Peripherally alkyl‐substituted aromatic molecules are of interest because they are predicted to promote the rapid vectorial conduction of electronic charge. It is shown—using the example of HHTT, see Figure—that the results obtained by flash‐photolysis time‐of‐flight conductivity and pulse‐radiolysis time‐resolved microwave conductivity measurements are complementary, allowing the charge‐carrier mobility to be determined in all four phases of HHTT. magnified image
Charge‐carrier transport in organic materials is the fundamental physical process behind devices such as laser printers. Charge‐carrier mobility data are presented for hexabutyloxytriphenylene (H4T), which exhibits an unusually high charge‐carrier mobility, which can be traced to the formation of a plastic discotic phase. The Figure shows the normal discotic hexagonal texture with six‐fold symmetry observed for H4T at 144°C; this symmetry disappears at lower temperatures (see also the cover). magnified image
A one-dimensional numerical model for the quantitative simulation of multilayer organic light emitting diodes (OLEDs) is presented. It encompasses bipolar charge carrier drift with field-dependent mobilities and space charge effects, charge carrier diffusion, trapping, bulk and interface recombination, singlet exciton diffusion and quenching effects. Using field-dependent mobility data measured on unipolar single layer devices, reported energetic levels of highest occupied and lowest unoccupied molecular orbitals, and realistic assumptions for experimentally not direct accessible parameters, current density and luminance of state-of-the-art undoped vapor-deposited two- and three-layer OLEDs with maximum luminance exceeding 10000 cd/m2 were successfully simulated over 4 orders of magnitude. For an adequate description of these multilayer OLEDs with energetic barriers at interfaces between two adjacent organic layers, the model also includes a simple theory of charge carrier barrier crossing and recombination at organic–organic interfaces. The discrete nature of amorphous molecular organic solids is reflected in the model by a spatial discretization according to actual molecule monolayers, with hopping processes for charge carrier and energy transport between neighboring monolayers.
Charge carrier transport in vapor-deposited films of 1,6,7,12-tetraphenoxy-N,N′-bis-(2,6-diisopropylphenyl)-perylene-3,4,9,10-bis(dicarboximide) was investigated using two different methods, the time-of-flight (TOF) technique and time-resolved electroluminescence. Electron mobilities of 10−5 cm2/V s were measured in the bulk using a time-of-flight technique. Hole transport was found to be dispersive and, thus, a transit time for holes could not be obtained. The above dye was also used to fabricate single layer light emitting diodes showing clearly visible red electroluminescence under ambient conditions. Our experiments on transit electroluminescence confirmed the measured electron mobility and ruled out the possibility that the transit time of holes is shorter than the time range investigated in our time-of-flight experiments.
We investigate electron injection and transport in single-layer devices of 8-hydroxyquinoline aluminum sandwiched between two electrodes. Electrodes comprising a thin lithium fluoride layer are compared with co-evaporated magnesium–silver cathodes and with pure aluminum cathodes. By employing both transient and quasistatic current measurements, the impact of the LiF-layer thickness on electron injection is investigated. It is demonstrated that contacts comprising 0.1–0.2 nm LiF and an aluminum capping layer are able to sustain space-charge-limited currents in 8-hydroxyquinoline aluminum. Further, steady-state current–voltage measurements as a function of temperature are discussed with respect to trap distributions in 8-hydroxyquinoline aluminum.
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