Browsing by Author "Sridharan, K."

Now showing 1 - 20 of 30

A robust photocatalyst using silver quantum clusters grafted in titanium dioxide nanotubes
(Elsevier B.V., 2022) Shenoy, S.; Sridharan, K.
Enhanced photocatalytic activity resulting from the direct electron transfer from noble metal nanoparticles coupled with semiconductor nanostructures is well reported. However, studies on the photocatalytic activity of semiconductor nanostructures coupled with noble metal clusters that exhibit fascinating chemical, optical, and electronic properties are still limited. In this context, we herein report the fabrication of silver quantum clusters grafted on titanium dioxide nanotubes (AgQCs-TNT) towards the photodegradation of ibuprofen and photoreduction of hexavalent chromium ions under visible light irradiation. The structural, chemical, morphological, and optical properties of the as-synthesized samples were studied through X-ray diffraction, energy-dispersive X-ray spectroscopy, transmission electron microscopy, and UV-visible diffuse reflectance spectroscopy. Interestingly, AgQCs-TNT exhibited excellent photocatalytic efficiency in the degradation of ibuprofen and the reduction of hexavalent chromium ions under visible light irradiation in comparison to their pristine counterparts. Role of scavengers and plausible mechanisms pertaining to the improved photocatalytic activity of AgQCs-TNT due to the synergy between the pristine counterparts are discussed. © 2022
Advanced two-dimensional heterojunction photocatalysts of stoichiometric and non-stoichiometric bismuth oxyhalides with graphitic carbon nitride for sustainable energy and environmental applications
(MDPI, 2021) Sridharan, K.; Shenoy, S.; Girish Kumar, S.G.; Terashima, C.; Fujishima, A.; Pitchaimuthu, S.
Semiconductor-based photocatalysis has been identified as an encouraging approach for solving the two main challenging problems, viz., remedying our polluted environment and the generation of sustainable chemical energy. Stoichiometric and non-stoichiometric bismuth oxyhalides (BiOX and BixOyXz where X = Cl, Br, and I) are a relatively new class of semiconductors that have attracted considerable interest for photocatalysis applications due to attributes, viz., high stability, suitable band structure, modifiable energy bandgap and two-dimensional layered structure capable of generating an internal electric field. Recently, the construction of heterojunction photocatalysts, especially 2D/2D systems, has convincingly drawn momentous attention practicably owing to the productive influence of having two dissimilar layered semiconductors in face-to-face contact with each other. This review has systematically summarized the recent progress on the 2D/2D heterojunction constructed between BiOX/BixOyXz with graphitic carbon nitride (g-C3N4). The band structure of individual components, various fabrication methods, different strategies developed for improving the photocatalytic performance and their applications in the degradation of various organic contaminants, hydrogen (H2) evolution, carbon dioxide (CO2) reduction, nitrogen (N2) fixation and the organic synthesis of clean chemicals are summarized. The perspectives and plausible opportunities for developing high performance BiOX/BixOyXz-g-C3N4 heterojunction photocatalysts are also discussed. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
Bimetallic nanoparticles grafted ZnO hierarchical structures as efficient visible light driven photocatalyst: An experimental and theoretical study
(Elsevier B.V., 2021) Shenoy, S.; Tarafder, K.; Sridharan, K.
Bimetallic nanoparticles (NPs) exhibiting novel properties due to synergy between the individual elements have sparkled significant interest as a co-catalyst in enhancing the photocatalytic efficiency of semiconductor materials. Here, we report the photocatalytic activity of NiAg NPs embedded on hierarchical ZnO structures (NiAg-ZnO). Structural and morphological investigations through X-ray diffraction and scanning electron microscopy confirmed the formation of NiAg-ZnO. UV-Vis diffuse reflectance spectroscopy revealed the decrease in the bandgap energy of NiAg-ZnO (2.65 eV) in comparison to pristine ZnO (3.1 eV). Interestingly, the rate of photodegradation of methylene blue and rhodamine B dye molecules under visible light irradiation are two to three times enhanced with NiAg-ZnO in comparison to Ag-ZnO. Enhanced visible light absorption and effective charge separation due to the synergistic metal-semiconductor interface formed by the embedment of NiAg bimetallic NPs on ZnO led to the improved photocatalytic activity. Experimental results are further confirmed through the first principle electronic band structure calculations. © 2021
Bismuth oxybromide nanoplates embedded on activated charcoal as effective visible light driven photocatalyst
(Elsevier B.V., 2020) Shenoy, S.; Sridharan, K.
Nanostructured bismuth oxybromide (BiOBr) are one among the most significantly researched visible light driven photocatalyst, but their low specific surface area hinders higher rate of photodegradation. Herein, a single-step solution based synthesis technique is adopted to embed BiOBr on very little quantities of activated charcoal (AC), thereby improving its specific surface area and visible light absorption range. Nanoplate morphology of BiOBr and their embedment on AC are confirmed from electron microscopy. Interestingly, the embedment of BiOBr on just 0.5 wt% of AC (BiOBr-AC0.5) significantly enhanced the rate of salicylic acid photodegradation, which was six-fold higher than that of pristine BiOBr. © 2020 Elsevier B.V.
Cadmium sulfide nanostructures: Influence of morphology on the photocatalytic degradation of erioglaucine and hydrogen generation
(2019) Shenoy, S.; Jang, E.; Park, T.J.; Gopinath, C.S.; Sridharan, K.
Size and shape of inorganic materials are known to have great effects on their physical and chemical properties. Here, for the first time we report the visible light driven photocatalytic degradation of erioglaucine a stable organic dye molecule in the presence of chemically synthesized nanoscale CdS with 1D (nanorods), 2D (nanosheets) and 3D (hierarchical) morphology. Visible light driven photocatalytic degradation efficiency of both 1D and 3D CdS in the removal of erioglaucine are identical. Surprisingly, with 5 min of sonication, the highly crystalline 3D CdS stacked with many thin nanowires containing numerous active surface sites exhibited four-fold enhanced photodegradation efficiency in comparison to 1D and 2D CdS. Scavenger studies revealed that electrons and superoxide radicals are primary reactive species involved in the photodegradation of erioglaucine, while cyclic photodegradation studies revealed the good stability of 3D CdS against photocorrosion. Further, the photocatalytic hydrogen evolution studies also revealed the excellent activity of 3D CdS in comparison to 1D and 2D CdS. Thus, we find that the morphology indeed influences the photocatalytic activity. These results reveal that 3D CdS nanostructures investigated in the present work are efficient photocatalysts that could be fine-tuned for both environmental remediation and hydrogen generation applications. 2019 Elsevier B.V.
Cadmium sulfide nanostructures: Influence of morphology on the photocatalytic degradation of erioglaucine and hydrogen generation
(Elsevier B.V., 2019) Shenoy, S.; Jang, E.; Park, T.J.; Gopinath, C.S.; Sridharan, K.
Size and shape of inorganic materials are known to have great effects on their physical and chemical properties. Here, for the first time we report the visible light driven photocatalytic degradation of erioglaucine – a stable organic dye molecule in the presence of chemically synthesized nanoscale CdS with 1D (nanorods), 2D (nanosheets) and 3D (hierarchical) morphology. Visible light driven photocatalytic degradation efficiency of both 1D and 3D CdS in the removal of erioglaucine are identical. Surprisingly, with 5 min of sonication, the highly crystalline 3D CdS stacked with many thin nanowires containing numerous active surface sites exhibited four-fold enhanced photodegradation efficiency in comparison to 1D and 2D CdS. Scavenger studies revealed that electrons and superoxide radicals are primary reactive species involved in the photodegradation of erioglaucine, while cyclic photodegradation studies revealed the good stability of 3D CdS against photocorrosion. Further, the photocatalytic hydrogen evolution studies also revealed the excellent activity of 3D CdS in comparison to 1D and 2D CdS. Thus, we find that the morphology indeed influences the photocatalytic activity. These results reveal that 3D CdS nanostructures investigated in the present work are efficient photocatalysts that could be fine-tuned for both environmental remediation and hydrogen generation applications. © 2019 Elsevier B.V.
Crystallization kinetics of Sn doped Ge20Te80?xSnx (0 ? x ? 4) chalcogenide glassy alloys
(2017) Fernandes, B.J.; Naresh, N.; Ramesh, K.; Sridharan, K.; Udayashankar, N.K.
Chalcogenide semiconductors have evolved as multifunctional materials due to their fascinating thermal, optical, electrical and mechanical properties. In this report, Ge20Te80?xSnx (0 ? x ? 4) glassy alloys are systematically studied in order to understand the effect of variation of Sn content on the thermal parameters such as glass transition (Tg) onset crystallization (Tc), peak crystallization (Tp), melting temperature (Tm), activation energy of glass transition (Eg), and crystallization (Ec). The values of Eg are calculated from the variation of Tg with the heating rate (?), according to Kissinger and Moynihan model, while the values of Ec are calculated from the variation of Tp with the heating rate (?), according to Kissinger, Takhor, Augis-Bennett and Ozawa model. Thermal stability and glass forming ability (GFA) are discussed for understanding the applicability of the synthesized materials in phase change memory (PCM) applications. Thermal parameters are correlated with the electrical switching studies to get an insight into the phase change mechanism. The results of the calculated thermal parameters reveal that the GFA of the synthesized Ge20Te80?xSnx (0 ? x ? 4) glassy alloys has a synchronous relationship with their thermal properties studied through differential scanning calorimetry, indicating their potential for phase-change memory device applications. 2017 Elsevier B.V.
Crystallization kinetics of Sn doped Ge20Te80?xSnx (0 ? x ? 4) chalcogenide glassy alloys
(Elsevier Ltd, 2017) Fernandes, B.J.; Naresh, N.; Ramesh, K.; Sridharan, K.; Udayashankar, N.K.
Chalcogenide semiconductors have evolved as multifunctional materials due to their fascinating thermal, optical, electrical and mechanical properties. In this report, Ge20Te80?xSnx (0 ? x ? 4) glassy alloys are systematically studied in order to understand the effect of variation of Sn content on the thermal parameters such as glass transition (Tg) onset crystallization (Tc), peak crystallization (Tp), melting temperature (Tm), activation energy of glass transition (Eg), and crystallization (Ec). The values of Eg are calculated from the variation of Tg with the heating rate (?), according to Kissinger and Moynihan model, while the values of Ec are calculated from the variation of Tp with the heating rate (?), according to Kissinger, Takhor, Augis-Bennett and Ozawa model. Thermal stability and glass forming ability (GFA) are discussed for understanding the applicability of the synthesized materials in phase change memory (PCM) applications. Thermal parameters are correlated with the electrical switching studies to get an insight into the phase change mechanism. The results of the calculated thermal parameters reveal that the GFA of the synthesized Ge20Te80?xSnx (0 ? x ? 4) glassy alloys has a synchronous relationship with their thermal properties studied through differential scanning calorimetry, indicating their potential for phase-change memory device applications. © 2017 Elsevier B.V.
Eliminated Phototoxicity of TiO2Particles by an Atomic-Layer-Deposited Al2O3Coating Layer for UV-Protection Applications
(2016) Jang, E.; Sridharan, K.; Park, Y.M.; Park, T.J.
We demonstrate the conformal coating of an ultrathin Al2O3layer on TiO2nanoparticles through atomic layer deposition by using a specifically designed rotary reactor to eliminate the phototoxicity of the particles for cosmetic use. The ALD reactor is modified to improve the coating efficiency as well as the agitation of the particles for conformal coating. Elemental and microstructural analyses show that ultrathin Al2O3layers are conformally deposited on the TiO2nanoparticles with a controlled thickness. Rhodamine B dye molecules on Al2O3-coated TiO2exhibited a long life time under UV irradiation, that is, more than 2 h, compared to that on bare TiO2, that is, 8 min, indicating mitigation of photocatalytic activity by the coated layer. The effect of carbon impurities in the film resulting from various deposition temperatures and thicknesses of the Al2O3layer on the photocatalytic activity are also thoroughly investigated with controlled experimental condition by using dye molecules on the surface. Our results reveal that an increased carbon impurity resulting from a low processing temperature provides a charge conduction path and generates reactive oxygen species causing the degradation of dye molecule. A thin coated layer, that is, less than 3 nm, also induced the tunneling of electrons and holes to the surface, hence oxidizing dye molecules. Furthermore, the introduction of an Al2O3layer on TiO2improves the light trapping thus, enhances the UV absorption. 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Eliminated Phototoxicity of TiO2Particles by an Atomic-Layer-Deposited Al2O3Coating Layer for UV-Protection Applications
(Wiley-VCH Verlag, 2016) Jang, E.; Sridharan, K.; Park, Y.M.; Park, T.J.
We demonstrate the conformal coating of an ultrathin Al2O3layer on TiO2nanoparticles through atomic layer deposition by using a specifically designed rotary reactor to eliminate the phototoxicity of the particles for cosmetic use. The ALD reactor is modified to improve the coating efficiency as well as the agitation of the particles for conformal coating. Elemental and microstructural analyses show that ultrathin Al2O3layers are conformally deposited on the TiO2nanoparticles with a controlled thickness. Rhodamine B dye molecules on Al2O3-coated TiO2exhibited a long life time under UV irradiation, that is, more than 2 h, compared to that on bare TiO2, that is, 8 min, indicating mitigation of photocatalytic activity by the coated layer. The effect of carbon impurities in the film resulting from various deposition temperatures and thicknesses of the Al2O3layer on the photocatalytic activity are also thoroughly investigated with controlled experimental condition by using dye molecules on the surface. Our results reveal that an increased carbon impurity resulting from a low processing temperature provides a charge conduction path and generates reactive oxygen species causing the degradation of dye molecule. A thin coated layer, that is, less than 3 nm, also induced the tunneling of electrons and holes to the surface, hence oxidizing dye molecules. Furthermore, the introduction of an Al2O3layer on TiO2improves the light trapping thus, enhances the UV absorption. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Graphitic C3N4/CdS composite photocatalyst: Synthesis, characterization and photodegradation of methylene blue under visible light
(Elsevier B.V., 2020) Shenoy, S.; Tarafder, K.; Sridharan, K.
Design and development of heterojunction photocatalysts is one among the main strategies for improving the photocatalytic activity of semiconductor materials. Here, we report the synthesis of a heterojunction photocatalyst by the embedment of cadmium sulphide (CdS) nanoparticles on the surface of graphitic carbon nitride (g-C3N4) layers through hydrothermal approach. The g-C3N4/CdS heterojunction photocatalyst exhibited two-fold and three-fold enhancement in the photodegradation efficiency in comparison to pristine CdS and g-C3N4, respectively in the removal of 20 ppm methylene blue dye molecules under visible light irradiation. The enhanced photocatalytic activity can be attributed to the formation of heterojunction and the synergistic effect of g-C3N4 and CdS in the promotion of charge separation and charge mobility that was tracked through photoluminescence spectroscopy. © 2020 Elsevier B.V.
Melt quenched vanadium oxide embedded in graphene oxide sheets as composite electrodes for amperometric dopamine sensing and lithium ion battery applications
(2017) Sreejesh, M.; Shenoy, S.; Sridharan, K.; Kufian, D.; Arof, A.K.; Nagaraja, H.S.
Electrochemical sensors and lithium-ion batteries are two important topics in electrochemistry that have attracted much attention owing to their extensive applications in enzyme-free biosensors and portable electronic devices. Herein, we report a simple hydrothermal approach for synthesizing composites of melt quenched vanadium oxide embedded on graphene oxide of equal proportion (MVGO50) for the fabrication of electrodes for nonenzymatic amperometic dopamine sensor and lithium-ion battery applications. The sensing performance of MVGO50 electrodes through chronoamperometry studies in 0.1 M PBS solution (at pH 7) over a wide range of dopamine concentration exhibited a highest sensitivity of 25.02 ?A mM ?1 cm ?2 with the lowest detection limit of 0.07 ?M. In addition, the selective sensing capability of MVGO50 was also tested through chronoamperometry studies by the addition of a very small concentration of dopamine (10 ?M) in the presence of a fairly higher concentration of uric acid (10 mM) as the interfering species. Furthermore, the reversible lithium cycling properties of MVGO50 are evaluated by galvanostatic charge-discharge cycling studies. MVGO50 electrodes exhibited enhanced rate capacity of up to 200 mAhg ?1 at a current of 0.1C rate and remained stable during cycling. These results indicate that MVGO composites are potential candidates for electrochemical device applications. 2017 Elsevier B.V.
Melt quenched vanadium oxide embedded in graphene oxide sheets as composite electrodes for amperometric dopamine sensing and lithium ion battery applications
(Elsevier B.V., 2017) Moolayadukkam, M.; Shenoy, S.; Sridharan, K.; Kufian, D.; Arof, A.K.; Nagaraja, H.S.
Electrochemical sensors and lithium-ion batteries are two important topics in electrochemistry that have attracted much attention owing to their extensive applications in enzyme-free biosensors and portable electronic devices. Herein, we report a simple hydrothermal approach for synthesizing composites of melt quenched vanadium oxide embedded on graphene oxide of equal proportion (MVGO50) for the fabrication of electrodes for nonenzymatic amperometic dopamine sensor and lithium-ion battery applications. The sensing performance of MVGO50 electrodes through chronoamperometry studies in 0.1 M PBS solution (at pH 7) over a wide range of dopamine concentration exhibited a highest sensitivity of 25.02 ?A mM ?1 cm ?2 with the lowest detection limit of 0.07 ?M. In addition, the selective sensing capability of MVGO50 was also tested through chronoamperometry studies by the addition of a very small concentration of dopamine (10 ?M) in the presence of a fairly higher concentration of uric acid (10 mM) as the interfering species. Furthermore, the reversible lithium cycling properties of MVGO50 are evaluated by galvanostatic charge-discharge cycling studies. MVGO50 electrodes exhibited enhanced rate capacity of up to 200 mAhg ?1 at a current of 0.1C rate and remained stable during cycling. These results indicate that MVGO composites are potential candidates for electrochemical device applications. © 2017 Elsevier B.V.
Memory type switching behavior of ternary Ge20Te80-xSnx (0 x 4) chalcogenide compounds
(2016) Fernandes, B.J.; Sridharan, K.; Munga, P.; Ramesh, K.; Udayashankar, N.K.
Chalcogenide compounds have gained huge research interest recently owing to their capability to transform from an amorphous to a crystalline phase with varying electrical properties. Such materials can be applied in building a new class of memories, such as phase-change memory and programmable metallization cells. Here we report the memory type electrical switching behavior of a ternary chalcogenide compound synthesized by doping Tin (Sn) in a germanium-telluride (Ge20Te80) host matrix, which yielded a composition of Ge20Te80-xSnx (0 x 4). Results indicate a remarkable decrease in the threshold switching voltage (V T) from 140 to 61 V when the Sn concentration was increased stepwise, which is attributed to the domination of the metallicity factor leading to reduced amorphous network connectivity and rigidity. Variation in the threshold switching voltage (V T) was noticed even when the sample thickness and temperature were altered, confirming that the memory switching process is of thermal origin. Investigations using x-ray diffraction (XRD) and scanning electron microscopy (SEM) revealed the formation of a crystalline channel that acts as the conduction path between the two electrodes in the switched region. Structural and morphological studies indicated that Sn metal remained as a micro inclusion in the matrix and hardly contributed to the rigid amorphous network formation in Ge20Te80-xSnx. Memory type electrical switching observed in these ternary chalcogenide compounds synthesized herein can be explored further for the fabrication of phase-change memory devices. 2016 IOP Publishing Ltd.
Memory type switching behavior of ternary Ge20Te80-xSnx (0 x 4) chalcogenide compounds
(Institute of Physics Publishing michael.roberts@iop.org, 2016) Fernandes, B.J.; Sridharan, K.; Pumlianmunga, P.; Ramesh, K.; Udayashankar, N.K.
Chalcogenide compounds have gained huge research interest recently owing to their capability to transform from an amorphous to a crystalline phase with varying electrical properties. Such materials can be applied in building a new class of memories, such as phase-change memory and programmable metallization cells. Here we report the memory type electrical switching behavior of a ternary chalcogenide compound synthesized by doping Tin (Sn) in a germanium-telluride (Ge20Te80) host matrix, which yielded a composition of Ge20Te80-xSnx (0 x 4). Results indicate a remarkable decrease in the threshold switching voltage (V T) from 140 to 61 V when the Sn concentration was increased stepwise, which is attributed to the domination of the metallicity factor leading to reduced amorphous network connectivity and rigidity. Variation in the threshold switching voltage (V T) was noticed even when the sample thickness and temperature were altered, confirming that the memory switching process is of thermal origin. Investigations using x-ray diffraction (XRD) and scanning electron microscopy (SEM) revealed the formation of a crystalline channel that acts as the conduction path between the two electrodes in the switched region. Structural and morphological studies indicated that Sn metal remained as a micro inclusion in the matrix and hardly contributed to the rigid amorphous network formation in Ge20Te80-xSnx. Memory type electrical switching observed in these ternary chalcogenide compounds synthesized herein can be explored further for the fabrication of phase-change memory devices. © 2016 IOP Publishing Ltd.
Microwave assisted growth of stannous ferrite microcubes as electrodes for potentiometric nonenzymatic H2O2 sensor and supercapacitor applications
(2016) Bindu, K.; Sridharan, K.; Ajith, K.M.; Lim, H.N.; Nagaraja, H.S.
Electrochemical sensors and supercapacitors are two noteworthy applications of electrochemistry. Herein, we report the synthesis of SnFe2O4 microcubes and Fe2O3 nanorods through a facile microwave assisted technique which are employed in fabricating the electrodes for nonenzymatic hydrogen peroxide (H2O2) sensor and supercapacitor applications. SnFe2O4 microcubes exhibited an enhanced specific capacitance of 172 Fg?1 at a scan rate of 5 mVs?1 in comparison to Fe2O3 nanorods (70 Fg?1). Furthermore, the H2O2 sensing performance of the fabricated SnFe2O4 electrodes through chronopotentiometry studies in 0.1 M PBS solution (at pH 7) with a wide linear range revealed a good sensitivity of 2.7 mV ?M?1 ?g?1 with a lowest detection limit of 41 nM at a signal-to-noise ratio of 3. These results indicate that SnFe2O4 microcubes are excellent materials for the cost effective design and development of efficient supercapacitors as well as nonenzymatic sensors. 2016 Elsevier Ltd
Microwave assisted growth of stannous ferrite microcubes as electrodes for potentiometric nonenzymatic H2O2 sensor and supercapacitor applications
(Elsevier Ltd, 2016) Bindu, K.; Sridharan, K.; Ajith, K.M.; Lim, H.N.; Nagaraja, H.S.
Electrochemical sensors and supercapacitors are two noteworthy applications of electrochemistry. Herein, we report the synthesis of SnFe2O4 microcubes and Fe2O3 nanorods through a facile microwave assisted technique which are employed in fabricating the electrodes for nonenzymatic hydrogen peroxide (H2O2) sensor and supercapacitor applications. SnFe2O4 microcubes exhibited an enhanced specific capacitance of 172 Fg?1 at a scan rate of 5 mVs?1 in comparison to Fe2O3 nanorods (70 Fg?1). Furthermore, the H2O2 sensing performance of the fabricated SnFe2O4 electrodes through chronopotentiometry studies in 0.1 M PBS solution (at pH 7) with a wide linear range revealed a good sensitivity of 2.7 mV ?M?1 ?g?1 with a lowest detection limit of 41 nM at a signal-to-noise ratio of 3. These results indicate that SnFe2O4 microcubes are excellent materials for the cost effective design and development of efficient supercapacitors as well as nonenzymatic sensors. © 2016 Elsevier Ltd
Nonlinear transmittance and optical power limiting in magnesium ferrite nanoparticles: effects of laser pulsewidth and particle size
(2016) Perumbilavil, S.; Sridharan, K.; Abraham, A.R.; Janardhanan, H.P.; Kalarikkal, N.; Philip, R.
We report comparative measurements of size dependent nonlinear transmission and optical power limiting in nanocrystalline magnesium ferrite (MgFe2O4) particles excited by short (nanosecond) and ultrashort (femtosecond) laser pulses. A standard sol-gel technique is employed to synthesize particles in the size range of 10-50 nm, using polyvinyl alcohol as the chelating agent. The structure and morphology of the samples are studied using X-ray diffraction, scanning electron microscopy and transmission electron microscopy. Growth of the particles in time is tracked through Fourier transform infrared spectroscopy. Nonlinear transmission measurements have been carried out using the open aperture Z-scan technique employing 532 nm, 5 nanosecond pulses and 800 nm, 100 femtosecond pulses, respectively. The measured optical nonlinearity is primarily of a reverse saturable absorption (RSA) nature, arising mostly from excited state absorption for nanosecond excitation, and two-photon absorption for femtosecond excitation. The optical limiting efficiency is found to increase with particle size for both cases. The calculated nonlinear parameters indicate that these materials are potential candidates for optical limiting applications. The Royal Society of Chemistry.
Nonlinear transmittance and optical power limiting in magnesium ferrite nanoparticles: effects of laser pulsewidth and particle size
(Royal Society of Chemistry, 2016) Perumbilavil, S.; Sridharan, K.; Abraham, A.R.; Janardhanan, H.P.; Kalarikkal, N.; Philip, R.
We report comparative measurements of size dependent nonlinear transmission and optical power limiting in nanocrystalline magnesium ferrite (MgFe2O4) particles excited by short (nanosecond) and ultrashort (femtosecond) laser pulses. A standard sol-gel technique is employed to synthesize particles in the size range of 10-50 nm, using polyvinyl alcohol as the chelating agent. The structure and morphology of the samples are studied using X-ray diffraction, scanning electron microscopy and transmission electron microscopy. Growth of the particles in time is tracked through Fourier transform infrared spectroscopy. Nonlinear transmission measurements have been carried out using the open aperture Z-scan technique employing 532 nm, 5 nanosecond pulses and 800 nm, 100 femtosecond pulses, respectively. The measured optical nonlinearity is primarily of a reverse saturable absorption (RSA) nature, arising mostly from excited state absorption for nanosecond excitation, and two-photon absorption for femtosecond excitation. The optical limiting efficiency is found to increase with particle size for both cases. The calculated nonlinear parameters indicate that these materials are potential candidates for optical limiting applications. © The Royal Society of Chemistry.
Novel N-substituted-5-phenyl-1H-pyrazole-4-ethyl carboxylates as potential NLO materials
(2013) Chandrakantha, B.; Isloor, A.M.; Sridharan, K.; Philip, R.; Shetty, P.; Padaki, M.
In the present investigation we have synthesized a novel series of N-substituted-5-phenyl-1H-pyrazole-4-ethyl carboxylates, which are characterized by 1H NMR, UV-Vis and FT-IR spectroscopy methods. The optical nonlinearity of the compounds in chloroform solution has been studied at 532nm using 5ns laser pulses, employing the open-aperture z-scan technique. It is found that compound 3c having carboxylic acid group and ester substituent has maximum nonlinearity. From measurements we conclude that compounds 3c (4-[4-(ethoxycarbonyl)-5-phenyl-1H-pyrazol-1-yl]benzoic acid) and 3e (ethyl 1-(2-bromophenyl)-5-phenyl-1H-pyrazole-4-carboxylate) are potential candidates for optical limiting applications. 2011.