Electrochemical determination of the ionization potential and electron affinity of poly(9,9-dioctylfluorene)
TL;DR: In this article, cyclic voltammetry measurements for the blue electroluminescent conjugated polymer poly(9,9-dioctylfluorene) were obtained and both oxidation and reduction potentials were determined and estimates of both the ionization potential Ip and electron affinity Ea of the polymer were obtained for the same sample under the same experimental conditions.
Abstract: We report cyclic voltammetry measurements for the blue electroluminescent conjugated polymer poly(9,9-dioctylfluorene). Both oxidation and reduction potentials are determined and thus estimates of both the ionization potential Ip and electron affinity Ea of the polymer are obtained for the same sample under the same experimental conditions. We estimate Ip=5.80 eV and Ea=2.12 eV. These results disagree with the common assumption that Ea is, to good approximation, given by the difference between Ip and the optical gap. Measurements on indium tin oxide/polyfluorene/calcium light emitting diode structures are consistent with the deductions from the electrochemical data.
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TL;DR: Research in the use of organic polymers as active semiconductors in light-emitting diodes has advanced rapidly, and prototype devices now meet realistic specifications for applications.
Abstract: Research in the use of organic polymers as the active semiconductors in light-emitting diodes has advanced rapidly, and prototype devices now meet realistic specifications for applications. These achievements have provided insight into many aspects of the background science, from design and synthesis of materials, through materials fabrication issues, to the semiconductor physics of these polymers.
5,653 citations
TL;DR: A comprehensive review of the literature on electron transport materials (ETMs) used to enhance the performance of organic light-emitting diodes (OLEDs) is presented in this article.
Abstract: A comprehensive review of the literature on electron transport materials (ETMs) used to enhance the performance of organic light-emitting diodes (OLEDs) is presented. The structure−property−performance relationships of many classes of ETMs, both small-molecule- and polymer-based, that have been widely used to improve OLED performance through control of charge injection, transport, and recombination are highlighted. The molecular architecture, electronic structure (electron affinity and ionization potential), thin film processing, thermal stability, morphology, and electron mobility of diverse organic ETMs are discussed and related to their effectiveness in improving OLED performance (efficiency, brightness, and drive voltage). Some issues relating to the experimental procedures for the estimation of relevant material properties such as electron affinity and electron mobility are discussed. The design of multifunctional electroluminescent polymers whereby light emission and electron- and hole-transport pro...
1,527 citations
TL;DR: In this paper, a review of conjugated polymers with 1D and 2D topological structures is presented, and a design approach for the alternating donor-acceptor (D-A) copolymers is proposed.
668 citations
TL;DR: In this article, a structural model based on intrachain ordering was proposed to account for the changes of the absorption spectrum of poly(9,9-dioctylfluorene) (PFO) films under certain physicochemical treatment protocols.
Abstract: From photophysical evidence, we suggest a structural model based on intrachain ordering that can account for the changes of the absorption spectrum of poly(9,9-dioctylfluorene) (PFO) films under certain physicochemical treatment protocols. We correlate this model to the results of X-ray fiber diffraction experiments.
615 citations
TL;DR: In this paper, a copolymerization of poly[(9,9-bis(3‘-(N,N-dimethylamino)propyl)-2,7-fluorene)-alt-2, 7-dioctylfluorene] (P1, P2, P4) was investigated and the resulting conjugated polyelectrolytes were used as emitting layers in device fabrication.
Abstract: Alternating copolymers poly[(9,9-bis(3‘-(N,N-dimethylamino)propyl)-2,7-fluorene)-alt-2,7-(9,9-dioctylfluorene)] (P1) and poly[(9,9-bis(3‘-(N,N-dimethylamino)propyl)-2,7-fluorene)-alt-1,4-phenylene] (P3) were synthesized by the palladium-catalyzed Suzuki coupling reaction and their quaternized ammonium polyelectrolyte derivatives (P2, P4) were obtained through a postpolymerization treatment on the terminal amino groups. The resulting conjugated polyelectrolytes (P2, P4) are soluble in polar solvents such as methanol, DMF, and DMSO while P4 is a water-soluble blue-emitting conjugated polyelectrolyte. The electrochemical and photophysics properties of the resulting copolymers were fully investigated. Both the neutral amino-functionalized polyfluorenes (P1, P3) and the quaternized ammonium salt functional conjugated polyelectrolytes derivatives (P2, P4) were used as the emitting layers in device fabrication. All these polymers show even higher external quantum efficiencies (QE) with the high work-function met...
567 citations
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TL;DR: In this paper, a cross-coupling reaction is proposed for coupling 1 -Alkenylboron Derivatives: Synthesis of Conjugated Dienes 6.
Abstract: B. Other Catalyti; Process by Transition-Metal Complexes IV. Cross-Coupling Reaction A. Coupling of 1 -Alkenylboron Derivatives: Synthesis of Conjugated Dienes 6. Coupling of Arylboron Derivatives: Synthesis of Biaryls C. Coupling of Alkylboron Derivatives D. Coupling with Triflates E. Synthesis of Vinylic Sulfides F. Coupling with lodoalkanes: Alkyl-Alkyl CouDlino G. Coupling with Other Organic Halides and Boron Reagents V. Head-to-Tail Coupling VI. Carbonylative Coupling VII. Alkoxycarbonylation and Dimerization VIII. Conclusion 2457 2458 2458
10,937 citations
IBM1
TL;DR: In this article, the authors demonstrate that poly(p-phenylene vinylene), prepared by way of a solution-processable precursor, can be used as the active element in a large-area light-emitting diode.
Abstract: CONJUGATED polymers are organic semiconductors, the semiconducting behaviour being associated with the π molecular orbitals delocalized along the polymer chain. Their main advantage over non-polymeric organic semiconductors is the possibility of processing the polymer to form useful and robust structures. The response of the system to electronic excitation is nonlinear—the injection of an electron and a hole on the conjugated chain can lead to a self-localized excited state which can then decay radiatively, suggesting the possibility of using these materials in electroluminescent devices. We demonstrate here that poly(p-phenylene vinylene), prepared by way of a solution-processable precursor, can be used as the active element in a large-area light-emitting diode. The combination of good structural properties of this polymer, its ease of fabrication, and light emission in the green–yellow part of the spectrum with reasonably high efficiency, suggest that the polymer can be used for the development of large-area light-emitting displays.
10,463 citations
TL;DR: In this paper, the valence effective Hamiltonian (VEH) technique is used to compute ionization potentials, optical transition energies, and electron affinities of oligomers and polymers in four conjugated systems: polyacetylene, poly@-phenylene), polythiophene, and polypyrrole.
Abstract: The valence effective Hamiltonian (VEH) technique is used to compute ionization potentials, optical transition energies, and electron affinities of oligomers and polymers in four conjugated systems: polyacetylene, poly@-phenylene), polythiophene, and polypyrrole. The theoretical results compare very favorably with experimental data on gas-phase ionization potentials, optical absorption, and electrochemical redox potentials. The latter case is especially important, and the calculated oxidation and reduction potentials are in remarkably good agreement with experiment. For polyacetylene the predicted oxidation potential is 0.4 V vs. SCE, and the predicted reduction potential is -1.1 V, both of which are in good agreement with experimentally observed oxidation and reduction onsets. In these systems, the electronic and electrochemical properties predicted by VEH theory for the oligomers extrapolate to those of the polymer with an inverse chain-length dependence.
1,135 citations
934 citations
TL;DR: In this article, a dioctyl-substituted polyfluorene was used as the emissive layer in combination with a polymeric triphenyldiamine hole transport layer.
Abstract: Efficient blue electroluminescence, peaked at 436 nm, is demonstrated from polymer light-emitting diodes operating at high brightness A dioctyl-substituted polyfluorene was used as the emissive layer in combination with a polymeric triphenyldiamine hole transport layer The luminance reaches 600 cd/m2 at a current density of 150 mA/cm2 for a bias voltage of 20 V, corresponding to an efficiency of 025 cd/A and a luminosity of 004 lm/W These values are optimized at a critical emissive layer thickness
614 citations