Highly luminescent and stable CH3NH3PbBr3 quantum dots with 91.7% photoluminescence quantum yield: Role of guanidinium bromide dopants

被引:14
作者
Jung, Kyungeun [2 ]
Choi, Hyungi [1 ]
Kim, Hyunkyu [1 ]
Park, Yun Chang [3 ]
Lee, Man-Jong [1 ,2 ]
机构
[1] Konkuk Univ, Dept Chem, Seoul 143701, South Korea
[2] Konkuk Univ, Dept Adv Technol Fus, Seoul 143701, South Korea
[3] Natl Nanofab Ctr NNFC, 53-3 Eoeun Dong, Daejeon 34141, South Korea
关键词
3 NH 3 PbBr 3 quantum dots; Guanidinium bromide; Recombination centers; Fluorescence lifetime imaging; Photoluminescence quantum yield; METAL-HALIDE PEROVSKITES; EFFICIENT; CATION; ENHANCEMENT; SIZE; BR; CL;
D O I
10.1016/j.jallcom.2020.154990
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
Although perovskite quantum dots (PQDs) have received considerable attention, defects in PQDs can signi ficantly degrade the properties and device performance. In this study, we report on an effective strategy for synthesizing highly luminescent CH 3 NH 3 PbBr 3 quantum dots (QDs) by a simple doping. To remove such defects, guanidinium bromide (GuBr) was doped into the CH 3 NH 3 PbBr 3 QDs synthesized by the ligand-assisted reprecipitation technique. From XRD and TEM studies, the doping of GuBr into the QD lattices was veri fied. In addition, the surfaces of PQDs with and without GuBr dopants were analyzed by XPS to trace the metallic Pb acting as a major recombination center. The GuBr doping resulted in the size uniformity of QDs and effectively eliminated defects and metallic Pb, which enhanced the photo- luminescence quantum yield (PLQY) through the inhibition of the non -radiative recombination pathway. Furthermore, the recombination dynamics in the QDs were examined by using time -resolved photo- luminescence and fluorescence lifetime imaging to verify the role of GuBr dopants. By optimizing the amount of GuBr doping, the CH 3 NH 3 PbBr 3 QDs with strong green emission achieved a maximum PLQY of 91.7%.
引用
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页数:7
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