Browsing by Author "Rao, V.J."

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Imidazole-Pyrene Hybrid Luminescent Materials for Organic Light-Emitting Diodes: Synthesis, Characterization & Electroluminescent Properties
(Elsevier B.V., 2021) Umasankar, G.; Ulla, H.; Madhu, C.; Gontu, G.R.; Shanigaram, B.; Nanubolu, J.B.; Bhanuprakash, B.; Karunakar, G.V.; Satyanarayan, M.N.; Rao, V.J.
A series of multichromophoric, pyrene-imidazole-phenyl based hybrid luminescent small molecules (PA, PI, PnB, PtB, PoM and PnDM) with different donating groups at the para position of the phenyl attached to N1 position of imidazole moiety were designed, synthesized, and characterized, for use in blue organic light-emitting diodes (OLEDs). The photophysical, thermal and electrochemical properties of the molecules were systematically investigated. All the molecules displayed delayed fluorescence at room temperature with a lifetime ranging from 7.1 to 8.5 µs. The synthesized fragment molecules (tetraphenyl-imidazoles: IA, IoM and InDM) revealed high triplet energies of ~ 2.90eV. Glass transition temperatures determined to range from 77°C to 123°C and decomposition temperatures are found to be above 280°C. The molecules possess appropriate HOMO and LUMO energy levels for effective charge injection. The crystal structure for PI is reported. OLED devices were fabricated based on the pyrene-imidazole-phenyl hybrids as emitters and as dopants with CBP as host. OLED devices with PI doped (5% wt.) with CBP exhibits excellent device performance with a current efficiency of 9.82 cd/A, the power efficiency of 8.32 lm/W and external quantum efficiency of 4.64%. © 2021
Optoelectronic properties of novel alkyl-substituted Triphenylamine derivatives
(2017) Fernandes, J.M.; Swetha, C.; Appalnaidu, E.; Navamani, K.; Rao, V.J.; Satyanarayan, M.N.; Umesh, G.
Hole transport characteristics in three new organic compounds based on triphenylamine (TPA) moiety are presented. The effect on electrical and optical properties of TPA, attached with methyl or tert-butyl side groups, has been investigated through measurement of current density versus voltage (J-V), capacitance versus voltage (C-V), frequency dependent capacitance, ac conductivity, Impedance spectroscopy, UV-Vis spectroscopy, Photoluminescence (PL) spectroscopy and X-Ray Diffraction (XRD) studies. These measurements reveal that, the attachment of methyl or tert-butyl group in the para-position of the TPA moiety leads to improved optoelectronic properties and greater molecular stability. XRD analysis of the samples indicates that the inter-molecular distance is the lowest for TPA with tert-butyl side group (3.43 ) as compared to pure TPA (3.57 ). This leads to stronger inter-molecular interaction as evidenced by the UV-Vis spectra. PL studies indicate significant Quantum Efficiency (?30%) for alkyl attached TPA. In order to get a better understanding of the charge transport phenomena, the effect of molecular structure dynamics on charge transfer kinetics is analyzed by evaluating the charge carrier hopping rate coefficient and dynamic state factor. The dynamic state factor b has higher value for lower bias voltage, corresponding to dc conductivity, whereas, at higher bias, the value of b is smaller, indicating the dominance of ac conductivity. Hopping conductivity is seen to be highest for the device with tert-butyl substitution in TPA moiety. Our experiments indicate an order of magnitude enhancement in charge carrier mobility for alkyl-substituted TPA. 2017 Elsevier B.V.
Optoelectronic properties of novel alkyl-substituted Triphenylamine derivatives
(Elsevier B.V., 2017) Fernandes, J.M.; Swetha, C.; Appalnaidu, E.; Navamani, K.; Rao, V.J.; Satyanarayan, M.N.; Umesh, G.
Hole transport characteristics in three new organic compounds based on triphenylamine (TPA) moiety are presented. The effect on electrical and optical properties of TPA, attached with methyl or tert-butyl side groups, has been investigated through measurement of current density versus voltage (J-V), capacitance versus voltage (C-V), frequency dependent capacitance, ac conductivity, Impedance spectroscopy, UV-Vis spectroscopy, Photoluminescence (PL) spectroscopy and X-Ray Diffraction (XRD) studies. These measurements reveal that, the attachment of methyl or tert-butyl group in the para-position of the TPA moiety leads to improved optoelectronic properties and greater molecular stability. XRD analysis of the samples indicates that the inter-molecular distance is the lowest for TPA with tert-butyl side group (3.43 Å) as compared to pure TPA (3.57 Å). This leads to stronger inter-molecular interaction as evidenced by the UV-Vis spectra. PL studies indicate significant Quantum Efficiency (?30%) for alkyl attached TPA. In order to get a better understanding of the charge transport phenomena, the effect of molecular structure dynamics on charge transfer kinetics is analyzed by evaluating the charge carrier hopping rate coefficient and dynamic state factor. The dynamic state factor b has higher value for lower bias voltage, corresponding to dc conductivity, whereas, at higher bias, the value of b is smaller, indicating the dominance of ac conductivity. Hopping conductivity is seen to be highest for the device with tert-butyl substitution in TPA moiety. Our experiments indicate an order of magnitude enhancement in charge carrier mobility for alkyl-substituted TPA. © 2017 Elsevier B.V.
Pyrene-Oxadiazoles for Organic Light-Emitting Diodes: Triplet to Singlet Energy Transfer and Role of Hole-Injection/Hole-Blocking Materials
(2016) Chidirala, S.; Ulla, H.; Valaboju, A.; Kiran, M.R.; Mohanty, M.E.; Satyanarayan, M.N.; Umesh, G.; Bhanuprakash, K.; Rao, V.J.
Three pyrene-oxadiazole derivatives were synthesized and characterized by optical, electrochemical, thermal, and theoretical investigations to obtain efficient multifunctional organic light emitting diode (OLED) materials. Synthesized molecules were used as emitters and electron transporters in three different device configurations, involving hole-injection/hole-blocking materials that showed good current and power efficiencies. To understand the underlying mechanisms involved in the application of these molecules as emitters and transporters, a detailed photophysical characterization of molecules 4-6 was carried out. The absorption, steady-state fluorescence, phosphorescence, fluorescence lifetime, and phosphorescence lifetime measurements were carried out. The high quantum yield and efficient reverse intersystem crossing leading to delayed fluorescence emission makes the molecule a good emitter, and the charge delocalization properties leading to excimer formation make them efficient electron transporters. Isoenergetic singlet and triplet states of the molecules make the reverse intersystem crossing feasible at room temperature even in the absence of thermal activation. 2015 American Chemical Society.
Pyrene-Oxadiazoles for Organic Light-Emitting Diodes: Triplet to Singlet Energy Transfer and Role of Hole-Injection/Hole-Blocking Materials
(American Chemical Society service@acs.org, 2016) Chidirala, S.; Ulla, H.; Valaboju, A.; Raveendra Kiran, M.R.; Mohanty, M.E.; Satyanarayan, M.N.; Umesh, G.; Bhanuprakash, K.; Rao, V.J.
Three pyrene-oxadiazole derivatives were synthesized and characterized by optical, electrochemical, thermal, and theoretical investigations to obtain efficient multifunctional organic light emitting diode (OLED) materials. Synthesized molecules were used as emitters and electron transporters in three different device configurations, involving hole-injection/hole-blocking materials that showed good current and power efficiencies. To understand the underlying mechanisms involved in the application of these molecules as emitters and transporters, a detailed photophysical characterization of molecules 4-6 was carried out. The absorption, steady-state fluorescence, phosphorescence, fluorescence lifetime, and phosphorescence lifetime measurements were carried out. The high quantum yield and efficient reverse intersystem crossing leading to delayed fluorescence emission makes the molecule a good emitter, and the charge delocalization properties leading to excimer formation make them efficient electron transporters. Isoenergetic singlet and triplet states of the molecules make the reverse intersystem crossing feasible at room temperature even in the absence of thermal activation. © 2015 American Chemical Society.