pseudocapacitive materials is crucial to achieving high-power and high-energy storage devices simultaneously. Herein, we synthesized a polyoxomolybdate-polypyrrole-graphene oxide nanohybrid via a one-pot reaction. The inclusion of polypyrrole enables a uniform distribution of the polyoxomolybdate clusters; it also confines the restacking of graphene oxide nanosheets. The structural and morphological analysis to unveil the nanohybrid architecture implies excellent interfacial contact, enabling fast redox reaction of polyanions, and a quick transfer of charge to the interfaces. Electrochemical characteristics tested under a two-electrode system exhibit the highest capacitance of 354 F g-1 with significantly high specific energy and power of 49.16 Wh kg-1 and 999.86 W kg-1, respectively. In addition, the cell possesses a high-rate capability and long cycle life by maintaining 96% of its capacitance over 5000 sweeping cycles. The highest specific power of ?10 »000 W kg-1 was computed with Coulombic efficiency of 92.30% at 5 A g-1 current density. Electrochemical impedance spectroscopy additionally reveals enhanced redox charge transfer due to double hybridization. Furthermore, it also demonstrates the impedance and capacitive behavior of supercapacitor cells over a definite frequency regime. ©Item Exploring the Synergy of B, Ce Dopants in Codoped Titanium Dioxide Multifunctional Photocatalysts for Antibiotic Degradation and Microbial Disinfection Under Solar Light(John Wiley and Sons Inc, 2022) Manjunatha, M.; Chandewar, P.R.; Mahalingam, H.An eco-friendly, controllable citrate-EDTA complexing sol–gel method is employed to systematically synthesize a series of BxCe1−xTiO2 (x = 0.9, 0.8, 0.7 at%) codoped photocatalysts. The degradation of ciprofloxacin (CIP) and norfloxacin (NOR) antibiotics, as well as Escherichia coli disinfection under sunlight, is assessed using these synthesized codoped photocatalysts. After physicochemical characterization of the synthesized catalysts for particle size, surface area, morphology, crystal structure, surface chemistry, bandgap energy values, and recombination, it is evident that the codoping has improved the visible light absorption, reduced the recombination, and promoted higher crystallinity as well as anatase phase content. The codoped catalysts also demonstrate an enhanced photocatalytic activity under solar light with regard to the degradation of the chosen antibiotics when compared to the performance of the monodoped counterparts or the latest generation catalysts from the literature. The highest degradation performance (≈98%) is shown by B0.8Ce0.2TiO2 in the case of CIP and B0.9Ce0.1TiO2 in the case of NOR. Also, in the case of microbial disinfection, these codoped catalysts are much better (by a factor of ≈10) than that of the monodoped catalysts. © 2021 Wiley-VCH GmbH.Item Vanadomanganate as a synergistic component in high-performance symmetric supercapacitor(Elsevier Ltd, 2022) Maity, S.; Anandan Vannathan, A.A.; Chandewar, P.R.; Shee, D.; Das, P.P.; Mal, S.S.Supercapacitor devices fabricated from capacitive and battery-type hybrid electrodes have been projected as a promising energy storage system because of their ability to produce high specific power and energy simultaneously. In this work, we have demonstrated a facile method of impregnation of faradaic type manganese (III) polyoxovanadate, [MnV14O40]−6 on the high surface area substrate of activated carbon (AC) as well as graphene oxide (GO). Materials and electrochemical characterizations data confirm the successful incorporation of capacitive and faradaic type manganese (III) polyoxovanadate into the nanohybrid electrode material. Furthermore, the synergic effect between the carbonaceous nanostructures (AC/GO) and redox-active oxometalate (MnV14) provides a better pathway for ion transport to the interface resulting in enhancement of the conductivity, diffusion ability of the nanohybrid. Moreover, the battery-type MnV14 clusters disperse in the micro/mesopores of AC, whereas the oxygen-containing functional groups in GO act as active sites for anchoring of MnV14 clusters. Thus, the surface modification with MnV14 clusters enhances the specific capacitance of nanohybrid with remarkable electrical and mechanical stability. The AC/MnV14 nanohybrid exhibits an enhanced specific capacitance of 547 F g−1 with specific energy and power of 76 Wh kg−1 and 1600 W kg−1, respectively, at 0.8 A g−1 current density. Additionally, GO/MnV14 shows a specific capacitance of 330 F g−1 with improved specific energy and power of 30 Wh kg−1 and 1276 W kg−1, respectively, at the same current density. Moreover, both the nanohybrids possess excellent cycle stability by retaining 92% (AC/MnV14) and 90.6% (GO/MnV14) of initial capacitance even after 5000 sweeping cycles. © 2021 Elsevier B.V.Item Phosphomolybdic acid embedded into biomass-derived biochar carbon electrode for supercapacitor applications(Elsevier B.V., 2023) J.e, M.; Chandewar, P.R.; Shee, D.; Mal, S.S.In high-performance, clean, safe, and cost-effective ways, supercapacitors are among the most promising ways to store and release nonfossil energy. In recent years, renewable biomass-derived activated carbon has been explored as a potential option for electrode material. It restricts their specific capacitance despite being environment-friendly and possessing intrinsic mechanical strength. In order to overcome this limitation and preserve all other properties, we are infusing polyoxometalate into the activated carbon; this increases specific capacitance with its fast reversible redox behaviour and preserves the carbon's characteristics. Beside suffusing phosphomolybdic acid (PMA) into biomass waste material, such as orange peel-derived activated carbon (OPAC), a new hybrid material (OPAC-PMA) was developed. The nanohybrid design was revealed by structural and morphological research, which showed high interfacial contact, allowing polyanions to redox rapidly. The novel hybrid electrode material (OPAC-PMA) has a capacitance value of 66% higher than the bare OPAC electrode. A further study showed that OPAC-PMA composite showed 88.23% cycle stability in 0.5 M H2SO4 electrolyte at 6 A g−1 for 4000 cycles. © 2023 Elsevier B.V.Item High-performance hybrid supercapacitor-immobilized Wells-Dawson polyoxometalates on activated carbon electrodes(Royal Society of Chemistry, 2023) Madhusree, J.E.; Chandewar, P.R.; Shee, D.; Mal, S.S.The nanofabrication of electroactive hybrid materials for next-generation energy storage devices is becoming increasingly significant as supercapacitor (SC) technology develops rapidly. The present study utilizes activated carbon (AC) templates reinforced with Wells-Dawson polyoxotungstates (POMs) to produce nanohybrid electrodes for high-performance supercapacitors. This study analyzes Wells-Dawson polyoxotungstates (P2W18) for the first time integrated with AC, and its structural and electrochemical performances are discussed. First, the electrochemical performances of symmetric supercapacitors were characterized in an acidic aqueous electrolyte (0.5 M H2SO4). It was observed that a supercapacitor cell containing the 5 wt% AC-P2W18 hybrid symmetric displayed a noteworthy specific capacitance of 289 F g−1 and a remarkable energy density of 40 W h kg−1. Moreover, 5% AC-P2W18 symmetric supercapacitor cells showed 89% cyclic stability over 4000 cycles. Three LED lights were charged onto the electrode. The LEDs continued to illuminate continuously for red until 160 seconds, yellow until 20 seconds, and blue until 10 seconds after removing the electrode from the electrochemical workstation, demonstrating the device's power and energy density. © 2023 The Royal Society of Chemistry.Item Synergistic Enhancement of Supercapacitor Performance: Vanadium-Substituted Phosphotungstic and Molybdic Acid Combined with Polypyrrole Using Pyridinium and Ammonium Ionic Containing Organic Cation Linkers with Improved Conductivity(John Wiley and Sons Inc, 2024) Puniyanikkottil, M.A.; Chandewar, P.R.; Shee, D.; Mal, S.S.High-performance energy-storage devices have emerged as a favored choice owing to their remarkable efficiency, sustainability, and environmental friendliness. Nowadays, polyoxometalate (POM)-based supercapacitor (SC) electrode materials have gained much attention. Herein, a few new POMs and ionic liquid (IL) composites incorporated into conducting polymer as electrode materials for SC applications are reported. The H6[PV3Mo9O40]⋅34H2O (PV3Mo9) and H6[PV3W9O40].34H2O (PV3W9) POMs are treated with tetrabutylammonium chloride and 1-butyl-4-methyl pyridinium chloride (BMP) and finally combined with polypyrrole (PPy) for the SC studies. An extensive array of analytical techniques is employed to delve into the interplay between the constituents within the composite materials, such as Fourier transform infrared spectroscopy, powder X-ray diffraction, thermogravimetric analysis, nuclear magnetic resonance (1H and 13C), Field-emission scanning electron microscopy, energy-dispersive X-ray stpectroscopy, X-ray photoelectron spectroscopy, and Brunauer-Emmett-Teller surface area. The combined application of these techniques enables us to understand the interaction dynamics within composite materials comprehensively. POM–ILs combination improves the solubility issues of POMs, and doping of PPy enhances the electrochemical performances of the materials. The PV3W9–BMP–PPy symmetric SC cell shows a specific capacitance of 294.79 F g−1 and an energy density of 28.89 Wh kg−1 at 1 A g−1 current density in 0.25 M H2SO4 medium followed by an excellent cycle life of 78.6% after 10,000 galvanostatic charge–discharge cycles. The fabricated SC device is performed to light up the bulbs of red, yellow, and green light emitting diodes for 50, 30, and 28 s, respectively. © 2024 Wiley-VCH GmbH.