Photo-stability of CsPbBr3 perovskite quantum dots for optoelectronic application

被引:215
作者
Chen, Junsheng [1 ,2 ]
Liu, Dongzhou [3 ,4 ]
Al-Marri, Mohammed J. [5 ]
Nuuttila, Lauri [6 ]
Lehtivuori, Heli [6 ]
Zheng, Kaibo [1 ,5 ]
机构
[1] Lund Univ, Dept Chem Phys & NanoLund, S-22100 Lund, Sweden
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Mol React Dynam, Dalian 116023, Peoples R China
[3] Agr Univ Hebei, Coll Sci, Baoding 071001, Peoples R China
[4] Hebei Univ, Coll Phys Sci & Technol, Baoding 071002, Peoples R China
[5] Qatar Univ, Coll Engn, Gas Proc Ctr, Doha, Qatar
[6] Univ Jyvaskyla, Dept Phys, Nanosci Ctr, Jyvaskyla, Finland
基金
芬兰科学院;
关键词
perovskite; quantum dots; photo-stability; ANION-EXCHANGE; NANOCRYSTALS; CSPBX3; PHOTOLUMINESCENCE; CONDUCTIVITY; EMISSION; GROWTH; BR; CL;
D O I
10.1007/s40843-016-5123-1
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Due to their superior photoluminescence (PL) quantum yield (QY) and tunable optical band gap, all-inorganic CsPbBr3 perovskite quantum dots (QDs) have attracted intensive attention for the application in solar cells, light emitting diodes (LED), photodetectors and laser devices. In this scenario, the stability of such materials becomes a critical factor to be revealed. We hereby investigated the long-termstability of as-synthesized CsPbBr3 QDs suspended in toluene at various environmental conditions. We found light illumination would induce drastic photo-degradation of CsPbBr3QDs. The steady-state spectroscopy, transmission electron microscopy (TEM), and X-ray diffraction (XRD) verified that CsPbBr3 QDs tend to aggregate to form larger particles under continuous light soaking. In addition, decreasing PL QY of the QDs during light soaking indicates the formation of trap sites. Our work reveals that the main origin of instability in CsPbBr3 QDs and provides reference to engineer such QDs towards optimal device application.
引用
收藏
页码:719 / 727
页数:9
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