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Nonconjugated Anionic Polyelectrolyte as an Interfacial Layer for the Organic Optoelectronic Devices
49
Citations
35
References
2013
Year
EngineeringOrganic ElectronicsOrganic Solar CellOptoelectronic DevicesPhotovoltaic DevicesChemistryPhotovoltaicsConducting PolymerChemical EngineeringElectronic DevicesCathode InterfacePolymer ChemistryFavorable Interface DipoleMaterials ScienceAnionic PolyelectrolyteElectrical EngineeringNonconjugated Anionic PolyelectrolyteSolar PowerOptoelectronic MaterialsOrganic SemiconductorOrganic Optoelectronic DevicesSemiconducting PolymerPolymer ScienceConjugated PolymerInterfacial LayerSolar Cells
A nonconjugated anionic polyelectrolyte, poly(sodium 4-styrenesulfonate) (PSS-Na), was applied to the optoelectronic devices as an interfacial layer (IFL) at the semiconducting layer/cathode interface. The ultraviolet photoelectron spectroscopy and the Kelvin probe microscopy studies support the formation of a favorable interface dipole at the organic/cathode interface. For polymer light-emitting diodes (PLEDs), the maximum luminance efficiency (LEmax) and the turn-on voltage (Von) of the device with a layer of PSS-Na spin-coated from the concentration of 0.5 mg/mL were 3.00 cd/A and 5.5 V, which are dramatically improved than those of the device without an IFL (LEmax = 0.316 cd/A, Von = 9.5 V). This suggests that the PSS-Na film at the emissive layer/cathode interface improves the electron injection ability. As for polymer solar cells (PSCs), the power conversion efficiency (PCE) of the device with a layer of PSS-Na spin-coated from the concentration of 0.5 mg/mL was 2.83%, which is a 16% increase compared to that of the PSC without PSS-Na. The PCE improvement is mainly due to the enhancement of the short-circuit current (12% increase). The results support that the electron collection and transporting increase by the introduction of the PSS-Na film at the photoactive layer/cathode interface. The improvement of the efficiency of the PLED and PSC is due to the reduction of the Schottky barrier by the formation of a favorable interface as well as the better Ohmic contact at the cathode interface.
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