Faculty Publications
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Item Facile hydrothermal synthesis of vanadium disulfide nanomaterial for supercapacitor application(SPIE, 2023) Mandal, A.; Pandey, N.; Pandey, S.K.; Yadav, A.K.; Chakrabarti, S.Vanadium disulfide (VS2) is a prominent metallic member of transition metal dichalcogenides (TMDs) family and has already demonstrated its flair in energy storage device applications such as supercapacitors and batteries. In this work, we have synthesized hexagonal shape VS2 nanomaterial using a facile one step hydrothermal route and investigated the phase, morphology and structural properties of the material. The formation of phase has been confirmed from the X-ray diffraction (XRD) plot by correlating with the database of Joint Committee on Powder Diffraction Standards (JCPDS) 00-036-1139 of 1T VS2. Further, the crystalline behavior of VS2 nanomaterial can be seen from the high resolution transmission electron microscopy (HRTEM) measurement. Moreover, the morphology of the synthesized material is obtained from the field emission gun-scanning electron microscopy (FEG-SEM). Also, the characteristic Raman peaks of 1T VS2 at 140.3 cm-1 and 192.3 cm-1 have been observed from the Raman spectrum indicating the metallic behavior of synthesized material. The peak at 281.8 cm-1 is attributed to the in-plane vibrational mode (E2g1) while the peak at 404.5 cm-1 represents the out-of-plane vibrational mode (A1g) of V-S bond. The Fourier transform infrared (FTIR) spectrum shows the V-S-V and V=S vibrational modes around 534 cm-1 and 982 cm-1 respectively. The study introduces a low cost, large scale, highly crystalline, and metallic VS2 nanomaterial with potential application for next generation supercapacitors and other energy storage devices. © 2023 SPIE.Item An insight into microscopy and analytical techniques for morphological, structural, chemical, and thermal characterization of cellulose(John Wiley and Sons Inc, 2022) Chakraborty, I.; Rongpipi, S.; Govindaraju, I.; Rakesh, B.; Mal, S.S.; Gomez, E.W.; Gomez, E.D.; Kalita, R.D.; Nath, Y.; Mazumder, N.Cellulose obtained from plants is a bio-polysaccharide and the most abundant organic polymer on earth that has immense household and industrial applications. Hence, the characterization of cellulose is important for determining its appropriate applications. In this article, we review the characterization of cellulose morphology, surface topography using microscopic techniques including optical microscopy, transmission electron microscopy, scanning electron microscopy, and atomic force microscopy. Other physicochemical characteristics like crystallinity, chemical composition, and thermal properties are studied using techniques including X-ray diffraction, Fourier transform infrared, Raman spectroscopy, nuclear magnetic resonance, differential scanning calorimetry, and thermogravimetric analysis. This review may contribute to the development of using cellulose as a low-cost raw material with anticipated physicochemical properties. Highlights: Morphology and surface topography of cellulose structure is characterized using microscopy techniques including optical microscopy, transmission electron microscopy, scanning electron microscopy, and atomic force microscopy. Analytical techniques used for physicochemical characterization of cellulose include X-ray diffraction, Fourier transform infrared spectroscopy, Raman spectroscopy, nuclear magnetic resonance spectroscopy, differential scanning calorimetry, and thermogravimetric analysis. © 2022 Wiley Periodicals LLC.Item Molybdenum based mixed oxide containing Mo0.65V 0.25W0.10 was investigated for the partial oxidation of methanol. The structural property and catalytic activity of the mixed oxide catalyst was studied by surface area (BET), scanning electron microscopy (SEM), energy dispersive X-ray (EDX), Fourier transform infra-red spectroscopy (FTIR) and X-ray diffraction (XRD). The thermal activation of the catalyst resulted increase in the conversion of methanol and the selectivity to formaldehyde. The thermal activation of the MoVW mixed oxide in nitrogen atmospheres induces partial crystallization of a Mo5O14-type oxide at 813 K. The SEM images of the thermally activated catalyst show needle like particles. These particles were agglomerates of platelet-like crystallites of a few hundreds of nanometers in size. SEM and EDX techniques show that the mixed oxide is characterized by an inhomogeneous elemental distribution on the length scale of a few microns. XRD of the thermally activated catalyst showed a nanocrystalline material identified as a mixture of Mo5O 14, MoO3 and MoO2-type MoVW oxides. The catalytic activity of the MoVW mixed oxide show a good conversion of methanol and selectivity to formaldehyde. © 2005 Springer Science+Business Media, Inc.(Partial oxidation of methanol to formaldehyde on molybdenum based mixed oxide catalyst) Badekai Ramachandra, B.; Choi, J.-S.; Choo, K.-Y.; Sung, J.-S.; Song, S.-D.; Kim, T.-H.2005Item 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.Item Third-order nonlinear optical susceptibilities of new copolymers containing alternate 3,4-dialkoxythiophene and (1,3,4-oxadiazolyl)pyridine moieties(Elsevier, 2009) Hegde, P.K.; Vasudeva Adhikari, A.V.; Manjunatha, M.G.; Poornesh, P.; Umesh, G.A new series of conjugated copolymers (P1-P3) consisting of alternate 3,4-dialkoxythiophene and (1,3,4-oxadiazolyl)pyridine moieties have been synthesized using the precursor polyhydrazide route. They have been characterized by FTIR, 1H NMR spectral and elemental analyses. These copolymers possess well defined structure and exhibit good thermal stability with the onset decomposition temperature in nitrogen at around 300 °C. Their molecular weights were determined by gel permeation chromatography (GPC). The optical and charge-transporting properties of the copolymers were investigated by UV-visible spectroscopy, fluorescence emission spectroscopy and cyclic voltammetry. Their UV-visible absorption spectra showed a ?max at around 342 nm and displayed bluish-green fluorescence in solution state. The band gaps were found to be at about 2.55 eV for all the copolymers. The third-order nonlinear optical properties (NLO) of these copolymers were studied by Z-scan technique. The measurements were performed at 532 nm with 7 ns laser pulses using a Nd:YAG laser in solution form. The real part of ?(3) were estimated to be -0.881 × 10-12, -0.901 × 10-12 and -1.030 × 10-12 esu for P1, P2 and P3 respectively. The imaginary part of ?(3) for the copolymers P1, P2 and P3 were determined to be 0.192 × 10-12, 0.253 × 10-12 and 0.272 × 10-12 esu respectively. The copolymers exhibit strong reverse saturable absorption and good optical limiting behaviour at 532 nm. © 2008 Elsevier B.V. All rights reserved.Item Miscibility of polymethylmethacrylate and polyethyleneglycol blends in tetrahydrofuran(2009) Muthu, M.S.; Bhat, D.K.; Renganathan, N.G.The miscibility of polymethylmethacrylate (PMMA) and polyethyleneglycol (PEG) blends in tetrahydrofuran. (THF) has been investigated by viscosity, density, refractive index, and ultrasonic velocity studies. Various interaction parameters such as polymer-solvent and blend-solvent interaction parameters and heat of mixing have been calculated using the viscosity, density, and ultrasonic velocity data. The results indicated the existence of positive interactions in the blend polymer solutions and that they are miscible in THF in the entire composition range. The study also revealed that variation in the temperature does not affect the miscibility of PMMA and PEG blends in THF significantly. The presence of hydrogen bonding in the blends in the solid state has also been indicated by FTIR studies. © 2008 Wiley Periodicals, Inc.Item Microwave-assisted synthesis and magnetic studies of cobalt oxide nanoparticles(2011) Bhatt, A.S.; Bhat, D.K.; Tai, C.-W.; Santosh, M.S.An efficient microwave-assisted route has been used to synthesize nanoparticles of cobalt oxide. The particles were well characterized by transmission electron microscopy (TEM) which showed that the average diameter of the particles is around 6 nm. X-ray diffraction (XRD) studies further confirmed the formation of the spinel Co3O4. Purity of the products was detected by Fourier transform infrared spectroscopy (FTIR) combined with thermal gravimetric analysis (TG/DTG). The magnetic measurements revealed a small hysteresis loop at room temperature indicating a weak ferromagnetic nature of the synthesized Co3O4 nanoparticles. The magnetic moment of the particles was measured to be 4.27 ?eff. © 2010 Elsevier B.V. All rights reserved.Item Characterization of poly(ethylene-co-vinyl acetate-co-carbon monoxide)/layered silicate clay hybrids obtained by melt mixing(2011) Anandhan, S.; Patil, H.G.; Babu, R.R.In recent times, polymer-layered silicate nanocomposites have drawn a great deal of attention because they often exhibit tremendous improvements in material properties compared with virgin polymers or conventional microor macro-composites. In the present study, nanocomposites were developed from organically modified clay and poly(ethylene-co-vinyl acetate-co-carbon monoxide) by melt mixing. FTIR spectroscopy reveals that the interaction between the organoclay and EVACO is thermodynamically favored. High resolution wide angle X-ray diffraction and transmission electron microscopy were used to study the morphology of the nanocomposites. Elemental mapping by scanning electron microscopy indicates good dispersion and distribution of the nanoclay in EVACO matrix. The mechanical properties of the nanocomposites are optimum at a clay loading of 3%. © Springer Science+Business Media, LLC 2011.Item Adsorption of benzene vapor onto activated biomass from cashew nut shell: Batch and column study(Bentham Science Publishers, 2012) Suresh, S.; Vijayalakshmi, G.; Rajmohan, B.; Subbaramaiah, V.The preparation of chemically modified activated cashew nut shell (ACNSB) of different impregnation ratios and their effects in adsorption of benzene vapor were studied. Effects of chemical pre-impregnation using phosphoric acid at different ratios (1:1 and 2:1) were investigated in order to patent. Physico-chemical characterization including surface area, scanning electron microscopy, energy dispersive X-ray spectroscopy, High-resolution Transmission Electron Microscopy and Fourier transform infrared spectroscopy of the ACNSB before and after benzene adsorption have been done to understand the adsorption mechanism. Optimum conditions for benzene removal were found to be, adsorbent dose m=10 g/l of solution and time (t) 120 min for the C0 range of 300-500 mg/l. Adsorption of benzene followed pseudosecond-order kinetics. Langmuir and R-P isotherms were found to best represented data for benzene adsorption onto ACSNB. In ACNSB column experiments, it can be concluded that concentration of benzene increases with the longer breakthrough time and hence higher adsorption capacity. ACSNB are many advantages includes simple and fast, organic solvent recovery, economical, energy savings, environmentally safe aspect and minimize the waste management problem. © 2012 Bentham Science Publishers.Item Synthesis of copper nanofluids using ascorbic acid reduction method via one step solution phase approach(ASTM International, 2012) Shenoy, S.U.; Nityananda Shetty, A.N.A simple one step solution phase approach to synthesize copper nanofluids has been developed, involving simultaneous in situ synthesis of nanoparticles and their dispersion in the base fluid. Copper nitrate has been reduced using ascorbic acid in ethylene glycol under thermal as well as microwave conditions. Sodium lauryl sulfate has been used to control the size of the particle as well as to act as a stabilizing agent. The effect of ratio of the reactants, pH, power of microwave, reaction time, and dilution on the size of the particles has been studied using X-ray diffraction, transmission electron microscopy, and field-emission scanning electron microscopy. The characterization of the fluids has also been done using Fourier transform infrared spectrometry, ultraviolet-visible spectroscopy, selected area electron diffraction, and energy dispersive X-ray analysis. The thermal conductivity and viscosity of the fluid were also measured at various particle concentrations. The copper particles in the fluid were found to have size less than 50nm and were well dispersed in the fluid. Thus this method was found to preserve the advantages of the polyol process and aqueous chemical reduction method as well. The fluid was stable up to 5 weeks under stationary conditions at room temperature. This method employs fast, inexpensive, extendible process for the synthesis of copper nanofluids and also overcomes the drawbacks of two step process. Copyright © 2012 by ASTM International.