Faculty Publications
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Item Third order nonlinear optical properties and two photon absorption in newly synthesized phenyl sydnone doped polymer(2007) Shettigar, S.; Umesh, G.; Chandrasekharan, K.; Kalluraya, B.We have investigated third order nonlinear optical properties of three newly synthesized 3-phenyl sydnones, doped into PMMA and determined both real and imaginary part of ?(3). The measurements were performed using nanosecond laser pulses at 532 nm wavelength by employing Z-Scan technique. The nonlinear refractive index is found to be of the order of 10-14 cm2/W. The magnitude of third order susceptibility is of the order of 10-13 esu. Their two photon absorption coefficient and absorption cross section have also been determined. The optical power limiting behavior of sydnone moieties doped PMMA was also investigated. The results suggest that among the three organic phenyl sydnone moieties, 2-benzylhydrazono-5-(3-p-tolylsydnone-4-yl)1,3,4,-thiadiazine doped PMMA is a promising class of nonlinear optical material due to its simple molecular structure with p-tolyl group. It also shows a very good optical limiting behaviour with a limiting threshold of 0.21 mJ/pulse. The nonlinear parameters obtained are comparable with the values obtained in stilbazolium like dye such as trans-4-[2-(pyrrl)vinyl]-1-methylpyridium iodide. Hence this material may be tailored suitably for applications such as optical power limiters, switches and modulators. © 2007 Elsevier B.V. All rights reserved.Item Synthesis, characterization and studies on the nonlinear optical parameters of hydrazones(2010) Naseema, K.; Sujith, K.V.; Manjunatha, K.B.; Kalluraya, B.; Umesh, G.; Rao, V.Three hydrazones, 2-(4-methylphenoxy)-N?-[(1E)-(4-nitrophenyl)methylene]acetohydrazide (compound-1), 2-(4-methylphenoxy)-N?-[(1E)-(4-methylphenyl)methylene]acetohydrazide ((compound-2) and N?-{(1E)-[4-(dimethylamino)phenyl]methylene}-2-(4-ethylphenoxy) acetohydrazide(compound-3) were synthesized and their third order nonlinear optical properties were investigated using a single beam z-scan technique with nanosecond laser pulses at 532 nm. Open aperture data obtained from the three compounds indicates two photon absorption at this wavelength. The nonlinear refractive index n2, the nonlinear absorption coefficient ?, the magnitude of the effective third order susceptibility ?(3), the second order hyperpolarizability ?h and the coupling factor ? have been estimated. The values obtained are comparable with the values obtained for 4-methoxy chalcone derivatives and dibenzylidene acetone derivatives. Among the compounds studied, compounds-1 and 3 exhibited the better optical power limiting behaviour at 532 nm. Our studies suggest that compounds-1, 2 and 3 are potential candidates for optical device applications such as optical limiters and optical switches. © 2009 Elsevier Ltd. All rights reserved.Item Synthesis, characterization and studies on nonlinear optical parameters of 4-amino-5-(4-nitrophenyl)-1, 2, 4-triazole-3-thione(2010) Naseema, K.; Rao, V.; Manjunatha, K.B.; Umesh, G.; Sujith, K.V.; Kalluraya, B.In this paper, we report the synthesis, characterization and third order nonlinear optical properties of a new organic NLO material of 4-amino-5-(4-nitrophenyl)-1, 2, 4-triazole-3-thione (ANIT). The material was characterized by UV-vis and FTIR studies. The third order nonlinear optical properties have been investigated in dimethyl formamide (DMF) solution at 532 nm by using the Z-scan technique with pulses of nanoseconds duration. Open aperture data demonstrates the presence of two photon absorption at this wavelength. The nonlinear absorption coefficient ?, the nonlinear refractive index n2, the magnitude of effective third order susceptibility ?(3) and the second order hyperpolarizability ?h have been estimated as 2.99 cm/GW, -2. 53?×?10-11 esu, 2.72?×?10 -13esu and 0.281?×?10-31esu respectively. The values obtained are comparable with the values obtained for 4-methoxy chalcone derivatives and dibenzylideneacetone derivatives. The value of coupling factor have been estimated to be 0.17, indicating that the nonlinearity is electronic in origin. The compound exhibits good optical limiting at 532 nm with the limiting threshold of 80 ?J/pulse. The comparatively high value obtained indicates that this material may be used in optical device applications like optical limiters and optical switches. © 2010 Optical Society of India.Item Third order optical nonlinearity and optical limiting studies of propane hydrazides(Elsevier B.V., 2012) Naseema, K.; Manjunatha, K.B.; Sujith, K.V.; Umesh, G.; Kalluraya, B.; Rao, V.Four hydrazones, 2-(4-isobutylphenyl)-N?-[phenylmethylene] propanehydrazide (P1), 2-(4-isobutylphenyl)-N?-[(4- tolyl)methylene] propane hydrazide (P2), 2-(4-isobutylphenyl)- N?-[1-(4- chlorophenyl)ethylidene] propanehydrazide (P3) and 2-(4-isobutylphenyl)-N?-[1-(4-Nitrrophenyl)ethylidene] propane hydrazide (P4) were synthesized and their third order nonlinear optical properties have been investigated using a single beam Z-scan technique with nanosecond laser pulses at 532 nm. The measurement on the compound-P1 is not reported as there is no detectable nonlinear response. Open aperture data of the other three compounds indicate two photon absorption at this wavelength. The nonlinear refractive index n2, nonlinear absorption coefficient ?, magnitude of effective third order susceptibility ?(3), the second order hyperpolarizability ?h and the coupling factor ? have been estimated. The values obtained are comparable with the values obtained for 4-methoxy chalcone derivatives and dibenzylideneacetone derivatives. The experimentally determined values of ?, n2, Re ?(3) and Im ?(3), ?h and ? of the compound-P4 are 1.42 cm/GW, -0.619 × 10-11 esu, -0.663 × 10-13 esu, 0.22 × 10-13 esu, 0.34 × 10-32 esu and 0.33 respectively. Further the compound-P4 exhibited the best optical power limiting behavior at 532 nm among the compounds studied. Our studies suggest that compounds P2, P3 and P4 are potential candidates for the optical device applications such as optical limiters and optical switches. © 2012 Elsevier B.V. All rights reserved.