Abstract:We report the characteristics of a series of polymer light-emitting diodes, fabricated with LiF/Al cathodes and differing only by the thickness of the LiF interlayer (0 nm⩽d⩽11 nm). Electroabsorption studies of the internal electrostatic potential give direct evidence of a sizable reduction of the cathodic barrier height brought about by the LiF films. These results also correlate with photoemission experiments [S. E. Shaheen, G. E. Jabbour, M. M. Morrell, Y. Kawabe, B. Kippelen, N. Peyghambarian, M. F. Nabor,… Show more
“…8,19) The use of both LiF and PEDOT-PSS in this way has proven effective in photovoltaic cells 20) and polymer light emitting diodes. 21,22) In fact, the use of alkali halide sandwich layers to improve injection at the cathode electrode has been used successfully in a wide variety of organic electronic devices, e.g., refs. 21, 23-26. In this work the cathode side is studied, particularly the beneficial effect that the LiF layer has on the interface between the Al and the active organic layer.…”
The surfaces and electrode interfaces of a polymer blend used in prototype solar cells have been characterized with photoelectron spectroscopy. The polymer blend in question is a 1 : 4 mixture of APFO-3 : PCBM. Based on surface analysis of the pristine film we can conclude that the surface of the blend is a 1 : 1 mixture of APFO-3 and PCBM. The electrode systems studied are the widely used Al and Al/LiF contacts. LiF prevents formation at the Al/organic interface of Al-organic complexes that destroy the -conjugation. In addition to this, there are two other beneficial, thickness dependent, effects. Decomposition of LiF occurs for thin enough layers in which the LiF species are in contact with both the organic film and the Al atoms, which creates a low workfunction contact. For thicker (multi)layers, the dipole formed at the LiF/organic interface is retained as no decomposition of the LiF occurs upon Al deposition.
“…8,19) The use of both LiF and PEDOT-PSS in this way has proven effective in photovoltaic cells 20) and polymer light emitting diodes. 21,22) In fact, the use of alkali halide sandwich layers to improve injection at the cathode electrode has been used successfully in a wide variety of organic electronic devices, e.g., refs. 21, 23-26. In this work the cathode side is studied, particularly the beneficial effect that the LiF layer has on the interface between the Al and the active organic layer.…”
The surfaces and electrode interfaces of a polymer blend used in prototype solar cells have been characterized with photoelectron spectroscopy. The polymer blend in question is a 1 : 4 mixture of APFO-3 : PCBM. Based on surface analysis of the pristine film we can conclude that the surface of the blend is a 1 : 1 mixture of APFO-3 and PCBM. The electrode systems studied are the widely used Al and Al/LiF contacts. LiF prevents formation at the Al/organic interface of Al-organic complexes that destroy the -conjugation. In addition to this, there are two other beneficial, thickness dependent, effects. Decomposition of LiF occurs for thin enough layers in which the LiF species are in contact with both the organic film and the Al atoms, which creates a low workfunction contact. For thicker (multi)layers, the dipole formed at the LiF/organic interface is retained as no decomposition of the LiF occurs upon Al deposition.
“…When incorporated into polymer light-emitting diodes ͑PLEDs͒, the LiF layer improves the device performance by increasing the electron attenuation length, by suppressing the interfacial reactions of the metal electrode with emissive layer during the cathode evaporation, and/or by reducing the barrier height of the electron injection through formation of a low work function interfacial layer at the cathode. 10,[13][14][15] The recent research using cationic systems [16][17][18] implies that anionic conjugated polyelectrolytes might offer several interesting opportunities for use in polymer-based optoelectronic devices. In light-emitting electrochemical cells ͑LECs͒, the mobile ions enable redox doping and the formation of ohmic contacts.…”
We report improved performance in polymer light-emitting diodes incorporating conjugated polyelectrolytes as an electron injection layer (EIL). When we introduce water soluble conjugated polymers, poly[9,9′-bis(4-sulfonatobutyl)fluorene-co-alt-1,4-phenylene] (anionic PFP), between the aluminum (Al) cathode and emissive layer, the devices show an increased electroluminescence efficiency with a lowered turn-on voltage. We believe the mobile Na+ ions in the EIL layer directly influences the device efficiency by forming a low work function layer at the interface between the EIL and Al cathode, thereby facilitating the electron injection into the emissive layer.
“…2 virtually inaccessible. 4,8,9 For a device that is connected to external terminals, the condition J = 0 by definition applies at zero bias. However, since the charge density in the vicinity of the contact is much higher than the densities associated with space-charge limited conduction ͑SCLC͒, it is reasonable to take the onset of SCLC, which occurs when flatband is reached in the bulk of the device, as a first-order approximation for the flatband condition ͓Fig.…”
The temperature dependence of the built-in voltage of organic semiconductor devices is studied. The results are interpreted using a simple analytical model for the band bending at the electrodes. It is based on the notion that, even at zero current, diffusion may cause a significant charge density in the entire device, and hence a temperature dependent band bending. Both magnitude and temperature dependence of the built-in potential of various devices are consistently described by the model, as the effects of a thin LiF layer between cathode and active layer.
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