Journal of the American Chemical Society · 1996 · 601 citations · 57 references
Natural SciencesChemistryMaterials ScienceElectrochemistryPolymer ChemistryPolymer MaterialsConducting PolymersConductive PolymersElectrochemical CellsElectrode MaterialsElectrolyte MaterialsPolymer Thin FilmsBand GapConjugated PolymersExternal Quantum EfficiencyIonic Conductivity In PolymersLuminescent PolymersPolymer ElectrodesQuantum EfficiencyThin Films Of Conductive Polymers
Solid-state polymer light-emitting electrochemical cells have been fabricated using thin films of blends of poly(1,4-phenylenevinylene) and poly(ethylene oxide) complexed with lithium trifluoromethanesulfonate. The cells contain three layers: the polymer film (as the emissive layer) and indium-tin oxide and aluminum films as the two contact electrodes. When externally biased, the conjugated polymers are p-doped and n-doped on opposite sides of the polymer layer, and a light-emitting p-n junction is formed in between. The admixed polymer electrolyte provides the counterions and the ionic conductivity necessary for doping. The p-n junction is dynamic and reversible, with an internal built-in potential close to the band gap of the redox-active conjugated polymer (2.4 eV for PPV). Green light emitted from the p-n junction was observed with a turn-on voltage of about 2.4 V. The devices reached 8 cd/m(2) at 3 V and 100 cd/m(2) at 4 V, with an external quantum efficiency of 0.3-0.4% photons/electron. The response speed of these cells was around 1 s, depending on the diffusion of ions. Once the light-emitting junction had been formed, the subsequent operation had fast response (microsecond scale or faster) and was no longer diffusion-controlled.
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