Highly luminescent and stable bright-blue CH3NH3Pb(Cl/Br)3 perovskite quantum dots with in-situ formed silica shell

被引:1
作者
Yang, Mu [1 ,2 ]
Dai, Qilin [3 ]
Tang, Aiwei [1 ]
Teng, Feng [1 ]
Peng, Hong-shang [2 ]
机构
[1] Beijing Jiaotong Univ, Inst Optoelect Technol, Key Lab Luminescence & Opt Informat, Minist Educ, Beijing 100044, Peoples R China
[2] Minzu Univ China, Sch Sci, Beijing 100081, Peoples R China
[3] Jackson State Univ, Dept Chem Phys & Atmospher Sci, Jackson, MS 39217 USA
关键词
CH3NH3Pb(Cl; Br)3; Postsynthetic; Silica shell; Defect passivation; Photostability; LIGHT-EMITTING-DIODES; ANION-EXCHANGE; EFFICIENT; NANOCRYSTALS; CSPBX3; BR; CL; EMISSION;
D O I
10.1016/j.materresbull.2022.112049
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Current chloride-bromine mixed perovskite quantum dots (PQDs) suffered from low luminescence efficiency and instability due to migration-nature of ionic species and high defect density. To tackle these challenges, herein a novel type of CH3NH3Pb(Cl/Br)3 PQDs (Cl/Br-PQDs) were synthesized via a two-step method. Briefly, pristine silane-capped Br-PQDs were prepared, followed by anion exchange using oleylammonium chloride (OAm-Cl) and in-situ formation of silica shell. The optimal feeding ratio of Cl/Br was determined to be 1:1, which yielded colloidal Cl/Br-PQDs possessing a strong 464-nm emission, a high photoluminescence quantum yield of 94.6% and ultrahigh stability. The high quantum yield was attributed to efficient defects passivation by doped Cl- ions and silica-shell-locked OAm+ ligands, whilst the high stability was to silica-shell-restricted migration of halogen ions. Such a combinational strategy of anion exchange and in-situ growth of silica shell may provide an effective solution for synthesis of mixed PQDs with high quality.
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页数:6
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