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Modulating the luminance of organic light-emitting diodes via optical stimulation of a photochromic molecular monolayer at transparent oxide electrode

DOI:10.1039/D0NR00724B 期刊:Nanoscale 出版年份:2020 更新时间:2025-09-19 17:13:59
摘要: Self-assembled monolayers (SAMs) deposited on bottom electrodes are commonly used to tune charge carrier injection or blocking in optoelectronic devices. Beside the enhancement of device performance, the fabrication of multifunctional devices in which the output can be modulated by multiple external stimuli remains a challenging target. In this work, we report the functionalization of an indium tin oxide (ITO) electrode with a SAM of a diarylethene derivative designed for optically control the electronic properties. Following the demonstration of dense SAM formation and its photochromic activity, as a proof-of-principle, an organic light-emitting diode (OLED) embedding the light-responsive SAM-covered electrode was fabricated and characterized. Optically addressing the two-terminal device by irradiation with ultraviolet light doubles the electroluminescence. The original value can be restored reversibly by irradiation with visible light. This expanded functionality is based on the photoinduced modulation of the electronic structure of the diarylethene isomers, which impact the charge carriers’ confinement within the emissive layer. This approach could be successfully exploited in the field of opto-communication technology, for example to fabricate opto-electronic logic circuits.
作者: Giovanni Ligorio,Giovanni F. Cotella,Aurelio Bonasera,Nicolas Zorn Morales,Giuseppe Carnicella,Bj?rn Kobin,Qiankun Wang,Norbert Koch,Stefan Hecht,Emil J.W. List-Kratochvil,Franco Cacialli
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Investigating the modulation of luminance in organic light-emitting diodes via optical stimulation of a photochromic molecular monolayer at a transparent oxide electrode.

The study successfully demonstrated that ITO electrodes in OLEDs can be modified with SAMs of photochromic switching molecules to add extra functionality, allowing for reversible modulation of luminance via optical stimulation. This approach expands the potential of SAM-treatment for dynamic energy tuning in two-terminal devices.

The study demonstrates the potential of using a single monolayer of photochromic molecules for dynamic control of OLED luminance, but the absolute EQE values were modest, indicating room for optimization. The approach is limited by the need for specific anchoring groups for different electrode materials.

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