Faculty Publications
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Item Hydrogen bond-driven columnar self-assembly of electroluminescent D-A-D configured cyanopyridones(Royal Society of Chemistry, 2018) Vinayakumara, D.R.; Ulla, H.; Kumar, S.; Pandith, A.; Satyanarayan, M.N.; Shankar Rao, D.S.S.; Prasad, S.K.; Vasudeva Adhikari, A.Herein, we report the design and synthesis of a new series of flying bird-shaped liquid crystalline (LC) cyanopyridone derivatives with a D-A-D architecture, CPO-1 to CPO-4. Their mesomorphic, photophysical, electrochemical, and electroluminescence characteristics have been investigated in detail. Here, the H-bonding interactions through a central lactam core were shown to be the key driving force for their self-assembly into columnar mesophases. The key role of H-bonding has been confirmed by using newly synthesized similar shaped compounds, MCP-1 to MCP-3. New CPO mesogens were found to be intense greenish blue light emitters with narrow band-gap energies. Conclusions were drawn based on theoretical studies also. Finally, the application potential of the selected mesogen CPO-2 as an emissive material has been demonstrated for the fabrication of doped and non-doped OLED devices with different device architectures, which displayed encouraging results. In fact, this is the first report on the use of emissive H-bond-assisted columnar liquid crystals in devices. The present results provide a new guideline and a versatile approach to the design of new LC molecules for the fabrication of efficient OLEDs. © 2018 The Royal Society of Chemistry.Item Enhancement in fluorescence quantum yield of MEH-PPV:BT blends for polymer light emitting diode applications(Elsevier B.V., 2018) K M, K.M.; Satyanarayan, M.N.; Umesh, G.We have investigated the effect of blending electron deficient heterocycle Benzothiadiazole (BT) on the photo-physical properties of conjugated polymer Poly [2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV). Quantum yield (QY) value has been found to increase from 37% for pure MEH-PPV to 45% for an optimum MEH-PPV:BT blend ratio of 1:3. This can be attributed to the efficient energy transfer from the wide bandgap BT (host) to the small bandgap MEH-PPV (guest). The FTIR spectrum of MEH-PPV:BT blended thin film indicates suppression of aromatic C-H out-of-plane and in-plane bending, suggesting planarization of the conjugated polymer chains and, hence, leading to increase in the conjugation length. The increase in conjugation length is also evident from the red-shifted PL spectra of MEH-PPV:BT blended films. Single layer MEH-PPV:BT device shows lower turn-on voltage than single layer MEH-PPV alone device. Further, the effect of electrical conductivity of PEDOT:PSS on the current-voltage characteristics is investigated in the PLED devices with MEH-PPV:BT blend as the active layer. PEDOT:PSS with higher conductivity as HIL reduces the turn on voltage from 4.5 V to 3.9 V and enhances the current density and optical output in the device. © 2018 Elsevier B.V.Item New cyanopyridine based conjugated polymers carrying auxiliary electron donors: From molecular design to blue emissive PLEDs(Elsevier Ltd, 2020) Pilicode, N.; Naik, P.; K M, K.M.; Acharya, M.; Satyanarayan, M.N.; Vasudeva Adhikari, A.V.Three new D-A (Donor-Acceptor) configured conjugated polymers, i.e. PPy1-3, centered on strong electron accepting cyanopyridine scaffold carrying varied auxiliary donors, viz. phenylene (PPy1), biphenyl (PPy2), and fluorene (PPy3) were designed and synthesized as blue emitters for PLEDs. The new polymers were subjected to spectral, thermal, photophysical and electrochemical characterization. Also, computational studies (DFT) were performed on the repeating units of polymer using Turbomole 7.2 V software package at the B3LYP/TZVP hybrid levels. Further, their weight average molecular masses were found to be 38.8 kDa, 38.9 kDa and 57.7 kDa, respectively as determined by GPC technique. Furthermore, the new polymers PPy1-3, were shown to be stable thermally up to 308–374 °C. Evidently, they exhibited good photophysical behavior with their optical energy band gaps of 2.53–2.64 eV. Finally, the polymers PPy1-3 were employed as an active emissive layer in standard ITO/PEDOT:PSS/Polymer/Al configured PLEDs. Interestingly, at 12 V all the newly fabricated devices exhibit a stable blue characteristic electroluminescence with low threshold voltages of 3.40–5.20 V, confirming an efficient injection of electrons in the diodes. From the results, it is clear that, the polymers PPy1-3, can be considered as prospective blue light emitters for PLED application. © 2019 Elsevier LtdItem Synthesis, characterization and electroluminescence studies of cyanopyridine-based ?-conjugative polymers carrying benzo[: C] [1,2,5]thiadiazole and naphtho[1,2- c:5,6- c ?]bis([1,2,5]thiadiazole) units(Royal Society of Chemistry orders@rsc.org, 2020) Pilicode, N.; Naik, P.; Acharya, M.; Vasudeva Adhikari, A.V.Four new donor-acceptor type cyanopyridine-based conjugative polymers, i.e.TDPy1-4, carrying different electron-donating aromatic/heteroaromatic moieties in the backbone were synthesized from their respective co-monomers by using the Suzuki cross-coupling polycondensation protocol. These polymers were designed to possess good control of color emission and to have balanced charge injection, and transport properties. Their structures were confirmed by spectroscopic studies and their thermal stability was evaluated using the TGA technique. The photophysical, electrochemical and electroluminescence properties of these materials were established in order to assess their suitability for PLED applications. DFT-based computational studies were performed to verify and elucidate the above-said properties. Evidently, they demonstrate good green fluorescence with optical band gap (Eg) values of 2.14-2.27 eV. Finally, new PLEDs based on TDPy1-4 were fabricated with a structure of ITO/PEDOT:PSS/polymer/Al, wherein they are able to act as green light emitters with stable electroluminescence behaviors. © 2020 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.Item New cyanopyridine-based ?-conjugative poly(azomethine)s: Synthesis, characterization and electroluminescence studies(John Wiley and Sons Ltd, 2021) Pilicode, N.; Naik, P.; K M, K.M.; Acharya, M.; Satyanarayan, M.N.; Vasudeva Adhikari, A.V.Four new Schiff-base type conjugative polymers (CPs), that is, Py1-4 carrying a strong electron-withdrawing cyanopyridine scaffold coupled with different electron-donating aromatic/heteroaromatic moieties were synthesized from their respective co-monomers by simple poly-condensation route. They were subjected to structural, thermal, photophysical, and electrochemical characterizations and theoretical investigations in order to identify their suitability in polymer light-emitting diode (PLED) application. All these polymers showed good film-forming ability and exhibited favorable photophysical behaviors with an optical bandgap in the order of 2.54-2.68 eV. Further, their electrochemical data were used to evaluate highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) levels. Finally, Py1-4 were successfully employed as blue-light emitter in the construction of new ITO/PEDOT:PSS/ Py1-4/Al configured light-emitting diodes (LED), and the fabricated devices demonstrated stable blue electroluminescence behavior endorsing an effective electrons injection in the PLEDs. © 2020 John Wiley & Sons LtdItem Utilization of newly configured carbazole-cyanopyridone structural hybrids towards achieving high-performance cyan fluorescent organic light-emitting diodes(Royal Society of Chemistry, 2024) Vishrutha, K.S.; Ulla, H.; Raveendra Kiran, M.; Badekai Ramachandra, B.R.; Vasudeva Adhikari, A.V.Herein, we report the synthesis, characterization, and device fabrication of novel D-A-D (donor-acceptor-donor) type cyanopyridone-based cyan light-emitting organic materials. These small molecules feature a strong electron-donating N-alkylated carbazole unit affixed to a powerful electron-withdrawing cyanopyridone core that is appended with varying secondary donor groups, producing bipolarity in their structures. All the synthesized molecules were well characterized by employing FT-IR, 1H NMR, and 13C NMR spectroscopy, followed by in-depth photophysical, thermal, electrochemical, and electroluminescent studies. Furthermore, we used the density functional theory (DFT) computational approach in the theoretical investigations to gain deeper insights into their electron cloud distributions and structural features. These fluorophores exhibit emission in the 489-510 nm range accompanied by high Stokes shift values, and their TGA data validate the excellent thermal stability (384 °C). As estimated by cyclic voltammetry, the HOMO and LUMO energy levels were found to be 5.35-5.69 eV and 2.92-3.02 eV, respectively, with band gaps of 2.36-2.74 eV. The optical and electrochemical properties of the luminogens have been successfully fine-tuned by varying the auxiliary donors at the carbazole-cyanopyridine hybrids. Electroluminescent studies proved the compatibility of the novel compounds to be an efficient cyan emissive layer with good performance characteristics. Interestingly, amongst the luminophores, Cz-CyP5 bearing a 4-hydroxyphenyl moiety exhibited a maximum current efficiency of 13.16 cd A−1, high power efficiency of 9.85 lm W−1, and good external quantum efficiency of 5.41%. © 2024 RSC.