Faculty Publications

Permanent URI for this communityhttps://idr.nitk.ac.in/handle/123456789/18736

Publications by NITK Faculty

Browse

Has files: NoSubject: search.filters.subject.Redox reactions

Search Results

Now showing 1 - 10 of 25
  • No Thumbnail Available
    Item
    N and p doped poly(3,4-ethylenedioxythiophene) electrode materials for symmetric redox supercapacitors
    (2007) Bhat, D.K.; Muthu, M.S.
    A symmetric redox supercapacitor has been fabricated based on n and p doped Poly(3,4-ethylenedioxythiophene)(PEDOT) coated on stainless steel (SS) electrodes. The characterization and performance of the supercapacitor has been studied by FTIR, Cyclic Voltammetry and AC Impedance spectroscopy. The supercapacitor showed a maximum specific capacitance of 121 F g-1 at a scan rate of 10 mV s-1. The time constant calculated for the supercapacitor through the active-reactive power behavior measurement was 12 milliseconds indicating the suitability of the system for efficient use at low frequency range. © 2007 Springer Science+Business Media, LLC.
  • No Thumbnail Available
    Item
    Development of low temperature stoichiometric solution combustion derived transparent conductive ternary zinc tin co-doped indium oxide electrodes
    (Royal Society of Chemistry, 2017) Pujar, P.; Gandla, S.; Singh, M.; Gupta, B.; Tarafder, K.; Gupta, D.; Noh, Y.-Y.; Mandal, S.
    Here, the development of transparent conductive zinc tin co-doped indium oxide (IZTO: In1.4Sn0.3Zn0.3O3) ternary electrodes is addressed through low temperature solution combustion processing. Optimization of fuel to oxidizer ratio offers low temperature (?130 °C) of combustion with balanced redox reaction. The thin films of IZTO annealed at different temperatures showed a decreasing trend in the resistivity with a fixed order of 10-2 ? cm and the film with a highest Hall mobility of 5.92 cm2 V-1 s-1 resulted at 400 °C. All the films with different temperatures of annealing were smooth (rms ? 2.42 nm) in nature and the IZTO film annealed at 200 °C is 83% transparent in the visible spectra. The effective band gap of 0.9 eV determined from first-principles density functional theory gives clear evidence for the conducting nature of IZTO. The thin film transistor fabricated with IZTO as a gate electrode with poly(methyl methacrylate) and pentacene as the dielectric and channel material, respectively, exhibited a saturation mobility of 0.44 cm2 V-1 s-1 and Ion/Ioff ratio of 103. Further, the printability of the IZTO combustible precursor is established which resulted in anti-edge deposition of the printed feature. © 2017 The Royal Society of Chemistry.
  • No Thumbnail Available
    Item
    Facile in situ formation of high conductive Ag and Cu x O y composite films: a role of aqueous spray combustion
    (Springer New York LLC barbara.b.bertram@gsk.com, 2019) Salian, A.; Pujar, P.; Mandal, S.
    In the present contribution, in situ formation of low-temperature high conductive composite films composed of pure silver and oxides of copper (Cu x O y where, x = y = 1 for CuO and x = 2, y = 1 for Cu 2 O), are presented through spray combustion with a balanced stoichiometric redox reaction. High electrical conductivity (~ 7.8 × 10 5  S/cm) was retained in the composite film at an annealing temperature of 170 °C with matrix silver phase being 50% by volume. Whereas electrical conductivity of spray combustion processed pure silver is found to be ~ 2 × 10 6  S/cm. In situ formation of the composite film directly from the silver and cupric nitrate aqueous precursor solution through spray combustion proves it to be compositionally tunable with minimal usage of noble metal. Presence of Ag and Cu x O y is confirmed by X-ray diffraction and X-ray photoelectron spectroscopy. The ratio of Cu 1+ /Cu 2+ in the composite is found to be 0.54 and 0.43 at an annealing temperature of 170 °C and 400 °C respectively. The transformation of Cu 2 O to CuO is highly a thermally activated phenomenon; as the vacancy driven electrical conductivity is more in Cu 2 O than CuO, stabilization of Cu 2 O at a lower temperature is desired. The composite electrode can have potential applications in optoelectronics, printed electronics and catalysis. © 2018, Springer Science+Business Media, LLC, part of Springer Nature.
  • No Thumbnail Available
    Item
    High-performance low voltage operation of indium zinc tin oxide thin film transistors using chemically derived sodium ?-alumina dielectric
    (Springer, 2019) Pujar, P.; Gupta, D.; Mandal, S.
    We present high performance, low voltage (< 3 V) operation of thin film transistors (TFTs) with indium zinc tin oxide (IZTO: In4Sn4ZnO15)-semiconductor. The film of IZTO was fabricated via low-temperature (200 °C) solution combustion processing without incorporating an external fuel. As 2-methoxyethanol is a widely used organic solvent due to its high dissolution capability, serve the purpose of both the solvent and the fuel. On quantification from the balanced redox reaction, 0.3% of 2-methoxyethanol assisted for the action of fuel and helped in the formation of metal oxide, and the rest (99.7%) served the purpose of being dissolution medium. The balanced redox chemistry yielded a significant fraction of (56.5%) metal oxide at 200 °C confirmed via high-resolution oxygen 1 y spectrum. Further, the chemically derived thin film of sodium ss-alumina with a dielectric constant of ~ 21, while annealing at 350 °C incorporated in the TFT for the realization of low voltage operation. The performance assessment is systematically carried out both silicon dioxide (SiO2) and sodium ss-alumina and found that the TFTs with SiO2 and IZTO exhibited a saturation mobility (µ^), Ion/Ioff ratio and the threshold voltage (Vth) of 0.50 ± 0.02 cm2 V-1 s-1, 1.25 x 104 and 6.6 ± 0.79 V respectively. While changing the dielectric to sodium ss-alumina presented a µsat, Ion/Ioff ratio and Vth of 4.21 ± 0.18 cm2 V-1 s-1, 1.4 x 102 and 0.47 ± 0.08 V respectively. © Springer Science+Business Media, LLC, part of Springer Nature 2019.
  • No Thumbnail Available
    Item
    Biological Treatment of 3,6-Dichloro-2-Methoxybenzoic Acid Using Anaerobic-Aerobic Sequential Batch Reactor
    (Springer Basel info@birkhauser-science.com, 2019) Mahesh, G.B.; Manu, B.
    A sequential anaerobic-aerobic batch reactor was used to treat 3,6-dichloro-2-methoxybenzoic acid (dicamba) during a long operation period of 340 days in the presence of disodium anthraquinone-2,6-disulphonate (AQS) as redox mediator. The sludge activity was evaluated for different dosages of dicamba over constant hydraulic retention time (HRT), neutral pH (6.5–7.5) and at ambient reactor temperature. Effects of increased dicamba concentration, solids retention time (SRT) and oxidation reduction potential (ORP) on the biodegradation of dicamba was monitored and compared with control reactor containing no dicamba. Results revealed that long operation period, long SRT and ORP were playing important role in the breakdown of dicamba to its transformation products and subsequent removal in the system. The system was capable of degrading the compound completely during long operation period, long SRT and at low ORP in the presence of AQS. Reducing condition in the anaerobic reactor significantly contributed to the treatment process through demethylation, dehalogenation and dechlorination reactions in the presence of different reducing bacteria. The results of GC-HRMS identified the anaerobic transformation products of dicamba as oleic acid (C18H34O2), 9-Octadecenoic acid (Z), 2-hydroxy-1-(hydroxymethyl)ethyl ester (C21H40O4), trans-13-Ocatadecenoic acid (C18H34O2) compounds which were then oxidised in the aerobic reactor. © 2019, Springer Nature Switzerland AG.
  • No Thumbnail Available
    Item
    Influence of cations in MFe2O4 (M: Fe, Zn, Ni, Sn) ferrite nanoparticles on the electrocatalytic activity for application in hydrogen peroxide sensor
    (Institute of Physics Publishing helen.craven@iop.org, 2019) Bindu, K.; Nagaraja, H.S.
    Hydrothermally prepared MFe2O4 (M: Fe, Zn, Ni and Sn) nanoparticles have been characterized by XRD, SEM and BET. The ferrite nanoparticles have been tested for their electrocatalytic activity and application towards the reduction and sensing of hydrogen peroxide using cyclic voltammetry and chronoamperometry techniques. ZnFe2O4 and SnFe2O4 reveal superior H2O2 sensing performance than Fe3O4 and NiFe2O4, which can be attributed to the lower redox potential of Sn2+/Sn4+ couple, lower charge-transfer resistance and higher specific surface area. ZnFe2O4 and SnFe2O4 have a sensitivity of 4.411 and 3.915 ?AmM-1 ?g-1, respectively, which is greater than that of Fe3O4 (0.434 ?AmM-1 ?g-1) and NiFe2O4 (0.644 ?AmM-1 ?g-1). SnFe2O4 has the lowest limit of detection (2.6 (M) with good selectivity towards H2O2 in the presence of other interference agents. © 2019 IOP Publishing Ltd.
  • No Thumbnail Available
    Item
    Improved electrochemical performance of graphene oxide supported vanadomanganate (IV) nanohybrid electrode material for supercapacitors
    (Elsevier Ltd, 2020) Kumari, S.; Maity, S.; Anandan Vannathan, A.A.; Shee, D.; Das, P.P.; Mal, S.S.
    Graphene oxide (GO)-supported polyoxometalates (POMs) have been considered as promising electrode materials for energy storage applications due to their ability to undergo fast and reversible redox reactions. Herein, vanadomanganate-GO composites (K7MnIVV13O38.18H2O-GO with 2:1 and 4:1 ratio) were investigated for use as potential electrode materials in supercapacitors (SCs). The K7MnIVV13O38.18H2O (MnV13) was synthesized and anchored on GO through electron transfer interaction and electrostatic interaction to make the composite electrodes for the present study. All synthesized electrode materials were fully characterized by various techniques, e.g., Fourier Transform Infrared (FTIR) Spectroscopy, Powder X-ray Diffraction (XRD), Scanning Electron Microscopy/Energy Dispersive X-ray Spectroscopy (SEM/EDS) and High Resolution-Transmission Electron Microscopy (HR-TEM). The electrochemical properties of MnV13/GO composites with different MnV13/GO ratios were investigated by two-electrode cyclic voltammetry (CV) and galvanostatic charge/discharge (GCD) in different electrolytes. The MnV13/GO composite of ratio 2:1 in 1 M LiCl electrolyte and that of ratio 4:1 in 1 M Na2SO4 electrolyte showed significant specific capacitance values of 269.15 F/g and 387.02 F/g, respectively and energy density of 37.38 Wh/kg and 53.75 Wh/kg, respectively for a scan rate of 5 mV/s. Interestingly, the 1:1 (MnV13/GO) composite in 1 M Na2SO4 and 1 M LiCl electrolytes showed very low specific capacitance values as the deposition of MnV13 on GO was not sufficient, as indicated by FTIR and SEM. Thus, it is evident that the specific capacitance value of these composite materials depends on the amount of MnV13 deposited on GO and these composite materials exhibit the potential to improve the performance of GO-based SCs. © 2019
  • No Thumbnail Available
    Item
    Improving hydrogen evolution reaction and capacitive properties on CoS/MoS2 decorated carbon fibers
    (Elsevier Ltd, 2020) Sangeetha, D.N.; Krishna Bhat, D.; Senthil Kumar, S.; Muthu, M.
    We report a facile method to transform abundantly dumped banana stem fibers into carbon fibers (CFs) useful for energy applications. The CFs surface area is increased by varying the quantity of KOH activation to 488 m2g-1. The solvothermal method is used to synthesize CoS, CoS/MoS2 and also grown on the activated carbon fibers (ACFs). Nano nodules of CoS arranged into sheets and layers of MoS2 stacked together were found in FESEM analysis. The morphology of the CoS/MoS2 differs when grown on ACFs. The growth of CoS/MoS2 along the ACFs length prevents any stacking of the pseudocapacitance materials. The ternary composite ACFs/CoS/MoS2 exhibits superior supercapacitor behavior as well as hydrogen evolution reaction (HER) due to the synergetic effect of the conducting ACF surface and redox active CoS/MoS2. A maximum specific capacitance of 733 Fg-1, energy and power density of 33 WhKg?1 and 999 WKg-1 respectively are obtained. A low Tafel slope value of 61 mVdec?1 is obtained for the ACFs/CoS/MoS2 ternary composite electrode. The present work therefore offers a fresh insight into the effective conversion of waste materials into electrode material for energy storage and conversion applications. © 2019 Hydrogen Energy Publications LLC
  • No Thumbnail Available
    Item
    Combustion aided in situ consolidation of high strength porous ceramic structures with a minimum thermal budget
    (Elsevier B.V., 2020) Pujar, P.; Pal, A.; Mandal, S.
    The exothermic reaction between a pair of combustible pore formers (urea-ammonium nitrate) is the driving force in realizing low-temperature consolidation of hydroxyapatite (HA) particles. The particles are allowed to sinter in the proximity to the combustible pore formers. The exothermic (?H°rea = -898 kJ/mol) redox reaction between combustible pore formers is successfully utilized in deriving high compressive strength (~24 MPa) of HA at 300 °C. The evolution of gaseous products of combustion results in an interconnected porous network of HA. The estimated compressive strength of sintered HA at 300 °C is comparable with high temperature (1100 °C) conventionally sintered HA, at a fixed open porosity (~40%); which depicts nearly ~82% achievement with a reduction of sintering temperature by ~72%. Also, the pellets sintered at 600 °C have shown ~90% achievement in compressive strength of sintered HA. Further, the saturated pore area of 15% requires a sintering time of 9.58 h at a sintering temperature of 600 °C. Thus, combustion-assisted sintering is an alternative technique proves its potentiality in achieving remarkable compressive strength and paves the way for low-cost porous ceramics. © 2020 Elsevier B.V.
  • No Thumbnail Available
    Item
    Redox-Active Vanadium-Based Polyoxometalate as an Active Element in Resistive Switching Based Nonvolatile Molecular Memory
    (Wiley-VCH Verlag info@wiley-vch.de, 2020) Sterin, N.S.; Basu, N.; Cahay, M.; Satyanarayan, M.N.; Mal, S.S.; Das, P.P.
    Resistive switching (RS)-based random access memory has been envisaged as a viable alternative to existing memory technology due to its nonvolatility, high switching speed, high endurance/retention, and considerably low operating voltage. Herein, a new uniform, repetitive, and stable RS phenomenon is demonstrated based on very low-cost two-terminal metal–insulator–metal stack fabricated using a highly redox-active vanadium-based polyoxometalate (POM) molecular clusters, [V10O28]6?—belonging to polyoxovanadate (POV) family. The RS is observed to be unipolar and nonvolatile in nature, and occur at a fairly low operating bias voltage (less than 2 V), making it suitable for low-power operations. The switching event is attributed to the cycling between formation and rupture of tiny conductive nanofilaments formed due to trapping and detrapping of positively charged ionized oxygen vacancy sites present in the active switching layer of [V10O28]6?. POMs, in their rich abundance, are highly stable early transition-metal oxide nanosized clusters, capable of storing as well as releasing a large number of electrons. In addition, they can undergo fast and reversible redox reactions (both in solid and liquid electrolyte media) in “stepwise” manner—a property that makes them a promising candidate for ultrafast and multi-level nonvolatile molecular memory for high-density data storage. Preliminary investigations on the POV-based memory cells result in device resistance ratio ?25, endurance for more than 200 cycles, and stable retention time around 2200 s, in fully open air condition. © 2020 Wiley-VCH GmbH