In this study we present research results on interdigitated organic / small molecule photoconductors. We investigated
photoconductivity in interdigitated lateral photoconductors with aluminum contacts, using (1) a spin-coated organic
blend and (2) evaporated organic multilayers as the active layer. The spin-coated devices were made with a blend of a
poly[2-methoxy-5-(2-ethylhexyl-oxy)-1,4-phenylene-vinylene]
[MEH-PPV] and {6}-1-(3-(methoxycarbonyl)
propyl)-{5}-1-phenyl-[6,6]-C61 [PCBM]. In spin-cast devices, the quantum efficiency was limited by the dissociation of the
excitons. The field dependence of the dissociation of the excitons was explained using a modified Onsager model for
charge dissociation. The evaporated devices were made from layers of alpha-sexithiophene [α-6T] and C60. In the
evaporate devices, trap sites in the active layer limited the quantum efficiency. By modeling the quantum efficiency
based on exciton diffusion to the interface and the dissociation of the excitons, the experimental quantum efficiency was
explained by a trapping model with a charge carrier lifetime of 0.002s.
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