Grinding Synthesis of APbX3 (A = MA, FA, Cs; X = Cl, Br, I) Perovskite Nanocrystals

被引:90
作者
Chen, Daqin [1 ,2 ,3 ,4 ]
Li, Junni [2 ]
Chen, Xiao [2 ]
Chen, Jiangkun [1 ,3 ,4 ]
Zhong, Jiasong [2 ]
机构
[1] Fujian Normal Univ, Coll Phys & Energy, Fujian Prov Key Lab Quantum Manipulat & New Energ, Fuzhou 350117, Fujian, Peoples R China
[2] Hangzhou Dianzi Univ, Coll Mat & Environm Engn, Hangzhou 310018, Zhejiang, Peoples R China
[3] Fujian Prov Engn Technol Res Ctr Solar Energy Con, Fuzhou 350117, Fujian, Peoples R China
[4] Fujian Prov Collaborat Innovat Ctr Optoelect Semi, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
perovskite; CsPbBr3; optical materials; luminescence; LED; CESIUM LEAD HALIDE; COLLOIDAL CH3NH3PBX3 X; QUANTUM DOTS; ANION-EXCHANGE; BRIGHTLY LUMINESCENT; WHITE LEDS; CSPBX3; PHOTOLUMINESCENCE; PHASE; EFFICIENT;
D O I
10.1021/acsami.8b19002
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Currently, metal halide perovskite nanocrystals have been extensively explored due to their unique optoelectronic properties and wide application prospects. In the present work, a facile grinding method is developed to prepare whole-family APbX(3) (A = MA, FA, and Cs; X = Cl, Br, and I) perovskite nanocrystals. This strategy alleviates the harsh synthesis conditions of precursor dissolution, atmosphere protection, and high temperature. Impressively, the as-prepared perovskite nanocrystals are evidenced to have halogen-rich surfaces and yield visible full-spectral emissions with maximal photoluminescence quantum yield up to 92% and excellent stability. Additionally, the grinding method can be extended to synthesize widely concerned Mn2+-doped CsPbCl3 nanocrystals with dual-modal emissions of both excitons and dopants. As a proof-of-concept experiment, the present perovskite nanocrystals are demonstrated to be applicable as blue/green/red color converters in UV-excitable white-light-emitting diodes.
引用
收藏
页码:10059 / 10067
页数:9
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