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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 2031-2037 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Optical absorption and photoluminescence spectroscopy have been carried out on a new class of (phenylene) ring substituted p-pyridylvinylenephenylenevinelyne polymers used as active materials in light emitting diodes. The effects of the ring substitutions on the optical absorption and photoluminescence energies are qualitatively explained through the use of semiempirical quantum chemical modeling of the ring torsion angles. Reduced aggregation through the use of "strap" substituents on the phenylene rings also is discussed. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 78 (1995), S. 4264-4266 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We have fabricated unilayer electroluminescent devices from soluble poly(p-pyridine) (PPy). The solubility of PPy in weak acids allows direct spin casting of the polymer films. The electroluminescence spectrum peaks at 2.5 eV (497 nm) corresponding to white light weighted towards the blue end of the spectrum. The photoluminescence spectrum peaks at 2.35 eV (530 nm). The operating voltages of the devices ranged from 4 to 12 V with current densities of 6 to 8 mA/mm2. We compare our devices with similar blue emitting devices based on poly(p-phenylene). © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 108 (1998), S. 7842-7848 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present photoluminescence and electroluminescence studies of bilayers and blends formed from poly(vinyl carbazole) (PVK) and poly(pyridyl vinylene phenylene vinylene) (PPyVPV) copolymer derivatives. Bilayers of PVK and the PPyVPV copolymers have a photoluminescence emission which cannot be assigned to either the photoluminescence of PVK or the PPyVPV layer. The blends of the two polymers show a similar new photoluminescence emission for a large range of concentrations. Absorption and photoluminescence excitation spectra confirm that the additional feature is an excited state species which results from an exciplex at the polymer/polymer interface. Bilayer light-emitting devices utilizing the PPyVPV copolymers show an electroluminescence spectrum consistent with emission from the exciplex. The efficiency of the bilayer devices as compared to single layer devices increases by over three orders of magnitude due to the exciplex formation and the elimination of exciton formation near the luminescence quenching electrodes. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 68 (1996), S. 894-896 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Most polymer electroluminescent devices to date are represented as tunnel diodes and operate under direct-current (dc) driving field. Here we report the fabrication of symmetrically configured alternating-current (ac) light-emitting (SCALE) devices based on conjugated polymers. The new devices consist of an emissive polymer layer sandwiched between two redox polymer layers. This configuration enables the SCALE devices to work under both forward and reverse dc bias as well as in ac modes. The nearly ohmic electrode/redox polymer contacts improve the charge injection efficiency significantly and make the SCALE device operation insensitive to electrode work functions. Symmetric operation supports the key role of redox polymer/emissive polymer interface states. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 70 (1997), S. 3215-3217 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: There is increased interest in developing color variable light emitting devices. We report here the fabrication of color variable bipolar/ac light-emitting devices based on conjugated polymers. The devices consist of blends of pyridine-phenylene and thiophene-phenylene based copolymers sandwiched between the emeraldine base form and the sulfonated form of polyaniline. ITO and Al are used as electrodes. The devices operate under either polarity of driving voltage with different colors of light being emitted, red under forward bias, and green under reverse bias. The relative fast time response allows the rapid switching of colors and ac operation. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 70 (1997), S. 1644-1646 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Photoluminescent and electroluminescent studies of bilayer heterojunctions formed from a poly(pyridyl vinylene phenylene vinylene) (PPyVPV) derivative and poly(vinyl carbazole) (PVK) show an emission peak which cannot be ascribed to either the PPyVPV derivative or PVK layer. Through studies of absorption and photoluminescence excitation (PLE) spectra we demonstrate that the additional feature results from an exciplex at the bilayer interface. The photoluminescence efficiency of the exciplex is greater than 20%. The electroluminescence spectrum from the bilayer devices is entirely due to exciplex emission, with internal efficiencies initially achieved exceeding 0.1%. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
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