The effect of magnetic field on the intensity of electroluminescence from devices made of a polyp-phenylenevinylene ͑PPV͒ copolymer was investigated. The emission intensity was enhanced by the application of magnetic field, and the magnitude of the increase depended on operational voltages. When the device was operated under application of low voltages, the intensity increased with magnetic field and reached an 8.5% increase at about 100 mT. With the increase of the operational voltage, the effect of magnetic field was lessened. In addition, when measured at high voltages with increasing magnetic field, the emission intensity started to decrease after passing a maximum, then leveled off. This saturation value was slightly higher than that observed in the absence of magnetic field. These findings suggest that two processes sensitive to magnetic field are included in the emission processes. They are assigned to the charge recombination ͑CR͒ of anion and cation radicals and triplet-triplet annihilation ͑TTA͒ processes. From the analysis of the effects of magnetic field on the emission intensity based on a kinetic model, we quantitatively determined the fractions of singlet and triplet excitons generated through the CR process to be 0.17 and 0.83, respectively. With the increase of the concentration of triplet excitons in the organic layer, production of singlet excitons through the TTA process was enhanced, and the total yield of the singlet excitons exceeded 0.5 under normal device operational conditions. We conclude that this high yield is responsible for the high emission efficiency observed in the light-emitting devices based on PPVs.

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Organic solar cells were fabricated by stacking aromatic amine and C60 layers. The energy conversion efficiency of these solar cells was low because of poor photoabsorption by these layers and short diffusion length of excitons. However, the photocurrent density was increased by about 3 times by the application of heat treatment to the stacked organic layers at 140 °C, and the maximum energy conversion efficiency reached 1.1 % under AM 1.5, 100 mW cm–2 simulated solar light. The internal quantum efficiency of the photocurrent after the annealing reached about 45 %. When the aromatic amine layer was about 100 nm thick, the organic layers after the annealing showed a wrinkled structure under an optical microscope. The annealing temperature needed for the formation of this structure was in good agreement with the temperature needed for the increase in the photocurrent. The morphological change caused by the annealing was attributed to infiltration of the amorphous aromatic amine compound into grain boundaries of the microcrystalline C60 layer, resulting in expansion of the C60 layer and the wrinkled structure of the organic layers. From observation by electron microscopy, the mixed form of these two compounds near the interface was found to be suited to solar cells because the C60 and aromatic amine phases wedge each other in a direction normal to two electrodes. However, the annealing slightly lowered photovoltage of the solar cell. This effect was attributed to a partial contact of the C60 layer with a counter electrode through the aromatic amine layer.

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