Faculty Publications
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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 isoelectronic tungsten doping on molybdenum selenide nanostructures and their graphene hybrids for supercapacitors(Elsevier Ltd, 2019) Bhat, K.S.; Nagaraja, H.S.Electrochemical supercapacitors are vital for the advancement of energy storage devices. Herein, we report the synthesis of molybdenum selenide (MoSe 2 ), tungsten-doped molybdenum selenide (W–MoSe 2 ) and their graphene (G) composites (W–MoSe 2 /G) via a facile hydrothermal method. Physiochemical properties of the as-synthesized samples are examined using X-ray diffraction, Raman spectroscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, Brunauer–Emmett–Teller measurements, scanning electron microscopy, high resolution transmission electron microscopy and energy dispersive X-ray spectroscopy measurements. Used as working electrodes for supercapacitors, MoSe 2 nanostructures could deliver the specific capacitance of 106 F g ?1 at 2 mV s ?1 scan rate. Further, doping with tungsten (W) demonstrates the variation of specific capacitances with 2 M % of tungsten as the optimum doping amount, delivering the maximum specific capacitance of 147 F g ?1 . Furthermore, graphene composites of these nanostructures deliver the enhanced specific capacitances of 248 F g ?1 and complimented with excellent capacitance retention capability of 102% for 20000 cycles. © 2019 Elsevier LtdItem Two-Dimensional Cadmium Hydroxide Nanosheets for Electrochemical Capacitors Under High Operating Voltage(Springer, 2020) Bhat, K.S.; Huvinahalli, B.R.; Nagaraja, H.S.Abstract: Electrochemical capacitors are deemed to be the most prospective energy storage devices in the field of alternative energy sources. Here, cadmium hydroxide (Cd(OH)2) nanosheets are hydrothermally synthesized and used as electrodes for supercapacitors. Physiochemical properties of the as-synthesized materials are examined using powder x-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy and energy-dispersive x-ray spectroscopy measurements. Electrochemical investigations reveal an excellent operating potential window of 1.5 V, with the specific capacitance of ? 71 F g?1 at a scan rate of 2 mV s?1. In addition, the Cd(OH)2 electrodes are complemented by good cyclic retention for 2000 cycles. Further, the analysis of the type of charge-storage mechanism reveals prominent contributions from the diffusion-controlled processes. Graphic Abstract: [Figure not available: see fulltext.]. © 2019, The Minerals, Metals & Materials Society.Item ZnWO4/SnO2@r-GO nanocomposite as an anode material for high capacity lithium ion battery(Elsevier Ltd, 2020) Brijesh, K.; Vinayraj, S.; Dhanush, P.C.; Bindu, K.; Nagaraja, H.S.Lithium ion battery (LIB) is widely used energy storage device. Herein, we report the preparation of ZnWO4/SnO2 nanocomposite and ZnWO4/SnO2@r-GO nanocomposite via solvothermal method. The structural, elemental and morphological properties of the prepared samples are characterized using x-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDAX), high-resolution transmission electron microscopy (HR-TEM), Brunauer-Emmett-Teller (BET) measurements, Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) techniques. The prepared samples are tested as an anode for LIB. The ZnWO4/SnO2 (5%) nanocomposite delivers initial discharge capacity of 882 mAh g?1 at a current density of 100 mA g?1, while, the specific capacity increases with the increase of SnO2 upto 10% tested in present case. Further, ZnWO4/SnO2@r-GO nanocomposite exhibits a discharge capacity of 1486 mAh g?1 which is higher than that of ZnWO4/SnO2 nanocomposite. In addition, after 500 cycles ZnWO4/SnO2@r-GO nanocomposite exhibits 89.8% cycle life and 98% of discharge capacity retention. These results indicate that, ZnWO4/SnO2@r-GO nanocomposite is a promising anode material for LIB. © 2020 Elsevier LtdItem Effect of binary zinc-magnesium oxides on polyphenylsulfone/cellulose acetate derivatives hollow fiber membranes for the decontamination of arsenic from drinking water(Elsevier B.V., 2021) Kumar, M.; Isloor, A.M.; Todeti, S.R.; Nagaraja, H.S.; A.F., A.F.; Susanti, R.Arsenic contamination is continuously threatening the safety of drinking water in many parts of the world. The consumption of chronic arsenic contaminated drinking water can cause serious health related issues. Therefore, the synthesis of novel materials is very much essential for the selective removal of arsenic from aqueous solution. In the present investigation, the effect of increased concentrations (0.6, 1.0 and 1.5 wt%) of binary zinc-magnesium oxide (ZnO-MgO) on cellulose acetate (CA)/polyphenylsulfone (PPSU) and cellulose acetate phthalate (CAP)/PPSU hollow fiber membranes for arsenic removal was performed. As used ZnO-MgO was characterized by using x-ray diffraction (XRD), transmission electron microscopy (TEM) and particle size distribution. Fabricated hollow fiber membranes were characterized using scanning electron microscopy (SEM), atomic force microscopy (AFM), zeta potential, fourier transform infrared (FTIR), x-ray photoelectron spectrophotometer (XPS), thermogravimetric analysis (TGA) and antifouling studies. The results revealed that, there is significant enhancement in the overall performance of the ZnO-MgO containedmembranes. An enhancement of arsenic removal properties was demonstrated from 0.6 wt% of ZnO-MgO in CAP/PPSU (ZMCAP-0.6) membrane was 81.31% with the retention permeability of 69.58 L/m2h bar respectively. Similarly, 1 wt% of ZnO-MgO in CA/PPSU (ZMCA-1) was found to be 78.48% and 198.47 L/m2h bar respectively using 1 ppm laboratory prepared aqueous arsenic solution (pH 6.8 ± 0.2) at 1 bar transmembrane pressure. In addition, improved antifouling properties was noticed with an increased flux recovery ratio and enhanced thermal stability from ZnO-MgO contained membranes. Therefore, as fabricated ZnO-MgO contained membranes provided enhanced arsenic removal tendency without compromising the retention permeability. © 2020Item Synergistic boost in Fe3O4 anode performance for li-ion batteries via Zn and Cu double doping and multi-walled carbon nanotube composite integration(Elsevier B.V., 2024) Kumar, A.; Mukesh, P.; Lakshmi Sagar, G.; Hegde, A.; Nagaraja, H.S.In this study, a novel nanocomposite material comprising pure Fe3O4 (FO), doped Zn0.5Cu0.5Fe2O4-3 (ZCFO-3), and Zn0.5Cu0.5Fe2O4-3@ Multi-walled carbon nanotube (ZCFO-3@MWCNT) nanocomposite material is carefully prepared using a simple one-step hydrothermal process. Comprehensive surface and morphological analysis are conducted using X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), and High-resolution transmission electron microscopy (HRTEM), while compositional studies are investigated through Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). The electrochemical performance is fully analyzed through Cyclic voltammetry (CV), Electrochemical impedance spectroscopy (EIS), rate capability tests, discharge/charge capacity, and cyclic stability evaluations. Among these three nanomaterials, ZCFO-3@MWCNT nanocomposite at 100 mA g−1 current density reveals the best performance, with a discharge capacity of 1974 mAh g–1, ZCFO-3 and FO reveal 1340 mAh g–1 and 1317 mAh g–1 respectively. After 800 cycles at 500 mA g−1 current density, ZCFO-3@MWCNT stays strong with a discharge capacity of 646 mAh g–1, while ZCFO-3 manages only 362 mAh g–1 and FO only 111 mAh g–1. After 1200 cycles at 500 mA g−1, the nanocomposite still delivers 518 mAh g–1. This study suggests that ZCFO-3@MWCNT could be a promising anode material for lithium-ion batteries. © 2024 Elsevier B.V.Item Novel Ag2Cu2O3 nanorods as stable anode material for lithium-ion battery(Elsevier B.V., 2025) Kumar, A.; Sagar G, L.; P, M.; Hegde, A.P.; Nagaraja, H.S.In this research novel Ag2Cu2O3 nanorods was prepared, for lithium-ion battery as anode, using facile co-precipitation method with four different stirring time and correspondingly Ag2Cu2O3 named ACO – 30 M, ACO – 12 H, ACO – 24 H, and ACO – 36 H. Field Emission Scanning Electron Microscopy (FESEM) and High-Resolution Transmission Electron Microscopy (HRTEM) analyze surface and morphology, while X-ray Diffraction (XRD) examines structural properties. Compositional analysis is carried out using X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. The electrochemical analysis is evaluated by cyclic stability, rate capability, discharge/charge capacity, electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV). The ACO – 24 H nanomaterial demonstrates an initial discharge capacity of 943 mAh g?1 at a current density of 50 mA g?1. Among the four materials tested, ACO – 24 H shows superior cycling performance, with a discharge capacity of 174 mAh g?1 at 200 mA g?1 after 1003 cycles. In comparison, ACO – 30 M, ACO – 12 H, and ACO – 36 H exhibit capacities of 134 mAh g?1, 91 mAh g?1, and 43 mAh g?1, respectively, under the same conditions. This study suggests that ACO – 24 H is a promising anode material for lithium-ion battery applications. © 2025 Elsevier B.V.