Faculty Publications
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Item 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.Item Polarity dependent photoisomerization of ether substituted azodyes: Synthesis and photoswitching behavior(Elsevier, 2015) Gan, S.M.; Pearl, Z.F.; Yuvaraj, A.R.; Lutfor, M.R.; Hegde, H.Two new ether substituted azodyes were synthesized and characterized by different spectral analysis such as 1H NMR, 13C NMR, FTIR and UV/Vis. Synthesized compounds were used to study the photoisomerization phenomenon by using UV-Vis spectro-photometer. Interesting polarity dependent effect is observed for the first time on these materials. Trans-cis (E-Z) and cis-trans (Z-E) conversion occurred within 41 s and 445 min, respectively for both the compounds in solutions. Polarizing optical microscopy studies revealed that there is no liquid crystal phase for both the compounds. The dramatic variation in the optical property is speculated to be the polarity of the chemical species. These derivatives are useful to fabricate optical data storage devices. © 2015 Published by Elsevier B.V.Item Fabrication, characterization and catalytic activity of ?-MnO2 nanowires for dye degradation of reactive black 5(Elsevier B.V., 2016) Ramesh, M.; Nagaraja, H.S.; Rao, M.P.; Anandan, S.; Huang, N.M.?-MnO2 nanowires (NWs) prepared by hydrothermal method are characterized using XRD and FT-IR. The crystallite size, surface area of NWs increases, whereas dislocation density and band gap decreases with an increase in oxidizer molarity. The band gap decreases from 2.55 to 1.27 eV. The above observations correlate well with the enhanced catalytic activity of MnO2 NWs for degradation of azo dye reactive black 5 (RB5). About 70% of the dye were successfully removed in 60 min using 20 mg of MnO2 NWs in the presence of 6 mL of H2O2. MnO2 NWs show a good reusability, suggesting it as an effective and recyclable catalyst. © 2016 Elsevier B.V. All rights reserved.Item 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.Item TiO2 nanosheet-graphene oxide based photocatalytic hierarchical membrane for water purification(Elsevier B.V., 2017) Nair, A.K.; JagadeeshBabu, J.There is a rising concern over the toxicity of nanomaterials which emphasizes the need for reforms in application of nanomaterials in water treatment. A hierarchical membrane with a thin layer of photocatalyst coated on top of the membrane surface has emerged as a better alternate for immobilization of photocatalyst. Studies have revealed that nanoparticles are not pliable for synthesis of hierarchical membranes due to their smaller size and low stability after deposition. TiO2 nanosheets serve as better alternate due their thin structure which enables stable layer formation. Integrating the nanosheets with modifiers like graphene oxide can further enhance the photocatalytic activity. The sheet structure of graphene oxide enhances stable film formation and also acts as support for interconnecting TiO2 nanosheets. In the present work, TiO2 nanosheets are modified with graphene oxide and used to develop a hierarchical membrane by depositing a catalyst coating on a support membrane. The hierarchical membrane performance was studied using Congo red dye as model pollutant and the effect of catalyst loading on the permeate flux and dye removal were analyzed. © 2017 Elsevier B.V.Item Chemical free synthesis of graphene oxide in the preparation of reduced graphene oxide-zinc oxide nanocomposite with improved photocatalytic properties(Elsevier B.V., 2018) Meti, S.; Rahman, M.R.; Ahmad, M.I.; Bhat, K.U.In the present investigation, the reduced graphene oxide – zinc oxide (rGO-ZnO) was prepared by rapid microwave-assisted hydrothermal technique. The chemical free graphene oxide (GO), synthesized by Tang Lau technique, was used in the preparation of rGO-ZnO nanocomposite. The GO gets reduced to rGO during microwave irradiation and provides the necessary nucleation site for the ZnO nanorods to grow in [0 0 0 1] direction. These ZnO nanorods were completely wrapped with rGO sheets, confirmed by the synchrotron XRD and TEM techniques. The phases and cell parameters were calculated by Rietveld method. The prepared composite was used for the photodegradation of methyl orange (MO) dye from water under UV light. Investigation revealed that the incorporation of rGO into the ZnO increased the photodegradation ability of the bare ZnO. The performance of the composite is also compared with the rGO-ZnO nanocomposite, where rGO was prepared by Hummer's method. rGO obtained from Tang Lau method formed stable and efficient composite with ZnO and exhibited higher activity compared to the composite, wherein rGO was prepared from conventional Hummer's method. Under UV light, the ZnO liberates photoelectrons which reacts with surface oxygen to form superoxide radicals (O ? 2 ) and (OH ? ) in the water medium. The rGO nanosheets could reduce the charge recombination during the reaction. The active species adsorbs the MO molecules and degrades into CO 2 , H 2 O and other byproducts. More than 3.5 times increase in the rate constant was observed for rGO-ZnO compared to the bare ZnO. © 2018 Elsevier B.V.Item Highly fluorescent materials derived from ortho-vanillin: Structural, photophysical electrochemical and theoretical studies(Elsevier B.V., 2019) Poojary, S.; Acharya, M.; Abdul Salam, A.A.; Kekuda, D.; Nayek, U.; Madan Kumar, S.; Vasudeva Adhikari, A.V.; Dhanya, D.Small-molecule organic fluorophores are highly in demand attributed to their extensive prospective in material and biomedical applications. Particularly, luminescent ?-conjugated organic molecules that possess an efficient solid-state emission are excellent candidates for optoelectronic devices. Focusing on high demand of organic fluorophores, we herein report the synthesis of three organic fluorescent materials derived from o?vanillin, viz. an ester (F1), an azine (F2) and an azo dye (F3). Interestingly, F2 exhibited very intense luminescence in its aggregate phase due to the restriction in intra-molecular rotation (RIR), as demonstrated by solution thickening studies. Further, its Single Crystal X-ray Crystallography (SCXRD) study suggested the existence of various intra and inter molecular interactions and gave evidences for locked intra-molecular rotations of the benzene rings in the rigid conformation of the molecule. The bathochromic shift in fluorescence from solution to solid phase was confirmed by its thin-film emission spectrum, which evidences the formation of J-aggregates. The observed RIR, development of J-aggregates and high conjugation in F2 impart an excellent fluorescence in its aggregated state. Thin films of both F2 and F3 on ITO plates exhibited a bathochromic shift with a deep orange to red photoluminescence on UV excitation. Furthermore, the morphological characterization revealed the presence of clear dense grains in case of F2 and F3, while the DSC analysis indicated phase transitions of all the derivatives. As seen from dielectric measurement studies, the azo dye F3 exhibited the highest dielectric constant among the three derivatives. The electronic and photophysical data based on Density Functional Theory (DFT) and Time Dependent-DFT (TD-DFT) calculations are in agreement with the experimental results. All the above data clearly advocate that, the synthesized fluorophoric o?vanillin derivatives are excellent candidates for electro-optical devices. © 2018 Elsevier B.V.Item Effect of methyl orange dye molecule on the structural, optical and electrical properties of the KHOOD single crystals(Springer, 2020) Mahendra, K.; Pujar, S.; Udayashankar, N.K.In the present investigation, synthesis of pristine and methyl orange dye-doped potassium hydrogen oxalate oxalic acid dihydrate (KHOOD) single crystals are reported. In this study, the structural properties of the crystals were investigated using powder XRD and the effect of dye incorporation on the KHOOD crystal was explored in detail. The effect of dye molecule on the optical absorption of the crystal was studied and the optical band gap was calculated using Tauc relation and presented in detail. Further, the effect on emission and mechanical properties of the crystals were also explored after doping with the dye molecule. Furthermore, the crystals were also studied electrically by subjecting to varying electrical frequencies (A.C) and the properties of pristine and doped crystals were compared and explained in detail. The modulus properties of the crystals were studied and compared. © 2020, Springer-Verlag GmbH Germany, part of Springer Nature.Item Visible light mediated photocatalytic dye degradation using Ag2O/AgO-TiO2nanocomposite synthesized by extracellular bacterial mediated synthesis - An eco-friendly approach for pollution abatement(Elsevier Ltd, 2021) Kulal, D.; Shetty K, V.A large quantity of dyes released with textile industry effluents has raised a lot of concern due to their harmful and toxic effect on the ecosystem. The present study reports a novel method for the synthesis of visible light active photocatalyst by a bacterial based synthesis approach for the degradation of dyes. Ag2O/AgO-TiO2 nanocomposite particles with an average crystallite size of 38» nm, containing rutile TiO2 were synthesized using the cell free supernatant of the culture broth of Alcaligenes aquatilis. The particles were spherical, distinct with average particle size of 39.6» nm. The particles were found to be visible light active with the band gap energy value of 1.5» eV and photocatalytically active in the degradation of Reactive Blue 220 (RB 220). Around 96% of 100» ppm dye could be degraded in 90» min under visible light irradiation using the biosynthesized Ag2O/AgO-TiO2 nanocomposites. The biosynthesized nanocomposite exhibited good solar photocatalytic activity not only in the degradation of RB 220, but also in degrading the azo dyes, such as Acid Yellow 17 and Methyl Orange. The activity of biosynthesized nanocomposite was found to be better than that of Bio-TiO2. These results demonstrated an eco-friendly, potentially economical and greener method for the synthesis of Ag2O/AgO-TiO2 nanocomposites, with involvement of minimum technical challenges in terms of downstream processing and less energy consumption, with a broad scope of application in solar light mediated photocatalytic treatment of waste water. © 2021 Elsevier Ltd.Item Polypyrrole functionalized Cobalt oxide Graphene (COPYGO) nanocomposite for the efficient removal of dyes and heavy metal pollutants from aqueous effluents(Elsevier B.V., 2021) Anuma, S.; Mishra, P.; Badekai Ramachandra, B.R.A cobalt oxide graphene nanocomposite functionalized with polypyrrole (COPYGO) having a heterogenous porous structure was synthesized using hydrothermal method. Microscopic imaging of the COPYGO surface revealed its highly porous and ordered features. The adsorption performance of the COPYGO composite was systemically investigated for Methylene Blue (MB), Congo red (CR) dyes and toxic lead (Pb(II)) and Cadmium (Cd(II)) metals. These were selected as they are the common pollutants in industrial wastewater. The COPYGO was found to be thermally stable up to 195 oC with a specific surface area of 133 m2 g?1. Experimental data indicates that the COPYGO follows Langmuir and Temkin adsorption isotherm. The COPYGO was efficient in removing MB (92.8%), CR (92.2%), Pb(II) (93.08%) and Cd(II) (95.28%) pollutants at pH 7.2, 5.0, 5.5 and 6.1 respectively from the simulated effluents. The maximum adsorption capacity (Qmax) observed for MB 663.018 mg g-1, CR 659.056 mg g-1, Pb(II) 780.363 mg g?1 and Cd(II) 794.188 mg g?1 pollutants. The thermodynamic analysis of the COPYGO indicates that the adsorption is endothermic and spontaneous in nature. COPYGO showed very high efficient removal rate for the pollutants in simulated effluents which guaranteed its benefits and efficacy in industrial wastewater treatment. © 2021 Elsevier B.V.