Colloidal CsPbBr3 Perovskite Nanocrystals: Luminescence beyond Traditional Quantum Dots

被引:946
|
作者
Swarnkar, Abhishek [1 ]
Chulliyil, Ramya [2 ]
Ravi, Vikash Kumar [1 ]
Irfanullah, Mir [2 ]
Chowdhury, Arindam [2 ]
Nag, Angshuman [1 ]
机构
[1] IISER, Dept Chem, Pune 411008, Maharashtra, India
[2] Indian Inst Technol, Dept Chem, Bombay 400076, Maharashtra, India
关键词
blinking; colloidal quantum dots; CsPbBr3; luminescence; nanocrystals; perovskites; ORGANOMETAL HALIDE PEROVSKITES; LIGHT-EMITTING DEVICES; FLUORESCENCE INTERMITTENCY; CDSE NANOCRYSTALS; LEAD BROMIDE; SOLAR-CELLS; BLINKING; GROWTH; TRANSISTORS; DISPLAY;
D O I
10.1002/anie.201508276
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Traditional CdSe-based colloidal quantum dots (cQDs) have interesting photoluminescence (PL) properties. Herein we highlight the advantages in both ensemble and single-nanocrystal PL of colloidal CsPbBr3 nanocrystals (NCs) over the traditional cQDs. An ensemble of colloidal CsPbBr3 NCs (11 nm) exhibits ca. 90% PL quantum yield with narrow (FWHM=86 meV) spectral width. Interestingly, the spectral width of a single-NC and an ensemble are almost identical, ruling out the problem of size-distribution in PL broadening. Eliminating this problem leads to a negligible influence of self-absorption and Forster resonance energy transfer, along with batch-to-batch reproducibility of NCs exhibiting PL peaks within +/- 1 nm. Also, PLpeak positions do not alter with measurement temperature in the range of 25 to 100 degrees C. Importantly, CsPbBr3 NCs exhibit suppressed PL blinking with ca. 90% of the individual NCs remain mostly emissive (on-time > 85%), without much influence of excitation power.
引用
收藏
页码:15424 / 15428
页数:5
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