Sequential Ligand Exchange of All-Inorganic CsPbI3 Perovskite Quantum Dots for Pure-Red Light-Emitting Diodes

被引:1
|
作者
Cheng, Huiyuan [1 ,2 ]
Zheng, Yifan [2 ]
Steele, Julian A. [1 ,3 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
[2] Chinese Acad Sci, Shanghai Inst Opt & Fine Mech, Key Lab Mat High Power Laser, Shanghai 201800, Peoples R China
[3] Univ Queensland, Sch Math & Phys, Brisbane, Qld 4072, Australia
来源
ACS MATERIALS LETTERS | 2024年 / 7卷 / 01期
基金
澳大利亚研究理事会; 中国国家自然科学基金;
关键词
NANOCRYSTALS;
D O I
10.1021/acsmaterialslett.4c01880
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Metal halide perovskite quantum dots (PQDs) are promising for next-generation optical displays, yet challenges persist in achieving pure-red emission (620-640 nm) due to a lack of effective ligand exchange methods for enhancing charge carrier transfer and stabilizing the PQDs structure/size during post-treatment. Herein, we report spectrally stable and efficient pure-red light-emitting diodes (LEDs) realized through sequential ligand post-treatment of all-inorganic CsPbI3 PQDs. The as-synthesized CsPbI3 PQDs (similar to 4 nm) undergo sequential purification steps, employing trioctylphosphine oxide (TOPO) and guanidinium iodide (GUAI) as ligands. This approach preserves the size and structure of the CsPbI3 PQDs after two purification washes, improving the optoelectronic properties of CsPbI3 PQD films and enables a stable electroluminescent emission centered at 640 nm with an external quantum efficiency (EQE) peaking near 15%. Our sequential ligand post-treatment successfully prevents the aggregation and coarsening of PQDs, presenting a novel approach toward enhancing the stability and efficiency of PQD-based LED technologies.
引用
收藏
页码:93 / 100
页数:8
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