Highly bright and low turn-on voltage CsPbBr3 quantum dot LEDs via conjugation molecular ligand exchange

被引:56
作者
Li, Guopeng [1 ]
Huang, Jingsheng [2 ]
Li, Yanqing [2 ]
Tang, Jianxin [2 ]
Jiang, Yang [1 ]
机构
[1] Hefei Univ Technol, Sch Mat Sci & Engn, Hefei 230009, Anhui, Peoples R China
[2] Soochow Univ, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Inst Funct Nano & Soft Mat FUNSOM, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
CsPbBr3 quantum dots; perovskite; light-emitting diodes; ligand exchange; -conjugation; LIGHT-EMITTING-DIODES; HALIDE PEROVSKITE NANOCRYSTALS; HIGH-EFFICIENCY; ANION-EXCHANGE; ENERGY LANDSCAPE; CESIUM; CSPBX3; BR; PHOTOLUMINESCENCE; STABILIZATION;
D O I
10.1007/s12274-018-2187-5
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
All-inorganic CsPbBr3 perovskite quantum dots (QDs) hold great promise as candidate materials for next-generation electroluminescent displays owing to their excellent optoelectronic properties. However, the long insulating ligands on the surface of CsPbBr3 QDs originating from the synthesis process hinder the fabrication of high-performance optoelectronic devices. Herein, an efficient ligand-exchange route is proposed with the use of perovskite-precursor-based halide ligands, including a series of phenalkylammonium bromides with a -conjugation benzene ring and different branch lengths. Based on the ligand-exchange method, the conductivity of the CsPbBr3 QD layer is significantly improved owing to ligand shortening and the insertion of the -conjugation benzene ring. As a result, high brightness (up to 12,650 cd/m(2)) and low turn-on voltage (as low as 2.66 V) can be realized in CsPbBr3 QD light-emitting diodes (QLEDs), leading to dramatic improvements in device performance with a current efficiency of 13.43 cd/A, power efficiency of 12.05 lm/W, and external quantum efficiency of 4.33%.
引用
收藏
页码:109 / 114
页数:6
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