A Conjugated Carboranyl Main Chain Polymer with Aggregation-Induced Emission in the Near-Infrared

Materials exhibiting aggregation-induced emission (AIE) are both highly emissive in the solid state and prompt a strongly red-shifted emission and should therefore pose as good candidates toward emerging near-infrared (NIR) applications of organic semiconductors (OSCs). Despite this, very few AIE ma...

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Veröffentlicht in:Journal of the American Chemical Society 2024-05, Vol.146 (19), p.13607-13616
Hauptverfasser: Aniés, Filip, Hamilton, Iain, De Castro, Catherine S. P., Furlan, Francesco, Marsh, Adam V., Xu, Weidong, Pirela, Valentina, Patel, Adil, Pompilio, Michele, Cacialli, Franco, Martín, Jaime, Durrant, James R., Laquai, Frédéric, Gasparini, Nicola, Bradley, Donal D. C., Heeney, Martin
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Sprache:eng
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Zusammenfassung:Materials exhibiting aggregation-induced emission (AIE) are both highly emissive in the solid state and prompt a strongly red-shifted emission and should therefore pose as good candidates toward emerging near-infrared (NIR) applications of organic semiconductors (OSCs). Despite this, very few AIE materials have been reported with significant emissivity past 700 nm. In this work, we elucidate the potential of ortho-carborane as an AIE-active component in the design of NIR-emitting OSCs. By incorporating ortho-carborane in the backbone of a conjugated polymer, a remarkable solid-state photoluminescence quantum yield of 13.4% is achieved, with a photoluminescence maximum of 734 nm. In contrast, the corresponding para and meta isomers exhibited aggregation-caused quenching. The materials are demonstrated for electronic applications through the fabrication of nondoped polymer light-emitting diodes. Devices employing the ortho isomer achieved nearly pure NIR emission, with 86% of emission at wavelengths longer than 700 nm and an electroluminescence maximum at 761 nm, producing a significant light output of 1.37 W sr–1 m–2.
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.4c03521