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Critical role of additive-induced molecular interaction on the operational stability of perovskite light-emitting diodes

  1. 1.
    SYSNO ASEP0541446
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleCritical role of additive-induced molecular interaction on the operational stability of perovskite light-emitting diodes
    Author(s) Kuang, C. (SE)
    Hu, Z. (SE)
    Yuan, Z. (SE)
    Wen, K. (CN)
    Qing, J. (SE)
    Kobera, Libor (UMCH-V) RID, ORCID
    Abbrent, Sabina (UMCH-V) RID, ORCID
    Brus, Jiří (UMCH-V) RID, ORCID
    Yin, C. (SE)
    Wang, H. (SE)
    Xu, W. (SE)
    Wang, J. (CN)
    Bai, S. (SE)
    Gao, F. (SE)
    Source TitleJoule. - : Cell Press - ISSN 2542-4351
    Roč. 5, č. 3 (2021), s. 618-630
    Number of pages13 s.
    Languageeng - English
    CountryUS - United States
    Keywordsmetal halide perovskite ; light-emitting diode ; operational stability
    Subject RIVCD - Macromolecular Chemistry
    OECD categoryPolymer science
    Method of publishingOpen access
    Institutional supportUMCH-V - RVO:61389013
    UT WOS000630098300012
    EID SCOPUS85102345653
    DOI10.1016/j.joule.2021.01.003
    AnnotationDespite rapid improvements in efficiency and brightness of perovskite light-emitting diodes (PeLEDs), the poor operational stability remains a critical challenge hindering their practical applications. Here, we demonstrate greatly improved operational stability of high-efficiency PeLEDs, enabled by incorporating dicarboxylic acids into the precursor for perovskite depositions. We reveal that the dicarboxylic acids efficiently eliminate reactive organic ingredients in perovskite emissive layers through an in situ amidation process, which is catalyzed by the alkaline zinc oxide substrate. The formed stable amides prohibit detrimental reactions between the perovskites and the charge injection layer underneath, stabilizing the perovskites and the interfacial contacts and ensuring the excellent operational stability of the resulting PeLEDs. Through rationally optimizing the amidation reaction in the perovskite emissive layers, we achieve efficient PeLEDs with a peak external quantum efficiency of 18.6% and a long half-life time of 682 h at 20 mA cm−2, presenting an important breakthrough in PeLEDs.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2022
    Electronic addresshttps://www.sciencedirect.com/science/article/pii/S2542435121000039?via%3Dihub
Number of the records: 1  

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