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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 89 (2001), S. 3343-3351 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The perfect injecting contact for any semiconductor device is, by definition, an ohmic contact. When such a contact is made to an organic semiconductor the current density is limited by bulk space-charge effects. In the absence of charge carrier traps, J reaches the ultimate, trap-free, space-charge-limited value, JTFSCLC=(9/8)cursive-epsilonμV2/d3. Knowledge of the mobility μ, permittivity cursive-epsilon, applied bias V, and film thickness d, thus allows the maximum possible current density to be calculated. The absolute injection efficiency of any specific contact can then be quantified via a figure of merit, χ=J/JTFSCLC, namely the ratio of the actual current density to that expected for the ideal trap-free, space-charge-limited current. In this article we report on the injection efficiency of positive carriers into poly(9,9-dioctylfluorene) (PFO) and two representative copolymers, poly(9,9-diocytlfluorene-co-bis-N,N′-(4-methoxyphenyl)-bis-N, N′-phenyl-1,4-phenylenediamine) (PFMO) and poly(9,9-dioctylfluorene-co-benzothiadiazole) (BT). Time-of-flight photocurrent, dark injection transient current, and current density–voltage (J–V) measurements were each performed on indium tin oxide (ITO)/polymer/Au or Al diode structures. The hole injection efficiency of various pretreated ITO electrodes and of the top Au and Al contacts was investigated. ITO coated glass substrates were cleaned by washing with solvents and then either not subjected to further treatment (untreated), exposed to an oxygen plasma (O2 plasma), or coated in a poly(ethylenedioxythiophene)/polystyrenesulphonic acid (PEDOT/PSS) blend. The steady-state J–V characteristics for the different device structures were compared to the expected JTFSCLC and the figure of merit χ was calculated. At an applied field of 5×105 V/cm, the absolute injection efficiencies of holes into PFMO (ionization potential, Ip=4.98 eV) from untreated, O2 plasma treated, and PEDOT/PSS treated ITO were found to be χ=10−3, 1, and 1, respectively. For PFO (Ip=5.8 eV) the same contacts gave χ=10−7, 10−6, and 10−3, respectively. For BT (Ip=5.9 eV) hole transport is highly dispersive, precluding determination of the hole mobility and hence an analysis of the injection efficiency. The injected current densities are, however, comparable to (within a factor of 5 of) those for PFO. The top Au and Al contacts exhibited injection limited behavior (10−8〈χ〈10−2). Heat treatment of the Au top contacts did not improve injection, contrary to previous observations for a molecularly doped xerographic polymer system. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 76 (2000), S. 1734-1736 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We report detailed measurements on diode structures containing the electroluminescent polyfluorene copolymer poly(9,9-dioctylfluorene-co-bis-N,N′-(4-methoxyphenyl)-bis-N,N′-phenyl-1,4 phenylenediamine). Ohmic injection of holes is achieved with an oxygen plasma cleaned indium tin oxide (ITO) electrode, untreated ITO coated with a film of poly(ethylenedioxythiophene)/polystyrenesulphonic acid (PEDOT/PSS) and plasma cleaned ITO with PEDOT/PSS. Transient dark injection and time-of-flight mobility measurements and steady state current density versus voltage measurements are then entirely consistent with a positive carrier, trap-free, space-charge-limited current. Injection limited behavior is observed, however, for untreated ITO without PEDOT/PSS and for evaporated Au contacts. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 79 (2001), S. 3872-3874 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Unbalanced carrier transport is known to strongly affect the efficiency of polymer light-emitting diodes. Here, we report the results of time-of-flight (TOF), current density–voltage, and electroluminescence (EL) quantum efficiency measurements on single-layer poly(9,9-dioctylfluorene) (PFO) devices doped with the red-emitter tetraphenylporphyrin (TPP). TOF shows that PFO is a unipolar conductor, with hole transport much better than electron transport. At a field of 5×105 V/cm, a nondispersive hole mobility of 4×10−5–5×10−4 cm2/V s, dependent on sample morphology, is obtained. Upon the addition of 5% by weight TPP, hole transport becomes as highly dispersive as electron transport, having no measurable average mobility. This results in a decrease in the current for a given applied bias but an increase in the external EL quantum efficiency. TPP acts as a strong hole trap, reducing the dominant hole current and producing more balanced carrier transport. At TPP concentrations above 6%, the device characteristics start to revert to those found at lower TPP concentrations. This is due to the onset of efficient hole transport between the dopant molecules that reestablishes a transport imbalance. © 2001 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 79 (2001), S. 2133-2135 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Here, we report results of both traditional current mode and current integration mode time-of-flight (TOF) measurements on the electroluminescent polyfluorene copolymer poly(9,9-dioctylfluorene-co-benzothiadiazole) (BT). Current mode TOF shows a strong but dispersive electron transport signal. The mobility derived from the current integration mode transit time (tQ) increases with decreasing film thickness as expected for dispersive transport. The fastest carriers in the photogenerated carrier packet are estimated to have mobilities of order 10−3 cm2/V s at applied fields of 0.5 MV/cm. Holes are heavily trapped close to the interface at which they are photogenerated. The TOF signals decay with repeated measurement and tQ remains constant with applied field. The transport properties of BT are thus in complete contrast to those of other polyfluorenes which show high-mobility nondispersive hole transport but weak and highly dispersive electron transport. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 109-112 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polydiacetylene xBCMU and 9PA crystals, solutions and solution-cast films vary in colour due to differences in backbone order and planarity. Associated with the colour changes are increases in the Raman frequencies of the triple and double backbone bond vibrational modes from those values found in the highly ordered single crystals. These increases are strongly correlated and the ratio of the change in the frequency of the triple bond mode to that of the double bond mode is found to be 1.6 (±0.1) over a wide variation in order. This ratio is compared with the values of 0.3 found under uniform strain and 1.1 predicted by a model of acetylenic to butatrienic delocalisation. The relationship between the Raman frequencies of the yellow solutions and melts and those of the crystal phases suggests that in the former the backbone has a continuous and smoothly curving ‘worm-like’ conformation. Models involving the break-up of the conjugated system by large-angle bond rotations appear to be incorrect for polydiacetylenes. These results have important consequences for theoretical models that predict the dependence of electron delocalisation on backbone order and planarity in polydiacetylenes.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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