Faculty Publications
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Item Progress in Electrochemical Trifluoromethylation Reactions(Wiley-VCH Verlag, 2020) Bhaskaran, R.P.; Babu, B.P.The importance of fluorinated organic molecules in drugs and pharmaceuticals led to the development of several synthetic methods for introducing fluorine into bioactive molecules and trifluoromethylation is one of the key approaches for the same. Electrochemical organic synthesis has emerged as one of the most sustainable, green synthetic strategies in recent years and new developments in electroorganic synthesis also focus on electrochemical trifluoromethylation of organic compounds. A considerable number of reports have appeared in recent literature and this review surveys all the recent developments in electrochemical trifluoromethylation reactions. This highly sustainable trifluoromethylating protocol will emerge further soon and pave the way for more energy-efficient and green protocols. (Figure presented.). © 2020 Wiley-VCH GmbHItem Polyvinyl alcohol-polystyrene sulphonic acid blend electrolyte for supercapacitor application(2009) Muthu, M.S.; Bhat, D.K.A new polymer blend electrolyte based on poly vinyl alcohol and poly styrene sulphonic acid has been studied as an electrolyte for supercapcitors. A carbon-carbon supercapacitor has been fabricated using this electrolyte and its electrochemical characteristics and performance have been studied. The conductivity has been calculated using the bulk impedance obtained through impedance spectroscopy. The real and imaginary parts of the electrical modulus of samples show a long tail feature, which can be attributed to high capacitance of the material. The super capacitor showed a fairly good specific capacitance of 40 F g- 1 and a time constant of 5 s. © 2008 Elsevier B.V. All rights reserved.Item LiClO4-doped plasticized chitosan as biodegradable polymer gel electrolyte for supercapacitors(2009) Muthu, M.S.; Bhat, D.K.Studies on redox supercapacitors using electronically conducting polymers are of great importance for hybrid power sources and pulse power applications. In this study, electrochemical properties of a chitosan-based biodegradable polymer gel electrolyte (PGE) and a p/p polypyrrole supercapacitor fabricated using this electrolyte have been investigated. The variation of conductivity and dielectric properties of the electrolyte film with temperature has also been measured. The PGE film chosen for the study exhibited a specific conductivity of 5.5 × 10-3 S cm~. The electric modulus of the electrolyte film exhibits a long tail feature indicative of good capacitance. The fabricated supercapacitor showed a fairly good specific capacitance of 120 F g-1 and a time constant of 1 s. © 2009 Wiley Periodicals, Inc.Item Electrolytic Synthesis and Characterization of Electrocatalytic Ni-W Alloy(Springer New York LLC barbara.b.bertram@gsk.com, 2015) Elias, L.; Scott, K.; Hegde, A.Inspired by the more positive (about 0.38 V nobler) discharge potential of hydrogen on Ni-W alloy compared to that on both Ni and W, a Ni-W alloy has been developed electrolytically as an efficient electrode material for water electrolysis. The deposition conditions, for peak performance of the electrodeposits for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in 1.0 M KOH medium have been optimized. Electrocatalytic activity of the coatings, deposited at different current densities (c.d.’s) for water splitting reactions of HER and OER was tested by cyclic voltammetry and chronopotentiometry. It was found that Ni-W alloys deposited, at 4.0 A/dm2 (having about 12.49 wt.% W) and 1.0 A/dm2 (having about 0.95 wt.% W) are good electrode materials as cathode (for HER) and anode (for OER), respectively. A dependency of the electrocatalytic activity for HER and OER with relative amount of Ni and W, in the deposit was found. The variation of electrocatalytic activity with W content showed the existence of a synergism between high-catalytic property of W (due to low hydrogen overvoltage) and Ni (having increased adsorption of OH? ions), for hydrogen (as cathode) and oxygen (as anode) evolution, respectively. Electrocatalytic activities of the coatings, developed at different c.d.’s were explained in the light of their phase structure, surface morphology, and chemical composition, confirmed by XRD, FESEM, and EDX analysis. The effect of c.d. on thickness, hardness, composition, HER, and OER was analyzed, and results were discussed with possible mechanisms. © 2015, ASM International.Item Effects of electric potential, NaCl, pH and distance between electrodes on efficiency of electrolysis in landfill leachate treatment(Taylor and Francis Inc. 325 Chestnut St, Suite 800 Philadelphia PA 19106, 2017) Erabee, I.K.; Ahsan, A.; Jose, B.; Arunkumar, T.; Sathyamurthy, R.; Idrus, S.; Daud, N.N.N.This study investigated the effects of different parameters on the removal efficiencies of organic and inorganic pollutants in landfill leachate treatment by electrolysis. Different parameters were considered such as the electric potential (e.g., 24, 40 and 60 V), hydraulic retention time (HRT) (e.g., 40, 60, 80, 100 and 120 min), sodium chloride (NaCl) concentration (e.g., 1, 3, 5 and 7%), pH (e.g., 3, 7 and 9), electrodes materials [e.g., aluminum (Al) and iron (Fe)] and distance between electrodes (e.g., 1, 2 and 3 cm). The best operational condition of electrolysis was then recommended. The electric potential of 60 V with HRT of 120 min at 5% of NaCl solution using Al as anode and Fe as cathode (kept at a distance of 3 cm) was the most efficient condition which increased the removal efficiencies of various parameters such as turbidity, salinity, total suspended solids (TSS), total dissolved solids (TDS), biochemical oxygen demand (BOD), chemical oxygen demand (COD) and heavy metals (e.g., Zn and Mn). The higher removal percentages of many parameters, especially COD (94%) and Mn (93%) indicated that the electrolysis is an efficient technique for multi-pollutants (e.g., organic, inorganic and heavy metals) removal from the landfill leachate. © 2017 Taylor & Francis Group, LLC.Item Adsorptive Treatment of Landfill Leachate using Activated Carbon Modified with Three Different Methods(Springer Verlag service@springer.de, 2018) Erabee, I.K.; Ahsan, A.; Jose, B.; Aziz, M.M.A.; Ng, A.W.M.; Idrus, S.; Daud, N.N.N.Activated Carbon (AC) is an adsorbent having high surface area which makes the process of removing heavy metals from wastewater (such as landfill leachate) very effective. This study explored the utilization of three methods of modification of AC produced from coconut shell by treating it with nitric acid (HNO3), potassium permanganate (KMnO4) and heating at 600°C to improve the adsorption capacity. The AC can remove multi-pollutants in the filtration process which was used to treat landfill leachate. The water quality parameters such as pH, TSS, Ammonia-Nitrogen and a few heavy metals were considered in the present study. Results showed that the removal of these parameters was proportional with the increase of contact time and the bed depth of AC. The isotherm analysis of the adsorption of modified AC showed the best Removal Efficiency (RE) can be achieved when AC treated with KMnO4 for NH3-N, zinc, TSS and sulphide. The morphology of the AC was studied through Scanning Electron Microscopy (SEM), Energy Dispersive X-ray spectroscopy (EDX) pattern analysis and Fourier Transform Infrared (FTIR) analysis. It was found that various types of oxygen functional groups were introduced onto the surface of coconut shell derived AC through oxidation using HNO3. FTIR was used to characterize the surface oxygen functional groups. The surface functional groups such as N-H and C-H stretching played a significant role in heavy metals adsorption. Hence, it can be concluded that the hybrid technique by using electrolysis process with AC adsorption be an effective way to remove the suspended solids and heavy metals from landfill leachate and thus able to reduce environmental pollution. © 2018, Korean Society of Civil Engineers.Item Polymorph nickel titanate nanofibers as bifunctional electrocatalysts towards hydrogen and oxygen evolution reactions(Royal Society of Chemistry, 2019) Kumar, B.; Tarafder, K.; Shetty, A.R.; Hegde, A.C.; Gudla, V.C.; Ambat, R.; Kalpathy, S.K.; Anandhan, S.Producing pure H2 and O2 to sustain the renewable energy sources with minimal environmental damage is a key objective of photo/electrochemical water-splitting research. Metallic Ni-based electrocatalysts are expensive and eco-hazardous. This has rendered the replacement or reduction of Ni content in Ni-based electrocatalysts a decisive criterion in the development of bifunctional electrocatalytic materials. In the current study, spinel/ilmenite composite nickel titanate (NTO) nanofibers were synthesised using sol-gel assisted electrospinning followed by pyrolysis at different soaking temperatures (viz., 773, 973, and 1173 K). The presence of a defective spinel NTO phase (SNTO) distributed uniformly along the nanofibers was confirmed by X-ray photoelectron and Raman spectroscopy. The electron micrographs revealed the morphological change of NTO nanofibers from a mosaic to bamboo structure with an increase in pyrolysis soaking temperature. The electrocatalytic activity of NTO nanofibers obtained at different pyrolysis soaking temperatures for alkaline water-splitting was studied. The highly defective SNTO manifests properties similar to metallic Ni and favours H2 evolution through the hydrogen evolution reaction (HER) by adsorbing more H+ ions on active sites. In contrast, the ilmenite NTO favours O2 discharge. These results are explained based on the morphology of the NTO nanofibers. The mosaic structure which has higher porosity and greater SNTO content shows excellent HER performance. In contrast, the large bamboo structured NTO nanofibers which have lesser porosity and SNTO content cage the bigger (OH)ads ions at their catalytic sites to facilitate OER performance. 2019 © The Royal Society of Chemistry.Item Electrochemical characterization of electrolyte supported solid oxide electrolysis cell during CO2/H2O co-electrolysis(Springer Science and Business Media Deutschland GmbH, 2024) Shirasangi, R.; Prasad Dasari, H.P.; Saidutta, M.B.High-temperature co-electrolysis is studied on electrolyte-supported NiO-YSZ/NiO-SDC/ScSZ/LSCF-GDC/LSCF (NiO: Nickel Oxide, YSZ: Yttria-stabilized zirconia, SDC: Samarium-doped ceria, ScSZ: Scandia-stabilized zirconia, LSCF: Lanthanum Strontium Cobalt Ferrite, GDC: Gadolinium-doped ceria) button cell. Electrochemical impedance spectroscopy (EIS) was recorded under open-circuit voltage (OCV) and co-electrolysis mode over various operating conditions, including temperature, water vapor content, and applied voltage. Interfacial polarization resistance (Rp) is obtained from peak arcs located in the three regions: gas conversion resistance (Region I (0.01 to 0.1 Hz)), gas diffusion resistance (Region II (0.1 to 100 Hz)) and air electrode charge transfer resistance (Region III (100 to 10,000 Hz)). As the temperature increased from 700 to 850 oC, Rp decreased from 18.15 to 3.32 Ω.cm2 at 1.3 V for 10%CO2/3%H2O. From the Distribution of relaxation times (DRT) studies, one additional peak, P5 (fuel gas conversion or gas-phase diffusion in the pores of the air electrode), is observed, and Region III (100 to 10,000 Hz) consists of two additional peaks: P1 (ionic transport coupled with gas diffusion close to triple phase boundaries (TPBs)) and P2 (fuel electrode charge transfer reaction), which were not clearly distinguished from EIS. Region II dominates in the overall polarization resistance. At 800 oC, for 10%CO2/3%H2O, the Rp decreased from 6.78 to 4.82 Ω.cm2, with an increase in the applied voltage from 1.3 to 1.5 V. At 800oC/1.5 V, the Rp values are 4.41, 8.09, and 6.77 Ω.cm2 for H2O, CO2, and co-electrolysis. At 800 ºC/1.5 V, with an increase in the water vapor content from 3%H2O to 15%H2O, there is not much change in the Rp value; therefore, 10%H2O is sufficient. H2 consumption is between 23 and 36%, depending on the temperature at OCV. At 800 °C for (10%H2/10%CO2/10%H2O), co-electrolysis occurs at applied voltage, along with Reverse water gas shift (RWGS) reaction. Graphical Abstract: (Figure presented.) © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024.Item Nano-composites of NiFe-LDH/V Se2 heterostructures for effective water splitting electrocatalyst(Elsevier Ltd, 2024) Hegde, A.; Mukesh, P.; G, L.S.; Kumar, A.; Nagaraja, H.S.In the realm of sustainable and environmentally friendly “green-hydrogen” fuel demand, water electrolysis stands as a pathway of hope for the extraction of renewable hydrogen. However, the durability and efficiency of electrocatalysts have been a major challenge in this process, owing to factors like the high costs of noble catalysts (Pt, Ir, Ru, etc.) and their limited stability. Layered Nickel-iron double hydroxides (NiFe-LDH) have shown potential as low-cost and efficient electrocatalysts because of their suitable electronic configuration and distinguished orbital confinement. However, their durability In the realm of sustainable and environmentally friendly “green-hydrogen” fuel demand, water electrolysis stands as a pathway of hope for the extraction of renewable hydrogen. However, the durability and efficiency of electrocatalysts have been a major challenge in this process, owing to factors like the high costs of noble catalysts (Pt, Ir, Ru, etc.) and their limited stability. Layered Nickel-iron double hydroxides (NiFe-LDH) have shown potential as low-cost and efficient electrocatalysts because of their suitable electronic configuration and distinguished orbital confinement. However, their performance and durability in corrosive alkaline water at high current density remain limited. In this regard, one can make the nano-composites of this NiFe-LDH with high electronic conductivity materials and layered structures like VSe2. With this motivation, this work presents a novel electrocatalyst, NiFe-LDH, supported with VSe2 nanosheets (V Se2/NiFe−LDH), designed to address these challenges and enhance water splitting efficiency. Experimental results demonstrate that the heterostructure synergistically reduces charge transfer resistance, increases exposure of active sites, and enhances oxygen gas evolution ability. Consequently, the V Se2/NiFe−LDH electrocatalyst demonstrated superior sustainability, maintaining an elevated current density (500mAcm−2) for over 50 h of continuous electrolysis without noticeable degradation. This research opens up new possibilities and shows that nano-compositing can be a good option for achieving efficient and durable electrocatalysts in alkaline water splitting, thereby contributing to sustainable hydrogen production. © 2024 Hydrogen Energy Publications LLCItem Growth of octahedral structured AgBiS2 single crystals and its insights on the high performance electrocatalytic hydrogen generation(Elsevier Ltd, 2024) Jauhar, R.O.M.; Ramachandran, K.; Deepapriya, S.; Joshi, S.; Ghfar, A.A.; Rao, L.; Badekai Ramachandra, B.R.; Udayashankar, N.K.; Vadivel, V.; Raji, R.; Kim, B.C.; Rodney, J.D.Given the enormous depletion of fossil fuels and growing environmental concerns, there is an immediate need to develop alternative and clean energy sources. Hydrogen (H2), recognized for its cleanliness and renewability, is poised to meet future energy requirements. Consequently, ongoing research is focused on the development of electro-active, durable, and cost-effective catalysts to replace expensive noble metal-based electrocatalysts. In this study, microscale AgBiS2 chalcogenide derived from a single crystal is reported as promising electrocatalysts for the Hydrogen Evolution Reaction (HER) with a remarkably low overpotential. The physico-chemical characterization of the AgBiS2 catalyst has been investigated using various analytical techniques. The synthesized AgBiS2 catalyst exhibits excellent HER activity, manifesting a low overpotential of 86 mV at a current density of 10 mA cm−2 and a Tafel slope of 44 mV dec−1, along with superior stability even after 24 h in HER at a very high current density. The developed AgBiS2 also showcased stable production when subjected to a two-electrode system. The enhanced alkaline HER activity of AgBiS2 can be attributed to its phase purity, high crystallinity, and the presence of high active sites. The observed high electrochemical performance and stability position AgBiS2 as a potential electrocatalyst for the hydrogen evolution reaction. This finding holds significant promise in the quest for efficient, durable, and economically viable catalysts to drive the shift towards clean and renewable energy sources. © 2024 Hydrogen Energy Publications LLC