Synthesis of Zwitterionic CsPbBr3 Nanocrystals with Controlled Anisotropy using Surface-Selective Ligand Pairs

被引:5
|
作者
Zhu, Hua [1 ]
Kick, Matthias [1 ]
Ginterseder, Matthias [1 ]
Krajewska, Chantalle J. [1 ]
Sverko, Tara [1 ]
Li, Ruipeng [2 ]
Lu, Yongli [1 ]
Shih, Meng-Chen [1 ]
Van Voorhis, Troy [1 ]
Bawendi, Moungi G. [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
[2] Brookhaven Natl Lab, Natl Synchrotron Light Source 2, Upton, NY 11973 USA
基金
美国国家科学基金会;
关键词
anisotropy; colloidal nanocrystals; density functional theory; metal halide perovskite; zwitterionic ligand; PEROVSKITE NANOCRYSTALS; LEAD; NUCLEATION; KINETICS; CSPBX3; SHAPE; BASE; ACID; BR;
D O I
10.1002/adma.202304069
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mechanistic studies of the morphology of lead halide perovskite nanocrystals (LHP-NCs) are hampered by a lack of generalizable suitable synthetic strategies and ligand systems. Here, the synthesis of zwitterionic CsPbBr3 NCs is presented with controlled anisotropy using a proposed "surface-selective ligand pairs" strategy. Such a strategy provides a platform to systematically study the binding affinity of capping ligand pairs and the resulting LHP morphologies. By using zwitterionic ligands (ZwL) with varying structures, majority ZwL-capped LHP NCs with controlled morphology are obtained, including anisotropic nanoplatelets and nanorods, for the first time. Combining experiments with density functional theory calculations, factors that govern the ligand binding on the different surface facets of LHP-NCs are revealed, including the steric bulkiness of the ligand, the number of binding sites, and the charge distance between binding moieties. This study provides guidance for the further exploration of anisotropic LHP-NCs.
引用
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页数:10
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