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A Conjugated Carboranyl Main Chain Polymer with Aggregation-Induced Emission in the Near-Infrared.
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.
Affiliation
  • Aniés F; Department of Chemistry, Centre for Processable Electronics, Molecular Sciences Research Hub, Imperial College London, 80 Wood Lane, London, W12 0BZ, U.K.
  • Hamilton I; KAUST Solar Center, King Abdullah University of Science and Technology, Thuwal, 23955-6900, Saudi Arabia.
  • De Castro CSP; KAUST Solar Center, King Abdullah University of Science and Technology, Thuwal, 23955-6900, Saudi Arabia.
  • Furlan F; Department of Chemistry, Centre for Processable Electronics, Molecular Sciences Research Hub, Imperial College London, 80 Wood Lane, London, W12 0BZ, U.K.
  • Marsh AV; KAUST Solar Center, King Abdullah University of Science and Technology, Thuwal, 23955-6900, Saudi Arabia.
  • Xu W; Department of Chemistry, Centre for Processable Electronics, Molecular Sciences Research Hub, Imperial College London, 80 Wood Lane, London, W12 0BZ, U.K.
  • Pirela V; POLYMAT University of the Basque Country UPV/EHU, Av. de Tolosa 72, Donostia-San Sebastián, 20018, Spain.
  • Patel A; Department of Physics and Astronomy, London Centre for Nanotechnology, University College London, London, WC1E 6BT, U.K.
  • Pompilio M; Department of Physics and Astronomy, London Centre for Nanotechnology, University College London, London, WC1E 6BT, U.K.
  • Cacialli F; Department of Physics and Astronomy, London Centre for Nanotechnology, University College London, London, WC1E 6BT, U.K.
  • Martín J; Department of Engineering, Free University of Bozen-Bolzano, Università 5, Bolzano, I-39100, Italy.
  • Durrant JR; Universidade da Coruña, Campus Industrial de Ferrol, CITENI, Esteiro, Ferrol, 15471, Spain.
  • Laquai F; Department of Chemistry, Centre for Processable Electronics, Molecular Sciences Research Hub, Imperial College London, 80 Wood Lane, London, W12 0BZ, U.K.
  • Gasparini N; KAUST Solar Center, King Abdullah University of Science and Technology, Thuwal, 23955-6900, Saudi Arabia.
  • Bradley DDC; Department of Chemistry, Centre for Processable Electronics, Molecular Sciences Research Hub, Imperial College London, 80 Wood Lane, London, W12 0BZ, U.K.
  • Heeney M; KAUST Solar Center, King Abdullah University of Science and Technology, Thuwal, 23955-6900, Saudi Arabia.
J Am Chem Soc ; 146(19): 13607-13616, 2024 May 15.
Article in En | MEDLINE | ID: mdl-38709316
ABSTRACT
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.