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.
Power efficiency is an important parameter for all OLEDs, and is particularly critical for lighting applications. To
maximize the power efficiency one must optimize charge injection, carrier transport, and radiative quantum efficiency,
while minimizing energy losses. In this work we discuss how isoelectronic dopants can be used to address these
problems. It can be difficult to produce efficient electrical contacts, particularly to large energy gap organic materials,
and thus the contacts often limit the performance and stability of OLEDs . Recent results by several groups have
attributed improved hole injection in poly (9,9' dioctylfluorene) [PFO] based LEDs to charge trapping, but the origin of
the traps is unknown. In order to understand the role of traps in improving injection we studied poly[2-methoxy, 5-(2'-
ethyl-hexyloxy)-1,4-phenylene vinylene] (MEH-PPV) devices with C60 molecules at the anode to improve hole
injection. Isoelectronic dopants are used widely as recombination centers in organic light emitting diodes (OLEDs). In
these systems one wants to maximize quantum efficiency by effectively trapping charges on the emitting dopants, while
at the same time maximizing power efficiency by maintaining good charge transport. An understanding of the influence
of the depth of the dopant on charge capture, and charge transport will aid in optimizing doped organic LEDs. We have
looked at the OLED system consisting of the polymer PFO, and the organometallic molecule PhqIr. We show that PhqIr
acts as a shallow hole trap in PFO, and that the charge transport and luminescence properties of this system are described
by quasi-equilibrium statistics.
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