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Article: Side-Chain-Promoted Polymer Architecture Enabling Stable Mixed-Halide Perovskite Light-Emitting Diodes

TitleSide-Chain-Promoted Polymer Architecture Enabling Stable Mixed-Halide Perovskite Light-Emitting Diodes
Authors
Issue Date10-May-2024
PublisherAmerican Chemical Society
Citation
ACS Energy Letters, 2024, v. 9, n. 5, p. 2118-2127 How to Cite?
AbstractMixed-halide perovskite nanocrystals (PeNCs) featuring bandgap-tunable luminescence with narrow bandwidth have emerged as promising electroluminescent materials for light-emitting diodes (LEDs) to satisfy the color standard of Rec. 2100. However, the phase segregation of mixed-halide perovskites severely restricts the spectral stability and lifetime of perovskite LEDs (PeLEDs). Here, we report that the introduction of multifunctional side-chain-promoted polymer architectures in the synthesis of I/Br-mixed PeNCs to suppress halide segregation and enable electroluminescent stability of the PeLEDs up to ∼2500 min, which is the longest to our knowledge. Meanwhile, the PeLEDs exhibit the pure-red electroluminescence spectrum with Commission Internationale de l’Eclairage coordinates (0.705, 0.292) at one of the highest external quantum efficiencies reported to date, 23.6%. Fundamentally, the as-proposed polymer ligand architecture simultaneously offers long-term nanocrystal dispersion, good charge transport, defect elimination, and phase segregation suppression. Overall, the work demonstrates the potential of the multifunctionalized polymer ligands for developing high-performance PeLEDs toward practical applications.
Persistent Identifierhttp://hdl.handle.net/10722/350456

 

DC FieldValueLanguage
dc.contributor.authorLyu, Benzheng-
dc.contributor.authorLin, Hong-
dc.contributor.authorLi, Dongyu-
dc.contributor.authorSergeev, Aleksandr-
dc.contributor.authorWang, Qiang-
dc.contributor.authorJiang, Zhengyan-
dc.contributor.authorHuo, Lijun-
dc.contributor.authorSu, Haibin-
dc.contributor.authorWong, Kam Sing-
dc.contributor.authorWang, Yufeng-
dc.contributor.authorChoy, Wallace C.H.-
dc.date.accessioned2024-10-29T00:31:41Z-
dc.date.available2024-10-29T00:31:41Z-
dc.date.issued2024-05-10-
dc.identifier.citationACS Energy Letters, 2024, v. 9, n. 5, p. 2118-2127-
dc.identifier.urihttp://hdl.handle.net/10722/350456-
dc.description.abstractMixed-halide perovskite nanocrystals (PeNCs) featuring bandgap-tunable luminescence with narrow bandwidth have emerged as promising electroluminescent materials for light-emitting diodes (LEDs) to satisfy the color standard of Rec. 2100. However, the phase segregation of mixed-halide perovskites severely restricts the spectral stability and lifetime of perovskite LEDs (PeLEDs). Here, we report that the introduction of multifunctional side-chain-promoted polymer architectures in the synthesis of I/Br-mixed PeNCs to suppress halide segregation and enable electroluminescent stability of the PeLEDs up to ∼2500 min, which is the longest to our knowledge. Meanwhile, the PeLEDs exhibit the pure-red electroluminescence spectrum with Commission Internationale de l’Eclairage coordinates (0.705, 0.292) at one of the highest external quantum efficiencies reported to date, 23.6%. Fundamentally, the as-proposed polymer ligand architecture simultaneously offers long-term nanocrystal dispersion, good charge transport, defect elimination, and phase segregation suppression. Overall, the work demonstrates the potential of the multifunctionalized polymer ligands for developing high-performance PeLEDs toward practical applications.-
dc.languageeng-
dc.publisherAmerican Chemical Society-
dc.relation.ispartofACS Energy Letters-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleSide-Chain-Promoted Polymer Architecture Enabling Stable Mixed-Halide Perovskite Light-Emitting Diodes-
dc.typeArticle-
dc.identifier.doi10.1021/acsenergylett.4c00355-
dc.identifier.scopuseid_2-s2.0-85190850294-
dc.identifier.volume9-
dc.identifier.issue5-
dc.identifier.spage2118-
dc.identifier.epage2127-
dc.identifier.eissn2380-8195-
dc.identifier.issnl2380-8195-

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