Faculty Publications
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Item Synergistic effect of gelatin and glycerol on electrodeposition of Zn-Ni alloy(2013) Rao, V.R.; Hegde, A.C.The use of organic compounds which improves corrosion resistance has attracted growing interest in electroplating technology. In this direction, this article presents the experimental results of electrodeposition of Zn-Ni alloy on mild steel (MS) from acid chloride bath using gelatin and glycerol as additives. The bath composition and operating parameters have been optimized by the conventional Hull cell method. The effect of gelatin and glycerol, individually and in combination on the deposition process, was identified by a cyclic voltammetry (CV) study at different scan rates. Bright deposition of Zn-Ni alloy was found at optimal current density (c.d.) due to the preferential deposition of gelatin and glycerol by controlling the Ni content of the alloy. The CV study demonstrated that alloy deposition is diffusion controlled when additives were used individually and is adsorption controlled when used in combination. Corrosion behaviors at different current densities (c.d.s) were evaluated by potentiodynamic polarization and electrochemical impedance (EIS) methods. The surface morphology and phase structure of the coatings were analyzed by field emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD) studies. The experimental results revealed that both gelatin and glycerol have synergistic effects in improving the electrocrystallization process and, hence, the corrosion stability of the coatings. At an optimal c.d. (3.0 A dm-2), the Zn-Ni alloy coating showed peak performance against corrosion with the least corrosion rate. Better corrosion protection at optimal c.d., which was attributed to specific Zn(101), ?-(411,330), and Zn(103) reflections, is evidenced by the XRD study. © 2013 The Minerals, Metals & Materials Society and ASM International.Item Novel Co-Ni-graphene composite electrodes for hydrogen production(Royal Society of Chemistry, 2015) Subramanya, B.; Ullal, Y.; Shenoy, S.U.; Bhat, D.; Hegde, A.C.Active, stable and cost-effective electrocatalysts are key to water splitting for hydrogen production through electrolysis. Herein, we report the facile preparation of highly porous Co-Ni-graphene (Co-Ni-G) composite electrodes by electrodeposition for electrocatalytic applications. The incorporation of graphene into the Co-Ni matrix enhances the catalyst's activity for the hydrogen evolution reaction (HER) in an alkaline solution. The best coating exhibits a maximum current density of -850 mA cm-2 at -1.6 V, which is approximately 4 times better than that of the binary Co-Ni alloy indicating higher activity for hydrogen production. The addition of graphene to an electrolyte bath results in a porous encapsulated bundle of alloy nano-particles within the graphene network which effectively increases the electrochemically active surface area. As indicated by XPS analysis results, on addition of graphene the Co(0) and Ni(0) content in the deposit increases and as a result both cobalt/cobalt oxide and nickel/nickel oxide sites are evenly distributed on the Co-Ni-G electrode surface which is responsible for increased HER activity. The Tafel slope analysis showed that the HER follows a Volmer-Tafel mechanism. The structure-property relationship of the Co-Ni-G composite coating has been discussed by interpreting field emission scanning electron microscopy (FESEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) analysis results. © The Royal Society of Chemistry 2015.Item Development of multilayer Sn-Ni alloy coating by pulsed sonoelectrolysis for enhanced corrosion protection(Royal Society of Chemistry, 2016) Shetty, S.; Mohamed, M.J.; Bhat, D.; Hegde, A.C.Multilayer Sn-Ni alloy coating has been developed electrochemically on mild steel using an ultrasound effect, as a tool to modulate mass transfer process at electrical double layer, during deposition. Sn-Ni coatings having alternate layers of alloys of different compositions were developed on a nano/micrometric scale by pulsing sonicator ON (tON) and OFF (tOFF), periodically. The composition modulated multilayer alloy (CMMA) Sn-Ni coatings have been deposited by inducing the ultrasound field periodically at optimal current density. Corrosion performances of ultrasound-assisted multilayer Sn-Ni alloy coatings have been evaluated by electrochemical methods. Corrosion data revealed that CMMA Sn-Ni coating, developed using pulsed ultrasonic field and having 150 layers, represented as (Sn-Ni)2/2/150, is the most corrosion resistant, compared to its monolayer alloy coatings developed by both with/without ultrasound effect. Corrosion protection efficacy of multilayer coatings was found to be decreased at high degree of layering due to diffusion of layers. Improved corrosion resistance of multilayer Sn-Ni coatings is attributed to an increase in the number of layers, or interfaces separating alloys of the same metals, but of different composition, surface morphologies and phase structures, supported by energy dispersive spectroscopy, field emission scanning electron microscopy and X-ray diffraction study, respectively. The better corrosion protection of CMMA Sn-Ni coatings, compared to monolayer counterparts, is attributed to an increase in the number of layers, hence phase boundaries between layers, and experimental results are discussed. © 2018 The Royal Society of Chemistry.Item Sol-gel electrospun ZnMn2O4 nanofibers as bifunctional electrocatalysts for hydrogen and oxygen evolution reactions(Institute of Physics Publishing helen.craven@iop.org, 2019) Shamitha, C.; Shetty, A.R.; Hegde, A.C.; Anandhan, S.Electrochemical water-splitting has gained significant attention for the development of next generation fuels. The present work is an investigation on the electrocatalytic activity towards both Oxygen Evolution Reaction (OER) and Hydrogen Evolution Reaction (HER) of ZnMn2O4 (ZMO) nanofabrics synthesized by sol-gel electrospinning followed by calcination (at 500, 600 and 700 °C). Poly(styrene-co-acrylonitrile) was used as the polymeric binder for the production of nanofabrics. The morphological features of ZMO nanofabrics were studied by scanning electron microscopy and field emission scanning electron microscopy. The electrocatalytic behavior of ZMO nanofabrics obtained at different calcination temperatures was evaluated using chrono-potentiometry, cyclic voltammetry, and linear sweep voltammetry in an alkaline medium (1 M KOH). The ZMO nanofabrics calcined at 500 °C exhibited the maximum electrocatalytic activity towards HER. This can be ascribed to their superior specific surface area (79.5 m2 g-1). The nanofabrics calcined at 700 °C displayed the least potential for O2 evolution and hence they are considered to be effective for OER. The results prove that ZMO nanofabrics are promising candidates as bifunctional electrocatalysts for water-splitting applications. © 2019 IOP Publishing Ltd.