Faculty Publications

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    Highly efficient catalytic reductive degradation of various organic dyes by Au/CeO2-TiO2 nano-hybrid
    (Springer India sanjiv.goswami@springer.co.in, 2017) Saikia, P.; Miah, A.T.; Das, P.P.
    Highly improved catalytic reductive degradation of different organic dyes, in the presence of excess NaBH4 over Au/CeO2-TiO2 nano-hybrid as the catalyst is reported in this study. CeO2-TiO2 nanocomposite was prepared by a facile co-precipitation method using ultra-high dilute aqueous solutions. Small amount of Au (only 1 wt%) was loaded onto the nanocomposite material by deposition-precipitation with urea (DPU) method to fabricate the ternary Au/CeO2-TiO2 nano-hybrid. The catalysts were characterized by the representative techniques like XRD, BET surface area, ICP-AES, UV-Vis diffuse reflectance spectroscopy, TEM and XPS. The Au/CeO2-TiO2 nano-hybrid along with NaBH4 exhibited remarkable catalytic activities towards all the probed dyes, namely Methylene Blue, Methyl Orange, Congo Red, Rhodamine B and Malachite Green, with a degradation efficiency of ?100% in a short reaction time. The degradation reaction followed pseudo-first-order kinetics with respect to the concentration of the dye. Different parameters that affect the rate of the reaction are discussed. A plausible mechanism for methylene blue degradation has also been proposed. [Figure not available: see fulltext.] © 2017, Indian Academy of Sciences.
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    Copper complex with N-,O- architecture grafted graphene oxide nanosheet as a heterogeneous catalyst for Suzuki cross coupling reaction
    (Taiwan Institute of Chemical Engineers, 2019) Anuma, S.; Mishra, P.; Badekai Ramachandra, B.R.
    We report a straight forward synthesis of a heterogeneous catalyst by covalently immobilizing copper Schiff base complex on the surface of amino functionalized graphene oxide (AGO) for the Suzuki coupling of substituted aryl halides with arylboronic acids. The as-synthesized complex and subsequent catalyst were characterized for their structural features using suitable techniques. The analysis confirmed that the Cu bound to Schiff base (L) ligand via bi(N-,O-) linkage and Cu-L immobilization on AGO was due to its amino functionality. The catalyst exhibited excellent yield of 94% for Suzuki coupling reactions as analyzed by gas chromatography. The catalyst was recycled for 5 successive reactions with insignificant loss in efficiency. ICP-AES analysis showed the catalyst retained 87.5% of its active metal center after 5th iteration. High yield, environmentally benign, easy work-up procedure, easy separation of catalyst and mild reaction conditions are some of the important facets this catalyst offer. © 2018 Taiwan Institute of Chemical Engineers
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    The catalytic effect of chromium-doped ceria-praseodymium on soot oxidation activity and its kinetics
    (Springer, 2024) Patil, S.S.; Prasad Dasari, H.P.
    Soot generated from the partial combustion of diesel significantly contributes to air pollution, and catalytic oxidation is currently an effective method for removing diesel soot particles. The chromium-doped ceria-praseodymium (Cr-CP) catalyst system is synthesized via solution combustion synthesis and evaluated for soot oxidation activity, with a subsequent kinetics study conducted. The XRD analysis of the catalysts indicated a decrease in crystallite size and increased lattice strain and reactive facet ratios for all Cr-doped CP samples. Raman analysis verified the existence of oxygen vacancy peaks in all chromium-doped CP catalysts. X-ray photoelectron spectroscopy (XPS) revealed the presence of adsorbed H2O or molecular water peaks in the O1s spectra for the 5 Cr-CP catalyst, which also exhibited a high concentration of surface Cr3+ ions. Thermogravimetric analysis (TGA) of soot oxidation indicated that 5 Cr-CP exhibited a superior T50 of 393 ± 2 °C, mostly attributed to the presence of reducible surface Cr3+ ion species. Kinetic analysis was performed on all Cr-doped CP catalysts to assess the kinetic triplets: activation energy, pre-exponential factor, and reaction model. The activation energy was low (87 kJ mol−1, Ozawa method) for 15 Cr-CP, while the pre-exponential factor was higher for 5 Cr-CP (7.39 × 1010 min−1). The Cr-CP catalyst system adhered to a power law, indicating a phase boundary-controlled reaction characterized by nucleation and growth mechanisms. The consistency between experimental and calculated curves confirmed that the developed catalysts adhered to the Avrami-Erofeev equation (Am) or the nucleation and growth model. Graphical Abstract: (Figure presented.) © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024.
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    Utilization of newly configured carbazole-cyanopyridone structural hybrids towards achieving high-performance cyan fluorescent organic light-emitting diodes
    (Royal Society of Chemistry, 2024) Vishrutha, K.S.; Ulla, H.; Raveendra Kiran, M.; Badekai Ramachandra, B.R.; Vasudeva Adhikari, A.V.
    Herein, we report the synthesis, characterization, and device fabrication of novel D-A-D (donor-acceptor-donor) type cyanopyridone-based cyan light-emitting organic materials. These small molecules feature a strong electron-donating N-alkylated carbazole unit affixed to a powerful electron-withdrawing cyanopyridone core that is appended with varying secondary donor groups, producing bipolarity in their structures. All the synthesized molecules were well characterized by employing FT-IR, 1H NMR, and 13C NMR spectroscopy, followed by in-depth photophysical, thermal, electrochemical, and electroluminescent studies. Furthermore, we used the density functional theory (DFT) computational approach in the theoretical investigations to gain deeper insights into their electron cloud distributions and structural features. These fluorophores exhibit emission in the 489-510 nm range accompanied by high Stokes shift values, and their TGA data validate the excellent thermal stability (384 °C). As estimated by cyclic voltammetry, the HOMO and LUMO energy levels were found to be 5.35-5.69 eV and 2.92-3.02 eV, respectively, with band gaps of 2.36-2.74 eV. The optical and electrochemical properties of the luminogens have been successfully fine-tuned by varying the auxiliary donors at the carbazole-cyanopyridine hybrids. Electroluminescent studies proved the compatibility of the novel compounds to be an efficient cyan emissive layer with good performance characteristics. Interestingly, amongst the luminophores, Cz-CyP5 bearing a 4-hydroxyphenyl moiety exhibited a maximum current efficiency of 13.16 cd A−1, high power efficiency of 9.85 lm W−1, and good external quantum efficiency of 5.41%. © 2024 RSC.
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    A comparative analysis of crustacean exoskeletons: structural, microstructural, morphological, and UV absorption studies
    (Institute of Physics, 2024) Nowl, M.S.; Praveen, L.L.; Ambili, V.; Singh, S.; Samad, U.; Seikh, A.H.; Dutta, S.; Mandal, S.
    This study aims to investigate the structural, thermal, and spectral characteristics, along with the ultra-violet (UV) absorption of various marine benthos exoskeletons, such as various species of crabs (Portunus sanguinolentus, Portunus pelagicus, Charybdis feriata) and mantis shrimp (Oratosquilla oratoria). Their unique properties and ability to survive in harsh oceanic environments make them interesting research subjects. This research utilized powder x-ray diffraction (XRD) analysis to determine the crystal structure of the benthic varieties. The sample surface was analyzed using high-resolution micrographs obtained from field-emission scanning electron microscopy (FESEM), which identified the presence of chitin and calcite in the marine benthos. This was further confirmed by differential scanning calorimetry (DSC), and Fourier transform infrared spectroscopy (FTIR). The optical characteristics were investigated using UV-visible spectroscopy. The proximate analysis revealed high protein content in the mantis shrimp exoskeleton compared to other crab species, highlighting its excellent UV absorption characteristics. Overall, this research has the potential to broaden our understanding of marine organisms, which can have potential applications in biotechnology and materials science to develop nature-inspired innovative materials sustainably. © 2024 The Author(s). Published by IOP Publishing Ltd.
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    Investigation of structural, thermal, magnetic, and dielectric properties of Yb+3 doped nickel cobalt ferrite nanomaterial for electro-magnetic applications
    (Springer, 2024) Patil, S.; Meti, S.; Anandalli, M.; Badiger, H.; Bhajantri, R.F.; Pratheek, L.; Muhiuddin, M.; Rahman, M.R.; Hegde, B.G.
    Herein, we report the synthesis of ytterbium (Yb) (with concentration x = 0.01, 0.015, 0.02, 0.025 and 0.03) doped in to nickel cobalt ferrite (NCYFO: YbxNi0.5Co0.5Fe2-xO4) nanoparticles at temperature 500 °C with phase pure spinel using solution combustion technique. The phase purity and effect of doping on NCYFO complex oxide on structural, thermal, magnetic and dielectric properties have been determined by various characterization techniques. The FTIR data reveal that strong metal oxide linkages can be observed in the tetrahedral and octahedral sites at wavenumbers 460 to 410 cm−1 and 595 to 540 cm−1. The X-ray diffraction (XRD) studies confirmed the spinel structure. The crystallite sizes and lattice parameters were estimated to be in the range of 31 to 22 nm and 8.32 to 8.35 Å, respectively. The X-ray photoelectron spectroscopy (XPS) study confirmed that the increase in Yb concentration results in accumulation of Yb in the grain boundaries of NCYFO in the form of Yb2O3. The thermal stability of nanoparticles were investigated using TGA/DSC method. Transmission Electron microscopy (TEM) studies and Field emission scanning electron microscopy (FESEM) used to study the particle size distribution and elemental composition within the nanomaterial. In addition, the dielectric properties, such as, dielectric constant and dielectric loss were investigated for all the NCYFO nanomaterial. The saturation magnetization of the NCYFO is determined using vibrating sample magnetometer (VSM) analysis and is maximum for x = 0.03 (Ms = 97.56 emu/g) sample. The high magnetic behaviour and better dielectric properties of the NCYFO nanomaterials are suitable for electro-magnetic applications. © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2024.
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    Unveiling the mass-loading effect on the electrochemical performance of Mn3O4 thin film electrodes: a combined computational and experimental study
    (Institute of Physics, 2024) Pramitha, A.; Hegde, S.S.; Badekai Ramachandra, B.R.; Yadav K, C.; Chakraborty, S.; Ravikumar, A.; George, S.D.; Sudhakar, Y.N.; Raviprakash, Y.
    The remarkable storage performance of manganese oxide (Mn3O4) makes it an appealing option for use as electrodes in electrochemical capacitors. However, the storage kinetics were significantly influenced by the mass loading of the electrode. Herein, we have inspected the dependency of mass loading on the storage performance of the spray pyrolyzed Mn3O4 thin film electrodes along with the correlation of structural and morphological characteristics. X-ray diffraction and Raman spectroscopic studies proven the formation of spinel Mn3O4 with a tetragonal structure. Morphological analysis revealed that all films exhibited fibrous structures with interconnected patterns at higher mass loadings. Moreover, the surface roughness and wettability of the electrode surface were influenced by variations in mass loading. Notably, thin-film electrode with a mass loading of 0.4 mg cm?2 exhibited the highest specific capacitance value of 168 F g?1 at 5 mV s?1 in a three-electrode system. Further, electrochemical impedance spectroscopic studies showed that there were noticeable changes in the capacitive behaviour of the electrode with respect to variations in mass loading. Moreover, the Dunn approach was employed to differentiate the underlying storage mechanism of the Mn3O4 electrode. Additionally, first-principles Density Functional Theory (DFT) studies were carried out in connection with the experimental study to comprehend the structure and electronic band structure of Mn3O4. This study underscores the critical importance of mass loading for enhancing the storage performance of Mn3O4 thin-film electrodes. © 2024 The Author(s). Published by IOP Publishing 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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    Pyrene carbaldehyde derived carbon dots for detecting water in alcohol and security printing
    (Elsevier B.V., 2024) Ullal, N.; Sahoo, B.; Dhanya, D.; Kulkarni, S.D.; Bhat K, U.; Anand
    This study focuses on preparing Carbon dots (CDs) from Pyrene-1-carbaldehyde (PCA) using a solvothermal method and further purification using column chromatography. The aggregation-induced emission (AIE) of CDs was systematically investigated in a THF/water medium. The CDs showed red shifts in their photoluminescence (PL) spectra upon increase in water content. Scanning electron microscopic (SEM) images revealed the formation of aggregates, while X-ray diffraction (XRD) confirmed that the d-spacing values remains unchanged. The NMR spectrum of the CDs displayed peaks corresponding to aromatic carbon, which disappeared upon addition of water due to ?-? stacking, indicating aggregate formation. Based on the aggregation-induced fluorescence emission mechanism, detection of water content in alcohol is demonstrated. Moreover, the synthesized CDs were used as fluorescent colorant in screen inks along with polyvinyl alcohol (PVA) and hydroxyethyl cellulose (HEC) as binders. The print proofs obtained on UV-dull paper using PVA-based screen ink exhibited fluorescence emission at longer wavelengths and showcased desirable photostability under prolonged UV exposure compared to the prints obtained using HEC-based ink. Moreover, though the PVA based print appeared blue or cyan fluorescent, the actual yellow emissions from the CDs can be visualised using UV block filter. Such features, masked to the forger, but known to the user can be utilised in checking the authenticity of the print. © 2024 The Authors
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    Photocatalytic Degradation of Chlorpyrifos and Tetracycline in Aqueous Medium Using Silver Titanate Perovskite Nanoparticles
    (Springer Science and Business Media Deutschland GmbH, 2024) Joseph, A.; Raval, K.; Manirethan, V.
    Near-infrared (NIR) active silver titanate perovskite (AgTiO3)-based photocatalysis is a potential method for degrading organic pollutants due to its unique structural features, compositional flexibility, and affordability. Herein, we have synthesized novel NIR-active AgTiO3 nanoparticles with a low band gap of 0.92 eV via the hydrothermal method using Ananas comosus leave extract, which is a major agricultural waste worldwide. The produced AgTiO3 nanoparticles were characterized using Fourier Transform Infrared (FTIR) spectroscopy investigations, X-ray photoelectron spectroscopy (XPS), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM) and Energy dispersive X-ray spectroscopy (EDS). The photocatalytic activities of the AgTiO3 nanoparticles toward the degradation of tetracycline and chlorpyrifos under UV, visible, NIR, and solar light irradiation were carefully examined, and the photocatalytic mechanism was proposed using liquid chromatography-mass spectrometry (LC-MS) and high-performance liquid chromatography (HPLC). AgTiO3 nanoparticles completely degraded tetracycline and chlorpyrifos within 27 min and 21 min, respectively. The increased efficiency of AgTiO3 nanoparticles produced by green synthesis over conventional photocatalysts points to a potential advancement avenue for water treatment systems. Furthermore, using agricultural waste like leftover pineapple leaves not only lessens the impact on the environment but also solves the issue of cost when putting these technologies into practice on a larger scale. © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2024.