A-Site Cation Influence on the Structural and Optical Evolution of Ultrathin Lead Halide Perovskite Nanoplatelets

被引:6
作者
Krajewska, Chantalle J. [1 ]
Kick, Matthias [1 ]
Kaplan, Alexander E. K. [1 ]
Berkinsky, David B. [1 ]
Zhu, Hua [1 ]
Sverko, Tara [1 ]
Van Voorhis, Troy [1 ]
Bawendi, Moungi G. [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
perovskites; nanoplatelet; quantum confinement; crystal structure; diffraction; excitons; THERMAL-EXPANSION; BR; NANOCRYSTALS; EXCITONS; CSPBX3; CL;
D O I
10.1021/acsnano.3c12286
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Imposing quantum confinement has the potential to significantly modulate both the structural and optical parameters of interest in many material systems. In this work, we investigate strongly confined ultrathin perovskite nanoplatelets APbBr(3). We compare the all-inorganic and hybrid compositions with the A-sites cesium and for mamidinium, respectively. Compared to each other and their bulk counterparts, the materials show significant differences in variable-temperature structural and optical evolution. We quantify and correlate structural asymmetry with the excitonic transition energy, spectral purity, and emission rate. Negative thermal expansion, structural and photoluminescence asymmetry, photoluminescence full width at half-maximum, and splitting between bright and dark excitonic levels are found to be reduced in the hybrid composition. This work provides composition- and structure-based mechanisms for engineering of the excitons in these materials.
引用
收藏
页码:8248 / 8258
页数:11
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