Solution-processed approach to highly luminescent trigonal Cs4PbBr6 nanodisks and their underlying shape evolution

被引:15
作者
Huang, Kaixiang [1 ]
Li, Dongmei [1 ]
Yang, Liu [1 ]
Liu, Song [1 ]
Yang, Fan [1 ]
机构
[1] Shanghai Univ, Sch Mat Sci & Engn, Dept Electron Informat Mat, Shanghai 200444, Peoples R China
关键词
Colloidal nanocrystal; Nanodisks; Perovskite; Trigonal; Surface chemistry; CESIUM LEAD HALIDE; LIGHT-EMITTING-DIODES; INORGANIC PEROVSKITE NANOCRYSTALS; ANION-EXCHANGE REACTIONS; QUANTUM DOTS; HIGH-QUALITY; SEMICONDUCTOR NANOCRYSTALS; COLLOIDAL SYNTHESIS; ROOM-TEMPERATURE; ENERGY-TRANSFER;
D O I
10.1016/j.jallcom.2016.12.201
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
All-inorganic cesium lead halide, a kind of promising semiconductor materials with fantastic properties for photoelectronic and photovoltaic applications, emerged recently. Herein, we report new strategies for synthesizing of trigonal Cs4PbBr6 nanodisks (NDs), which are also of ultrahigh luminescent (PLQY reached 85%). The key points to the high-yield synthesis of perovskite NDs are the elevated concentration of Cs precursor and proper temperature. Transmission electron microscopy studies of reaction products at various stages of the synthesis reveal that the Cs4PbBr6 NDs are built due to a selectivity of the ligands capping the different facets of a seed. Particularly, we find that by using cesium acetate as cesium source instead of cesium carbonate, the geometric construction of NDs is more defined, which indicates that the extra anions have a substantial effect on the perovskite crystal growth kinetics and their morphologies. Our work presents a new opportunity for better understanding the effect of composition, surface chemistry and intrinsic efficient luminescence in perovskite nanoparticles. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:244 / 252
页数:9
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