钙钛矿(结构)
量子点
材料科学
油胺
氢氟酸
氟
光致发光
光电子学
氟化物
氟化氢
量子产额
离子
纳米技术
化学稳定性
二极管
兴奋剂
化学工程
发光二极管
八面体
纳米晶
异质结
无机化学
量子效率
介孔材料
光化学
作者
Jianxun Wang,Huang Tao,Shuo Li,Ruoxi Wang,Jingyu Qian,Xiaoyu Zhang
标识
DOI:10.1021/acs.chemmater.6c00080
摘要
Fluorine ion doping serves as an effective strategy for enhancing the stability of perovskite quantum dots (QDs), which is crucial for constructing high-performance and highly stable optoelectronic devices. However, conventional fluorination methods often rely on highly toxic fluorine sources, such as hydrofluoric acid (HF), posing safety hazards and limiting large-scale fabrication. Herein, we propose a simple and universal in situ fluorination strategy based on the reaction between benzoyl fluoride and oleylamine under mild conditions, which safely generates HF and enables efficient fluorine doping. The incorporated fluoride ions enter the CsPbI 3 lattice, effectively suppressing octahedral tilting and thereby enhancing structural stability. The resulting F-doped CsPbI 3 QDs achieve a photoluminescence quantum yield close to unity and exhibit a 15-fold improvement in T 95 under light illumination stability testing. Deep-red light-emitting diodes fabricated from these QDs deliver a peak external quantum efficiency of 25.7% and show a 20-fold enhancement in operational lifetime. Furthermore, this approach is successfully extended to green- and blue-emitting perovskite QD systems, demonstrating its broad potential for full-color display applications. This work provides a rational and scalable chemical pathway to address the intrinsic instability of perovskite QDs, paving the way toward efficient and durable optoelectronic devices.
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