Faculty Publications

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    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.
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    Nickel selenide nanostructures as an electrocatalyst for hydrogen evolution reaction
    (Elsevier Ltd, 2018) Bhat, K.S.; Nagaraja, H.S.
    Electrochemical water splitting has gained momentum for the development of alternative energy sources. Herein, we report the synthesis of two different nickel selenide nanostructures of different morphology and composition employing hydrothermal method. NiSe2 nanosheets were obtained by the anion-exchange reaction of Ni(OH)2 with Se ions for 15 h. On the other hand, NiSe nanoflakes were synthesized by the direct selenization of nickel surface with the reaction time of 2 h. Tested as an electrocatalyst for hydrogen evolution reaction, NiSe2 nanosheets and NiSe nanoflakes can afford a geometric current density of 10 mA cm?2 at an overpotential of 198 mV and 217 mV respectively. The measured Tafel slope values of NiSe nanoflakes are 28.6 mV dec?1, which is three times lower as compared with NiSe2 nanosheets (72.1 mV dec?1). These results indicates the HER kinetics of NiSe nanoflakes are at par with the state-of-the-art Pt/C catalyst and also complimented with the short synthesis time of 2 h. Further, both nickel selenides exhibit ultra-long term stability for 30 h as evident from constant current chronopotentiometry and electrochemical impedance spectroscopy results. © 2018 Hydrogen Energy Publications LLC
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    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 Ltd
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    Performance evaluation of molybdenum dichalcogenide (MoX2; X= S, Se, Te) nanostructures for hydrogen evolution reaction
    (Elsevier Ltd, 2019) Bhat, K.S.; Nagaraja, H.S.
    Hydrogen evolution reaction (HER) using transition metal dichalcogenides (TMDs) have gained interest owing to their low-cost, abundancy and predominant conductivity. However, forthright comparisons of transition metal chalcogenides for HER are scarcely conducted. In this work, we report the synthesis of series of molybdenum chalcogenide nanostructures MoX2 (X = S, Se, Te) via a facile hydrothermal method. Used as an electrocatalyst for HER, MoS2 nanograins, MoSe2 nanoflowers and MoTe2 nanotubes could afford the benchmark current densities of 10 mA cm?2 at the overpotentials of ?173 mV, ?208 mV and ?283 mV with the measured Tafel slope values of 109.81 mV dec?1, 65.92 mV dec?1 and 102.06 mV dec?1, respectively. Besides other factors influencing HER, the role of electronic conductivity in HER of these molybdenum dichalcogenides are elucidated. In addition, the presented molybdenum dichalcogenides in this work are also complimented with robustness as determined from high-current density stability measurements. © 2019 Hydrogen Energy Publications LLC
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    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.