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Published on: October 1, 2019
Highly luminescent red emissive perovskite quantum dots-embedded composite films: ligands capping and caesium
Xian-Gang Wu1, Jialun Tang, Feng Jiang
1Beijing Key Laboratory of Nanophotonics and Ultrafine Optoelectronic Systems, School of Materials & Engineering, Beijing Institute of Technology, 5 Zhongguancun South Street, Beijing 100081, Haidian District, China. hzzhong@bit.edu.cn.
Abstract:
Perovskite quantum dots (PQDs) are emerging as functional luminescence down-shifting materials for light conversion applications. The incorporation of PQDs into a polymeric matrix is a key step to improving their stability, thus facilitating device integration. Compared to the conventional way of mixing the pre-synthesized PQDs into a polymer, the in situ fabrication of perovskite quantum dots-embedded composite films (PQDCFs) is an efficient and cost-effective method, which yields enhanced photoluminescence properties. This method has been successfully developed for green emissive CH3NH3PbBr3 PQDCFs, whereas the red CH3NH3PbI3 PQDCFs only show the photoluminescence quantum yields (PLQYs) less than 15%. By means of combining transmittance electron microscopy (TEM) and absorption spectrum analysis, we showed that the "perovskite red wall" in PQDCFs was mainly related to the phase separation, formation of large-sized particles and incomplete chemical conversion of precursors. These problems are caused by the solubility variance of perovskite precursors in the solvent as well as the solvation compatibility between perovskite precursors and the polymer during the crystallization process. Based on these findings, we introduced Cs+ as a dopant and 3,3-diphenylpropyamine (DPPA) as capping ligands, respectively, to decrease the solubility variance of the precursors and improve the compatibility between PQDs and the polymer. Consequently, highly luminescent red emissive PQDCFs with a PLQY of 91% were achieved with this strategy.
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