Diarylethenes in Optically Switchable Organic Light‐Emitting Diodes: Direct Investigation of the Reversible Charge Carrier Trapping Process
Advanced Optical Materials, vol. 10
Abstract
Abstract The design, fabrication, and characterization of optically switchable organic light‐emitting diodes (OSOLEDs) based on the combination of the commercially available light‐emitting polymer poly(9,9′‐dioctylfluorene‐alt‐benzothiadiazole), F8BT, doped with a diarylethene derivative is reported. The photochromic activity of the dopant in the solid state has been investigated both via UV/vis absorption and photoluminescence spectroscopy, whereas the morphology of different blends is investigated via atomic force microscopy. OSOLEDs embedding dopant loadings of 1, 5, and 10 wt% exhibit optical responsivity with a maximum reversible optical threshold voltage shift of 4 V. The best performing devices containing 5 wt% dopant show a maximum current density and luminance ON/OFF ratio of ≈20 and ≈90, respectively. For the first time, the impact of the diarylethene isomerization on hole and electron transport has been decoupled and directly investigated, via the design, fabrication, and characterization of single‐carrier switchable devices based on the same blends. Not only do these results confirm the photo‐responsive trapping activity of the diarylethenes on both charge carriers, but they also demonstrate its asymmetry, with a predominant effect on electron transport that is over 3.4 times larger as compared to hole transport.
Authors 6
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London Centre for Nanotechnology · University College London
Affiliation as printed
Department of Physics and Astronomy (CMMP Group) and London Centre for Nanotechnology University College London London WC1E 6BT UK
Department of Physics and Astronomy (CMMP Group) and London Centre for Nanotechnology, University College London, London, WC1E 6BT UK
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Aurelio Bonasera corresponding
Humboldt-Universität zu Berlin · National Interuniversity Consortium of Materials Science and Technology · University of Palermo
Affiliation as printed
Department of Chemistry & IRIS Adlershof Humboldt‐Universität zu Berlin Brook‐Taylor‐Str. 2 12489 Berlin Germany
Department of Physics and Chemistry–Emilio Segrè University of Palermo, and INSTM–Palermo Research Unit viale delle Scienze, bdg. 17 Palermo 90128 Italy
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London Centre for Nanotechnology · University College London
Affiliation as printed
Department of Physics and Astronomy (CMMP Group) and London Centre for Nanotechnology University College London London WC1E 6BT UK
Department of Physics and Astronomy (CMMP Group) and London Centre for Nanotechnology, University College London, London, WC1E 6BT UK
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London Centre for Nanotechnology · University College London
Affiliation as printed
Department of Physics and Astronomy (CMMP Group) and London Centre for Nanotechnology University College London London WC1E 6BT UK
Department of Physics and Astronomy (CMMP Group) and London Centre for Nanotechnology, University College London, London, WC1E 6BT UK
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Humboldt-Universität zu Berlin · DWI – Leibniz Institute for Interactive Materials · RWTH Aachen University
Affiliation as printed
DWI–Leibniz Institute for Interactive Materials Forckenbeckstr. 50 52074 Aachen Germany
Department of Chemistry & IRIS Adlershof Humboldt‐Universität zu Berlin Brook‐Taylor‐Str. 2 12489 Berlin Germany
Institute of Technical and Macromolecular Chemistry RWTH Aachen University Worringer Weg 2 52074 Aachen Germany
Department of Chemistry & IRIS Adlershof Humboldt‐Universität zu Berlin Brook‐Taylor‐Str. 2 12489 Berlin Germany
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Franco Cacialli corresponding
London Centre for Nanotechnology · University College London
Affiliation as printed
Department of Physics and Astronomy (CMMP Group) and London Centre for Nanotechnology University College London London WC1E 6BT UK
Department of Physics and Astronomy (CMMP Group) and London Centre for Nanotechnology, University College London, London, WC1E 6BT UK
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