Stable CsPbBr3 Nanoclusters Feature a Disk-like Shape and aDistorted Orthorhombic Structure

被引:22
作者
Zhang, Baowei [1 ,2 ]
Altamura, Davide [3 ]
Caliandro, Rocco [3 ]
Giannini, Cinzia [3 ]
Peng, Lucheng [1 ]
De Trizio, Luca [1 ]
Manna, Liberato [1 ]
机构
[1] Ist Italiano Tecnol IIT, Nanochem Dept, I-16163 Genoa, Italy
[2] Univ Genoa, Dipartimento Chim & Chim Ind, I-16146 Genoa, Italy
[3] Ist Cristallografia Consiglio Nazl Ric IC CNR, I-70126 Bari, Italy
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
OPTICAL-PROPERTIES; 2-STEP NUCLEATION; CDSE CLUSTERS; GROWTH; NANOCRYSTALS; SIZE; TRANSFORMATION; NANOCLUSTERS; PHOTOLUMINESCENCE; PRECURSORS;
D O I
10.1021/jacs.1c13544
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CsPbBr3nanoclusters have been synthesized byseveral groups and mostly employed as single-source precursors forthe synthesis of anisotropic perovskite nanostructures or perov-skite-based heterostructures. Yet, a detailed characterization ofsuch clusters is still lacking due to their high instability. In thiswork, we were able to stabilize CsPbBr3nanoclusters by carefullyselecting ad hoc ligands (benzoic acid together with oleylamine) topassivate their surface. The clusters have a narrow absorption peakat 400 nm, a band-edge emission peaked at 410 nm at roomtemperature, and their composition is identified as CsPbBr2.3.Synchrotron X-ray pair distribution function measurementsindicate that the clusters exhibit a disk-like shape with a thicknesssmaller than 2 nm and a diameter of 13 nm, and their crystalstructure is a highly distorted orthorhombic CsPbBr3. Based on small- and wide-angle X-ray scattering analyses, the clusters tend toform a two-dimensional (2D) hexagonal packing with a short-range order and a lamellar packing with a long-range order.
引用
收藏
页码:5059 / 5066
页数:8
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