CsPbBr3 Quantum Dots 2.0: Benzenesulfonic Acid Equivalent Ligand Awakens Complete Purification

被引:408
作者
Yang, Dandan [1 ]
Li, Xiaoming [1 ]
Zhou, Wenhan [1 ]
Zhang, Shengli [1 ]
Meng, Cuifang [1 ]
Wu, Ye [1 ]
Wang, Yue [1 ]
Zeng, Haibo [1 ]
机构
[1] Nanjing Univ Sci & Technol, Coll Mat Sci & Engn, Inst Optoelect & Nanomat, MIIT Key Lab Adv Display Mat & Devices, Nanjing 210094, Jiangsu, Peoples R China
关键词
benzenesulfonic acid; CsPbBr3 quantum dots; equivalent ligand; high stability; quantum yield; HALIDE PEROVSKITE NANOCRYSTALS; LIGHT-EMITTING-DIODES; HIGHLY LUMINESCENT; HYDRODYNAMIC FRICTION; DEFECT-TOLERANCE; CSPBX3; STABILITY; BR; PASSIVATION; PERFORMANCE;
D O I
10.1002/adma.201900767
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The stability and optoelectronic device performance of perovskite quantum dots (Pe-QDs) are severely limited by present ligand strategies since these ligands exhibit a highly dynamic binding state, resulting in serious complications in QD purification and storage. Here, a "Br-equivalent" ligand strategy is developed in which the proposed strong ionic sulfonate heads, for example, benzenesulfonic acid, can firmly bind to the exposed Pb ions to form a steady binding state, and can also effectively eliminate the exciton trapping probability due to bromide vacancies. From these two aspects, the sulfonate heads play a similar role as natural Br ions in a perfect perovskite lattice. Using this approach, high photoluminescence quantum yield (PL QY) > 90% is facilely achieved without the need for amine-related ligands. Furthermore, the prepared PL QYs are well maintained after eight purification cycles, more than five months of storage, and high-flux photo-irradiation. This is the first report of high and versatile stabilities of Pe-QD, which should enable their improved application in lighting, displays, and biologic imaging.
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页数:8
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