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Browsing by Author "Udayashankar, N.K."

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    A novel approach to the synthesis of semiorganic ammonium hydrogen oxalate oxalic acid dihydrate single crystal and its characterization
    (Springer Science and Business Media B.V., 2021) Mahendra, K.; Fernandes, J.M.; Udayashankar, N.K.
    A different approach used in the synthesis of ammonium hydrogen oxalate oxalic acid dihydrate (NH4H3(C4O8)·2H2O) single crystals is presented. The crystals are synthesized using solvent evaporation technique. The analysis of the synthesized NH4H3(C4O8)·2H2O single crystals has been carried out through measurements such as single-crystal X-ray diffraction (SCXRD), powder XRD, UV–Vis and photoluminescence spectroscopy, Fourier transform infrared spectroscopy, thermogravimetric and differential thermal analysis (TG–DTA), Vickers microhardness measurements and current versus voltage (I–V) characteristics. The evaluation of the molecular structure of the crystals using SCXRD shows that they belong to the triclinic crystal system with space group P-1. The structural properties of the crystals are also evaluated using powder XRD measurements on their finely crushed powder. These measurements corroborate the results of SCXRD and confirm the triclinic system of the crystals. The optical properties like absorbance and emission of these crystals are determined using UV–Vis and photoluminescence spectroscopy, respectively. These measurements show that the crystals exhibit substantial emission in the blue region. The thermal stability and the decomposition mechanism of the crystals is studied using TG–DTA analysis. The mechanical strength of the crystals is determined using Vickers microhardness technique. The photoresponse of the NH4H3(C4O8)·2H2O crystals is analyzed from light-dependent I–V characteristics, and it is observed that the crystals exhibit photoresistive behavior. © 2020, Akadémiai Kiadó, Budapest, Hungary.
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    A novel effective immobilization of glucose oxidase on Ni0.25Zn0.25Cu0.25Co0.25La0.06Fe1.94O4 – Chitosan nanocomposite as an enzymatic glucose biosensor
    (Elsevier B.V., 2023) Deepapriya, S.; Rodney, J.D.; John, J.; Joshi, S.; Udayashankar, N.K.; Lakshmi Devi, S.; Jerome das, S.
    An effectual enzymatic glucose biosensor has drawn significant attention in the natural world due to its continuous glucose monitoring systems on human beings. A need for accurate and dependable glucose biosensors is needed and has notably augmented the keen interest to synthesize new non-invasive glucose monitoring systems in the recent phase. A novel Ni0.25Zn0.25Cu0.25Co0.25La0.06Fe1.94O4 nanocomposite has been synthesized via the combustion method to develop an appreciable glucose biosensor. The glucose biosensor was fabricated by immobilization of glucose oxidase (GOx) onto chitosan (CH)-Ni0.25Zn0.25Cu0.25Co0.25La0.06Fe1.94O4 heterojunction nanocomposite on FTO glass substrate. The performance of the as-prepared enzymatic glucose biosensor was estimated using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The electrochemical studies revealed an enhanced diffusion of molecules on the electrode surface, superior charge transfer rate, high sensitivity, and fast response time. The Ni0.25Zn0.25Cu0.25Co0.25La0.06Fe1.94O4-CH bi-junction conjoining with GOx exhibits a higher sensitivity of 52.76 µAmM-1cm−2 in a comprehensive undeviating range. The catalytic properties of the electrode in the H2O2 solution were studied using cyclic voltammetry, which showed a good linear response with an increase in scan rate and peak current resulting in enriched electrostatic interaction. In addition, the fabricated biosensor with a low Michaelis-Menten constant contributes a better affinity of the electrode surface towards glucose oxide. © 2023 Elsevier B.V.
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    A study on structural, optical, thermal and electrical properties of the amaranth dye-doped KHOOD single crystal
    (World Scientific Publishing Co. Pte Ltd wspc@wspc.com.sg, 2020) Mahendra, K.; Udayashankar, N.K.
    Influence of amaranth dye on the potassium hydrogen oxalate oxalic acid dihydrate (KHOOD) single crystal is investigated. The structural studies were carried out to understand the crystal behavior after dye incorporation. Optical studies were performed to investigate the photon absorption of the crystal with or without the presence of dye molecule. The absorption of pure crystals were also compared with that of amaranth dye-doped crystals and the bandgap was estimated. The surface morphology and the presence of dye molecules are investigated using scanning electron microscope (SEM) and EDX analysis. The elemental mapping was carried out to understand the distribution of elements in the crystal surface. The thermal behavior of the crystal was studied and compared with that of KHOOD and dye-doped KHOOD crystals in detail. The emission properties of the crystals were studied and compared crystal. Field-dependent I-V studies were performed to study the conductivity of the crystals and results were discussed in detail. © 2020 World Scientific Publishing Company.
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    Aging time correlation in DC magnetron sputtered Ni60Ti40 thin films
    (Elsevier Ltd, 2017) Reddy, B.; Udayashankar, N.K.
    In this work, Intermetallic NiTi thin films have been prepared using glancing angle DC magnetron sputtering technique on Si (1 0 0) substrate maintained at room temperature with separate elemental targets Ni and Ti. The films were solution treated (annealed) at 600 °C for 1 h followed by aging at 500 °C for 2 h, 4 h and 6 h. The degree of crystallinity increases with subsequent solution treatment followed by aging at different times. The hardness and elastic modulus increased from 8.32 to 9.41 GPa and from 148.92 to 163.13 GPa, respectively, with respect to the increase in aging time. From HR-XPS (High Resolution X-ray Photoelectron Spectroscopy) investigations, it was found that the films aged at different times have shown strong tendency to form thicker surface layer TiO2 (metal oxide) onto the film surface due to higher thermodynamic reactivity by leaving Ni-rich precipitates in the matrix immediately behind the metal oxide layer. © 2016 Elsevier Ltd
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    An insight into noticeable dielectric response and effect of fe doping on photocatalytic efficiency (visible light) of ZnO nanoparticles synthesized through solution precipitation for harmful textile dye degradation
    (Springer Science and Business Media B.V., 2024) Mahendra, K.; Fernandes, J.M.; James, A.; B.s, N.; Pattar, J.; Sunitha, D.V.; Gopal, K.; Udayashankar, N.K.
    Iron (Fe)-incorporated zinc oxide (ZnO) nanoparticles (NPs) were synthesized via chemical precipitation technique and studied using powder X-ray diffraction (PXRD), field emission scanning electron microscopy (FESEM), and UV–vis diffuse reflectance spectroscopy. PXRD analysis reveals a hexagonal wurtzite structure for all the synthesized samples. UV–visible measurements demonstrate a reduction in the bandgap of ZnO with an increase in Fe concentration. The ZnO and Fe-incorporated ZnO NPs are studied for the degradation of organic textile dye under visible light irradiation. All the nanoparticles are thoroughly investigated using impedance and dielectric measurements in the frequency range of 20 Hz to 1 MHz. The results obtained are compared, interpreted, and presented in this paper. © The Author(s), under exclusive licence to Springer Nature B.V. 2024.
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    Bi-functional LaMxFe1-xO3 (M = Cu, Co, Ni) for photo-fenton degradation of methylene blue and photoelectrochemical water splitting
    (Elsevier Ltd, 2023) James, A.; Rodney, J.D.; Rao, L.; Badekai Ramachandra, B.R.; Udayashankar, N.K.
    Due to growing concern over environmental remediation and the energy crisis, perovskite nanoparticles have gained wide interest in converting solar energy to sustainable fuel and also in degrading organic effluents. Herein, we report the synthesis and bi-functional activity of one-pot-glycine combustion derived LaMxFe1-xO3 (M = Cu, Co, Ni; x = 0, 0.01) for photo-Fenton degradation of Methylene Blue (MB) and photoelectrochemical water splitting. When used as a photocatalyst, with partial substitution of Cu even at a lower concentration, LaCu0.01Fe0.99O3 has exhibited excellent degradation efficiency of 96.4% in 90 min, which is 2.5 times better than the LaFeO3. On the other hand, Co and Ni modified LaFeO3 photocatalysts have demonstrated prominent activities with degradation efficiency of 93.8% and 74.8% respectively within 180 min of visible light irradiation. The retention and reusability analysis showed that LaCu0.01Fe0.99O3 is stable against photo corrosion and remains unchanged after 5 consecutive cycles of MB dye degradation. In addition, LaCu0.01Fe0.99O3 is complimented as a single catalyst for dual functions such as photocatalysis and electrocatalysis, both of which are assisted by visible light. Under illumination, the overpotential (η) improved from 507.6 mV vs RHE (dark) to 498.1 mV vs RHE (light) for O2 evolution and 220.5 mV vs RHE (dark) to 182.8 mV vs RHE (light) for H2 generation respectively. The light response of the catalyst and improvement in activity is validated by the significant enhancement in current density under exposure at both half cycle of chronoamperometry. © 2023 Hydrogen Energy Publications LLC
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    Cerium-Modulated Zinc Oxide for enhanced Photoelectrochemical Non-Enzymatic biosensing of Cholesterol: An experimental and First Principle Analysis
    (Elsevier B.V., 2024) Rao, L.; Rodney, J.D.; Joy, A.; Shivangi Nileshbhai, C.; James, A.; S, S.; Joyline Mascarenhas, F.; Udayashankar, N.K.; Anjukandi, P.; Chul Kim, B.; Badekai Ramachandra, B.R.
    Herein, we synthesized CexZn1-xO (x = 0.00, 0.01, 0.02, and 0.03) using the wet chemical method. The investigation explores photoelectrochemical (PEC) biosensors for enzyme-free detection of cholesterol, employing Ce0.03Zn0.97O (CZO3)/Nickel Foam (NF) as the active material. The investigation revealed notable enhancements in sensitivity for cholesterol detection, with a recorded activity of 2.812 mA.mM?1.cm?2, marking a twofold increase in comparison to dark mode (1.37 mA.mM?1.cm?2). The Limit of Detection (LOD) was determined to be 17 µM (light) and 28 µM (dark), while the Limit of Quantification (LOQ) was measured at 54 µM (light) and 98 µM (dark) in 0.1 M KOH solution. These findings demonstrate a linear detection range spanning from 80 µM to 2 mM. Ab-initio calculations based on Density Functional Theory (DFT) were carried out on 101 surfaces of both pristine ZnO and CZO3 to understand how the doping affected the pristine ZnO band gap. The findings indicate that CZO3 exhibits superior activity compared to pristine ZnO, underscoring its enhanced performance and potential for sensing application. The CZO3/NF photoelectrochemical (PEC) biosensor displayed notable cyclic stability, retaining 97 % of its performance over a 60-day period. This underscores its potential for reliable and enduring operation in biosensing applications. Additionally, CZO3/NF exhibited robust sensing capabilities when utilized with human serum samples, showcasing consistent performance in both dark and illuminated conditions. © 2024 Elsevier B.V.
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    Cobalt-doped LaFeO3 for photo-Fenton degradation of organic pollutants and visible-light-assisted water splitting
    (Springer, 2024) James, A.; Rodney, J.D.; Manojbabu, A.; Joshi, S.; Rao, L.; Badekai Ramachandra, B.R.; Udayashankar, N.K.
    The increasing demand for clean energy sources and the growing concerns about environmental pollution have led to a significant interest in developing efficient photocatalytic and photoelectrochemical systems. Here, we report the visible-light-induced photo-Fenton catalytic degradation of Methylene Blue (MB) dye over LaFeO3 and LaCo xFe1−xO3 (x = 0.01, 0.05, 0.1) catalysts synthesized via the facile combustion method. The LaCo0.01Fe0.99O3 has significantly enhanced the photo-Fenton catalytic efficiency of LaFeO3 from 67.75 to 93.85% for MB dye removal after 180 min of light irradiation. The rate constants calculated via the pseudo-first-order kinetics mechanism are found to be 0.00532/min for LaFeO3 and 0.01476/min for LaCo0.01Fe0.99O3, respectively. In addition, the most effective LaCo0.01Fe0.99O3 catalyst has demonstrated remarkable degradation performance towards Tetracycline (TC) and Methyl Orange (MO) dye with an efficacy of 93.81% and 69.67%, respectively, indicating its versatility. Further, the pristine and doped LaFeO3 were structurally optimized using DFT, and the computed band gaps were following the experimental data. Interestingly, the same catalyst can be employed as a light-induced electrocatalyst in addition to water treatment by taking advantage of its dual functionality. The LaCo0.01Fe0.99O3 catalyst achieved a benchmark current density of 10 mA/cm2 for H2 evolution at an overpotential of 297 mV vs. RHE which further improved to 190 mV vs. RHE under illumination. This work provides valuable insights on partial Co incorporation at the B-site of LaFeO3 for the development of visible-light-induced photocatalytic and electrocatalytic systems, which is hoped to contribute to the advancement of sustainable energy production and environmental remediation. © 2024, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
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    Contact angle measurement studies on porous anodic alumina membranes prepared using different electrolytes
    (VBRI Press editorialoffice@vbripress.com, 2016) Ramana Reddy, P.R.; Ajith, K.M.; Udayashankar, N.K.
    This paper investigates the effect of pore widening duration on the wetting properties of nanostructured porous anodic alumina (PAA) membranes fabricated using sulphuric and oxalic acid as electrolytes by two step anodization process. XRD analysis shows that prepared PAA membranes were amorphous in nature. With increasing of pore widening durations from 0 to 120 min, the contact angle of PAA membranes varied from 21 to 78°. It was noticed that PAA membranes were hydrophilic in nature in the present of water medium. In the presence of acetone medium, PAA membranes prepared with 1hr pore widening time showed super hydrophilic behaviour. © 2016 VBRI Press.
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    Crystal structure of semiorganic antimony thiourea bromide monohydrate crystals: a redetermination
    (2009) Upadhya, M.K.; Udayashankar, N.K.
    The growth of antimony thiourea bromide monohydrate (ATBM) single crystals by evaporation technique at room temperature is reported here. Antimony thiourea bromide monohydrate crystallizes in the orthorhombic space group Cmca with unit cell parameters a = 12.320(7) A, b = 11.668(7) A, c = 18.615(11), and z = 8. The structure has been solved by direct methods and refined to a final R value of 0.0239.
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    Crystallization kinetics of Si20Te80?xBix (0???x???3) chalcogenide glasses
    (Elsevier Ltd, 2019) Fernandes, B.J.; Ramesh, K.; Udayashankar, N.K.
    In this report, we investigate the crystallization kinetics of Si20Te80?xBix (0 ? x ? 3) chalcogenide glassy systems using differential scanning calorimetry (DSC) technique. Systematic studies are carried out in order to understand the variation of thermal parameters such as glass transition temperature (Tg), onset crystallization temperature (Tc) and peak crystallization temperature (Tp) as a function of composition. Activation energy for glass transition (Eg) and crystallization (Ec) has been calculated based on the relevant statistical methods. Furthermore, thermal parameters such as change in specific heat (?Cp), fragility index (F), thermal stability (?T)& (S), enthalpy (?Hc), entropy (?S) are deduced to interpret distinct material behaviour as a function of composition. Structural evaluation like thermal devitrification studies elucidate the restricted glass formability of the studied glass system. Conclusively, a relationship has been established between the obtained thermal parameters and electrical switching characteristics. © 2019 Elsevier B.V.
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    Crystallization kinetics of Sn doped Ge20Te80?xSnx (0 ? x ? 4) chalcogenide glassy alloys
    (Elsevier Ltd, 2017) Fernandes, B.J.; Naresh, N.; Ramesh, K.; Sridharan, K.; Udayashankar, N.K.
    Chalcogenide semiconductors have evolved as multifunctional materials due to their fascinating thermal, optical, electrical and mechanical properties. In this report, Ge20Te80?xSnx (0 ? x ? 4) glassy alloys are systematically studied in order to understand the effect of variation of Sn content on the thermal parameters such as glass transition (Tg) onset crystallization (Tc), peak crystallization (Tp), melting temperature (Tm), activation energy of glass transition (Eg), and crystallization (Ec). The values of Eg are calculated from the variation of Tg with the heating rate (?), according to Kissinger and Moynihan model, while the values of Ec are calculated from the variation of Tp with the heating rate (?), according to Kissinger, Takhor, Augis-Bennett and Ozawa model. Thermal stability and glass forming ability (GFA) are discussed for understanding the applicability of the synthesized materials in phase change memory (PCM) applications. Thermal parameters are correlated with the electrical switching studies to get an insight into the phase change mechanism. The results of the calculated thermal parameters reveal that the GFA of the synthesized Ge20Te80?xSnx (0 ? x ? 4) glassy alloys has a synchronous relationship with their thermal properties studied through differential scanning calorimetry, indicating their potential for phase-change memory device applications. © 2017 Elsevier B.V.
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    Cu- and Bi-codoped LaFeO3-Decorated MXene Nanosheets for Photo-Fenton Catalysis and Hydrogen Evolution
    (American Chemical Society, 2025) James, A.; Ray, S.; Rodney, J.D.; Carva, K.; Udayashankar, N.K.; Kim, B.C.
    The increasing release of contaminants into the environment and the demand for sustainable energy solutions have prompted the exploration of advanced oxidation methods such as photo-Fenton and photoelectrochemical water splitting. Herein, hierarchical heterostructures of Cu- and Bi-codoped LaFeO3(Bi0.05La0.95Cu0.1Fe0.9O3) (LFOBC)-decorated Ti3C2(MXene) nanosheets were developed by a low-cost one-pot combustion approach. The optimized LFOBC/Mx-7 (Bi0.05La0.95Cu0.1Fe0.9O3/Ti3C2-7) composite demonstrated superior photo-Fenton degradation of tetracycline (TC), achieving 1.69 times higher efficiency than LFOBC and 10.65 times more efficiency than pristine LaFeO3(LFO). This enhanced performance is attributed to strong interfacial coupling, which suppressed photoexcited carrier recombination, as confirmed by PL, TRPL, EIS, and photocurrent studies. Experimental and theoretical work function analyses revealed band bending and the formation of an Ohmic junction at the interface. Furthermore, a degradation mechanism and a reaction pathway were proposed, and the reduction in toxicity levels was identified. The LFOBC/Mx-7 catalyst also exhibited promising results for H2evolution with an overpotential of 156 mV vs RHE under visible-light illumination, which was 2.37 times less than that of LFOBC. These results, therefore, showcase the LFOBC/Mx composite as a multifunctional photocatalyst for both pollutant degradation and sustainable energy generation. © 2025 American Chemical Society
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    Defect-engineered single crystal Bi2Te3 via Sb and Se doping for enhanced thermoelectric performance
    (Springer, 2025) Puthran, S.; Hegde, G.S.; Prabhu, A.N.; Wang, Y.-L.; Kuo, Y.K.; Joshi, S.; Udayashankar, N.K.; Nayak, R.
    The limitation of the single crystal melt growth method to tune the microstructure of the materials in a controlled way and the need for enhancing the thermoelectric properties of single crystal grown Bismuth telluride (Bi2Te3), through defect and microstructural engineering, has motivated this work. In this work, we address this limitation through a controlled doping strategy using antimony (Sb) and selenium (Se) to introduce targeted defects and microstructural modifications within single-crystalline Bi2Te3. Sb and Se substitutions create atomic scale strain, point defects, and micro-grain structures, enhancing phonon scattering without significantly disrupting the crystalline order. The resulting defect-engineered single crystals exhibit improved thermoelectric performance, with a notable reduction in lattice thermal conductivity and retention of excellent electrical properties. The co-doped compositions, Bi2Te2.7Se0.3 and (Bi0.98Sb0.02)2Te2.7Se0.3, exhibited significantly enhanced thermoelectric performance, with Seebeck coefficients reaching ~ 253 ?V/K and ? 211 ?V/K, respectively, over the 10–400 K range. The power factor improved remarkably, showing a ~ 30-fold increase for Bi2Te2.7Se0.3 and ~ 20-fold for the Sb-doped variant, while the figure of merit (ZT) improved by ~ 28.5 and ~ 14 times, respectively. Further, a flexible thermoelectric device fabricated from these optimized materials generated output power of 2.7 nW and 3.35 nW at ambient temperature. The non-monotonic variation of the Seebeck coefficient with Sb content, showing an optimal enhancement at x = 0.04, highlights the delicate balance between carrier concentration and band structure modification, emphasizing moderate Sb substitution achieves the most favorable conditions for thermoelectric performance. Our results present a scalable strategy for bridging the performance gap between pristine single crystals and heavily nanostructured thermoelectrics, opening new avenues for high-efficiency energy harvesting devices. © The Author(s) 2025.
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    Defect-induced measurements of semi-organic ammonium hydrogen oxalate oxalic acid dihydrate single crystals using gamma irradiation
    (Taylor and Francis Ltd., 2022) Mahendra, K.; Maria Fernandes, J.; Udayashankar, N.K.
    The structural, optical, mechanical and electrical properties of pure and 5—20-kGy gamma-irradiated semi-organic single crystals of ammonium hydrogen oxalate oxalic acid dihydrate (NH4H3(C4O8).2H2O) are presented. The crystals were synthesized at room temperature using facile solvent evaporation technique. Powder XRD measurements indicate gradual enhancement in crystallinity and lattice defect annihilation for low radiation dosage. Radiation-induced increase in optical band gap (4.01–4.16 eV) indicates high damage threshold of the crystals. Quenching of photoluminescence is attributed to the lowering of surface defect density with radiation. The influence of gamma radiation on the functional vibrations of the crystals is studied using FTIR-Raman spectroscopy. Vickers microhardness measurements show gradual enhancement in crystal hardness with the increase in radiation. An increase in forward resistance with irradiation is observed from I–V measurements and is attributed to high transparency of the crystals. These results indicate the viability of NH4H3(C4O8) 2H2O crystals in potential space optoelectronic applications. © 2022 Informa UK Limited, trading as Taylor & Francis Group.
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    Defects Enriched p-type Zinc Stannate for Selective Detection of ppb-Level NO2 Gas at Ambient Temperature
    (American Chemical Society, 2024) Pawar, N.; Nath, V.G.; Rodney, J.D.; Joshi, S.; Subramanian, A.; Udayashankar, N.K.
    In this study, we explore the synthesis and gas-sensing capabilities of zinc stannate (Zn2SnO4) in three morphologies─spherical nanoparticles, urchins, and octahedrons─aiming to investigate the influence of morphology on sensing properties. The fabricated devices exhibit a significant resistance decrease upon exposure to NO2 at room temperature (24 °C), indicating p-type sensing behavior. Among these morphologies, the spherical nanoparticle-based sensor exhibits the highest sensor response of 57% to 6 ppm of NO2, outperforming urchins and octahedrons by approximately 1.2 and 4.1 times, respectively. This superior performance, with response and recovery times of 6.3 s and 224 s, is attributed to enhanced redox reactions from a larger surface area and a higher proportion of oxygen interstitials. The spherical nanoparticle-based sensor also demonstrates exceptional selectivity for NO2 over SO2, CO, NH3, and CH4, with a detection limit of 200 ppb. Furthermore, the sensor exhibits excellent reversibility with only 2% variation across 20 consecutive test cycles and demonstrates remarkable long-term stability, with a performance fluctuation of approximately 2.3% over 63 days without significant degradation. © 2024 American Chemical Society.
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    Development of titanium nitride thin film microheaters using laser micromachining
    (Elsevier Ltd, 2022) M.a, M.A.; Lakshmi Ganapathi, K.L.; Ambresh, M.; Nukala, P.; Udayashankar, N.K.; Mohan, S.
    In this paper, we report the fabrication and characterization of titanium nitride (TiN) thin-film-based microheaters. TiN thin films have been optimized on Si and SiO2 substrates for their optimum electrical resistivities by controlling the process parameters, including argon:nitrogen (Ar:N2) ratio in reactive pulsed DC magnetron sputter (PDCMS) deposition technique. An optical emission spectroscope (OES) was used for monitoring the plasma characteristics at various nitrogen flow rates. The microstructural and surface properties of the TiN films have been investigated and correlated with the electrical properties. It has been observed that the amount of nitrogen flux in the TiN plasma plays an essential role in the microstructural, surface, and electrical properties of the TiN thin films. Micro-heaters have been fabricated with TiN thin films with low electrical resistivity using laser engraving techniques instead of conventional lithographic and micromachining techniques. The TiN microheater has shown excellent performance. A temperature of 406 °C has been achieved by applying an input power of 8 W. This work paves the path for developing scalable and economic TiN microheaters using laser micromachining techniques. © 2021
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    Development of Zn-Co alloy coatings by pulsed current from chloride bath
    (2008) Thangaraj, V.; Udayashankar, N.K.; Hegde, A.
    Zinc-M (where M = Ni, Co and Fe) alloy is of great interest owing to their better mechanical and corrosion properties compared with pure zinc coatings. Corrosion resistance of Zn-Co alloy coatings can be improved considerably by pulse plating. The paper details the optimization of Zn-Co alloy bath using pulsed current and details the superiority of pulse plating over direct current plating. Electroplating of Zn-Co alloys over mild steel was carried out under different conditions of pulse parameters like duty cycle, frequency and peak current density. The production and properties of the deposits were found to be influenced by pulse parameters employed. Within the ranges studied, the bath follows anomalous codeposition with preferential deposition of less noble zinc. The influence of current density on %wt. of Co in the deposit and cathode current efficiencies was studied. It was observed that the deposit at average current density of 5.0 A.dm-2, 50% duty cycle and 100 Hz frequency showed excellent corrosion resistance with fine structure. The peak performance of pulse electrodeposit against corrosion was attributed to the change in the surface homogeneity as evidenced by scanning electron microscope (SEM) image. The drastic decrease of corrosion rate in pulse electrodeposit was attributed to the formation of semiconductor films on the surface as supported by impedance spectroscopy signals.
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    Effect of aging and protective coating on the corrosion behavior of 6061 Al / SiCp composite in chloride solutions
    (2011) Rajasekaran, S.; Udayashankar, N.K.; Nayak, J.
    Metal matrix composites considered especially for marine application are typically aluminum-based. Utilization of the composites in marine environments requires adequate corrosion resistance. In this work, the effect of aging and aluminum as resistive coating on the corrosion behavior of 6061 Al / SiC p composite in 1N and 3.5N NaCl solution in the temperature range of 30�C-50�C is studied by means of electrochemical techniques, scanning electron microscope (SEM) and weight loss measurements. Aging results in precipitation of intermetallics in the matrix, this in turn leads to galvanic and pitting corrosion. Pitting initiation and propagation as the main corrosion mechanism was driven by the aging kinetics which is ruled by the reduction in the retained vacancy concentration and at the same time by dislocation density due to the presence of SiCp. Sputtered aluminum coating on the composite effectively resists the pitting initiation and propagation and hence corrosion process. Also the intermetallic precipitates are unexposed to the Chloride solution by the presence of aluminum coating. Hence aluminum coating acts as corrosion resistive coating for the 6061 Al / SiCp aged composites. � (2011) Trans Tech Publications.
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    Effect of aging and protective coating on the corrosion behavior of 6061 Al / SiCp composite in chloride solutions
    (Trans Tech Publications Ltd ttp@transtec.ch, 2011) Rajasekaran, S.; Udayashankar, N.K.; Nayak, J.
    Metal matrix composites considered especially for marine application are typically aluminum-based. Utilization of the composites in marine environments requires adequate corrosion resistance. In this work, the effect of aging and aluminum as resistive coating on the corrosion behavior of 6061 Al / SiC p composite in 1N and 3.5N NaCl solution in the temperature range of 30°C-50°C is studied by means of electrochemical techniques, scanning electron microscope (SEM) and weight loss measurements. Aging results in precipitation of intermetallics in the matrix, this in turn leads to galvanic and pitting corrosion. Pitting initiation and propagation as the main corrosion mechanism was driven by the aging kinetics which is ruled by the reduction in the retained vacancy concentration and at the same time by dislocation density due to the presence of SiCp. Sputtered aluminum coating on the composite effectively resists the pitting initiation and propagation and hence corrosion process. Also the intermetallic precipitates are unexposed to the Chloride solution by the presence of aluminum coating. Hence aluminum coating acts as corrosion resistive coating for the 6061 Al / SiCp aged composites. © (2011) Trans Tech Publications.
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