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- Birgerson, J., et al.
(författare)
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Doped polymeric cathodes for PPV/Al based LEDs
- 2002
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Ingår i: Synthetic metals. - 0379-6779 .- 1879-3290. ; 132:1, s. 57-61
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Tidskriftsartikel (refereegranskat)abstract
- The effect of Li-doping in poly(para-phenylenevinylene) (PPV) based light emitting devices has been studied. In a standard structure with an indium tin oxide (ITO) anode, poly(3,4-ethylenedioxythiophene) doped with poly(4-styrenesulfonate) (PEDOT-PSS)-layer and an active PPV-layer, the effects of a thin (around 1 Å) Li-layer and a thin layer, (50 Å), of a large bandgap polymer, poly(2,5-diheptyl-1,4-phenylene-alt-1,4-naphthylene) (P14NHP) between the PPV and the aluminum cathode have been studied in terms of IV-characteristics and efficiency. The Li-atoms dope the interfacial layer of the PPV as seen by photoelectron spectroscopy. A thin layer of Li improves the charge balance by decreasing the energy barrier for injection of electrons for the Al/Li/PPV/PEDOT-PSS/ITO device. The efficient electron injection originates from a Fermi level alignment between the doped polymer and the aluminum cathode, which reduces the energy barrier. A thin layer of the large bandgap polymer P14NHP, between the PPV and Al contact, increases the light output and efficiency by blocking the holes. In addition, it may also reduce the light quenching by moving the region of recombination away from the Al-contact. The addition of a Li-layer on top of P14NHP leads to an increase of the quantum efficiency, because of better electron injection. © 2002 Elsevier Science B.V. All rights reserved.
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| 2. |
- Crispin, Xavier, et al.
(författare)
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Conductivity, Morphology, Interfacial Chemistry, and Stability of Poly(3,4- ethylene dioxythiophene)–Poly(styrene sulfonate) : A Photoelectron Spectroscopy Study
- 2003
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Ingår i: Journal of Polymer Science Part B. - : John Wiley & Sons. - 0887-6266 .- 1099-0488. ; 41:21, s. 2561-2583
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Forskningsöversikt (refereegranskat)abstract
- X-ray photoelectron spectroscopy (XPS) has been used to characterize poly(3,4-ethylene dioxythiophene)-poly(styrene sulfonate) (PEDT/PSS), one of the most common electrically conducting organic polymers. A correlation has been established between the composition, morphology, and polymerization mechanism, on the one hand, and the electric conductivity of PEDT/PSS, on the other hand. XPS has been used to identify interfacial reactions occurring at the polymer-on-ITO and polymer-on-glass interfaces, as well as chemical changes within the polymer blend induced by electrical stress and exposure to ultraviolet light.
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| 3. |
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| 4. |
- Jönsson, Stina, et al.
(författare)
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The effects of solvents on the morphology and sheet resistance in poly(3,4-ethylenedioxythiophene)–polystyrenesulfonic acid (PEDOT–PSS) films
- 2003
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Ingår i: Synthetic metals. - 0379-6779 .- 1879-3290. ; 139:1, s. 1-10
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Tidskriftsartikel (refereegranskat)abstract
- Films of poly(3,4-ethylenedioxythiophene)–polystyrenesulfonic acid (PEDOT–PSS), prepared by coating the aqueous PEDOT–PSS dispersion and by coating a mixture of the PEDOT–PSS dispersion and different solvents, have been studied using four-point probe conductivity measurements, atomic force microscopy and photoelectron spectroscopy. The electrical conductivity of thin films of the second type (further on called PEDOT–PSS–solvents) was increased by a factor of about 600 as compared to films of the first type (further on called PEDOT–PSS–pristine). Morphological and physical changes occur in the polymer film due to the presence of the solvent mixture, the most striking being that the ratio of PEDOT-to-PSS in the surface region of the films is increased by a factor of ∼2–3. This increase of PEDOT at the surface indicates that the thickness of the insulating PSS ‘shell’ that surrounds the conducting PEDOT–PSS grains is reduced. The (partial) reduction of the excess PSS layer that surrounds the conducting PEDOT–PSS grains is proposed to lead to an increased and improved connectivity between such grains in the film and hence a higher conductivity. When PEDOT–PSS–solvents receives a post-coating heat treatment, the increased PEDOT-to-PSS ratio at the surface is maintained or even slightly improved, as is the increase in electrical conductivity, even though spectroscopy show that the solvent molecules are removed. This suggests that screening or doping by the solvents throughout the film are not likely to be the key mechanisms for the improved conductivity and supports our proposed mechanism of improved conductivity through improved connectivity between the conducting grains.
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