Faculty Publications
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Item Growth and morphology of mixed K1-x(NH4)xH2PO4 crystals(Elsevier Ltd, 2010) Shenoy, P.; Bangera, K.V.; Shivakumar, G.K.Mixed crystals of ammonium dihydrogen orthophosphate (ADP) and potassium dihydrogen orthophosphate (KDP), i.e., potassium ammonium dihydrogen phosphate, K1-x(NH4)xH2PO4 have been grown by slow evaporation from the supersaturated solution at an ambient temperature 26 ± 1 °C for ammonium concentration x in the range 0.0 ? x ? 1.0. The morphology changes from tetragonal prism to needles when the concentration of either of the components approaches that of the other. Induction periods were measured for various compositions of mixed crystals of ADP and KDP by the direct vision method. Crystal compositions were determined by flame atomic absorption spectroscopy and also by chemical analysis. Results of the X-ray analysis of the grown crystals are also reported. Maximum size of the grown mixed crystal was around 16 × 10 × 4 mm3. © 2010 Elsevier B.V. All rights reserved.Item LiClO4-doped plasticized chitosan and poly(ethylene glycol) blend as biodegradable polymer electrolyte for supercapacitors(Institute for Ionics, 2013) Sudhakar, Y.N.; Muthu, M.; Bhat, D.K.Biodegradable polymer electrolyte comprising the blend of chitosan (CS) and poly(ethylene glycol) (PEG) plasticized with ethylene carbonate and propylene carbonate, as host polymer, and lithium perchlorate (LiClO4), as a dopant, was prepared by solution casting technique. The ionic conductivity has been calculated using the bulk impedance obtained through impedance spectroscopy. The variation of conductivity and dielectric properties has been investigated as a function of polymer blend ratio, plasticizer content and LiClO4 concentration at temperature range of 298-343 K. The DSC thermograms show two broad peaks for CS/PEG blend and increased with increase in the LiClO4 content. The maximum conductivity has been found to be 1. 1 × 10-4 S cm-1 at room temperature for 70:30 (CS/PEG) concentration. The electric modulus of the electrolyte film exhibits a long tail feature indicative of good capacitance. The activation energy of all samples was calculated using the Arrhenius plot, and it has been found to be 0. 12 to 0. 38 eV. A carbon-carbon supercapacitor has been fabricated using this electrolyte, and its electrochemical characteristics and performance have been studied. The supercapacitor showed a fairly good specific capacitance of 47 F g-1. © 2012 Springer-Verlag.Item Porous nickel telluride nanostructures as bifunctional electrocatalyst towards hydrogen and oxygen evolution reaction(Elsevier Ltd, 2017) Bhat, K.S.; Barshilia, H.C.; Nagaraja, H.S.Electrochemical water splitting technology has attracted researchers for the development of next generation fuels. Herein, we report the synthesis of nanostructured porous hollow nickel telluride nanosheets and their use as bifunctional electrocatalyst towards hydrogen and oxygen evolution reaction, anticipating an enhanced performance owing to their 2D sheet like morphology, conductivity, porous nature providing larger catalytic surface for water splitting reaction. In this regard, nickel telluride nanostructures were synthesized via an anion-exchange-reaction between pre-synthesized nickel hydroxide hexagonal nanosheets and tellurium ions under hydrothermal conditions. The as-synthesized nanostructures were characterized for structural, morphological and compositional properties using X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, high resolution transmission electron microscopy and energy dispersive X-ray spectroscopy. Nickel telluride modified electrodes were tested as bifunctional electrocatalyst under acidic and alkaline conditions, through linear sweep voltammetry and constant current chronopotentiometry methods. The modified electrodes revealed an onset potential of ?422 mV and 87.4 mV dec?1 Tafel slope towards HER and overpotential of 679 mV and 151 mV dec?1 Tafel slope towards OER. The lower onset potentials are complimented with excellent electrocatalytic stability. © 2017 Hydrogen Energy Publications LLCItem Porous cobalt chalcogenide nanostructures as high performance pseudo-capacitor electrodes(Elsevier Ltd, 2017) Bhat, K.S.; Shenoy, S.; Nagaraja, H.S.; Sridharan, K.Electrochemical supercapacitor is an essential technology that is pivotal for the development of reliable energy storage devices. Herein, we report the fabrication of supercapacitor electrodes using nanostructured porous cobalt chalcogenide (CoTe2 and CoSe2) electrodes, anticipating an enhanced performance owing to their higher contact area with electrolyte and large pore volume enabling shorter diffusion paths for ion exchange. In this regard, we synthesized CoTe2 and CoSe2 nanostructures via an anion-exchange-reaction between pre-synthesized Co(OH)2 hexagonal nanosheets and chalcogen (tellurium and selenium) ions under hydrothermal conditions. Structural, morphological and compositional properties of the as-synthesized materials are examined using X-ray diffraction, Raman spectroscopy, scanning electron microscopy, high resolution transmission electron microscopy and energy dispersive X-ray spectroscopy. Pseudo-capacitive properties of CoTe2 and CoSe2 nanostructures as working electrodes are studied through cyclic voltammetry and galvanostatic charge-discharge methods using an electrochemical workstation. CoSe2 electrode delivered a specific capacitance of 951 F g?1 at a scan rate of 5 mV s?1, which surprisingly is almost three times higher in comparison to CoTe2 electrode (360 F g?1). Both CoTe2 and CoSe2 electrodes exhibited good capacitance retention capability for 2500 CV cycles. The superior electrochemical performance of the nanoporous CoSe2 electrode indicate their applicability for high-performance energy storage device applications. © 2017 Elsevier LtdItem Effect of oxygen substitution and phase on nickel selenide nanostructures for supercapacitor applications(Institute of Physics Publishing helen.craven@iop.org, 2018) Bhat, K.S.; Nagaraja, H.S.Electrochemical supercapacitors are the eminent technology for the progress of energy storage devices. The current manuscript deals with the formation of oxygen substituted nickel selenide nanostructures and their use as active electrode material for supercapacitor, expecting an enhanced performance owing to their sheet-like geometry, high specific surface area and porous assembly. In this context, Ni(OH)2 (nickel hydroxide) nanostructures were synthesized employing one-pot hydrothermal method and the ion-exchange reaction of Ni(OH)2 nanostructures with selenium resulted in cubic-NiSe2 (nickel selenide) nanostructures. Further, annealing NiSe2 nanostructures at intermediate pressure (10-3 Torr) has realized the partial oxygen substitution in place of selenium, resulting in NiSe/NiO nanostructures along with phase change from cubic-NiSe2 to hexagonal-NiSe. Supercapacitor electrodes fabricated using NiSe/NiO nanostructures delivered the specific capacitance of 83.5 F g-1 at the scan rate of 2 mV s-1, which is surprisingly more than a double as compared with pristine NiSe2 electrodes (37.4 F g-1). Annealing at intermediate pressure and high temperature significantly enhanced the specific capacitances of the nanostructured electrodes and also accompanied with the good capacitance retention of 94% for 5000 CV cycles. © 2018 IOP Publishing Ltd.Item An electroactive ?-phase polyvinylidene fluoride as gel polymer electrolyte for magnesium–ion battery application(Elsevier B.V., 2019) Singh, R.; Janakiraman, S.; Khalifa, M.; Anandhan, S.; Ghosh, S.; Adyam, A.; Biswas, K.The gel polymer electrolytes (GPEs) are currently interesting research area in rechargeable batteries. In the present study, synthesis and characterization of electroactive gel polymer electrolyte (EGPE) for Mg-ion batteries application have been investigated. The bead free electroactive polyvinylidene fluoride (PVDF) with high porosity is achieved by an electrospinning process. The ?-phase of PVDF is polar and electroactive with a high dipole moment. Electroactive ?-phase is confirmed by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). Field emission scanning electron microscopy (FESEM) study is done to analyze the structure and morphology of the electroactive membrane. The electroactive gel polymer electrolyte is formed by immersing an electroactive PVDF membrane in 0.3 M magnesium perchlorate (MgClO4) and propylene carbonate (PC) solution. The ionic conductivity of electroactive ?-phase PVDF membrane is achieved to be 1.49 mS cm?1 at 30 °C, which is higher than commercial available polypropylene (PP) Celgard. Tortuosity of electroactive gel polymer electrolyte is found to be 1.44. The voltage stability of the EGPE is stable up to a high voltage of 5.0 V against Mg+2/Mg. The total ionic transference number and magnesium ion transference number of EGPE are also investigated to confirm high ionic conductivity. © 2019 Elsevier B.V.Item A high thermally stable polyacrylonitrile (PAN)-based gel polymer electrolyte for rechargeable Mg-ion battery(Springer, 2020) Singh, R.; Janakiraman, S.; Khalifa, M.; Anandhan, S.; Ghosh, S.; Adyam, A.; Biswas, K.The ionic conductivity and thermal stability of the electrolyte-separator system is an essential parameter for improving battery performance and safety. The present work addresses the high thermally stable gel polymer electrolyte (GPE) using polyacrylonitrile (PAN) as a polymer membrane and magnesium perchlorate in propylene carbonate (Mg(ClO4)2-PC) as a liquid electrolyte. The PAN based polymer membrane is prepared by electrospinning process which produces a bead free and uniformly distributed nanofibers. The electrospun PAN based GPE is characterized by different physical and electrochemical techniques like X-ray diffraction, field emission scanning electron microscopy, thermogravimetric analysis, differential scanning calorimetry, ionic conductivity, linear sweep voltammetry, magnesium ion transference number and electrochemical impedance spectroscopy. The ionic conductivity of PAN is 3.28 mS cm?1, compared to that of PP Celgard is 1.97 × 10–4 mS cm?1 at 30 °C. The electrochemical stability of PAN is 4.6 V and also exhibits excellent interfacial stability with magnesium metal. The results showed that the PAN-based GPE has higher ionic conductivity and thermal stability than the polypropylene (PP) Celgard membrane. © 2020, Springer Science+Business Media, LLC, part of Springer Nature.Item Impact of copper doping on the electrochemical response of MnSe2 as anode for lithium-ion battery(Springer, 2024) Mukesh, P.; Lakshmi Sagar, G.; Brijesh, K.; Kumawat, S.; Hegde, A.; Kumar, A.; Nagaraja, H.S.Transition Metal Chalcogenides (TMC), due to their unique physicochemical properties, are studied in various fields and have potent applications in energy storage applications. This work is based on the synthesis and characterization of copper-doped manganese di-selenide and the effect of its doping on electrochemical performance as anode material for lithium-ion battery applications using the solvothermal method. The characterization techniques used are X-ray diffraction, Raman spectroscopy, field-emission scanning electron microscopy, XPS, UV–visible absorption spectroscopy, and electrochemical analysis. The XRD data confirms the formation of MnSe2 exhibiting Cubic crystal geometry. The FESEM images show the micro-cube-like structure with agglomerated nanocluster nanostructures on the surface with a dimension of 100–200 nm. The doping of the copper has decreased the band gap of the MnSe2, as studied by the UV–visible absorption spectrum. The electrochemical performance is analyzed as anode material for lithium-ion batteries. The charge/discharge measurements show a specific capacity of 706 mAh g−1 as the initial discharge capacity and 336 mAh g−1 as the initial charge capacity at 0.1 A g−1 current density. Meanwhile, 3% Copper-doped MnSe2 showed a better specific capacity of 878 mAh g−1 as the initial discharge capacity and 461 mAh g−1 as the initial charge capacity at 0.1 A g−1 current density. Cyclic stability, rate capability, and electrochemical impedance spectroscopy were performed, and it shows that 3% copper-doped MnSe2 has good stability and better conductivity and charge kinetics, indicating copper doping has enhanced the electrochemical performance of pristine MnSe2. © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2024.