The Quantum Efficiency Roll-Off Effect in Near-Infrared Organic Electroluminescent Devices with Iridium Complexes Emitters

Abstract

The electroluminescence quantum efficiency roll-off in iridium(III)-based complexes, namely Ir(iqbt)2(dpm) and Ir(iqbt)3 (iqbt = 1 (benzo[b]thiophen-2-yl)-isoquinolinate, dpm = 2,2,6,6-tetramethyl-3,5-heptanedionate) utilized as near-infrared emitters in organic light emitting diodes with remarkable external quantum efficiencies, up to circa 3%, 1.5% and 1%, are measured and analyzed. With a 5–6 weight% of emitters embedded in a host matrix, the double-layer solution-processed structure as well as analogous three-layer one extended by a hole-conducting film are investigated. The triplet-polaron, the Onsager electron-hole pair dissociation and the triplet-triplet annihilation approaches were used to reproduce the experimental data. The mutual annihilation of triplets in iridium emitters was identified as prevailingly controlling the moderate roll-off, with the interaction between those of iridium emitters and host matrixes found as being less probable. Following the fitting procedure, the relevant rate constant was estimated to be ( 0.5 − 12 ) × 10 − 12 cm3/s, values considered to be rather too high for disordered organic systems, which was assigned to the simplicity of the applied model. A coexistence of some other mechanisms is therefore inferred, ones, however, with a less significant contribution to the overall emission quenching.