Faculty Publications

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    Surface modification by multilayered Zn-Co alloy coatings
    (2012) Yogesha, S.; Udupa, K.R.; Hegde, A.
    Nanostructured multilayer alloy or composition modulated multilayer alloy coatings of Zn-Co have been developed, and their corrosion behaviours were studied by potentiodynamic polarization and electrochemical impedance spectroscopy methods. The coatings were developed galvanostatically using square, triangular and sawtooth current pulses through single bath technique. The cyclic cathode current density and the numbers of layers have been optimised for peak performance of the coatings against corrosion. Under optimal conditions, the coatings developed using square, triangular and sawtooth current pulses were found to be respectively y100, 80 and 90 times more corrosion resistant than monolithic alloy of same thickness. The better corrosion resistances of the composition modulated multilayer alloy coatings were attributed to the dielectric barrier at the interface, as evidenced by dielectric spectroscopy. Surface morphology, multilayer formation and surface after corrosion tests were examined by scanning electron microscopy. © 2012 Institute of Materials, Minerals and Mining.
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    Magnetic property and corrosion resistance of electrodeposited nanocrystalline iron-nickel alloys
    (Elsevier B.V., 2012) Pavithra, G.P.; Hegde, A.
    In the present investigation we have galvanostatically synthesized nanocrystalline Fe-Ni alloys on copper substrate. The effect of current density (c.d.) on composition, surface morphology and phase structure were studied for explaining the magnetic and electrochemical properties of the nanocrystalline alloy. The bath found to exhibit the preferential deposition of less noble Fe than Ni, and at no conditions of c.d., the deposition has changed from anomalous to normal type. Surface morphology and structural characteristics of the deposits were examined using scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis. As composition of the alloy varied, consequent to the current density a change of body centered cubic structure (bcc) to face centered cubic structure (fcc) was observed for nanocrystalline materials. Finally, the conditions responsible for peak magnetic property and corrosion resistance were optimized. Factors responsible for improved functional properties were explained in terms of surface morphology and crystalline grain size of the coatings. © 2012 Elsevier B.V.
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    Effect of surfactant on high capacitance of galvanostatically deposited MnO2
    (Elsevier B.V., 2012) Suhasini; Hegde, A.
    Manganese dioxide has been galvanostatically deposited on stainless-steel substrate from an aqueous acidic solution of manganese sulphate (1 M) in presence of a surface active agent (surfactant), namely, sodium lauryl sulphate (SLS), for supercapacitor applications. The deposits have been developed under different conditions of SLS and their specific capacitance is measured by cyclic voltammetry (CV) and also by galvanostatic charge/discharge cycle. The oxide film (?0.1 mg cm-2) anodized from the manganese solution at 2.0 mA cm-2 has shown the highest specific capacitance of 255.8 F g -1, at scan rate of 10 mV s-1. It is observed that the capacitance increased by about 40% compared to the oxide prepared in the absence of SLS. Improved specific capacitance is due to the effect of the surfactant molecules in the deposit, causing high surface area of the deposit. The deposit is found to display good cycleability, even up to 1500 cycles. The structure and surface morphology of the deposits have been studied by means of X-ray diffraction (XRD) analysis and Scanning Electron Microscopy (SEM). XRD study reveals that crystallinity of the deposit with SLS remains unchanged, both are amorphous in nature. The surface area of the deposit is found to increase considerably due to the effect of SLS, as evident by SEM study.© 2012 Elsevier B.V. All rights reserved.
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    Production of layer by layer Zn-Fe compositional multilayer alloy coatings using triangular current pulses for better corrosion protection
    (Maney Publishing, 2015) Bhat, R.S.; Hegde, A.
    Multiple-layer coatings of Zn-Fe alloy having alternatively the same compositions have been developed galvanostatically on mild steel (MS) from a single plating bath using triangular current pulses. Thiamine hydrochloride (THC) and citric acid (CA) were used as additives. Multiple-layer coatings were developed under different conditions of cyclic cathode current density (CCCD) and number of layers. Cyclic voltammetry demonstrated that the addition of THC and CA improves the deposit character by increasing the Ni content (through suppressing the deposition of Zn) via preferential adsorption on the cathode surface. The corrosion behaviours of the coatings were evaluated by electrochemical AC and DC methods. The optimum multiple-layer coating, represented as (Zn-Fe)3.0/5.0/300, was found to exhibit about four to five times better corrosion resistance when compared with monolayer (Zn-Fe)3.0 alloy, developed from the same bath for the same duration. Distinct phase structures responsible for interface formation between successive layers (which changes alternatively) were confirmed by X-ray diffraction analysis. Better corrosion resistance afforded by multiple-layer coating was attributed to the increased specific surface area of the coating because of layering. A synergistic effect of both structural difference between layers and individual layer thickness is responsible for enhanced corrosion resistance of the multiple-layer coatings. The formation of multiple layers and corrosion mechanism were analysed by scanning electron microscopy. © 2015 Institute of Materials Finishing.
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    Novel Fe-Ni-Graphene composite electrode for hydrogen production
    (Elsevier Ltd, 2015) Badrayyana, S.; Bhat, D.K.; Shenoy, U.S.; Ullal, Y.; Hegde, A.
    We have developed a novel, efficient and economical composite electrode for hydrogen production. The electrode has been formed by embedding graphene in the Fe-Ni matrix via room temperature electrodeposition. The obtained active coatings have been tested for their efficiency and performance as electrode surfaces for hydrogen evolution reaction (HER) in 6 M KOH by cyclic voltammetry and chronopotentiometry techniques. The coating obtained at 60 mA cm-2 exhibited approximately 3 times higher activity for hydrogen production than that of binary Fe-Ni alloy. Addition of graphene to electrolyte bath resulted in porous 3D projections of nano-sized spheres of Fe-Ni on the surface of graphene, which effectively increased the electrochemically active surface area. XPS analysis results showed the equal distribution of both Ni metal and NiO active sites on the composite. The addition of graphene favoured the deposition of metallic nickel, which accelerated the rate determining proton discharge reaction. All these factors remarkably enhanced the HER activity of Fe-Ni-Graphene (Fe-Ni-G) composite electrode. The Tafel slope analysis showed that the HER follows Volmer-Tafel mechanism. The structure-property relationship of Fe-Ni-G coating has been discussed by interpreting field emission scanning electron microscopy (FESEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) analysis results. © 2015 Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
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    Electrodeposition of laminar coatings of Ni-W alloy and their corrosion behaviour
    (Elsevier, 2015) Elias, L.; Hegde, A.
    The attractiveness of electroplating for the synthesis of advanced materials is linked to large selection of plating conditions coupled with different mass transfer processes towards the cathode, and this allows the tailoring of different properties of many electrodeposited coatings. This theme has been exploited effectively in the development of a new class of coatings; called composition modulated multilayered (CMM), or in short laminar coatings. The work embodied in this paper is to demonstrate how the corrosion resistance of monolayer Ni-W alloys can be increased to many fold of its magnitude by multilayer deposition. Ni-W coatings have been deposited on mild steel (MS) in a laminar multilayer pattern from a citrate bath using single bath technique (SBT). Electrodeposits having alternate layers of alloys, having different compositions were developed by modulating the direct current (DC). CMM coating configurations have been optimized from a newly developed bath, in terms of current pulse height and thickness of each layer to maximize its corrosion protection ability, in relation to its monolayer coating, developed from same bath for same time. The process and product of the Ni-W coatings have been characterized using different instrumental methods, such as cyclic voltammetry (CV), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and X-ray diffraction (XRD) study. The better corrosion resistance behaviour of CMM Ni-W coatings has been analysed in the light of increased surface areas of the coatings due to layering, and results are discussed. © 2015 Elsevier B.V.
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    Development of nanolaminated multilayer Ni-P alloy coatings for better corrosion protection
    (Royal Society of Chemistry, 2016) Elias, L.; Bhat, K.U.; Hegde, A.
    Nanolaminated multilayer Nickel-Phosphorous (Ni-P) alloy coatings were developed on mild steel from a citrate bath using glycerol as an additive. Multilayer Ni-P alloy coatings having nanolaminated layers of alloys of alternatively different compositions have been developed using pulsed direct current (DC) by cyclic modulation of the cathode current density. The composition and number (hence thickness) of the layers were tailored by periodic modulation of the current density (c.d.) and time using a programmable power source. The deposition conditions were optimized for both the composition and thickness of the individual layers for the best performance of the coatings against corrosion. Electrochemical corrosion study, evaluated by potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) demonstrated that the multilayer Ni-P alloy coating with 300 nanolaminated layers, represented as (Ni-P)1.0/4.0/300 showed several fold better corrosion resistance compared to its monolayer counterpart (deposited using regular DC) from the same electrolytic bath. Drastic improvement in the corrosion protection efficacy of the nanolaminated multilayer Ni-P alloy coatings were attributed to an increase in number of interfaces, separating layers of alloys having different morphologies, compositions and phase structures, which was supported by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and X-ray diffraction (XRD) analyses, respectively. The corrosion rates of the multilayer Ni-P alloy coatings were decreased with increasing number of layers, only up to an optimal level and then increased. The increase in corrosion rates at a higher degree of layering were attributed to the diffusion of layers, due to the very short deposition time of each layer. © The Royal Society of Chemistry 2016.
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    Magnetoelectrodeposition of Ni-W alloy coatings for enhanced hydrogen evolution reaction
    (Royal Society of Chemistry, 2016) Elias, L.; Cao, P.; Hegde, A.
    The electrocatalytic efficiency of electrodeposited (ED) Ni-W alloy coatings for the hydrogen evolution reaction (HER) has been improved drastically through magnetoelectrodeposition (MED) approach. Ni-W alloy coatings have been developed under different conditions of magnetic field intensity 'B' (applied perpendicular in the range of 0.1-0.4 T), and their electrocatalytic activity for the HER has been tested using cyclic voltammetry (CV) and chronopotentiometry (CP) techniques in 1.0 M KOH solution. A drastic improvement in the electrocatalytic behavior of the MED coating, represented as (Ni-W)B=0.2 T was found as compared to its conventional Ni-W alloy coatings. Improved performance of the MED coatings was explained on the basis of differences in the process of electrocrystallization affected due to the applied magnetic field, supported by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) analyses. A magnetic field has been used advantageously for the first time to increase the W content of the alloy. Increased activity of the MED coatings was attributed to the increased W content in the alloy, characterized by the unique (220) reflection, explained by the magnetohydrodynamic (MHD) effect due to Lorentz force. © 2016 The Royal Society of Chemistry.
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    Ultrasound induced multilayer Ni-Co alloy coatings for better corrosion protection
    (Elsevier B.V., 2017) Shetty, A.R.; Hegde, A.
    Ultrasound induced multilayer Ni-Co alloy coatings have been developed galvanostatically by periodic modulation of ultrasound effect, parallel to the process of conventional electroplating. Multilayer Ni-Co alloy having alternative layers of different composition were developed by turning the sonicator probe, ON and OFF periodically, while keeping the current density (c.d.) constant. The deposition conditions, in terms of pulsing power density (p.d.) and degree of layering have been optimized for the highest performance of coating against corrosion, evaluated by electrochemical testing methods. Corrosion data revealed that under optimal conditions, multilayer Ni-Co alloy coating having 150 layers, represented as (Ni-Co)2/2/150 is about 11 times more corrosion resistant than its homogeneous coating, represented as (Ni-Co)4.0 A dm ? 2, deposited from the same bath for same duration of time. Improved corrosion resistance of multilayer Ni-Co alloy coatings was attributed to an increase in the number of interfaces, separating the layers of alloys of different composition, affected due to periodic pulsing of the sonicator. The dependence of corrosion behaviors at different combination of c.d. and p.d., on surface morphology, composition and phase structures were analyzed, using scanning electron microscopy (SEM), energy dispersion spectroscopy (EDS) and X-ray diffraction (XRD) technique, respectively. Experimental results are compared, and discussed. © 2017 Elsevier B.V.
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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.