量子点
配体(生物化学)
密度泛函理论
化学
对偶(语法数字)
纳米技术
量子
材料科学
光电子学
物理
计算化学
量子力学
生物化学
文学类
艺术
受体
作者
Jongbeom Kim,Ye In Kim,Hengquan Guo,Dongryeol Lee,Jinkyu Yang,Dongeun Kim,Su Seok Choi,Junzhi Ye,Robert L. Z. Hoye,Robert A. Taylor,Seung Geol Lee,Myoung Hoon Song
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-08-18
卷期号:10 (9): 4402-4409
被引量:1
标识
DOI:10.1021/acsenergylett.5c01958
摘要
Weakly bonded native ligands severely degrade the performance of perovskite quantum dot (PeQD) light-emitting diodes (LEDs). While conventional approaches can be used to strengthen ligand binding, they fail to achieve complete ligand exchange, leaving residual ligands that promote degradation. Herein, we present a dual-functional fluorinated benzyl phosphonic acid (F-BPA) ligand that modulates the acidity and enhances the binding affinity between the phosphonate groups of F-BPA and the perovskite surface compared to BPA due to a significant redistribution of the electrostatic potential of the molecule induced by fluorination. The F-BPA treatment facilitates effective ligand exchange and obtains well-passivated CsPbI3 PeQDs with improved stability under thermal, light, and polar solvent stress. Red-emissive LEDs achieved a maximum external quantum efficiency of 24.0% with improved device stability (half-lifetime of 1,020 min at 100 cd m–2). This study demonstrates a dual-functional ligand strategy and opens a new pathway toward PeQDs for next-generation display technologies.
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