Faculty Publications

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    Synthesis, characterization and nonlinear optical properties of 2-[(E)-2-(4-ethoxyphenyl)ethenyl]-1-methylquinolinium 4-substitutedbenzenesulfonate compounds
    (2010) Ruanwas, P.; Kobkeatthawin, T.; Chantrapromma, S.; Fun, H.-K.; Philip, R.; Smijesh, N.; Padaki, M.; Isloor, A.M.
    In the present investigation, 2-[(E)-2-(4-ethoxyphenyl)ethenyl]-1-methylquinolinium 4-substituted benzenesulfonate (X = CH3 (1), X = OCH3 (2), X = Cl (3), X = Br (4)) have been synthesized and characterized by 1H NMR, UV-Vis and FT-IR spectroscopy methods. In addition compound 3 was also characterized by single crystal X-ray diffraction (XRD) and found that it crystallized out in the monoclinic space group P21 with cell parameters, a = 9.8072(9) Å, b = 6.4848(5) Å, c = 19.4405(16) Å, ? = 90°, ? = 103.421(5)°, ? = 90°, z = 2 and V = 1202.61(17) Å3. The nonlinear optical absorption of the samples has been studied at 532 nm using 5 ns laser pulses, employing the open-aperture z-scan technique. It is found that some of the samples are potential candidates for optical limiting applications. © 2009 Elsevier B.V. All rights reserved.
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    Solar light induced photocatalytic degradation of Reactive Blue 220 (RB-220) dye with highly efficient Ag@TiO2 core-shell nanoparticles: A comparison with UV photocatalysis
    (2014) Khanna, A.; Shetty K, K.
    Ag core-TiO2 shell (Ag@TiO2) structured nanoparticles with Ag to TiO2 molar ratio of 1:1.7 were synthesized using one pot synthesis method and post calcination was carried out at 450°C for 3h to convert it from amorphous to crystalline form. The Ag core and TiO2 shell formation was confirmed by TEM and AFM. The particle size analysis revealed the average size of Ag@TiO2 as approximately around 30nm. EDS spectra showed the presence of O, Ag, and Ti elements. The improvement in optical properties was proved by DRS which showed significant red shift by Ag core in visible region. Ag@TiO2 exhibited better photocatalytic activity as compared to Degussa P25-TiO2, synthesized TiO2, and the Ag doped TiO2 photocatalysts under UV and solar light irradiation for degradation of Reactive Blue 220 (RB-220) dye. Higher rate of photocatalysis of RB-220 with Ag@TiO2 was obtained under solar light irradiation as compared to UV light irradiation, confirming the capability of the catalyst to absorb both UV and visible light. The kinetics of degradation of dye was found to follow modified Langmuir Hinshelwood (L-H) kinetic model. Ag@TiO2 can be recycled without much decline in the efficacy. Ag@TiO2 has been found to be the effective photocatalyst for degradation of water contaminated with azo dyes under both UV and solar light irradiations. © 2013 Elsevier Ltd.
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    Influence of Sn doping on photoluminescence and photoelectrochemical properties of ZnO nanorod arrays
    (Kluwer Academic Publishers, 2014) Santhosh Kumar, A.S.; Huang, N.M.; Nagaraja, H.S.
    Herein, the nanostructured Sn containing ZnO is directly synthesized on the surface of substrate by modified sol gel approach under low-temperature condition. The samples are characterized by scanning electron microscopy (SEM), x-ray diffraction (XRD), Raman-scattering, photoluminescence (PL) and photoelectrochemical analyses. The SEM micrographs show that the undoped and 1 at. % Sn doped films are composed of nanorods and the concentration of 2 at. % Sn doping hinders the rod-like structure's growth and modulates into granular nature. The investigations of XRD reveal that the synthesized undoped and Sn doped ZnO nanorods possess a perfect hexagonal growth habit of wurtzite zinc oxide, along the (002) direction of preference. The Raman spectra demonstrate that the vibrational mode of E1(LO), which is very weak in undoped and 1at. % Sn doped ZnO, is strongly enhanced with 2 at. % Sn doping into ZnO lattice. PL spectra show that strong UV emission in pure and 1 at. % Sn doped ZnO, while there is dominant green emission in 2 at. % Sn doped ZnO. Moreover, all the samples are photo electrochemically active and exhibit the highest photocurrent of 28 ?A for the 1 at. % Sn doped ZnO nanorod arrays in 0.2M Na2SO4 electrolyte, on light irradiation. Time dependent photoresponse tests are carried out by measuring the photocurrent under chopped light irradiation. © 2014 The Korean Institute of Metals and Materials and Springer Science+Business Media Dordrecht.
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    New luminescent 2-methoxy-6-(4-methoxy-phenyl)-4-p-tolyl-nicotinonitrile: Synthesis, crystal structure, DFT and photophysical studies
    (2014) Ahipa, T.N.; Kamath, P.R.; Kumar, V.; Vasudeva Adhikari, A.V.
    In the current communication, we report the synthesis, spectroscopic, crystal structure, DFT and photophysical studies of a new nicotinonitrile derivative, viz. 2-methoxy-6-(4-methoxy-phenyl)-4-p-tolyl-nicotinonitrile (2) as a potential blue light emitting material. The compound 2 was synthesized in good yield via a simple route. The acquired spectral and elemental analysis data were in consistent with the chemical structure of 2. The single crystal study further confirms its three dimensional structure, molecular shape, and nature of short contacts. Its DFT calculations reveal that compound 2 possesses a non-planar structure and its theoretical IR spectral data are found to be in accordance with experimental values. In addition, its UV-visible and fluorescence spectral measurements prove that the compound exhibits good absorption and fluorescence properties. Also, it shows positive solvatochromic effect when the solvent polarity was varied from non-polar to polar. © 2014 Elsevier B.V. All rights reserved.
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    Novel RGO-ZnWO4-Fe3O4 nanocomposite as high performance visible light photocatalyst
    (Royal Society of Chemistry, 2016) Mohamed, M.M.J.; Shenoy, U.S.; Bhat, D.K.
    A novel RGO-ZnWO4-Fe3O4 nanocomposite is synthesized by a microwave irradiation method and its catalytic activity for the photo degradation of Methylene Blue (MB) is investigated. The prepared nanocomposites are characterized by powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), high resolution transmission electron microscopy (HRTEM), transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), Raman spectroscopy, photoluminescence spectroscopy (PL) and UV-visible spectroscopy. The visible light photocatalytic activities of the prepared nanocomposites are investigated using a MB dye solution. It is noteworthy that RGO-ZnWO4-Fe3O4 nanocomposites exhibited relatively high photocatalytic activity compared to ZnWO4-RGO and pure ZnWO4 on MB in aqueous solution. This enhanced rate is due to the ability of the graphene in the RGO-ZnWO4-Fe3O4 composite to support carrier exploitation efficiently by tolerating the photo excited electron-hole pairs and thus encouraging oxidative degradation of the pollutants. This work could be extended to other organic pollutants as well and could provide new insights into ternary nanocomposites as high performance photocatalysts and their application in waste water treatment. © 2016 The Royal Society of Chemistry.
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    D-A conjugated polymers containing substituted thiophene, 1,3,4-oxadiazole and non-conjugation linkers: Synthesis and study of optical and electrochemical properties
    (Springer India sanjiv.goswami@springer.co.in, 2016) Prashanth Kumar, K.R.; Udayakumar, D.; Siji Narendran, N.K.; Chandrasekharan, K.; Srivastava, R.
    In this communication, we report synthesis and characterization of new D-A conjugated polymers (P1-P3) consisting of electron-donating (D) 3,4-didodecyloxythiophene, electron-accepting (A) 1,3,4-oxadiazole unit and non-conjugation linkers. The conjugated segment in P1-P3 contains only five aromatic rings resulting in short conjugation length, but has an alternate D-A arrangement which significantly enhances the intramolecular charge transfer (ICT) interaction within the segment. As a result, these polymers exhibited low optical band gap in the range 2.51–2.76 eV. Fluorescence emission studies revealed that the polymer thin films emit intense blue light with emission maxima in the wavelength rage 430–480 nm. All three polymers undergo both oxidation and reduction processes under electrochemical conditions. Further, these polymers (P1–P3) exhibit low-lying HOMO and LUMO levels as a result of D-A structure of the conjugated segment. Polymer light-emitting devices were fabricated using these polymers as emissive layer with a device configuration of ITO/MoO 3/polymer/LiF/Al. The test device based on P2 emitted blue light with a low threshold voltage of 5 V. Z-scan studies reveal that the polymers exhibit a strong optical limiting behavior. The value of the nonlinear absorption coefficient (?) of polymers is of the order 10 ?11m/W which indicates that these materials may be accomplished for fabricating optical limiters. [Figure not available: see fulltext.] © 2016, Indian Academy of Sciences.
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    Use of light emitting diodes (LEDs) for enhanced lipid production in micro-algae based biofuels
    (Elsevier B.V., 2017) Severes, A.; Hegde, S.; D'Souza, L.; Hegde, S.
    Microalgae are an alternative source for renewable energy to overcome the energy crises caused by exhaustion of fuel reserves. Algal biofuel technology demands a cost effective strategy for net profitable productivity. Inconsistent illumination intensities hinder microalgal growth. The light-utilizing efficiency of the cells is critical. Light scarcity leads to low production and high intensities cause photo-inhibition. We report effective usage of LEDs of different band wavelengths on the growth of microalgae in a closed, controlled environment to generate biomass and lipid yields. Among the different intensity and wavelengths tested. The light intensities of 500 lx of blue-red combination gave maximum biomass in terms of cell density. LED of red light 220 lx wavelength doubled the lipid dry weight from 30% (w/w) in white light to 60% (w/w). Thin layer lipid chromatogram demonstrated a dense and prominent spot of triacylglycerols in the red light, 220 lx grown cultures. The FTIR profile indicates that different wavelength exposure did not alter the functional groups or change the chemical composition of the extracted lipids ensuring the quality of the product. We reiterate the fact that combination of red and blue LEDs is favoured over white light illumination for generation of biomass. In addition, we report an exciting finding of exposure to LEDs of red wavelength post-biomass generation lead to enhanced lipid production. This simple process doubled the lipid content harvested in 20 days culture period. © 2017 Elsevier B.V.
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    Synthesis, photophysical and electroluminescence studies of new triphenylamine-phenanthroimidazole based materials for organic light emitting diodes
    (Elsevier B.V., 2018) Tagare, J.; Ulla, H.; Satyanarayan, M.N.; Sivakumar, S.
    In this work, two star-shaped small conjugated materials, namely tris(4-(1-phenyl-1H-phenanthro[9,10-d]imidazol-2-yl)phenyl) amine (PIPTPA) and tris(4-(1-p-tolyl-1H-phenanthro[9,10-d]imidazol-2-yl)phenyl)amine (PITTPA) with donor-?-acceptor (D-?-A) structures, were designed and synthesized by combining three phenanthroimidazole arms into an triphenylamine core. A detailed photophysical, thermal, electrochemical and related properties were systematically studied. Furthermore, theoretical calculations (DFT and TD-DFT) were performed to get a better understanding of the electronic structures. Both the materials were found to exhibit high glass transition temperatures (~ 238 °C) and high thermal stabilities with decomposition temperatures up to 298 °C. OLEDs using these materials as emissive materials showed excellent device performance (7.42 cd A?1, 5.77 lm W?1, 4.14% at 100 cd m?2) with green emission and low turn-on voltages. The results demonstrate that TPA integrated with phenthroimdazole plays an important role in the device performance. © 2017 Elsevier B.V.
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    Visible light-induced photocatalytic degradation of Reactive Blue-19 over highly efficient polyaniline-TiO2 nanocomposite: a comparative study with solar and UV photocatalysis
    (Springer Verlag service@springer.de, 2018) Kalikeri, S.; Kamath, N.; Gadgil, D.J.; Shetty K, V.
    Polyaniline-TiO2 (PANI-TiO2) nanocomposite was prepared by in situ polymerisation method. X-ray diffractogram (XRD) showed the formation of PANI-TiO2 nanocomposite with the average crystallite size of 46 nm containing anatase TiO2. The PANI-TiO2 nanocomposite consisted of short-chained fibrous structure of PANI with spherical TiO2 nanoparticles dispersed at the tips and edge of the fibres. The average hydrodynamic diameter of the nanocomposite was 99.5 nm. The band gap energy was 2.1 eV which showed its ability to absorb light in the visible range. The nanocomposite exhibited better visible light-mediated photocatalytic activity than TiO2 (Degussa P25) in terms of degradation of Reactive Blue (RB-19) dye. The photocatalysis was favoured under initial acidic pH, and complete degradation of 50 mg/L dye could be achieved at optimum catalyst loading of 1 g/L. The kinetics of degradation followed the Langmuir-Hinshelhood model. PANI-TiO2 nanocomposite showed almost similar photocatalytic activity under UV and visible light as well as in the solar light which comprises of radiation in both UV and visible light range. Chemical oxygen demand removal of 86% could also be achieved under visible light, confirming that simultaneous mineralization of the dye occurred during photocatalysis. PANI-TiO2 nanocomposites are promising photocatalysts for the treatment of industrial wastewater containing RB-19 dye. © 2017, Springer-Verlag GmbH Germany, part of Springer Nature.
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    Solar light-driven photocatalysis using mixed-phase bismuth ferrite (BiFeO3/Bi25FeO40) nanoparticles for remediation of dye-contaminated water: kinetics and comparison with artificial UV and visible light-mediated photocatalysis
    (Springer Verlag service@springer.de, 2018) Kalikeri, S.; Shetty K, V.
    Mixed-phase bismuth ferrite (BFO) nanoparticles were prepared by co-precipitation method using potassium hydroxide as the precipitant. X-ray diffractogram (XRD) of the particles showed the formation of mixed-phase BFO nanoparticles containing BiFeO3/Bi25FeO40 phases with the crystallite size of 70 nm. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) revealed the formation of quasi-spherical particles. The BFO nanoparticles were uniform sized with narrow size range and with the average hydrodynamic diameter of 76 nm. The band gap energy of 2.2 eV showed its ability to absorb light even in the visible range. Water contaminated with Acid Yellow (AY-17) and Reactive Blue (RB-19) dye was treated by photocatalysis under UV, visible, and solar light irradiation using the BFO nanoparticles. The BFO nanoparticles showed maximum photocatalytical activity under solar light as compared to UV and visible irradiations, and photocatalysis was favored under acidic pH. Complete degradation of AY-17 dyes and around 95% degradation of RB-19 could be achieved under solar light at pH 5. The kinetics of degradation followed the Langmuir–Hinshelhood kinetic model showing that the heterogeneous photocatalysis is adsorption controlled. The findings of this work prove the synthesized BFO nanoparticles as promising photocatalysts for the treatment of dye-contaminated industrial wastewater. © 2018, Springer-Verlag GmbH Germany, part of Springer Nature.